| geneid | 128153 |
|---|---|
| ensemblid | ENSG00000162814.11 |
| hgncid | 25184 |
| symbol | SPATA17 |
| name | spermatogenesis associated 17 |
| refseq_nuc | NM_138796.4 |
| refseq_prot | NP_620151.1 |
| ensembl_nuc | ENST00000366933.5 |
| ensembl_prot | ENSP00000355900.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 217631344 |
| end | 217871696 |
| strand | + |
| ver | v1.2 |
| region | chr1:217631344-217871696 |
| region5000 | chr1:217626344-217876696 |
| regionname0 | SPATA17_chr1_217631344_217871696 |
| regionname5000 | SPATA17_chr1_217626344_217876696 |
| 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 | 1/1 | 361 | 242 | 77 | 43 | 83 | 12 | 25 | 63 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0002 | 0/0 | 361 | 5 | 0 | 0 | 4 | 0 | 1 | 3 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0003 | 0/0 | 361 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0004 | 0/0 | 361 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0005 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| 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 | 0/0 | 1086 | 124 | 32 | 29 | 39 | 8 | 16 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| c0002 | 1/0 | 1086 | 67 | 20 | 9 | 28 | 3 | 6 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| c0003 | 0/1 | 1086 | 24 | 4 | 2 | 13 | 1 | 3 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| c0004 | 0/0 | 1086 | 16 | 14 | 2 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| c0005 | 0/0 | 1086 | 5 | 4 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| c0006 | 0/0 | 1086 | 5 | 0 | 0 | 4 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| c0007 | 0/0 | 1086 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| c0008 | 0/0 | 1086 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| c0009 | 0/0 | 1086 | 2 | 1 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| c0010 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| c0011 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| c0012 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| c0013 | 0/0 | 1086 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| 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 | 4712 | 85 | 10 | 13 | 45 | 2 | 15 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0002 | 0/0 | 4711 | 25 | 0 | 11 | 10 | 4 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0003 | 0/1 | 4711 | 20 | 1 | 3 | 14 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0004 | 0/0 | 4711 | 12 | 11 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0005 | 0/0 | 4711 | 10 | 7 | 2 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0006 | 0/0 | 4710 | 7 | 0 | 4 | 0 | 2 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0007 | 0/0 | 4711 | 6 | 6 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0008 | 0/0 | 4711 | 5 | 5 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0009 | 0/0 | 4711 | 5 | 4 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0010 | 0/0 | 4712 | 5 | 0 | 2 | 2 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0011 | 0/0 | 4711 | 4 | 0 | 3 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0012 | 0/0 | 4712 | 4 | 1 | 1 | 0 | 0 | 2 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0013 | 0/0 | 4710 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0014 | 0/0 | 4712 | 3 | 0 | 1 | 2 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0015 | 0/0 | 4711 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0016 | 0/0 | 4711 | 3 | 0 | 0 | 2 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0017 | 0/0 | 4712 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0018 | 0/0 | 4711 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0019 | 0/0 | 4712 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0020 | 0/0 | 4712 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0021 | 0/0 | 4713 | 2 | 0 | 0 | 1 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0022 | 0/0 | 4711 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0023 | 0/0 | 4712 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0024 | 0/0 | 4711 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0025 | 0/0 | 4711 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0026 | 0/0 | 4712 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0027 | 0/0 | 4711 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0028 | 0/0 | 4711 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0029 | 0/0 | 4710 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0030 | 0/0 | 4710 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0031 | 0/0 | 4711 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0032 | 0/0 | 4710 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0033 | 0/0 | 4710 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0034 | 0/0 | 4711 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0035 | 0/0 | 4711 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0036 | 0/0 | 4711 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0037 | 0/0 | 4711 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0038 | 0/0 | 4712 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0039 | 0/0 | 4712 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0040 | 0/0 | 4712 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0041 | 0/0 | 4712 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0042 | 0/0 | 4712 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0043 | 0/0 | 4712 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0044 | 0/0 | 4712 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0045 | 0/0 | 4712 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0046 | 0/0 | 4712 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0047 | 1/0 | 4713 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0048 | 0/0 | 4713 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0049 | 0/0 | 4713 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0050 | 0/0 | 4713 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0051 | 0/0 | 4713 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0052 | 0/0 | 4710 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0053 | 0/0 | 4711 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0054 | 0/0 | 4711 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0055 | 0/0 | 4712 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0056 | 0/0 | 4710 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0057 | 0/0 | 4712 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| t0058 | 0/0 | 4712 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| 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 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| 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 | 0/0 | 1086 | 124 | 32 | 29 | 39 | 8 | 16 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002 | 1/0 | 1086 | 67 | 20 | 9 | 28 | 3 | 6 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0003 | 0/1 | 1086 | 24 | 4 | 2 | 13 | 1 | 3 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0004 | 0/0 | 1086 | 16 | 14 | 2 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0005 | 0/0 | 1086 | 5 | 4 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0008 | 0/0 | 1086 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0009 | 0/0 | 1086 | 2 | 1 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0011 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0012 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0002c0006 | 0/0 | 1086 | 5 | 0 | 0 | 4 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0003c0007 | 0/0 | 1086 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0004c0013 | 0/0 | 1086 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0005c0010 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5797 | 50 | 7 | 11 | 21 | 1 | 10 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0002 | 0/0 | 5796 | 24 | 0 | 10 | 10 | 4 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0003 | 0/0 | 5796 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0004 | 0/0 | 5796 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0005 | 0/0 | 5796 | 5 | 4 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0006 | 0/0 | 5795 | 7 | 0 | 4 | 0 | 2 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0007 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0008 | 0/0 | 5796 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0009 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0010 | 0/0 | 5797 | 4 | 0 | 2 | 1 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0011 | 0/0 | 5796 | 2 | 0 | 1 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0012 | 0/0 | 5797 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0015 | 0/0 | 5796 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0016 | 0/0 | 5796 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0018 | 0/0 | 5796 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0020 | 0/0 | 5797 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0023 | 0/0 | 5797 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0024 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0035 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0036 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0040 | 0/0 | 5797 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0041 | 0/0 | 5797 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0042 | 0/0 | 5797 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0043 | 0/0 | 5797 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0046 | 0/0 | 5797 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0048 | 0/0 | 5798 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0050 | 0/0 | 5798 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0056 | 0/0 | 5795 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0057 | 0/0 | 5797 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0001t0058 | 0/0 | 5797 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0001 | 0/0 | 5797 | 26 | 0 | 1 | 22 | 1 | 2 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0002 | 0/0 | 5796 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0003 | 0/0 | 5796 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0005 | 0/0 | 5796 | 2 | 1 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0007 | 0/0 | 5796 | 5 | 5 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0009 | 0/0 | 5796 | 2 | 1 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0010 | 0/0 | 5797 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0011 | 0/0 | 5796 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0012 | 0/0 | 5797 | 3 | 0 | 1 | 0 | 0 | 2 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0013 | 0/0 | 5795 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0014 | 0/0 | 5797 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0016 | 0/0 | 5796 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0017 | 0/0 | 5797 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0019 | 0/0 | 5797 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0020 | 0/0 | 5797 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0021 | 0/0 | 5798 | 2 | 0 | 0 | 1 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0022 | 0/0 | 5796 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0025 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0026 | 0/0 | 5797 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0028 | 0/0 | 5796 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0030 | 0/0 | 5795 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0039 | 0/0 | 5797 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0044 | 0/0 | 5797 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0045 | 0/0 | 5797 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0047 | 1/0 | 5798 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0049 | 0/0 | 5798 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0002t0054 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0003t0001 | 0/0 | 5797 | 3 | 1 | 0 | 0 | 0 | 2 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0003t0003 | 0/1 | 5796 | 16 | 1 | 2 | 11 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0003t0014 | 0/0 | 5797 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0003t0024 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0003t0029 | 0/0 | 5795 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0003t0031 | 0/0 | 5796 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0003t0038 | 0/0 | 5797 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0004t0001 | 0/0 | 5797 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0004t0004 | 0/0 | 5796 | 6 | 6 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0004t0005 | 0/0 | 5796 | 2 | 1 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0004t0008 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0004t0027 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0004t0032 | 0/0 | 5795 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0004t0034 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0004t0052 | 0/0 | 5795 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0004t0053 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0004t0055 | 0/0 | 5797 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0005t0001 | 0/0 | 5797 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0005t0004 | 0/0 | 5796 | 2 | 1 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0005t0023 | 0/0 | 5797 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0008t0014 | 0/0 | 5797 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0008t0051 | 0/0 | 5798 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0009t0001 | 0/0 | 5797 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0009t0019 | 0/0 | 5797 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0011t0037 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0001c0012t0004 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0002c0006t0001 | 0/0 | 5797 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0002c0006t0003 | 0/0 | 5796 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0002c0006t0018 | 0/0 | 5796 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0003c0007t0005 | 0/0 | 5796 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0003c0007t0009 | 0/0 | 5796 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0004c0013t0033 | 0/0 | 5795 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| a0005c0010t0001 | 0/0 | 5797 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | copy fasta | chr1 | 217626344 | 217876696 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0010g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0010g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0010g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0011g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0011g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0012g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0015g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0015g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0015g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0016g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0016g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0018g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0020g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0023g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0024g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0035g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0036g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0040g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0041g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0042g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0043g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0046g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0048g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0050g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0056g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0057g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0001t0058g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0009g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0010g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0011g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0011g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0012g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0012g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0012g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0013g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0013g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0013g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0014g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0016g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0017g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0017g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0017g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0019g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0020g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0021g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0021g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0022g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0022g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0025g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0026g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0028g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0030g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0039g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0044g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0045g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0047g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0049g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0002t0054g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0014g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0024g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0029g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0031g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0003t0038g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0027g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0032g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0034g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0052g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0053g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0004t0055g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0005t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0005t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0005t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0005t0023g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0008t0014g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0008t0051g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0009t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0009t0019g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0011t0037g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0001c0012t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0002c0006t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0002c0006t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0002c0006t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0002c0006t0018g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0002c0006t0018g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0003c0007t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0003c0007t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0003c0007t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0004c0013t0033g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| a0005c0010t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | GBR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0131 | EUR | GBR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | GBR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00140 | hp2 | a0001 | c0002 | t0005 | g0078 | EUR | GBR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00280 | hp1 | a0001 | c0001 | t0043 | g0155 | EUR | FIN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00280 | hp2 | a0001 | c0003 | t0003 | g0221 | EUR | FIN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | FIN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0205 | EUR | FIN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | CHS | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00558 | hp2 | a0001 | c0001 | t0016 | g0172 | EAS | CHS | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00609 | hp1 | a0001 | c0003 | t0003 | g0214 | EAS | CHS | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00609 | hp2 | a0005 | c0010 | t0001 | g0169 | EAS | CHS | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00639 | hp2 | a0001 | c0002 | t0028 | g0079 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0133 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00733 | hp2 | a0001 | c0001 | t0010 | g0157 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0109 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01069 | hp1 | a0001 | c0003 | t0003 | g0218 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0202 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01074 | hp2 | a0001 | c0004 | t0001 | g0219 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0201 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01106 | hp1 | a0001 | c0001 | t0011 | g0227 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01109 | hp1 | a0001 | c0004 | t0005 | g0233 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0118 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01167 | hp2 | a0001 | c0002 | t0012 | g0018 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01168 | hp1 | a0004 | c0013 | t0033 | g0095 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01261 | hp1 | a0001 | c0005 | t0004 | g0245 | AMR | CLM | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01361 | hp1 | a0001 | c0003 | t0003 | g0098 | AMR | CLM | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01433 | hp2 | a0001 | c0002 | t0009 | g0076 | AMR | CLM | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01891 | hp1 | a0001 | c0004 | t0053 | g0239 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01891 | hp2 | a0001 | c0002 | t0007 | g0062 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0096 | AMR | PEL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01981 | hp2 | a0001 | c0002 | t0011 | g0199 | AMR | PEL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0161 | AMR | PEL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02004 | hp2 | a0001 | c0002 | t0011 | g0198 | AMR | PEL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | KHV | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02055 | hp1 | a0001 | c0002 | t0026 | g0048 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02129 | hp2 | a0001 | c0002 | t0010 | g0125 | EAS | KHV | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CDX | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CDX | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02165 | hp1 | a0001 | c0003 | t0003 | g0223 | EAS | CDX | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CDX | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02257 | hp1 | a0003 | c0007 | t0009 | g0117 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02257 | hp2 | a0001 | c0002 | t0005 | g0056 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02258 | hp1 | a0001 | c0002 | t0054 | g0050 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02258 | hp2 | a0003 | c0007 | t0009 | g0116 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02280 | hp1 | a0001 | c0002 | t0007 | g0067 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02280 | hp2 | a0001 | c0005 | t0023 | g0100 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0049 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02451 | hp2 | a0001 | c0002 | t0007 | g0061 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | KHV | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02523 | hp2 | a0002 | c0006 | t0003 | g0014 | EAS | KHV | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02572 | hp1 | a0001 | c0001 | t0023 | g0053 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02572 | hp2 | a0001 | c0003 | t0024 | g0243 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02615 | hp1 | a0001 | c0002 | t0020 | g0070 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02615 | hp2 | a0001 | c0004 | t0005 | g0250 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02622 | hp1 | a0001 | c0004 | t0004 | g0248 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02622 | hp2 | a0001 | c0002 | t0049 | g0055 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02630 | hp1 | a0001 | c0002 | t0022 | g0196 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02630 | hp2 | a0001 | c0004 | t0032 | g0186 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0064 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0136 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0142 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02723 | hp1 | a0001 | c0002 | t0007 | g0060 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02723 | hp2 | a0001 | c0004 | t0004 | g0240 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02735 | hp1 | a0001 | c0001 | t0011 | g0034 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0220 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02886 | hp2 | a0001 | c0004 | t0004 | g0246 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02895 | hp1 | a0001 | c0001 | t0056 | g0075 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0141 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0231 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02896 | hp2 | a0001 | c0001 | t0015 | g0093 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02965 | hp1 | a0001 | c0002 | t0022 | g0194 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0045 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0068 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02970 | hp2 | a0001 | c0001 | t0020 | g0094 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02976 | hp1 | a0001 | c0001 | t0015 | g0058 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02976 | hp2 | a0001 | c0003 | t0038 | g0244 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03041 | hp1 | a0001 | c0002 | t0013 | g0121 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03041 | hp2 | a0001 | c0004 | t0004 | g0247 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03098 | hp1 | a0001 | c0002 | t0039 | g0057 | AFR | MSL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03098 | hp2 | a0001 | c0001 | t0048 | g0110 | AFR | MSL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03130 | hp1 | a0001 | c0001 | t0036 | g0187 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03130 | hp2 | a0001 | c0012 | t0004 | g0042 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03139 | hp1 | a0001 | c0001 | t0035 | g0085 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03139 | hp2 | a0001 | c0002 | t0013 | g0193 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03195 | hp1 | a0001 | c0011 | t0037 | g0249 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0192 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03225 | hp1 | a0001 | c0004 | t0052 | g0238 | AFR | MSL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03225 | hp2 | a0001 | c0002 | t0030 | g0232 | AFR | MSL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03239 | hp1 | a0001 | c0001 | t0057 | g0200 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03453 | hp1 | a0001 | c0001 | t0024 | g0040 | AFR | MSL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0084 | AFR | MSL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03486 | hp1 | a0001 | c0002 | t0025 | g0195 | AFR | MSL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03516 | hp1 | a0001 | c0002 | t0019 | g0066 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03516 | hp2 | a0001 | c0001 | t0042 | g0035 | AFR | ESN | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03540 | hp1 | a0001 | c0001 | t0012 | g0188 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0120 | AFR | MSL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03579 | hp2 | a0001 | c0004 | t0055 | g0242 | AFR | MSL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03688 | hp1 | a0002 | c0006 | t0001 | g0105 | SAS | STU | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0215 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03710 | hp2 | a0001 | c0002 | t0012 | g0080 | SAS | PJL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0144 | SAS | BEB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03831 | hp2 | a0001 | c0001 | t0058 | g0150 | SAS | BEB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03927 | hp1 | a0001 | c0001 | t0040 | g0025 | SAS | BEB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03927 | hp2 | a0001 | c0002 | t0012 | g0077 | SAS | BEB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG04184 | hp1 | a0001 | c0002 | t0044 | g0091 | SAS | BEB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG04184 | hp2 | a0001 | c0001 | t0010 | g0029 | SAS | BEB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG04199 | hp1 | a0001 | c0002 | t0021 | g0122 | SAS | STU | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0203 | SAS | STU | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG04204 | hp2 | a0001 | c0003 | t0029 | g0063 | SAS | STU | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18612 | hp1 | a0001 | c0003 | t0003 | g0229 | EAS | CHB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | CHB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18906 | hp1 | a0003 | c0007 | t0005 | g0115 | AFR | YRI | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18906 | hp2 | a0001 | c0005 | t0004 | g0071 | AFR | YRI | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18941 | hp1 | a0001 | c0008 | t0014 | g0213 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18942 | hp1 | a0001 | c0003 | t0003 | g0211 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18946 | hp2 | a0001 | c0002 | t0017 | g0113 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18949 | hp1 | a0001 | c0008 | t0051 | g0234 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18951 | hp2 | a0001 | c0001 | t0041 | g0015 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18957 | hp2 | a0001 | c0003 | t0003 | g0222 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18959 | hp1 | a0001 | c0001 | t0018 | g0183 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18959 | hp2 | a0001 | c0001 | t0010 | g0043 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18960 | hp1 | a0001 | c0009 | t0001 | g0178 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18962 | hp1 | a0001 | c0002 | t0017 | g0151 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18968 | hp1 | a0001 | c0003 | t0003 | g0228 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18969 | hp1 | a0001 | c0003 | t0003 | g0210 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18969 | hp2 | a0001 | c0001 | t0016 | g0208 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18975 | hp1 | a0001 | c0002 | t0017 | g0152 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18975 | hp2 | a0001 | c0003 | t0003 | g0217 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18979 | hp2 | a0001 | c0001 | t0046 | g0153 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18990 | hp1 | a0001 | c0003 | t0003 | g0226 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18991 | hp1 | a0001 | c0002 | t0045 | g0145 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19003 | hp1 | a0001 | c0003 | t0014 | g0230 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19003 | hp2 | a0001 | c0002 | t0021 | g0160 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19005 | hp1 | a0001 | c0003 | t0003 | g0224 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19012 | hp2 | a0001 | c0001 | t0050 | g0017 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19043 | hp1 | a0001 | c0009 | t0019 | g0092 | AFR | LWK | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19043 | hp2 | a0001 | c0004 | t0004 | g0073 | AFR | LWK | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19063 | hp1 | a0001 | c0003 | t0003 | g0212 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19065 | hp1 | a0002 | c0006 | t0003 | g0185 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19066 | hp1 | a0001 | c0003 | t0031 | g0225 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19077 | hp1 | a0002 | c0006 | t0018 | g0139 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19087 | hp1 | a0002 | c0006 | t0018 | g0137 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0089 | AFR | YRI | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA19240 | hp2 | a0001 | c0004 | t0004 | g0252 | AFR | YRI | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ASW | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA20129 | hp2 | a0001 | c0004 | t0008 | g0241 | AFR | ASW | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0204 | EUR | TSI | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA20805 | hp2 | a0001 | c0002 | t0016 | g0074 | EUR | TSI | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01123 | hp1 | a0001 | c0002 | t0014 | g0102 | AMR | CLM | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG01123 | hp2 | a0001 | c0001 | t0010 | g0156 | AMR | CLM | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02486 | hp1 | a0001 | c0004 | t0027 | g0237 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02486 | hp2 | a0001 | c0001 | t0015 | g0059 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03471 | hp1 | a0001 | c0002 | t0007 | g0051 | AFR | MSL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG03471 | hp2 | a0001 | c0002 | t0013 | g0099 | AFR | MSL | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0052 | AFR | USA | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0189 | AFR | USA | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA20300 | hp1 | a0001 | c0004 | t0034 | g0251 | AFR | USA | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA20300 | hp2 | a0001 | c0003 | t0003 | g0235 | AFR | USA | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| NA21309 | hp2 | a0001 | c0002 | t0009 | g0072 | AFR | LWK | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0003 | g0097 | REF | REF | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0047 | g0088 | REF | REF | SPATA17_chr1_217626344_217876696 | SPATA17 | chr1 | 217626344 | 217876696 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:217631382
|
G | A | 1 | a0005 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.4G>A | p.Ala2Thr | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/11 | 39/5798 | 4/1086 | 2/361 | chr1 | 217631382 | ||
| chr1:217683280
|
A | G | 1 | a0002 | 5 | HG02523.hp2 HG03688.hp1 NA19065.hp1 others(2): Show |
missense_variant | MODERATE | c.314A>G | p.Tyr105Cys | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/11 | 349/5798 | 314/1086 | 105/361 | chr1 | 217683280 | ||
| chr1:217742054
|
G | A | 1 | a0004 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.475G>A | p.Asp159Asn | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/11 | 510/5798 | 475/1086 | 159/361 | chr1 | 217742054 | ||
| chr1:217782313
|
A | T | 1 | a0003 | 3 | HG02257.hp1 HG02258.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.863A>T | p.Asn288Ile | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/11 | 898/5798 | 863/1086 | 288/361 | chr1 | 217782313 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:217683284
|
G | A | 5 | a0001c0003a0001c0004a0001c0008others(2): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
synonymous_variant | LOW | c.318G>A | p.Arg106Arg | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/11 | 353/5798 | 318/1086 | 106/361 | chr1 | 217683284 | ||
| chr1:217741982
|
C | T | 3 | a0001c0003a0001c0009a0001c0012 | 27 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(24): Show |
synonymous_variant | LOW | c.403C>T | p.Leu135Leu | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/11 | 438/5798 | 403/1086 | 135/361 | chr1 | 217741982 | ||
| chr1:217774396
|
G | A | 8 | a0001c0001a0001c0003a0001c0004others(5): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
synonymous_variant | LOW | c.582G>A | p.Gln194Gln | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/11 | 617/5798 | 582/1086 | 194/361 | chr1 | 217774396 | ||
| chr1:217774519
|
T | A | 1 | a0001c0005 | 5 | HG01261.hp1 HG02280.hp2 HG02895.hp2 others(2): Show |
synonymous_variant | LOW | c.705T>A | p.Ile235Ile | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/11 | 740/5798 | 705/1086 | 235/361 | chr1 | 217774519 | ||
| chr1:217862824
|
A | G | 1 | a0001c0011 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1056A>G | p.Lys352Lys | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/11 | 1091/5798 | 1056/1086 | 352/361 | chr1 | 217862824 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:217867219
|
A | C | 1 | a0001c0001t0058 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*200A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 4365 | chr1 | 217867219 | |||||
| chr1:217867351
|
C | G | 2 | a0001c0001t0024a0001c0003t0024 | 2 | HG02572.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*332C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 4497 | chr1 | 217867351 | |||||
| chr1:217867707
|
C | T | 2 | a0001c0001t0023a0001c0005t0023 | 2 | HG02280.hp2 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*688C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 4853 | chr1 | 217867707 | |||||
| chr1:217867728
|
A | G | 1 | a0001c0001t0057 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*709A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 4874 | chr1 | 217867728 | |||||
| chr1:217867807
|
C | T | 1 | a0001c0001t0006 | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*788C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 4953 | chr1 | 217867807 | |||||
| chr1:217867958
|
G | T | 6 | a0001c0001t0004a0001c0001t0056a0001c0002t0022others(3): Show | 15 | HG01261.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*939G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5104 | chr1 | 217867958 | |||||
| chr1:217867981
|
T | G | 1 | a0001c0002t0025 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*962T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5127 | chr1 | 217867981 | |||||
| chr1:217868123
|
A | C | 2 | a0001c0001t0018a0002c0006t0018 | 3 | NA18959.hp1 NA19077.hp1 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1104A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5269 | chr1 | 217868123 | |||||
| chr1:217868263
|
A | G | 4 | a0001c0002t0054a0001c0004t0052a0001c0004t0053others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1244A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5409 | chr1 | 217868263 | |||||
| chr1:217868350
|
C | A | 1 | a0001c0002t0026 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1331C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5496 | chr1 | 217868350 | |||||
| chr1:217868612
|
A | G | 2 | a0001c0001t0024a0001c0003t0024 | 2 | HG02572.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1593A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5758 | chr1 | 217868612 | |||||
| chr1:217868664
|
GT | G | 35 | a0001c0001t0001a0001c0001t0010a0001c0001t0012others(32): Show | 119 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1671delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5836 | INFO_REALIGN_3_PRIME | chr1 | 217868664 | ||||
| chr1:217868664
|
GTT | G | 41 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(38): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1670_*1671delTT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5835 | INFO_REALIGN_3_PRIME | chr1 | 217868664 | ||||
| chr1:217868664
|
GTTT | G | 8 | a0001c0001t0006a0001c0001t0056a0001c0002t0013others(5): Show | 16 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1669_*1671delTTT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5834 | INFO_REALIGN_3_PRIME | chr1 | 217868664 | ||||
| chr1:217868674
|
T | G | 1 | a0001c0004t0027 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1655T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5820 | chr1 | 217868674 | |||||
| chr1:217868676
|
T | G | 1 | a0001c0002t0028 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1657T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5822 | chr1 | 217868676 | |||||
| chr1:217868677
|
T | G | 1 | a0001c0004t0027 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1658T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5823 | chr1 | 217868677 | |||||
| chr1:217868690
|
T | A | 13 | a0001c0001t0003a0001c0001t0008a0001c0002t0003others(10): Show | 32 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1671T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5836 | chr1 | 217868690 | |||||
| chr1:217868753
|
C | A | 1 | a0001c0004t0034 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1734C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5899 | chr1 | 217868753 | |||||
| chr1:217868836
|
A | T | 84 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(81): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*1817A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 5982 | chr1 | 217868836 | |||||
| chr1:217868870
|
C | T | 1 | a0001c0001t0057 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1851C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 6016 | chr1 | 217868870 | |||||
| chr1:217868896
|
G | A | 1 | a0001c0004t0027 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1877G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 6042 | chr1 | 217868896 | |||||
| chr1:217868961
|
C | T | 1 | a0001c0011t0037 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1942C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 6107 | chr1 | 217868961 | |||||
| chr1:217869270
|
T | C | 1 | a0001c0001t0015 | 3 | HG02486.hp2 HG02896.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2251T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 6416 | chr1 | 217869270 | |||||
| chr1:217869312
|
A | G | 2 | a0001c0001t0020a0001c0002t0020 | 2 | HG02615.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2293A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 6458 | chr1 | 217869312 | |||||
| chr1:217869367
|
G | A | 1 | a0001c0003t0038 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2348G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 6513 | chr1 | 217869367 | |||||
| chr1:217869484
|
T | C | 1 | a0001c0001t0048 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2465T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 6630 | chr1 | 217869484 | |||||
| chr1:217869496
|
T | C | 7 | a0001c0001t0005a0001c0001t0012a0001c0002t0005others(4): Show | 15 | HG00140.hp2 HG01109.hp1 HG01109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2477T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 6642 | chr1 | 217869496 | |||||
| chr1:217869566
|
G | A | 9 | a0001c0001t0002a0001c0001t0010a0001c0001t0011others(6): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2547G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 6712 | chr1 | 217869566 | |||||
| chr1:217869745
|
C | T | 1 | a0001c0001t0046 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2726C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 6891 | chr1 | 217869745 | |||||
| chr1:217869779
|
T | G | 1 | a0001c0001t0056 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2760T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 6925 | chr1 | 217869779 | |||||
| chr1:217869858
|
G | A | 1 | a0001c0004t0027 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2839G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7004 | chr1 | 217869858 | |||||
| chr1:217869889
|
A | C | 1 | a0001c0002t0045 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2870A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7035 | chr1 | 217869889 | |||||
| chr1:217869947
|
C | A | 2 | a0001c0001t0041a0001c0001t0050 | 2 | NA18951.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2928C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7093 | chr1 | 217869947 | |||||
| chr1:217870056
|
C | A | 2 | a0001c0001t0015a0001c0001t0036 | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3037C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7202 | chr1 | 217870056 | |||||
| chr1:217870258
|
A | G | 1 | a0001c0004t0027 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3239A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7404 | chr1 | 217870258 | |||||
| chr1:217870334
|
G | A | 10 | a0001c0001t0003a0001c0002t0003a0001c0002t0014others(7): Show | 26 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3315G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7480 | chr1 | 217870334 | |||||
| chr1:217870368
|
A | G | 3 | a0001c0002t0054a0001c0004t0052a0001c0004t0055 | 3 | HG02258.hp1 HG03225.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3349A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7514 | chr1 | 217870368 | |||||
| chr1:217870462
|
C | T | 1 | a0001c0001t0036 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3443C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7608 | chr1 | 217870462 | |||||
| chr1:217870493
|
G | T | 1 | a0001c0001t0036 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3474G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7639 | chr1 | 217870493 | |||||
| chr1:217870503
|
T | C | 1 | a0001c0002t0022 | 2 | HG02630.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3484T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7649 | chr1 | 217870503 | |||||
| chr1:217870506
|
G | T | 1 | a0001c0001t0015 | 3 | HG02486.hp2 HG02896.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3487G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7652 | chr1 | 217870506 | |||||
| chr1:217870646
|
A | C | 9 | a0001c0001t0002a0001c0001t0010a0001c0001t0011others(6): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3627A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7792 | chr1 | 217870646 | |||||
| chr1:217870650
|
T | C | 11 | a0001c0001t0002a0001c0001t0010a0001c0001t0011others(8): Show | 39 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3631T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7796 | chr1 | 217870650 | |||||
| chr1:217870710
|
A | G | 17 | a0001c0001t0002a0001c0001t0010a0001c0001t0011others(14): Show | 47 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3691A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7856 | chr1 | 217870710 | |||||
| chr1:217870740
|
C | A | 2 | a0001c0001t0035a0001c0002t0039 | 2 | HG03098.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3721C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 7886 | chr1 | 217870740 | |||||
| chr1:217870888
|
C | G | 1 | a0001c0004t0027 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3869C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 8034 | chr1 | 217870888 | |||||
| chr1:217870903
|
A | G | 1 | a0001c0001t0036 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3884A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 8049 | chr1 | 217870903 | |||||
| chr1:217870931
|
A | G | 1 | a0001c0001t0043 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3912A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 8077 | chr1 | 217870931 | |||||
| chr1:217871299
|
T | C | 1 | a0001c0004t0027 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4280T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 8445 | chr1 | 217871299 | |||||
| chr1:217871315
|
G | A | 1 | a0001c0001t0036 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4296G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 8461 | chr1 | 217871315 | |||||
| chr1:217871403
|
T | G | 14 | a0001c0001t0003a0001c0001t0008a0001c0001t0042others(11): Show | 33 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*4384T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 8549 | chr1 | 217871403 | |||||
| chr1:217871514
|
G | A | 3 | a0001c0002t0017a0001c0002t0045a0001c0008t0051 | 5 | NA18946.hp2 NA18949.hp1 NA18962.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4495G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 8660 | chr1 | 217871514 | |||||
| chr1:217871573
|
A | G | 1 | a0001c0004t0027 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4554A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 8719 | chr1 | 217871573 | |||||
| chr1:217871581
|
C | T | 1 | a0001c0003t0031 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4562C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 8727 | chr1 | 217871581 | |||||
| chr1:217871585
|
G | A | 1 | a0001c0004t0027 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4566G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 8731 | chr1 | 217871585 | |||||
| chr1:217871617
|
T | C | 8 | a0001c0001t0009a0001c0001t0024a0001c0002t0009others(5): Show | 12 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4598T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 8763 | chr1 | 217871617 | |||||
| chr1:217871677
|
A | G | 3 | a0001c0001t0011a0001c0001t0040a0001c0002t0011 | 5 | HG01106.hp1 HG01981.hp2 HG02004.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4658A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 11/11 | 8823 | chr1 | 217871677 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:217631613
|
T | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.68+167T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217631613 | ||||||
| chr1:217631793
|
A | C | 8 | a0001c0004t0004g0246a0001c0004t0004g0247a0001c0004t0004g0248others(5): Show | 8 | HG01261.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68+347A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217631793 | ||||||
| chr1:217631881
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.68+435C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217631881 | ||||||
| chr1:217631920
|
C | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.68+474C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217631920 | ||||||
| chr1:217632182
|
CAATA | C | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG01261.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.68+753_68+756delAA others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217632182 | |||||
| chr1:217632458
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.68+1012T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217632458 | ||||||
| chr1:217632670
|
A | G | 4 | a0001c0002t0005g0078a0001c0002t0012g0077a0001c0002t0012g0080others(1): Show | 4 | HG00140.hp2 HG00639.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+1224A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217632670 | ||||||
| chr1:217632882
|
G | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.68+1436G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217632882 | ||||||
| chr1:217633176
|
C | A | 1 | a0001c0002t0001g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.68+1730C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217633176 | ||||||
| chr1:217633197
|
CAAAT | C | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.68+1786_68+1789del others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217633197 | |||||
| chr1:217633197
|
CAAATAAA others(5): Show |
C | 4 | a0001c0002t0009g0076a0001c0004t0027g0237a0001c0004t0052g0238others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+1778_68+1789del others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217633197 | |||||
| chr1:217633288
|
G | A | 3 | a0001c0001t0008g0049a0001c0002t0009g0076a0001c0002t0026g0048 | 3 | HG01433.hp2 HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.68+1842G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217633288 | ||||||
| chr1:217633300
|
T | C | 3 | a0001c0001t0008g0049a0001c0002t0009g0076a0001c0002t0026g0048 | 3 | HG01433.hp2 HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.68+1854T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217633300 | ||||||
| chr1:217633325
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.68+1879T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217633325 | ||||||
| chr1:217633354
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.68+1908A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217633354 | ||||||
| chr1:217633400
|
A | AT | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.68+1959dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217633400 | |||||
| chr1:217633503
|
TGGGAGGC others(2): Show |
T | 29 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.68+2061_68+2069del others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217633503 | |||||
| chr1:217633517
|
A | T | 29 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.68+2071A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217633517 | ||||||
| chr1:217633962
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.68+2516A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217633962 | ||||||
| chr1:217634024
|
C | T | 3 | a0001c0001t0001g0206a0001c0001t0016g0208a0001c0002t0001g0207 | 3 | NA18944.hp1 NA18969.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.68+2578C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217634024 | ||||||
| chr1:217634063
|
A | G | 6 | a0001c0001t0001g0209a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 6 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+2617A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217634063 | ||||||
| chr1:217634241
|
T | C | 1 | a0001c0002t0001g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.68+2795T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217634241 | ||||||
| chr1:217634286
|
T | C | 4 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(1): Show | 4 | NA18941.hp1 NA18942.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.68+2840T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217634286 | ||||||
| chr1:217634309
|
A | G | 1 | a0001c0001t0057g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.68+2863A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217634309 | ||||||
| chr1:217634481
|
G | A | 1 | a0001c0002t0054g0050 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.68+3035G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217634481 | ||||||
| chr1:217634553
|
A | T | 3 | a0001c0004t0027g0237a0001c0004t0052g0238a0001c0004t0053g0239 | 3 | HG01891.hp1 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.68+3107A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217634553 | ||||||
| chr1:217634894
|
CT | C | 7 | a0001c0001t0001g0209a0001c0001t0005g0084a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+3453delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217634894 | |||||
| chr1:217634897
|
T | TTTG | 15 | a0001c0001t0001g0190a0001c0001t0001g0197a0001c0001t0008g0189others(12): Show | 15 | HG01168.hp1 HG01981.hp2 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.68+3487_68+3489dup others(3): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217634897 | |||||
| chr1:217634897
|
TTTG | T | 47 | a0001c0001t0001g0046a0001c0001t0001g0216a0001c0001t0002g0047others(44): Show | 47 | HG00280.hp2 HG00609.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.68+3487_68+3489del others(3): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217634897 | |||||
| chr1:217634897
|
TTTGTTG | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.68+3484_68+3489del others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217634897 | |||||
| chr1:217634897
|
TTTGTTGT others(2): Show |
T | 3 | a0001c0004t0027g0237a0001c0004t0052g0238a0001c0004t0053g0239 | 3 | HG01891.hp1 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.68+3481_68+3489del others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217634897 | |||||
| chr1:217635248
|
C | A | 6 | a0001c0001t0001g0190a0001c0001t0008g0189a0001c0001t0012g0188others(3): Show | 6 | HG02970.hp2 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.68+3802C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217635248 | ||||||
| chr1:217635423
|
G | T | 1 | a0001c0001t0015g0093 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.68+3977G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217635423 | ||||||
| chr1:217635696
|
T | C | 3 | a0001c0001t0006g0201a0001c0001t0006g0202a0001c0001t0006g0203 | 3 | HG01074.hp1 HG01099.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.68+4250T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217635696 | ||||||
| chr1:217635726
|
G | T | 1 | a0001c0002t0016g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.68+4280G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217635726 | ||||||
| chr1:217635727
|
T | C | 1 | a0001c0002t0016g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.68+4281T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217635727 | ||||||
| chr1:217635768
|
TA | T | 49 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0005g0084others(46): Show | 49 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.68+4324delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217635768 | |||||
| chr1:217635853
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.68+4407C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217635853 | ||||||
| chr1:217635860
|
A | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.68+4414A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217635860 | ||||||
| chr1:217635939
|
C | T | 1 | a0002c0006t0003g0185 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.68+4493C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217635939 | ||||||
| chr1:217636064
|
T | C | 1 | a0001c0002t0014g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.68+4618T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217636064 | ||||||
| chr1:217636107
|
T | A | 29 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.68+4661T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217636107 | ||||||
| chr1:217636126
|
C | T | 1 | a0001c0004t0004g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.68+4680C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217636126 | ||||||
| chr1:217636131
|
C | CA | 50 | a0001c0001t0001g0087a0001c0001t0001g0119a0001c0001t0001g0123others(47): Show | 50 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.68+4704dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217636131 | |||||
| chr1:217636131
|
C | CAA | 95 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.68+4703_68+4704dup others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217636131 | |||||
| chr1:217636131
|
C | CAAA | 26 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0046others(23): Show | 26 | HG01261.hp1 HG01361.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.68+4702_68+4704dup others(3): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217636131 | |||||
| chr1:217636131
|
C | CAAAA | 28 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(25): Show | 28 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.68+4701_68+4704dup others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217636131 | |||||
| chr1:217636131
|
CAAA | C | 45 | a0001c0001t0001g0082a0001c0001t0001g0148a0001c0001t0001g0154others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.68+4702_68+4704del others(3): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217636131 | |||||
| chr1:217636288
|
A | T | 1 | a0001c0004t0004g0252 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.68+4842A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217636288 | ||||||
| chr1:217636388
|
A | AATT | 26 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(23): Show | 26 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.68+4958_68+4960dup others(3): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217636388 | |||||
| chr1:217636388
|
AATT | A | 3 | a0001c0004t0027g0237a0001c0004t0052g0238a0001c0004t0053g0239 | 3 | HG01891.hp1 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.68+4958_68+4960del others(3): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217636388 | |||||
| chr1:217636475
|
G | C | 5 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093others(2): Show | 5 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.68+5029G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217636475 | ||||||
| chr1:217636479
|
T | C | 1 | a0002c0006t0003g0185 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.68+5033T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217636479 | ||||||
| chr1:217636768
|
T | A | 1 | a0001c0003t0003g0214 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.68+5322T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217636768 | ||||||
| chr1:217636794
|
C | T | 2 | a0001c0003t0003g0229a0001c0003t0014g0230 | 2 | NA18612.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.68+5348C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217636794 | ||||||
| chr1:217636903
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.68+5457A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217636903 | ||||||
| chr1:217636948
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.68+5502A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217636948 | ||||||
| chr1:217636964
|
G | C | 1 | a0001c0003t0001g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.68+5518G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217636964 | ||||||
| chr1:217636968
|
C | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.68+5522C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217636968 | ||||||
| chr1:217637212
|
A | G | 6 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0001g0206others(3): Show | 6 | NA18944.hp1 NA18959.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+5766A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217637212 | ||||||
| chr1:217637499
|
T | C | 1 | a0001c0005t0004g0245 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.68+6053T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217637499 | ||||||
| chr1:217637602
|
T | C | 29 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.68+6156T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217637602 | ||||||
| chr1:217637603
|
A | G | 1 | a0001c0001t0018g0183 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.68+6157A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217637603 | ||||||
| chr1:217637684
|
C | T | 3 | a0001c0004t0027g0237a0001c0004t0052g0238a0001c0004t0053g0239 | 3 | HG01891.hp1 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.68+6238C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217637684 | ||||||
| chr1:217637869
|
A | G | 1 | a0001c0008t0051g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.68+6423A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217637869 | ||||||
| chr1:217637917
|
C | T | 1 | a0001c0004t0004g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.68+6471C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217637917 | ||||||
| chr1:217637942
|
C | T | 1 | a0001c0001t0010g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.68+6496C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217637942 | ||||||
| chr1:217638103
|
G | A | 1 | a0001c0001t0002g0006 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.68+6657G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217638103 | ||||||
| chr1:217638314
|
TAA | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.68+6869_68+6870del others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217638314 | ||||||
| chr1:217638586
|
T | C | 49 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0005g0084others(46): Show | 49 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.68+7140T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217638586 | ||||||
| chr1:217638660
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.68+7214G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217638660 | ||||||
| chr1:217638973
|
G | T | 3 | a0001c0004t0027g0237a0001c0004t0052g0238a0001c0004t0053g0239 | 3 | HG01891.hp1 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.68+7527G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217638973 | ||||||
| chr1:217638982
|
T | A | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.68+7536T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217638982 | ||||||
| chr1:217639202
|
A | C | 7 | a0001c0001t0001g0190a0001c0001t0008g0189a0001c0001t0012g0188others(4): Show | 7 | HG02630.hp2 HG02970.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.68+7756A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217639202 | ||||||
| chr1:217639261
|
A | G | 2 | a0001c0004t0034g0251a0001c0005t0004g0245 | 2 | HG01261.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.68+7815A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217639261 | ||||||
| chr1:217639417
|
C | T | 1 | a0001c0002t0001g0111 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.68+7971C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217639417 | ||||||
| chr1:217639621
|
A | G | 3 | a0001c0001t0001g0041a0001c0001t0024g0040a0001c0012t0004g0042 | 3 | HG03130.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.68+8175A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217639621 | ||||||
| chr1:217639826
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.68+8380G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217639826 | ||||||
| chr1:217640221
|
A | G | 1 | a0001c0002t0001g0144 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.69-8661A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217640221 | ||||||
| chr1:217640275
|
A | G | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.69-8607A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217640275 | ||||||
| chr1:217640299
|
G | C | 1 | a0001c0001t0001g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.69-8583G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217640299 | ||||||
| chr1:217640397
|
GA | G | 17 | a0001c0001t0001g0065a0001c0001t0004g0069a0001c0001t0005g0068others(14): Show | 17 | HG00733.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.69-8484delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217640397 | ||||||
| chr1:217640503
|
C | T | 1 | a0001c0001t0002g0181 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.69-8379C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217640503 | ||||||
| chr1:217640542
|
C | G | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0048g0110 | 3 | HG02109.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.69-8340C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217640542 | ||||||
| chr1:217640645
|
A | G | 6 | a0001c0001t0001g0209a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 6 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.69-8237A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217640645 | ||||||
| chr1:217640768
|
C | A | 3 | a0001c0004t0027g0237a0001c0004t0052g0238a0001c0004t0053g0239 | 3 | HG01891.hp1 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.69-8114C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217640768 | ||||||
| chr1:217641006
|
G | A | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG01261.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.69-7876G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217641006 | ||||||
| chr1:217641101
|
G | T | 1 | a0001c0001t0002g0039 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.69-7781G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217641101 | ||||||
| chr1:217641134
|
C | T | 2 | a0001c0001t0016g0208a0001c0002t0001g0207 | 2 | NA18944.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.69-7748C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217641134 | ||||||
| chr1:217641270
|
A | G | 2 | a0001c0002t0001g0179a0001c0002t0001g0180 | 2 | NA18968.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.69-7612A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217641270 | ||||||
| chr1:217641341
|
G | A | 7 | a0001c0001t0058g0150a0001c0002t0001g0149a0001c0002t0001g0179others(4): Show | 7 | HG03831.hp2 NA18946.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.69-7541G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217641341 | ||||||
| chr1:217641388
|
T | C | 49 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0005g0084others(46): Show | 49 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.69-7494T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217641388 | ||||||
| chr1:217641417
|
A | G | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69-7465A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217641417 | ||||||
| chr1:217642074
|
C | T | 29 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.69-6808C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217642074 | ||||||
| chr1:217642139
|
T | C | 1 | a0001c0003t0003g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.69-6743T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217642139 | ||||||
| chr1:217642163
|
A | G | 1 | a0001c0005t0004g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69-6719A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217642163 | ||||||
| chr1:217642262
|
A | G | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.69-6620A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217642262 | ||||||
| chr1:217642301
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093 | 3 | HG02559.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.69-6581C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217642301 | ||||||
| chr1:217642331
|
A | G | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG01261.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.69-6551A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217642331 | ||||||
| chr1:217642663
|
C | G | 2 | a0001c0005t0001g0141a0001c0005t0023g0100 | 2 | HG02280.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69-6219C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217642663 | ||||||
| chr1:217642737
|
A | G | 1 | a0001c0002t0001g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.69-6145A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217642737 | ||||||
| chr1:217642757
|
TCCA | T | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0048g0110 | 3 | HG02109.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.69-6121_69-6119del others(3): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217642757 | |||||
| chr1:217642780
|
G | A | 1 | a0001c0003t0001g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.69-6102G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217642780 | ||||||
| chr1:217642898
|
A | G | 6 | a0001c0001t0001g0209a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 6 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.69-5984A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217642898 | ||||||
| chr1:217643021
|
G | T | 5 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093others(2): Show | 5 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-5861G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643021 | ||||||
| chr1:217643082
|
T | C | 1 | a0001c0002t0001g0112 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.69-5800T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643082 | ||||||
| chr1:217643096
|
G | T | 1 | a0001c0001t0056g0075 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.69-5786G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643096 | ||||||
| chr1:217643184
|
T | G | 1 | a0001c0002t0005g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.69-5698T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643184 | ||||||
| chr1:217643187
|
C | A | 7 | a0001c0001t0001g0209a0001c0001t0005g0084a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.69-5695C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643187 | ||||||
| chr1:217643674
|
G | C | 7 | a0001c0001t0001g0209a0001c0001t0005g0084a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.69-5208G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643674 | ||||||
| chr1:217643680
|
A | C | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.69-5202A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643680 | ||||||
| chr1:217643703
|
A | ACT | 4 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093others(1): Show | 4 | HG01070.hp1 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-5168_69-5167dup others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217643703 | |||||
| chr1:217643703
|
A | T | 3 | a0001c0004t0027g0237a0001c0004t0052g0238a0001c0004t0053g0239 | 3 | HG01891.hp1 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.69-5179A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643703 | ||||||
| chr1:217643714
|
CTA | C | 14 | a0001c0001t0005g0084a0001c0003t0024g0243a0001c0003t0038g0244others(11): Show | 14 | HG01261.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.69-5149_69-5148del others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217643714 | |||||
| chr1:217643714
|
CTATA | C | 3 | a0001c0004t0027g0237a0001c0004t0052g0238a0001c0004t0053g0239 | 3 | HG01891.hp1 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.69-5151_69-5148del others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217643714 | |||||
| chr1:217643716
|
A | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.69-5166A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643716 | ||||||
| chr1:217643718
|
A | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.69-5164A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643718 | ||||||
| chr1:217643720
|
A | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.69-5162A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643720 | ||||||
| chr1:217643722
|
A | C | 5 | a0001c0001t0002g0038a0001c0001t0008g0049a0001c0002t0009g0076others(2): Show | 5 | HG01261.hp2 HG01433.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.69-5160A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643722 | ||||||
| chr1:217643731
|
TATA | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-5148_69-5146del others(3): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217643731 | |||||
| chr1:217643732
|
AT | A | 6 | a0001c0001t0001g0209a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 6 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.69-5149delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643732 | ||||||
| chr1:217643735
|
A | AT | 5 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093others(2): Show | 5 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-5135dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217643735 | |||||
| chr1:217643735
|
A | T | 6 | a0001c0001t0001g0209a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 6 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.69-5147A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643735 | ||||||
| chr1:217643735
|
AT | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.69-5135delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217643735 | |||||
| chr1:217643736
|
T | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-5146T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643736 | ||||||
| chr1:217643791
|
C | T | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG01261.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.69-5091C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643791 | ||||||
| chr1:217643865
|
A | G | 1 | a0001c0009t0001g0178 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.69-5017A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643865 | ||||||
| chr1:217643957
|
A | G | 7 | a0001c0001t0001g0209a0001c0001t0005g0084a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.69-4925A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643957 | ||||||
| chr1:217643997
|
G | T | 6 | a0001c0001t0001g0190a0001c0001t0008g0189a0001c0001t0012g0188others(3): Show | 6 | HG02970.hp2 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.69-4885G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217643997 | ||||||
| chr1:217644050
|
C | T | 1 | a0001c0002t0020g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.69-4832C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217644050 | ||||||
| chr1:217644297
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0041g0015others(1): Show | 4 | NA18951.hp2 NA18984.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.69-4585A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217644297 | ||||||
| chr1:217644513
|
G | A | 1 | a0001c0003t0001g0231 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.69-4369G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217644513 | ||||||
| chr1:217644554
|
C | T | 2 | a0001c0001t0020g0094a0001c0001t0035g0085 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.69-4328C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217644554 | ||||||
| chr1:217644598
|
T | C | 29 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.69-4284T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217644598 | ||||||
| chr1:217644730
|
G | A | 7 | a0001c0001t0001g0209a0001c0001t0005g0084a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.69-4152G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217644730 | ||||||
| chr1:217644798
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.69-4084T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217644798 | ||||||
| chr1:217645029
|
C | T | 29 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.69-3853C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217645029 | ||||||
| chr1:217645065
|
G | T | 5 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093others(2): Show | 5 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-3817G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217645065 | ||||||
| chr1:217645122
|
A | G | 29 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.69-3760A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217645122 | ||||||
| chr1:217645185
|
T | C | 1 | a0001c0002t0013g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.69-3697T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217645185 | ||||||
| chr1:217645331
|
C | T | 1 | a0001c0002t0001g0138 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.69-3551C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217645331 | ||||||
| chr1:217645345
|
A | G | 1 | a0001c0004t0052g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.69-3537A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217645345 | ||||||
| chr1:217645489
|
A | G | 29 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.69-3393A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217645489 | ||||||
| chr1:217645536
|
A | T | 3 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093 | 3 | HG02559.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.69-3346A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217645536 | ||||||
| chr1:217646038
|
A | G | 49 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0005g0084others(46): Show | 49 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.69-2844A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217646038 | ||||||
| chr1:217646215
|
C | T | 49 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0005g0084others(46): Show | 49 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.69-2667C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217646215 | ||||||
| chr1:217646231
|
C | T | 2 | a0001c0003t0001g0231a0001c0004t0005g0233 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.69-2651C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217646231 | ||||||
| chr1:217646456
|
C | A | 2 | a0001c0004t0004g0240a0001c0004t0008g0241 | 2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.69-2426C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217646456 | ||||||
| chr1:217646515
|
G | A | 29 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.69-2367G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217646515 | ||||||
| chr1:217646621
|
G | A | 7 | a0001c0001t0001g0209a0001c0001t0005g0084a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.69-2261G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217646621 | ||||||
| chr1:217646679
|
G | A | 2 | a0001c0001t0015g0058a0001c0001t0015g0059 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.69-2203G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217646679 | ||||||
| chr1:217646818
|
C | T | 1 | a0001c0001t0015g0093 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.69-2064C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217646818 | ||||||
| chr1:217646825
|
C | T | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69-2057C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217646825 | ||||||
| chr1:217646891
|
T | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.69-1991T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217646891 | ||||||
| chr1:217646952
|
C | T | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.69-1930C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217646952 | ||||||
| chr1:217646982
|
C | T | 1 | a0002c0006t0018g0137 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.69-1900C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217646982 | ||||||
| chr1:217647122
|
A | T | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69-1760A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217647122 | ||||||
| chr1:217647301
|
G | C | 1 | a0001c0001t0056g0075 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.69-1581G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217647301 | ||||||
| chr1:217647353
|
T | C | 29 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.69-1529T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217647353 | ||||||
| chr1:217647658
|
T | C | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG01261.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.69-1224T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217647658 | ||||||
| chr1:217647664
|
C | T | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG01261.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.69-1218C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217647664 | ||||||
| chr1:217647725
|
A | AT | 14 | a0001c0003t0003g0214a0001c0003t0024g0243a0001c0003t0038g0244others(11): Show | 14 | HG00609.hp1 HG01261.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.69-1146dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 217647725 | |||||
| chr1:217647725
|
A | T | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69-1157A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217647725 | ||||||
| chr1:217647750
|
G | C | 1 | a0001c0002t0007g0060 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.69-1132G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217647750 | ||||||
| chr1:217647982
|
G | C | 49 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0005g0084others(46): Show | 49 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.69-900G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217647982 | ||||||
| chr1:217648172
|
A | T | 4 | a0001c0001t0004g0069a0001c0001t0005g0068a0001c0001t0015g0058others(1): Show | 4 | HG02055.hp2 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.69-710A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217648172 | ||||||
| chr1:217648438
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.69-444G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217648438 | ||||||
| chr1:217648481
|
G | A | 1 | a0001c0002t0003g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.69-401G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217648481 | ||||||
| chr1:217648584
|
C | G | 3 | a0001c0005t0001g0141a0001c0005t0001g0192a0001c0005t0023g0100 | 3 | HG02280.hp2 HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69-298C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217648584 | ||||||
| chr1:217648793
|
G | A | 29 | a0001c0001t0001g0216a0001c0001t0006g0096a0001c0001t0011g0227others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.69-89G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 1/10 | chr1 | 217648793 | ||||||
| chr1:217648974
|
A | G | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.158+3A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | chr1 | 217648974 | ||||||
| chr1:217649274
|
T | C | 1 | a0001c0001t0008g0189 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.158+303T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | chr1 | 217649274 | ||||||
| chr1:217649336
|
G | A | 4 | a0001c0001t0001g0190a0001c0001t0008g0189a0001c0001t0012g0188others(1): Show | 4 | HG03130.hp1 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+365G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | chr1 | 217649336 | ||||||
| chr1:217649733
|
C | CT | 14 | a0001c0001t0001g0216a0001c0003t0024g0243a0001c0003t0038g0244others(11): Show | 14 | HG01261.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.158+777dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 217649733 | |||||
| chr1:217649733
|
CT | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.158+777delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 217649733 | |||||
| chr1:217649835
|
A | G | 1 | a0001c0001t0004g0143 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158+864A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | chr1 | 217649835 | ||||||
| chr1:217649934
|
C | CT | 41 | a0001c0001t0001g0005a0001c0001t0001g0184a0001c0001t0006g0096others(38): Show | 41 | HG00280.hp1 HG00280.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.158+983dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 217649934 | |||||
| chr1:217649934
|
C | CTT | 12 | a0001c0001t0001g0216a0001c0001t0005g0084a0001c0004t0004g0240others(9): Show | 12 | HG01261.hp1 HG02615.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.158+982_158+983dup others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 217649934 | |||||
| chr1:217649934
|
CT | C | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0236others(18): Show | 21 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.158+983delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 217649934 | |||||
| chr1:217649936
|
T | C | 2 | a0001c0001t0020g0094a0001c0009t0019g0092 | 2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.158+965T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | chr1 | 217649936 | ||||||
| chr1:217649987
|
T | A | 6 | a0001c0001t0002g0101a0001c0001t0002g0158a0001c0001t0002g0159others(3): Show | 6 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+1016T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | chr1 | 217649987 | ||||||
| chr1:217650075
|
G | A | 1 | a0001c0001t0057g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.159-1022G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | chr1 | 217650075 | ||||||
| chr1:217650093
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.159-1004C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | chr1 | 217650093 | ||||||
| chr1:217650182
|
G | T | 7 | a0001c0001t0001g0209a0001c0001t0005g0084a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.159-915G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | chr1 | 217650182 | ||||||
| chr1:217650396
|
T | TTC | 3 | a0001c0001t0001g0184a0001c0002t0001g0103a0001c0002t0001g0108 | 3 | HG00438.hp1 NA19009.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.159-689_159-688dup others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 217650396 | |||||
| chr1:217650467
|
A | C | 3 | a0001c0001t0008g0049a0001c0002t0009g0076a0001c0002t0026g0048 | 3 | HG01433.hp2 HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.159-630A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | chr1 | 217650467 | ||||||
| chr1:217650506
|
TC | T | 3 | a0001c0004t0027g0237a0001c0004t0052g0238a0001c0004t0053g0239 | 3 | HG01891.hp1 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.159-588delC | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 217650506 | |||||
| chr1:217650695
|
A | G | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.159-402A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | chr1 | 217650695 | ||||||
| chr1:217650719
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.159-378C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | chr1 | 217650719 | ||||||
| chr1:217650898
|
A | C | 2 | a0001c0001t0004g0069a0001c0001t0005g0068 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.159-199A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 2/10 | chr1 | 217650898 | ||||||
| chr1:217651233
|
TACTC | T | 3 | a0001c0002t0005g0078a0001c0002t0012g0080a0001c0002t0028g0079 | 3 | HG00140.hp2 HG00639.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.240+59_240+62delCA others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217651233 | |||||
| chr1:217651273
|
T | C | 1 | a0001c0002t0001g0114 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.240+95T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217651273 | ||||||
| chr1:217651340
|
C | G | 1 | a0001c0002t0020g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.240+162C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217651340 | ||||||
| chr1:217651440
|
C | G | 3 | a0001c0001t0008g0049a0001c0002t0009g0076a0001c0002t0026g0048 | 3 | HG01433.hp2 HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.240+262C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217651440 | ||||||
| chr1:217651501
|
A | G | 3 | a0001c0002t0007g0051a0001c0002t0007g0067a0001c0002t0019g0066 | 3 | HG02280.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.240+323A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217651501 | ||||||
| chr1:217651728
|
T | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.240+550T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217651728 | ||||||
| chr1:217651742
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0012g0188 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.240+564T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217651742 | ||||||
| chr1:217651952
|
A | G | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG01261.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.240+774A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217651952 | ||||||
| chr1:217652224
|
A | C | 1 | a0001c0002t0009g0076 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.240+1046A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217652224 | ||||||
| chr1:217652253
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.240+1075A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217652253 | ||||||
| chr1:217652300
|
C | T | 3 | a0001c0001t0001g0065a0001c0002t0001g0064a0001c0003t0029g0063 | 3 | HG00733.hp1 HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.240+1122C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217652300 | ||||||
| chr1:217652308
|
C | T | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.240+1130C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217652308 | ||||||
| chr1:217652347
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.240+1169T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217652347 | ||||||
| chr1:217652361
|
A | C | 1 | a0001c0001t0008g0189 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.240+1183A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217652361 | ||||||
| chr1:217652378
|
C | G | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG01261.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.240+1200C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217652378 | ||||||
| chr1:217652491
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0044 | 2 | HG01993.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.240+1313C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217652491 | ||||||
| chr1:217652526
|
G | T | 3 | a0001c0001t0008g0049a0001c0002t0009g0076a0001c0002t0026g0048 | 3 | HG01433.hp2 HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.240+1348G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217652526 | ||||||
| chr1:217652530
|
G | C | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.240+1352G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217652530 | ||||||
| chr1:217652797
|
G | A | 1 | a0003c0007t0005g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.240+1619G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217652797 | ||||||
| chr1:217653380
|
C | T | 2 | a0001c0001t0006g0204a0001c0001t0006g0205 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.240+2202C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217653380 | ||||||
| chr1:217653412
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.240+2234C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217653412 | ||||||
| chr1:217653597
|
G | A | 1 | a0001c0002t0020g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.240+2419G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217653597 | ||||||
| chr1:217653599
|
G | A | 6 | a0001c0001t0001g0209a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 6 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+2421G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217653599 | ||||||
| chr1:217653621
|
T | TAAGAATC others(322): Show |
1 | a0001c0004t0055g0242 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.240+2456_240+2457i others(331): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217653621 | |||||
| chr1:217653621
|
T | TAAGAATC others(320): Show |
2 | a0001c0003t0024g0243a0001c0003t0038g0244 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.240+2456_240+2457i others(329): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217653621 | |||||
| chr1:217653621
|
T | TAAGAATC others(321): Show |
6 | a0001c0004t0004g0240a0001c0004t0004g0247a0001c0004t0004g0248others(3): Show | 6 | HG02615.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+2456_240+2457i others(330): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217653621 | |||||
| chr1:217653621
|
T | TAAGAATC others(322): Show |
4 | a0001c0004t0004g0246a0001c0004t0004g0252a0001c0004t0034g0251others(1): Show | 4 | HG01261.hp1 HG02886.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.240+2456_240+2457i others(331): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217653621 | |||||
| chr1:217653707
|
G | C | 6 | a0001c0001t0001g0209a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 6 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+2529G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217653707 | ||||||
| chr1:217653794
|
A | G | 2 | a0001c0002t0001g0179a0001c0002t0001g0180 | 2 | NA18968.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.240+2616A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217653794 | ||||||
| chr1:217653914
|
C | A | 1 | a0002c0006t0003g0185 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.240+2736C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217653914 | ||||||
| chr1:217653966
|
A | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.240+2788A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217653966 | ||||||
| chr1:217654142
|
CT | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0209a0001c0001t0005g0084others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.240+2976delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217654142 | |||||
| chr1:217654208
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0163 | 2 | HG00438.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.240+3030G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217654208 | ||||||
| chr1:217654216
|
C | T | 5 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093others(2): Show | 5 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+3038C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217654216 | ||||||
| chr1:217654331
|
G | C | 1 | a0001c0004t0055g0242 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.240+3153G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217654331 | ||||||
| chr1:217654368
|
G | A | 8 | a0001c0004t0004g0246a0001c0004t0004g0247a0001c0004t0004g0248others(5): Show | 8 | HG01261.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.240+3190G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217654368 | ||||||
| chr1:217654429
|
T | C | 1 | a0001c0002t0005g0078 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.240+3251T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217654429 | ||||||
| chr1:217654693
|
T | C | 7 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(4): Show | 7 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.240+3515T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217654693 | ||||||
| chr1:217654717
|
C | CT | 21 | a0001c0001t0001g0036a0001c0001t0001g0174a0001c0001t0002g0039others(18): Show | 21 | HG01261.hp1 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.240+3557dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217654717 | |||||
| chr1:217654717
|
CT | C | 6 | a0001c0001t0002g0007a0001c0001t0002g0019a0001c0002t0021g0160others(3): Show | 6 | HG00639.hp2 HG01168.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+3557delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217654717 | |||||
| chr1:217654747
|
C | T | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.240+3569C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217654747 | ||||||
| chr1:217654840
|
G | A | 1 | a0001c0005t0001g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.240+3662G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217654840 | ||||||
| chr1:217654879
|
ATTTTTGT others(1164): Show |
A | 1 | a0001c0004t0004g0247 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.240+3731_240+4901d others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217654879 | |||||
| chr1:217654990
|
G | A | 12 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(9): Show | 12 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.240+3812G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217654990 | ||||||
| chr1:217654992
|
G | A | 1 | a0001c0004t0053g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.240+3814G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217654992 | ||||||
| chr1:217654999
|
C | T | 1 | a0001c0001t0008g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.240+3821C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217654999 | ||||||
| chr1:217655110
|
T | C | 1 | a0001c0003t0003g0214 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.240+3932T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217655110 | ||||||
| chr1:217655113
|
T | A | 7 | a0001c0001t0058g0150a0001c0002t0001g0149a0001c0002t0001g0179others(4): Show | 7 | HG03831.hp2 NA18946.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.240+3935T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217655113 | ||||||
| chr1:217655206
|
A | G | 4 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035others(1): Show | 4 | HG02965.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+4028A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217655206 | ||||||
| chr1:217655232
|
T | C | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+4054T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217655232 | ||||||
| chr1:217655579
|
A | C | 6 | a0001c0001t0001g0135a0001c0002t0001g0106a0001c0002t0001g0107others(3): Show | 6 | NA18944.hp2 NA18946.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+4401A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217655579 | ||||||
| chr1:217655626
|
T | C | 2 | a0001c0001t0020g0094a0001c0001t0035g0085 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.240+4448T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217655626 | ||||||
| chr1:217655842
|
C | A | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+4664C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217655842 | ||||||
| chr1:217655953
|
T | C | 1 | a0001c0001t0006g0161 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.240+4775T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217655953 | ||||||
| chr1:217656041
|
G | A | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.240+4863G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217656041 | ||||||
| chr1:217656045
|
G | A | 43 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(40): Show | 43 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.240+4867G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217656045 | ||||||
| chr1:217656392
|
A | G | 1 | a0001c0002t0014g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.240+5214A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217656392 | ||||||
| chr1:217656546
|
A | ATATG | 42 | a0001c0001t0001g0022a0001c0001t0001g0082a0001c0001t0002g0023others(39): Show | 42 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.240+5400_240+5403d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217656546 | |||||
| chr1:217656546
|
A | ATATGTAT others(1): Show |
10 | a0001c0001t0001g0021a0001c0001t0001g0190a0001c0001t0002g0019others(7): Show | 10 | HG01168.hp2 HG01891.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.240+5396_240+5403d others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217656546 | |||||
| chr1:217656546
|
A | ATATGTAT others(5): Show |
7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.240+5392_240+5403d others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217656546 | |||||
| chr1:217656546
|
A | ATATGTAT others(9): Show |
2 | a0001c0001t0006g0204a0001c0004t0027g0237 | 2 | HG02486.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.240+5388_240+5403d others(18): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217656546 | |||||
| chr1:217656546
|
ATATG | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0033a0001c0001t0011g0034 | 3 | HG02004.hp1 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.240+5400_240+5403d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217656546 | |||||
| chr1:217656578
|
G | GTATGTAT others(1): Show |
3 | a0001c0003t0001g0231a0001c0004t0005g0233a0004c0013t0033g0095 | 3 | HG01109.hp1 HG01168.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.240+5403_240+5404i others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217656578 | |||||
| chr1:217656578
|
G | GTATT | 5 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(2): Show | 5 | HG02559.hp1 HG02896.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+5410_240+5413d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217656578 | |||||
| chr1:217656578
|
G | T | 2 | a0001c0001t0001g0173a0001c0005t0004g0245 | 2 | HG01261.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.240+5400G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217656578 | ||||||
| chr1:217656582
|
T | G | 1 | a0001c0012t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.240+5404T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217656582 | ||||||
| chr1:217656621
|
A | C | 3 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035 | 3 | HG02965.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.240+5443A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217656621 | ||||||
| chr1:217656749
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.240+5571C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217656749 | ||||||
| chr1:217656811
|
T | A | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.240+5633T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217656811 | ||||||
| chr1:217656816
|
A | G | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240+5638A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217656816 | ||||||
| chr1:217656836
|
A | G | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.240+5658A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217656836 | ||||||
| chr1:217656847
|
C | T | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.240+5669C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217656847 | ||||||
| chr1:217656988
|
C | T | 1 | a0001c0002t0012g0018 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.240+5810C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217656988 | ||||||
| chr1:217657145
|
T | C | 1 | a0001c0001t0046g0153 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.240+5967T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217657145 | ||||||
| chr1:217657399
|
G | A | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+6221G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217657399 | ||||||
| chr1:217657469
|
A | G | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.240+6291A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217657469 | ||||||
| chr1:217657594
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.240+6416T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217657594 | ||||||
| chr1:217657725
|
T | G | 8 | a0001c0002t0013g0099a0001c0002t0013g0193a0001c0002t0022g0194others(5): Show | 8 | HG02257.hp1 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.240+6547T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217657725 | ||||||
| chr1:217657886
|
T | A | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.240+6708T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217657886 | ||||||
| chr1:217657893
|
G | A | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.240+6715G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217657893 | ||||||
| chr1:217657956
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.240+6778G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217657956 | ||||||
| chr1:217658221
|
G | T | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.240+7043G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217658221 | ||||||
| chr1:217658275
|
T | G | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.240+7097T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217658275 | ||||||
| chr1:217658540
|
C | T | 7 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0015g0093others(4): Show | 7 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.240+7362C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217658540 | ||||||
| chr1:217658574
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.240+7396T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217658574 | ||||||
| chr1:217658580
|
T | A | 1 | a0001c0001t0002g0032 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.240+7402T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217658580 | ||||||
| chr1:217658671
|
T | C | 49 | a0001c0001t0001g0190a0001c0001t0008g0189a0001c0001t0012g0188others(46): Show | 49 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.240+7493T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217658671 | ||||||
| chr1:217658736
|
C | T | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.240+7558C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217658736 | ||||||
| chr1:217658933
|
C | T | 1 | a0001c0001t0002g0001 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.240+7755C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217658933 | ||||||
| chr1:217658995
|
A | T | 1 | a0001c0002t0049g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.240+7817A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217658995 | ||||||
| chr1:217659153
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0163 | 2 | HG00438.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.240+7975A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217659153 | ||||||
| chr1:217659187
|
A | AAC | 20 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0177others(17): Show | 20 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.240+8045_240+8046d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217659187 | |||||
| chr1:217659187
|
A | AACAC | 6 | a0001c0002t0007g0061a0001c0003t0024g0243a0001c0003t0038g0244others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+8043_240+8046d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217659187 | |||||
| chr1:217659187
|
A | AACACAC | 3 | a0001c0001t0008g0189a0001c0001t0012g0188a0001c0004t0055g0242 | 3 | HG03540.hp1 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.240+8041_240+8046d others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217659187 | |||||
| chr1:217659187
|
AAC | A | 9 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(6): Show | 9 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.240+8045_240+8046d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217659187 | |||||
| chr1:217659187
|
AACAC | A | 9 | a0001c0001t0001g0164a0001c0001t0008g0045a0001c0001t0024g0040others(6): Show | 9 | HG01168.hp1 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.240+8043_240+8046d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217659187 | |||||
| chr1:217659187
|
AACACAC | A | 27 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(24): Show | 27 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.240+8041_240+8046d others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217659187 | |||||
| chr1:217659472
|
T | C | 1 | a0001c0002t0017g0113 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.240+8294T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217659472 | ||||||
| chr1:217659701
|
G | A | 3 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035 | 3 | HG02965.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.240+8523G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217659701 | ||||||
| chr1:217659778
|
C | A | 1 | a0001c0001t0056g0075 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.240+8600C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217659778 | ||||||
| chr1:217659858
|
C | G | 30 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.240+8680C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217659858 | ||||||
| chr1:217659863
|
G | T | 1 | a0001c0001t0002g0031 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.240+8685G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217659863 | ||||||
| chr1:217660034
|
G | A | 3 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035 | 3 | HG02965.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.240+8856G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217660034 | ||||||
| chr1:217660068
|
T | C | 1 | a0001c0003t0029g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.240+8890T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217660068 | ||||||
| chr1:217660198
|
T | C | 4 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035others(1): Show | 4 | HG02965.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-8835T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217660198 | ||||||
| chr1:217660210
|
G | A | 1 | a0001c0002t0005g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.241-8823G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217660210 | ||||||
| chr1:217660493
|
G | A | 4 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035others(1): Show | 4 | HG02965.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-8540G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217660493 | ||||||
| chr1:217660670
|
G | A | 1 | a0001c0003t0003g0212 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.241-8363G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217660670 | ||||||
| chr1:217660770
|
T | C | 6 | a0001c0001t0001g0135a0001c0002t0001g0106a0001c0002t0001g0107others(3): Show | 6 | NA18944.hp2 NA18946.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-8263T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217660770 | ||||||
| chr1:217660874
|
A | C | 1 | a0001c0002t0012g0018 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.241-8159A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217660874 | ||||||
| chr1:217660897
|
T | G | 1 | a0001c0002t0003g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.241-8136T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217660897 | ||||||
| chr1:217660915
|
A | C | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-8118A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217660915 | ||||||
| chr1:217661170
|
A | G | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.241-7863A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217661170 | ||||||
| chr1:217661181
|
G | T | 1 | a0001c0002t0005g0078 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.241-7852G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217661181 | ||||||
| chr1:217661259
|
A | T | 1 | a0001c0001t0001g0182 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.241-7774A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217661259 | ||||||
| chr1:217661266
|
C | CAG | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.241-7766_241-7765d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217661266 | |||||
| chr1:217661305
|
T | C | 1 | a0001c0002t0005g0078 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.241-7728T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217661305 | ||||||
| chr1:217661495
|
G | A | 11 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(8): Show | 11 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.241-7538G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217661495 | ||||||
| chr1:217661602
|
G | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.241-7431G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217661602 | ||||||
| chr1:217661622
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.241-7411T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217661622 | ||||||
| chr1:217661648
|
A | G | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.241-7385A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217661648 | ||||||
| chr1:217661656
|
A | G | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.241-7377A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217661656 | ||||||
| chr1:217661821
|
C | T | 1 | a0001c0001t0046g0153 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.241-7212C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217661821 | ||||||
| chr1:217661868
|
A | G | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.241-7165A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217661868 | ||||||
| chr1:217661887
|
C | A | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-7146C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217661887 | ||||||
| chr1:217661976
|
G | A | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.241-7057G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217661976 | ||||||
| chr1:217662005
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.241-7028A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217662005 | ||||||
| chr1:217662178
|
A | C | 15 | a0001c0001t0004g0054a0001c0001t0008g0049a0001c0001t0023g0053others(12): Show | 15 | HG00140.hp2 HG00639.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.241-6855A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217662178 | ||||||
| chr1:217662409
|
A | G | 3 | a0001c0003t0001g0231a0001c0004t0005g0233a0001c0012t0004g0042 | 3 | HG01109.hp1 HG02896.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.241-6624A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217662409 | ||||||
| chr1:217662742
|
G | C | 4 | a0001c0001t0001g0190a0001c0001t0008g0189a0001c0001t0012g0188others(1): Show | 4 | HG03130.hp1 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-6291G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217662742 | ||||||
| chr1:217662757
|
T | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.241-6276T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217662757 | ||||||
| chr1:217662767
|
C | T | 1 | a0001c0003t0038g0244 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.241-6266C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217662767 | ||||||
| chr1:217662829
|
C | T | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.241-6204C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217662829 | ||||||
| chr1:217662916
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.241-6117A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217662916 | ||||||
| chr1:217662968
|
A | T | 1 | a0003c0007t0005g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.241-6065A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217662968 | ||||||
| chr1:217663129
|
T | A | 1 | a0001c0002t0001g0131 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.241-5904T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217663129 | ||||||
| chr1:217663168
|
G | A | 3 | a0001c0003t0003g0098a0001c0003t0003g0218a0001c0004t0001g0219 | 3 | HG01069.hp1 HG01074.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.241-5865G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217663168 | ||||||
| chr1:217663213
|
C | T | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.241-5820C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217663213 | ||||||
| chr1:217663318
|
G | A | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.241-5715G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217663318 | ||||||
| chr1:217663326
|
T | A | 2 | a0001c0002t0016g0074a0001c0002t0049g0055 | 2 | HG02622.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.241-5707T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217663326 | ||||||
| chr1:217663402
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0005g0118 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.241-5631G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217663402 | ||||||
| chr1:217663597
|
A | G | 3 | a0001c0001t0004g0054a0001c0001t0023g0053a0001c0002t0009g0072 | 3 | HG02572.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.241-5436A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217663597 | ||||||
| chr1:217663774
|
C | G | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.241-5259C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217663774 | ||||||
| chr1:217663937
|
C | T | 1 | a0001c0003t0003g0097 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.241-5096C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217663937 | ||||||
| chr1:217663938
|
A | G | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.241-5095A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217663938 | ||||||
| chr1:217663950
|
G | A | 3 | a0001c0002t0007g0051a0001c0002t0007g0067a0001c0002t0019g0066 | 3 | HG02280.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.241-5083G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217663950 | ||||||
| chr1:217664008
|
G | T | 3 | a0001c0002t0007g0060a0001c0002t0007g0061a0001c0002t0007g0062 | 3 | HG01891.hp2 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.241-5025G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217664008 | ||||||
| chr1:217664051
|
C | T | 3 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0010g0157 | 3 | HG00733.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.241-4982C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217664051 | ||||||
| chr1:217664083
|
G | A | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.241-4950G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217664083 | ||||||
| chr1:217664122
|
T | A | 1 | a0001c0004t0004g0247 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.241-4911T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217664122 | ||||||
| chr1:217664289
|
CT | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(195): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.241-4723delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217664289 | |||||
| chr1:217664289
|
CTTTTT | C | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-4727_241-4723d others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217664289 | |||||
| chr1:217664291
|
T | A | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.241-4742T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217664291 | ||||||
| chr1:217664357
|
A | G | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-4676A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217664357 | ||||||
| chr1:217664515
|
A | G | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.241-4518A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217664515 | ||||||
| chr1:217664918
|
A | T | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.241-4115A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217664918 | ||||||
| chr1:217665020
|
G | A | 3 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035 | 3 | HG02965.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.241-4013G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217665020 | ||||||
| chr1:217665238
|
ATGTGCCT others(5): Show |
A | 2 | a0001c0003t0024g0243a0001c0003t0038g0244 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.241-3790_241-3779d others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217665238 | |||||
| chr1:217665278
|
G | C | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.241-3755G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217665278 | ||||||
| chr1:217665346
|
T | C | 4 | a0001c0001t0001g0190a0001c0001t0008g0189a0001c0001t0012g0188others(1): Show | 4 | HG03130.hp1 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-3687T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217665346 | ||||||
| chr1:217665359
|
A | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.241-3674A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217665359 | ||||||
| chr1:217665402
|
C | A | 1 | a0001c0002t0009g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.241-3631C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217665402 | ||||||
| chr1:217665838
|
C | A | 3 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035 | 3 | HG02965.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.241-3195C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217665838 | ||||||
| chr1:217665859
|
C | A | 30 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.241-3174C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217665859 | ||||||
| chr1:217665894
|
A | T | 1 | a0001c0002t0014g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.241-3139A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217665894 | ||||||
| chr1:217666097
|
C | T | 1 | a0001c0001t0007g0142 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.241-2936C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217666097 | ||||||
| chr1:217666107
|
T | C | 1 | a0001c0004t0053g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.241-2926T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217666107 | ||||||
| chr1:217666120
|
C | T | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.241-2913C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217666120 | ||||||
| chr1:217666160
|
T | C | 1 | a0001c0003t0001g0220 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.241-2873T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217666160 | ||||||
| chr1:217666382
|
C | G | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.241-2651C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217666382 | ||||||
| chr1:217666488
|
T | G | 3 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093 | 3 | HG02559.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.241-2545T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217666488 | ||||||
| chr1:217666526
|
G | GT | 9 | a0001c0001t0001g0036a0001c0002t0012g0018a0001c0003t0003g0214others(6): Show | 9 | HG00609.hp1 HG01167.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.241-2496dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217666526 | |||||
| chr1:217666792
|
T | C | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-2241T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217666792 | ||||||
| chr1:217666838
|
A | G | 1 | a0001c0001t0002g0001 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.241-2195A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217666838 | ||||||
| chr1:217667001
|
A | G | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-2032A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217667001 | ||||||
| chr1:217667048
|
C | CT | 10 | a0001c0001t0001g0081a0001c0001t0001g0170a0001c0001t0011g0034others(7): Show | 10 | HG02129.hp1 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-1968dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217667048 | |||||
| chr1:217667048
|
CT | C | 60 | a0001c0001t0001g0011a0001c0001t0001g0090a0001c0001t0001g0209others(57): Show | 60 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.241-1968delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217667048 | |||||
| chr1:217667087
|
AC | A | 3 | a0001c0002t0017g0151a0001c0002t0017g0152a0001c0002t0045g0145 | 3 | NA18962.hp1 NA18975.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.241-1944delC | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217667087 | |||||
| chr1:217667114
|
C | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.241-1919C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217667114 | ||||||
| chr1:217667121
|
C | T | 1 | a0001c0002t0001g0147 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.241-1912C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217667121 | ||||||
| chr1:217667134
|
G | A | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-1899G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217667134 | ||||||
| chr1:217667251
|
G | A | 1 | a0001c0003t0029g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.241-1782G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217667251 | ||||||
| chr1:217667301
|
C | T | 1 | a0001c0003t0003g0212 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.241-1732C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217667301 | ||||||
| chr1:217667461
|
C | T | 1 | a0001c0002t0002g0133 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.241-1572C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217667461 | ||||||
| chr1:217667483
|
C | T | 1 | a0001c0001t0058g0150 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.241-1550C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217667483 | ||||||
| chr1:217667562
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.241-1471C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217667562 | ||||||
| chr1:217667786
|
TTAAAG | T | 3 | a0001c0001t0006g0201a0001c0001t0006g0202a0001c0001t0006g0203 | 3 | HG01074.hp1 HG01099.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.241-1242_241-1238d others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 217667786 | |||||
| chr1:217668078
|
G | T | 1 | a0001c0001t0001g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.241-955G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217668078 | ||||||
| chr1:217668099
|
C | T | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.241-934C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217668099 | ||||||
| chr1:217668109
|
A | C | 3 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0002g0176 | 3 | HG01952.hp1 HG02148.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.241-924A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217668109 | ||||||
| chr1:217668110
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0002g0176 | 3 | HG01952.hp1 HG02148.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.241-923C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217668110 | ||||||
| chr1:217668111
|
AATTAT | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0002g0176 | 3 | HG01952.hp1 HG02148.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.241-921_241-917del others(5): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217668111 | ||||||
| chr1:217668119
|
C | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0177a0001c0001t0002g0176 | 3 | HG01952.hp1 HG02148.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.241-914C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217668119 | ||||||
| chr1:217668175
|
A | G | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.241-858A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217668175 | ||||||
| chr1:217668323
|
A | T | 1 | a0001c0001t0020g0094 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.241-710A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217668323 | ||||||
| chr1:217668602
|
C | G | 3 | a0001c0001t0008g0049a0001c0002t0009g0076a0001c0002t0026g0048 | 3 | HG01433.hp2 HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.241-431C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217668602 | ||||||
| chr1:217668787
|
A | G | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.241-246A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217668787 | ||||||
| chr1:217668838
|
T | C | 8 | a0001c0002t0005g0078a0001c0002t0012g0077a0001c0002t0012g0080others(5): Show | 8 | HG00140.hp2 HG00639.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.241-195T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217668838 | ||||||
| chr1:217668881
|
A | G | 2 | a0001c0001t0020g0094a0001c0001t0035g0085 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.241-152A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217668881 | ||||||
| chr1:217668967
|
G | A | 2 | a0001c0001t0008g0045a0001c0001t0042g0035 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.241-66G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 3/10 | chr1 | 217668967 | ||||||
| chr1:217669233
|
C | A | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.291+150C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217669233 | ||||||
| chr1:217669436
|
G | T | 4 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0013others(1): Show | 4 | NA18747.hp1 NA18959.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+353G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217669436 | ||||||
| chr1:217669545
|
A | G | 53 | a0001c0001t0001g0041a0001c0001t0001g0082a0001c0001t0001g0130others(50): Show | 53 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.291+462A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217669545 | ||||||
| chr1:217669614
|
A | G | 1 | a0001c0003t0003g0212 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.291+531A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217669614 | ||||||
| chr1:217669713
|
AT | A | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+632delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217669713 | |||||
| chr1:217669782
|
T | C | 1 | a0001c0004t0004g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.291+699T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217669782 | ||||||
| chr1:217669831
|
C | T | 6 | a0001c0001t0004g0054a0001c0001t0008g0049a0001c0001t0023g0053others(3): Show | 6 | HG01433.hp2 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.291+748C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217669831 | ||||||
| chr1:217669937
|
C | T | 1 | a0001c0002t0022g0196 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.291+854C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217669937 | ||||||
| chr1:217670232
|
T | C | 1 | a0001c0009t0001g0178 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.291+1149T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217670232 | ||||||
| chr1:217670602
|
C | T | 1 | a0001c0002t0039g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.291+1519C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217670602 | ||||||
| chr1:217670945
|
C | T | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.291+1862C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217670945 | ||||||
| chr1:217670953
|
G | GA | 69 | a0001c0001t0001g0065a0001c0001t0001g0090a0001c0001t0002g0181others(66): Show | 69 | HG00280.hp2 HG00609.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.291+1889dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217670953 | |||||
| chr1:217670969
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0005g0118 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.291+1886A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217670969 | ||||||
| chr1:217671083
|
ATGGGGAT others(16): Show |
A | 1 | a0001c0001t0004g0143 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.291+2002_291+2024d others(25): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217671083 | |||||
| chr1:217671235
|
T | C | 1 | a0001c0001t0008g0189 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.291+2152T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217671235 | ||||||
| chr1:217671503
|
A | G | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.291+2420A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217671503 | ||||||
| chr1:217671633
|
G | T | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.291+2550G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217671633 | ||||||
| chr1:217671669
|
C | T | 1 | a0001c0002t0001g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.291+2586C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217671669 | ||||||
| chr1:217671711
|
G | A | 4 | a0001c0003t0001g0220a0001c0003t0003g0097a0001c0003t0003g0221others(1): Show | 4 | HG00280.hp2 HG02735.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+2628G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217671711 | ||||||
| chr1:217672237
|
C | T | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.291+3154C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217672237 | ||||||
| chr1:217672268
|
G | A | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.291+3185G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217672268 | ||||||
| chr1:217672272
|
A | T | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+3189A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217672272 | ||||||
| chr1:217672310
|
C | T | 2 | a0001c0001t0007g0142a0001c0001t0048g0110 | 2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.291+3227C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217672310 | ||||||
| chr1:217672311
|
G | A | 1 | a0001c0001t0012g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.291+3228G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217672311 | ||||||
| chr1:217672348
|
A | G | 27 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(24): Show | 27 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.291+3265A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217672348 | ||||||
| chr1:217672361
|
C | G | 2 | a0001c0001t0002g0013a0001c0001t0010g0043 | 2 | NA18959.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.291+3278C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217672361 | ||||||
| chr1:217672521
|
C | A | 2 | a0001c0001t0016g0208a0001c0002t0001g0207 | 2 | NA18944.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.291+3438C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217672521 | ||||||
| chr1:217672539
|
TCAAAGAG others(2947): Show |
T | 1 | a0001c0001t0008g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.291+3457_291+6410d others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217672539 | ||||||
| chr1:217673043
|
C | T | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.291+3960C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217673043 | ||||||
| chr1:217673250
|
C | T | 1 | a0001c0002t0001g0132 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.291+4167C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217673250 | ||||||
| chr1:217673341
|
A | G | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.291+4258A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217673341 | ||||||
| chr1:217673406
|
G | A | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.291+4323G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217673406 | ||||||
| chr1:217673762
|
G | A | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.291+4679G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217673762 | ||||||
| chr1:217673848
|
C | A | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.291+4765C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217673848 | ||||||
| chr1:217673984
|
C | A | 1 | a0001c0002t0001g0106 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.291+4901C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217673984 | ||||||
| chr1:217674383
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.291+5300C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217674383 | ||||||
| chr1:217674630
|
T | C | 4 | a0001c0001t0001g0190a0001c0001t0008g0189a0001c0001t0012g0188others(1): Show | 4 | HG03130.hp1 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+5547T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217674630 | ||||||
| chr1:217674656
|
G | T | 1 | a0001c0001t0001g0154 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.291+5573G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217674656 | ||||||
| chr1:217674744
|
G | C | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.291+5661G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217674744 | ||||||
| chr1:217674795
|
C | T | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.291+5712C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217674795 | ||||||
| chr1:217674827
|
T | C | 1 | a0001c0003t0003g0214 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.291+5744T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217674827 | ||||||
| chr1:217674911
|
G | A | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.291+5828G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217674911 | ||||||
| chr1:217674979
|
G | T | 1 | a0001c0003t0003g0228 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.291+5896G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217674979 | ||||||
| chr1:217675053
|
C | T | 1 | a0001c0003t0003g0214 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.291+5970C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675053 | ||||||
| chr1:217675090
|
T | C | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.291+6007T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675090 | ||||||
| chr1:217675280
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.291+6197G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675280 | ||||||
| chr1:217675374
|
A | T | 1 | a0001c0001t0001g0184 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.291+6291A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675374 | ||||||
| chr1:217675387
|
C | A | 2 | a0001c0001t0015g0058a0001c0001t0015g0059 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.291+6304C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675387 | ||||||
| chr1:217675409
|
C | T | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+6326C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675409 | ||||||
| chr1:217675444
|
C | T | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.291+6361C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675444 | ||||||
| chr1:217675494
|
G | A | 1 | a0001c0001t0008g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.291+6411G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675494 | ||||||
| chr1:217675499
|
A | G | 1 | a0001c0001t0056g0075 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.291+6416A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675499 | ||||||
| chr1:217675500
|
T | A | 1 | a0001c0001t0008g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.291+6417T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675500 | ||||||
| chr1:217675505
|
G | T | 1 | a0001c0001t0008g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.291+6422G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675505 | ||||||
| chr1:217675506
|
G | T | 1 | a0001c0001t0008g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.291+6423G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675506 | ||||||
| chr1:217675507
|
T | C | 1 | a0001c0001t0008g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.291+6424T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675507 | ||||||
| chr1:217675515
|
TGTGGCTG others(2273): Show |
T | 1 | a0001c0001t0008g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.291+6434_292-5462d others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217675515 | |||||
| chr1:217675738
|
G | A | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+6655G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675738 | ||||||
| chr1:217675760
|
A | G | 1 | a0001c0002t0012g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.291+6677A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217675760 | ||||||
| chr1:217676264
|
C | G | 1 | a0001c0004t0053g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.292-6994C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217676264 | ||||||
| chr1:217676319
|
T | C | 1 | a0001c0002t0001g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.292-6939T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217676319 | ||||||
| chr1:217676335
|
G | T | 1 | a0001c0001t0056g0075 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.292-6923G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217676335 | ||||||
| chr1:217676352
|
C | A | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-6906C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217676352 | ||||||
| chr1:217676439
|
A | G | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292-6819A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217676439 | ||||||
| chr1:217676455
|
A | G | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-6803A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217676455 | ||||||
| chr1:217676570
|
A | G | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.292-6688A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217676570 | ||||||
| chr1:217676677
|
G | A | 1 | a0001c0001t0005g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.292-6581G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217676677 | ||||||
| chr1:217676894
|
T | G | 1 | a0001c0001t0046g0153 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.292-6364T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217676894 | ||||||
| chr1:217676969
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.292-6289C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217676969 | ||||||
| chr1:217677364
|
G | A | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.292-5894G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217677364 | ||||||
| chr1:217677533
|
T | G | 3 | a0003c0007t0005g0115a0003c0007t0009g0116a0003c0007t0009g0117 | 3 | HG02257.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.292-5725T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217677533 | ||||||
| chr1:217677796
|
G | C | 1 | a0001c0001t0008g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.292-5462G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217677796 | ||||||
| chr1:217677811
|
G | A | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292-5447G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217677811 | ||||||
| chr1:217677877
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.292-5381T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217677877 | ||||||
| chr1:217677899
|
G | A | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-5359G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217677899 | ||||||
| chr1:217677955
|
G | A | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-5303G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217677955 | ||||||
| chr1:217677968
|
C | T | 1 | a0001c0001t0046g0153 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.292-5290C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217677968 | ||||||
| chr1:217678073
|
T | G | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-5185T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217678073 | ||||||
| chr1:217678074
|
C | A | 1 | a0001c0001t0001g0184 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.292-5184C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217678074 | ||||||
| chr1:217678096
|
T | C | 1 | a0001c0002t0016g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.292-5162T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217678096 | ||||||
| chr1:217678205
|
C | CT | 6 | a0001c0001t0004g0069a0001c0001t0005g0052a0001c0001t0010g0029others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.292-5032dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217678205 | |||||
| chr1:217678205
|
CT | C | 10 | a0001c0001t0001g0165a0001c0001t0002g0020a0001c0001t0036g0187others(7): Show | 10 | HG00323.hp1 HG02165.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.292-5032delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217678205 | |||||
| chr1:217678210
|
T | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.292-5048T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217678210 | ||||||
| chr1:217678239
|
T | C | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-5019T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217678239 | ||||||
| chr1:217678255
|
C | T | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-5003C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217678255 | ||||||
| chr1:217678463
|
C | T | 1 | a0001c0002t0001g0144 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.292-4795C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217678463 | ||||||
| chr1:217678918
|
C | CT | 62 | a0001c0001t0001g0090a0001c0001t0002g0171a0001c0001t0005g0084others(59): Show | 62 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.292-4330dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217678918 | |||||
| chr1:217678934
|
A | C | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-4324A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217678934 | ||||||
| chr1:217679031
|
C | T | 2 | a0001c0001t0008g0045a0001c0001t0042g0035 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.292-4227C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217679031 | ||||||
| chr1:217679067
|
C | A | 69 | a0001c0001t0001g0041a0001c0001t0001g0082a0001c0001t0001g0123others(66): Show | 69 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.292-4191C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217679067 | ||||||
| chr1:217679217
|
C | G | 1 | a0001c0001t0001g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.292-4041C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217679217 | ||||||
| chr1:217679335
|
C | T | 10 | a0001c0001t0001g0065a0001c0002t0001g0064a0001c0002t0007g0051others(7): Show | 10 | HG00733.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.292-3923C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217679335 | ||||||
| chr1:217679394
|
T | C | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.292-3864T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217679394 | ||||||
| chr1:217679424
|
G | A | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-3834G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217679424 | ||||||
| chr1:217679641
|
A | G | 1 | a0001c0002t0012g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.292-3617A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217679641 | ||||||
| chr1:217679724
|
A | C | 1 | a0001c0001t0005g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.292-3534A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217679724 | ||||||
| chr1:217679767
|
A | G | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-3491A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217679767 | ||||||
| chr1:217679801
|
A | G | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-3457A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217679801 | ||||||
| chr1:217679944
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.292-3314C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217679944 | ||||||
| chr1:217679949
|
C | G | 1 | a0002c0006t0003g0014 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.292-3309C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217679949 | ||||||
| chr1:217680059
|
C | T | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.292-3199C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217680059 | ||||||
| chr1:217680123
|
C | T | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-3135C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217680123 | ||||||
| chr1:217680578
|
C | T | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.292-2680C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217680578 | ||||||
| chr1:217680896
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.292-2362G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217680896 | ||||||
| chr1:217680922
|
T | TA | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.292-2312dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217680922 | |||||
| chr1:217680922
|
T | TAA | 13 | a0001c0001t0001g0005a0001c0001t0001g0036a0001c0001t0001g0037others(10): Show | 13 | HG01106.hp1 HG01168.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.292-2313_292-2312d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217680922 | |||||
| chr1:217680922
|
TA | T | 62 | a0001c0001t0001g0146a0001c0001t0001g0154a0001c0001t0001g0164others(59): Show | 62 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.292-2312delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217680922 | |||||
| chr1:217680922
|
TAA | T | 8 | a0001c0001t0001g0163a0001c0003t0038g0244a0001c0004t0004g0240others(5): Show | 8 | HG00558.hp1 HG02615.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.292-2313_292-2312d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217680922 | |||||
| chr1:217680922
|
TAAAA | T | 5 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(2): Show | 5 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-2315_292-2312d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217680922 | |||||
| chr1:217681000
|
AG | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.292-2256delG | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217681000 | |||||
| chr1:217681055
|
C | T | 2 | a0001c0001t0015g0058a0001c0001t0015g0059 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.292-2203C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217681055 | ||||||
| chr1:217681175
|
C | T | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.292-2083C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217681175 | ||||||
| chr1:217681188
|
C | T | 1 | a0001c0001t0004g0143 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.292-2070C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217681188 | ||||||
| chr1:217681227
|
AAAAT | A | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-2011_292-2008d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217681227 | |||||
| chr1:217681275
|
T | A | 1 | a0001c0001t0001g0016 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.292-1983T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217681275 | ||||||
| chr1:217681405
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.292-1853G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217681405 | ||||||
| chr1:217681469
|
G | T | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.292-1789G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217681469 | ||||||
| chr1:217681555
|
G | A | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.292-1703G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217681555 | ||||||
| chr1:217681624
|
C | T | 1 | a0001c0002t0001g0126 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.292-1634C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217681624 | ||||||
| chr1:217681798
|
G | A | 3 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035 | 3 | HG02965.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.292-1460G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217681798 | ||||||
| chr1:217681817
|
C | T | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.292-1441C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217681817 | ||||||
| chr1:217682022
|
A | G | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-1236A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217682022 | ||||||
| chr1:217682050
|
A | G | 2 | a0001c0002t0001g0179a0001c0002t0001g0180 | 2 | NA18968.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.292-1208A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217682050 | ||||||
| chr1:217682057
|
A | G | 1 | a0002c0006t0001g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.292-1201A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217682057 | ||||||
| chr1:217682095
|
C | T | 3 | a0001c0002t0007g0051a0001c0002t0007g0067a0001c0002t0019g0066 | 3 | HG02280.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.292-1163C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217682095 | ||||||
| chr1:217682163
|
G | A | 2 | a0001c0003t0024g0243a0001c0003t0038g0244 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.292-1095G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217682163 | ||||||
| chr1:217682364
|
CA | C | 12 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(9): Show | 12 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.292-881delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217682364 | |||||
| chr1:217682672
|
T | C | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.292-586T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217682672 | ||||||
| chr1:217682761
|
GTTA | G | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-494_292-492del others(3): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217682761 | |||||
| chr1:217682943
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.292-315C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217682943 | ||||||
| chr1:217683062
|
TTA | T | 4 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035others(1): Show | 4 | HG02965.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-194_292-193del others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 217683062 | |||||
| chr1:217683063
|
TA | T | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.292-194delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217683063 | ||||||
| chr1:217683091
|
A | G | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.292-167A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 4/10 | chr1 | 217683091 | ||||||
| chr1:217683445
|
A | AT | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.395+91dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217683445 | |||||
| chr1:217683461
|
T | C | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.395+100T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217683461 | ||||||
| chr1:217683512
|
C | T | 1 | a0001c0001t0056g0075 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.395+151C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217683512 | ||||||
| chr1:217683561
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010 | 3 | HG01070.hp2 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.395+200C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217683561 | ||||||
| chr1:217683588
|
G | A | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.395+227G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217683588 | ||||||
| chr1:217683631
|
G | A | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.395+270G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217683631 | ||||||
| chr1:217683701
|
A | G | 1 | a0001c0001t0002g0039 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.395+340A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217683701 | ||||||
| chr1:217683720
|
G | A | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.395+359G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217683720 | ||||||
| chr1:217683765
|
T | C | 1 | a0001c0001t0002g0001 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.395+404T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217683765 | ||||||
| chr1:217683903
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.395+542G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217683903 | ||||||
| chr1:217684186
|
C | T | 2 | a0001c0001t0015g0058a0001c0001t0015g0059 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.395+825C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217684186 | ||||||
| chr1:217684241
|
T | C | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.395+880T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217684241 | ||||||
| chr1:217684358
|
A | T | 1 | a0001c0012t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.395+997A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217684358 | ||||||
| chr1:217684372
|
C | T | 3 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0010g0157 | 3 | HG00733.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.395+1011C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217684372 | ||||||
| chr1:217684438
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.395+1077G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217684438 | ||||||
| chr1:217684456
|
G | T | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.395+1095G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217684456 | ||||||
| chr1:217684597
|
T | C | 1 | a0001c0002t0001g0104 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.395+1236T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217684597 | ||||||
| chr1:217684668
|
G | A | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+1307G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217684668 | ||||||
| chr1:217684708
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.395+1347G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217684708 | ||||||
| chr1:217684842
|
A | G | 3 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035 | 3 | HG02965.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.395+1481A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217684842 | ||||||
| chr1:217684897
|
T | A | 1 | a0001c0002t0049g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.395+1536T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217684897 | ||||||
| chr1:217684961
|
C | T | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.395+1600C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217684961 | ||||||
| chr1:217685063
|
C | CTGGCTGG others(11): Show |
61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.395+1708_395+1709i others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217685063 | |||||
| chr1:217685082
|
C | G | 1 | a0001c0001t0001g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.395+1721C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217685082 | ||||||
| chr1:217685098
|
T | C | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+1737T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217685098 | ||||||
| chr1:217685194
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.395+1833C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217685194 | ||||||
| chr1:217685640
|
A | T | 1 | a0001c0002t0014g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.395+2279A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217685640 | ||||||
| chr1:217685739
|
T | C | 1 | a0001c0002t0001g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.395+2378T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217685739 | ||||||
| chr1:217685753
|
G | A | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.395+2392G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217685753 | ||||||
| chr1:217685842
|
C | A | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+2481C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217685842 | ||||||
| chr1:217685898
|
A | G | 7 | a0001c0003t0003g0214a0001c0003t0003g0217a0001c0003t0003g0223others(4): Show | 7 | HG00609.hp1 HG02165.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+2537A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217685898 | ||||||
| chr1:217685966
|
A | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.395+2605A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217685966 | ||||||
| chr1:217686000
|
G | GGTAT | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+2649_395+2652d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217686000 | |||||
| chr1:217686125
|
T | C | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+2764T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217686125 | ||||||
| chr1:217686381
|
C | A | 50 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(47): Show | 50 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.395+3020C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217686381 | ||||||
| chr1:217686385
|
T | A | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+3024T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217686385 | ||||||
| chr1:217686539
|
TTTAAC | T | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+3182_395+3186d others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217686539 | |||||
| chr1:217686591
|
C | T | 1 | a0001c0008t0051g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.395+3230C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217686591 | ||||||
| chr1:217687056
|
A | G | 3 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035 | 3 | HG02965.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.395+3695A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217687056 | ||||||
| chr1:217687088
|
T | C | 1 | a0001c0002t0016g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.395+3727T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217687088 | ||||||
| chr1:217687103
|
C | T | 1 | a0001c0002t0011g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.395+3742C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217687103 | ||||||
| chr1:217687263
|
AT | A | 3 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093 | 3 | HG02559.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.395+3908delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217687263 | |||||
| chr1:217687296
|
A | G | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.395+3935A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217687296 | ||||||
| chr1:217687558
|
A | G | 2 | a0001c0001t0001g0065a0001c0002t0001g0064 | 2 | HG00733.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.395+4197A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217687558 | ||||||
| chr1:217687604
|
T | C | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.395+4243T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217687604 | ||||||
| chr1:217687888
|
T | C | 1 | a0001c0001t0005g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.395+4527T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217687888 | ||||||
| chr1:217688016
|
G | A | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+4655G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217688016 | ||||||
| chr1:217688051
|
T | C | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.395+4690T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217688051 | ||||||
| chr1:217688124
|
G | C | 1 | a0001c0004t0004g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.395+4763G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217688124 | ||||||
| chr1:217688261
|
A | AT | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+4906dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217688261 | |||||
| chr1:217688268
|
A | T | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+4907A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217688268 | ||||||
| chr1:217688283
|
A | C | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+4922A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217688283 | ||||||
| chr1:217688335
|
A | G | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+4974A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217688335 | ||||||
| chr1:217688563
|
T | G | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+5202T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217688563 | ||||||
| chr1:217688568
|
T | C | 50 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(47): Show | 50 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.395+5207T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217688568 | ||||||
| chr1:217688589
|
T | A | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+5228T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217688589 | ||||||
| chr1:217688737
|
T | C | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.395+5376T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217688737 | ||||||
| chr1:217688879
|
TG | T | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+5519delG | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217688879 | ||||||
| chr1:217688885
|
CT | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+5525delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217688885 | ||||||
| chr1:217688985
|
C | G | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+5624C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217688985 | ||||||
| chr1:217689032
|
G | C | 1 | a0001c0001t0001g0166 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.395+5671G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217689032 | ||||||
| chr1:217689135
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0041g0015others(1): Show | 4 | NA18951.hp2 NA18984.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.395+5774G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217689135 | ||||||
| chr1:217689139
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.395+5778C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217689139 | ||||||
| chr1:217689140
|
G | A | 1 | a0001c0002t0007g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.395+5779G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217689140 | ||||||
| chr1:217689221
|
C | CT | 136 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.395+5882dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217689221 | |||||
| chr1:217689221
|
C | CTT | 14 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0081others(11): Show | 14 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.395+5881_395+5882d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217689221 | |||||
| chr1:217689221
|
C | CTTTTT | 6 | a0001c0001t0001g0209a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 6 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.395+5878_395+5882d others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217689221 | |||||
| chr1:217689221
|
CTTTTTTT | C | 43 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(40): Show | 43 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.395+5876_395+5882d others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217689221 | |||||
| chr1:217689502
|
A | G | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+6141A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217689502 | ||||||
| chr1:217689537
|
C | T | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+6176C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217689537 | ||||||
| chr1:217689943
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0005g0118 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.395+6582G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217689943 | ||||||
| chr1:217689957
|
G | A | 1 | a0001c0001t0008g0189 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.395+6596G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217689957 | ||||||
| chr1:217689985
|
T | C | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+6624T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217689985 | ||||||
| chr1:217689986
|
C | A | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.395+6625C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217689986 | ||||||
| chr1:217689989
|
C | T | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+6628C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217689989 | ||||||
| chr1:217690041
|
G | T | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.395+6680G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217690041 | ||||||
| chr1:217690103
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0002g0171 | 2 | NA18939.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.395+6742A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217690103 | ||||||
| chr1:217690109
|
G | T | 14 | a0001c0001t0004g0054a0001c0001t0008g0049a0001c0001t0023g0053others(11): Show | 14 | HG00140.hp2 HG00639.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.395+6748G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217690109 | ||||||
| chr1:217690332
|
G | C | 2 | a0001c0003t0024g0243a0001c0003t0038g0244 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.395+6971G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217690332 | ||||||
| chr1:217690365
|
C | T | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.395+7004C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217690365 | ||||||
| chr1:217690473
|
AT | A | 68 | a0001c0001t0001g0041a0001c0001t0001g0123a0001c0001t0001g0130others(65): Show | 68 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.395+7126delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217690473 | |||||
| chr1:217690473
|
ATT | A | 7 | a0001c0001t0001g0082a0001c0001t0001g0163a0001c0001t0001g0175others(4): Show | 7 | HG00438.hp2 HG00558.hp1 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.395+7125_395+7126d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217690473 | |||||
| chr1:217690479
|
T | TA | 146 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.395+7118_395+7119i others(3): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217690479 | ||||||
| chr1:217690481
|
T | G | 1 | a0001c0001t0001g0182 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.395+7120T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217690481 | ||||||
| chr1:217690505
|
A | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0081 | 3 | HG01952.hp2 HG02129.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.395+7144A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217690505 | ||||||
| chr1:217690577
|
G | A | 30 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.395+7216G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217690577 | ||||||
| chr1:217690909
|
T | C | 1 | a0001c0003t0003g0098 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.395+7548T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217690909 | ||||||
| chr1:217690948
|
G | A | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.395+7587G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217690948 | ||||||
| chr1:217690993
|
G | C | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+7632G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217690993 | ||||||
| chr1:217691053
|
A | G | 2 | a0001c0003t0003g0222a0001c0003t0003g0228 | 2 | NA18957.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.395+7692A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691053 | ||||||
| chr1:217691176
|
A | G | 1 | a0001c0002t0014g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.395+7815A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691176 | ||||||
| chr1:217691202
|
T | C | 3 | a0001c0001t0004g0069a0001c0001t0005g0052a0001c0001t0005g0068 | 3 | HG02055.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.395+7841T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691202 | ||||||
| chr1:217691240
|
G | A | 5 | a0001c0005t0001g0141a0001c0005t0001g0192a0001c0005t0004g0071others(2): Show | 5 | HG01261.hp1 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+7879G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691240 | ||||||
| chr1:217691258
|
T | C | 1 | a0001c0002t0049g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.395+7897T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691258 | ||||||
| chr1:217691316
|
T | C | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.395+7955T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691316 | ||||||
| chr1:217691334
|
G | T | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+7973G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691334 | ||||||
| chr1:217691339
|
A | T | 251 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.395+7978A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691339 | ||||||
| chr1:217691482
|
C | G | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+8121C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691482 | ||||||
| chr1:217691544
|
T | G | 4 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035others(1): Show | 4 | HG02965.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.395+8183T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691544 | ||||||
| chr1:217691646
|
C | G | 1 | a0001c0001t0035g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.395+8285C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691646 | ||||||
| chr1:217691658
|
G | T | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+8297G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691658 | ||||||
| chr1:217691707
|
A | G | 5 | a0001c0005t0001g0141a0001c0005t0001g0192a0001c0005t0004g0071others(2): Show | 5 | HG01261.hp1 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+8346A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691707 | ||||||
| chr1:217691957
|
T | C | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+8596T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217691957 | ||||||
| chr1:217692247
|
G | C | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+8886G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217692247 | ||||||
| chr1:217692366
|
G | T | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+9005G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217692366 | ||||||
| chr1:217692395
|
A | AGACGATG others(2443): Show |
1 | a0001c0001t0015g0093 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.395+9050_395+9051i others(2452): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217692395 | |||||
| chr1:217692395
|
A | AGACGATG others(2437): Show |
1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.395+9050_395+9051i others(2446): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217692395 | |||||
| chr1:217692395
|
A | AGACGATG others(2444): Show |
2 | a0001c0001t0001g0090a0001c0001t0005g0089 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.395+9050_395+9051i others(2453): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217692395 | |||||
| chr1:217692395
|
A | AGACGATG others(2455): Show |
1 | a0004c0013t0033g0095 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.395+9050_395+9051i others(2464): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217692395 | |||||
| chr1:217692395
|
A | AGACGATG others(2452): Show |
1 | a0001c0002t0044g0091 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.395+9050_395+9051i others(2461): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217692395 | |||||
| chr1:217692399
|
G | A | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.395+9038G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217692399 | ||||||
| chr1:217692661
|
G | T | 5 | a0001c0001t0058g0150a0001c0002t0001g0149a0001c0002t0017g0151others(2): Show | 5 | HG03831.hp2 NA18946.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.395+9300G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217692661 | ||||||
| chr1:217692808
|
T | C | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+9447T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217692808 | ||||||
| chr1:217692881
|
G | T | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.395+9520G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217692881 | ||||||
| chr1:217692962
|
T | G | 1 | a0001c0004t0053g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.395+9601T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217692962 | ||||||
| chr1:217692997
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.395+9636T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217692997 | ||||||
| chr1:217693307
|
A | G | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+9946A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693307 | ||||||
| chr1:217693340
|
C | T | 1 | a0001c0004t0052g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.395+9979C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693340 | ||||||
| chr1:217693401
|
G | T | 24 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0003g0097others(21): Show | 24 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.395+10040G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693401 | ||||||
| chr1:217693407
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.395+10046G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693407 | ||||||
| chr1:217693500
|
G | T | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+10139G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693500 | ||||||
| chr1:217693515
|
A | G | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.395+10154A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693515 | ||||||
| chr1:217693556
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.395+10195C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693556 | ||||||
| chr1:217693585
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.395+10224C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693585 | ||||||
| chr1:217693586
|
G | T | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+10225G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693586 | ||||||
| chr1:217693666
|
C | T | 10 | a0001c0001t0001g0065a0001c0002t0001g0064a0001c0002t0007g0051others(7): Show | 10 | HG00733.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.395+10305C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693666 | ||||||
| chr1:217693667
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.395+10306G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693667 | ||||||
| chr1:217693797
|
C | T | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.395+10436C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693797 | ||||||
| chr1:217693878
|
C | T | 19 | a0001c0001t0016g0172a0001c0002t0001g0083a0001c0002t0001g0103others(16): Show | 19 | HG00438.hp1 HG00558.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.395+10517C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693878 | ||||||
| chr1:217693940
|
G | T | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+10579G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217693940 | ||||||
| chr1:217694009
|
C | T | 1 | a0001c0001t0012g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.395+10648C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694009 | ||||||
| chr1:217694010
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.395+10649G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694010 | ||||||
| chr1:217694055
|
G | T | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+10694G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694055 | ||||||
| chr1:217694099
|
G | A | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+10738G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694099 | ||||||
| chr1:217694114
|
T | G | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+10753T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694114 | ||||||
| chr1:217694185
|
G | T | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+10824G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694185 | ||||||
| chr1:217694190
|
T | C | 1 | a0001c0003t0003g0224 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.395+10829T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694190 | ||||||
| chr1:217694339
|
G | T | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.395+10978G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694339 | ||||||
| chr1:217694393
|
C | T | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+11032C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694393 | ||||||
| chr1:217694434
|
G | C | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+11073G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694434 | ||||||
| chr1:217694473
|
G | C | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.395+11112G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694473 | ||||||
| chr1:217694763
|
G | T | 1 | a0001c0004t0053g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.395+11402G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694763 | ||||||
| chr1:217694772
|
G | C | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+11411G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694772 | ||||||
| chr1:217694917
|
C | T | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+11556C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217694917 | ||||||
| chr1:217695013
|
G | T | 1 | a0001c0002t0016g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.395+11652G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695013 | ||||||
| chr1:217695111
|
G | A | 1 | a0001c0004t0004g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.395+11750G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695111 | ||||||
| chr1:217695188
|
A | G | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.395+11827A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695188 | ||||||
| chr1:217695285
|
C | A | 5 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.395+11924C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695285 | ||||||
| chr1:217695351
|
T | C | 2 | a0001c0003t0024g0243a0001c0003t0038g0244 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.395+11990T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695351 | ||||||
| chr1:217695359
|
C | T | 1 | a0001c0002t0011g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.395+11998C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695359 | ||||||
| chr1:217695383
|
T | G | 1 | a0001c0001t0001g0004 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.395+12022T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695383 | ||||||
| chr1:217695468
|
C | T | 3 | a0001c0001t0005g0084a0001c0002t0044g0091a0004c0013t0033g0095 | 3 | HG01168.hp1 HG03453.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.395+12107C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695468 | ||||||
| chr1:217695637
|
G | C | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+12276G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695637 | ||||||
| chr1:217695767
|
G | C | 1 | a0001c0003t0031g0225 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.395+12406G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695767 | ||||||
| chr1:217695774
|
T | C | 1 | a0001c0003t0031g0225 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.395+12413T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695774 | ||||||
| chr1:217695805
|
G | A | 7 | a0001c0001t0001g0154a0001c0001t0002g0101a0001c0001t0002g0158others(4): Show | 7 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.395+12444G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695805 | ||||||
| chr1:217695811
|
CA | C | 6 | a0001c0001t0002g0101a0001c0001t0002g0158a0001c0001t0002g0159others(3): Show | 6 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+12451delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695811 | ||||||
| chr1:217695815
|
A | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(213): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.395+12454A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695815 | ||||||
| chr1:217695817
|
T | C | 2 | a0001c0001t0024g0040a0001c0003t0031g0225 | 2 | HG03453.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.395+12456T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695817 | ||||||
| chr1:217695826
|
C | A | 1 | a0001c0001t0056g0075 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.395+12465C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695826 | ||||||
| chr1:217695833
|
G | A | 2 | a0001c0001t0024g0040a0001c0003t0031g0225 | 2 | HG03453.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.395+12472G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695833 | ||||||
| chr1:217695847
|
C | T | 1 | a0001c0003t0031g0225 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.395+12486C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695847 | ||||||
| chr1:217695872
|
T | C | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.395+12511T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695872 | ||||||
| chr1:217695936
|
C | T | 1 | a0001c0001t0005g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.395+12575C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695936 | ||||||
| chr1:217695962
|
C | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.395+12601C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695962 | ||||||
| chr1:217695971
|
G | T | 1 | a0001c0001t0001g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.395+12610G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695971 | ||||||
| chr1:217695998
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.395+12637C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217695998 | ||||||
| chr1:217696036
|
T | C | 2 | a0001c0001t0001g0165a0001c0002t0005g0056 | 2 | HG02257.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.395+12675T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696036 | ||||||
| chr1:217696090
|
G | A | 69 | a0001c0001t0001g0082a0001c0001t0001g0123a0001c0001t0001g0130others(66): Show | 69 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.395+12729G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696090 | ||||||
| chr1:217696102
|
C | G | 1 | a0001c0001t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.395+12741C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696102 | ||||||
| chr1:217696149
|
C | T | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.395+12788C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696149 | ||||||
| chr1:217696152
|
G | C | 2 | a0001c0004t0027g0237a0001c0004t0053g0239 | 2 | HG01891.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.395+12791G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696152 | ||||||
| chr1:217696243
|
G | A | 14 | a0001c0001t0004g0054a0001c0001t0008g0049a0001c0001t0023g0053others(11): Show | 14 | HG00140.hp2 HG00639.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.395+12882G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696243 | ||||||
| chr1:217696264
|
G | A | 3 | a0001c0001t0008g0049a0001c0002t0009g0076a0001c0002t0026g0048 | 3 | HG01433.hp2 HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.395+12903G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696264 | ||||||
| chr1:217696324
|
T | C | 1 | a0001c0005t0023g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.395+12963T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696324 | ||||||
| chr1:217696349
|
G | T | 1 | a0001c0001t0023g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.395+12988G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696349 | ||||||
| chr1:217696416
|
C | T | 4 | a0001c0002t0005g0078a0001c0002t0012g0077a0001c0002t0012g0080others(1): Show | 4 | HG00140.hp2 HG00639.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.395+13055C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696416 | ||||||
| chr1:217696447
|
C | T | 1 | a0001c0001t0058g0150 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.395+13086C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696447 | ||||||
| chr1:217696448
|
G | T | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.395+13087G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696448 | ||||||
| chr1:217696459
|
C | A | 1 | a0001c0002t0021g0160 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.395+13098C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696459 | ||||||
| chr1:217696464
|
C | T | 7 | a0001c0002t0007g0051a0001c0002t0007g0060a0001c0002t0007g0061others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.395+13103C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696464 | ||||||
| chr1:217696488
|
A | G | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.395+13127A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696488 | ||||||
| chr1:217696504
|
A | G | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.395+13143A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696504 | ||||||
| chr1:217696627
|
T | C | 2 | a0001c0001t0002g0026a0001c0001t0002g0032 | 2 | HG02015.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.395+13266T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696627 | ||||||
| chr1:217696696
|
C | A | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+13335C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696696 | ||||||
| chr1:217696915
|
A | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0033 | 2 | HG02004.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.395+13554A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217696915 | ||||||
| chr1:217697087
|
C | A | 1 | a0001c0001t0011g0227 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.395+13726C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217697087 | ||||||
| chr1:217697135
|
C | T | 1 | a0001c0002t0030g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.395+13774C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217697135 | ||||||
| chr1:217697267
|
C | G | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+13906C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217697267 | ||||||
| chr1:217697628
|
T | C | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.395+14267T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217697628 | ||||||
| chr1:217697861
|
A | G | 3 | a0001c0002t0007g0051a0001c0002t0007g0067a0001c0002t0019g0066 | 3 | HG02280.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.395+14500A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217697861 | ||||||
| chr1:217698158
|
G | C | 2 | a0001c0001t0020g0094a0001c0001t0035g0085 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.395+14797G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217698158 | ||||||
| chr1:217698163
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.395+14802G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217698163 | ||||||
| chr1:217698319
|
A | G | 1 | a0001c0002t0013g0121 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.395+14958A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217698319 | ||||||
| chr1:217698539
|
G | A | 55 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.395+15178G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217698539 | ||||||
| chr1:217698579
|
TA | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.395+15233delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217698579 | |||||
| chr1:217698579
|
TAA | T | 55 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.395+15232_395+1523 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217698579 | |||||
| chr1:217698673
|
A | G | 1 | a0001c0008t0014g0213 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.395+15312A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217698673 | ||||||
| chr1:217698722
|
G | A | 11 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(8): Show | 11 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+15361G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217698722 | ||||||
| chr1:217698854
|
C | T | 1 | a0001c0002t0007g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.395+15493C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217698854 | ||||||
| chr1:217698856
|
C | A | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+15495C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217698856 | ||||||
| chr1:217698908
|
C | A | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.395+15547C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217698908 | ||||||
| chr1:217699131
|
A | G | 27 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(24): Show | 27 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.395+15770A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217699131 | ||||||
| chr1:217699405
|
G | A | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+16044G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217699405 | ||||||
| chr1:217699436
|
T | C | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+16075T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217699436 | ||||||
| chr1:217699468
|
A | C | 1 | a0001c0001t0002g0171 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.395+16107A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217699468 | ||||||
| chr1:217699664
|
A | G | 1 | a0001c0002t0022g0196 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.395+16303A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217699664 | ||||||
| chr1:217699840
|
C | G | 1 | a0001c0002t0021g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.395+16479C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217699840 | ||||||
| chr1:217700077
|
C | A | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.395+16716C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217700077 | ||||||
| chr1:217700084
|
G | A | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+16723G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217700084 | ||||||
| chr1:217700762
|
C | CT | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.395+17416dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217700762 | |||||
| chr1:217700762
|
C | CTT | 63 | a0001c0001t0001g0065a0001c0001t0001g0090a0001c0001t0001g0209others(60): Show | 63 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.395+17415_395+1741 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217700762 | |||||
| chr1:217700762
|
C | T | 1 | a0001c0002t0044g0091 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.395+17401C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217700762 | ||||||
| chr1:217701017
|
C | G | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+17656C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701017 | ||||||
| chr1:217701047
|
T | G | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+17686T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701047 | ||||||
| chr1:217701071
|
T | C | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.395+17710T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701071 | ||||||
| chr1:217701097
|
G | C | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.395+17736G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701097 | ||||||
| chr1:217701119
|
C | T | 30 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.395+17758C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701119 | ||||||
| chr1:217701166
|
G | C | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+17805G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701166 | ||||||
| chr1:217701218
|
G | A | 1 | a0001c0001t0010g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.395+17857G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701218 | ||||||
| chr1:217701232
|
C | T | 2 | a0001c0004t0004g0240a0001c0004t0008g0241 | 2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.395+17871C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701232 | ||||||
| chr1:217701286
|
G | T | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+17925G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701286 | ||||||
| chr1:217701301
|
A | ATG | 8 | a0001c0001t0001g0090a0001c0001t0001g0119a0001c0001t0005g0084others(5): Show | 8 | HG01109.hp2 HG01168.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.395+17956_395+1795 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217701301 | |||||
| chr1:217701319
|
ATATATAT others(5): Show |
A | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.395+17972_395+1798 others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217701319 | |||||
| chr1:217701355
|
A | C | 1 | a0001c0001t0002g0020 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.395+17994A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701355 | ||||||
| chr1:217701500
|
C | T | 1 | a0001c0008t0051g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.395+18139C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701500 | ||||||
| chr1:217701504
|
A | G | 1 | a0001c0008t0051g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.395+18143A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701504 | ||||||
| chr1:217701505
|
T | C | 1 | a0001c0008t0051g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.395+18144T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701505 | ||||||
| chr1:217701530
|
C | T | 1 | a0001c0003t0003g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.395+18169C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701530 | ||||||
| chr1:217701682
|
T | A | 1 | a0001c0001t0001g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.395+18321T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701682 | ||||||
| chr1:217701733
|
A | G | 1 | a0001c0002t0005g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.395+18372A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701733 | ||||||
| chr1:217701802
|
C | T | 11 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(8): Show | 11 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.395+18441C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701802 | ||||||
| chr1:217701877
|
T | C | 1 | a0001c0002t0039g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.395+18516T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701877 | ||||||
| chr1:217701990
|
CTT | C | 4 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035others(1): Show | 4 | HG02965.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.395+18630_395+1863 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217701990 | ||||||
| chr1:217702032
|
G | GTA | 69 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.395+18689_395+1869 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217702032 | |||||
| chr1:217702032
|
G | GTATA | 36 | a0001c0001t0001g0065a0001c0001t0002g0007a0001c0001t0004g0054others(33): Show | 36 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.395+18687_395+1869 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217702032 | |||||
| chr1:217702032
|
G | GTATATA | 4 | a0001c0001t0004g0069a0001c0001t0024g0040a0001c0002t0012g0018others(1): Show | 4 | HG01167.hp2 HG02055.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.395+18685_395+1869 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217702032 | |||||
| chr1:217702097
|
G | A | 3 | a0001c0001t0006g0201a0001c0001t0006g0202a0001c0001t0006g0203 | 3 | HG01074.hp1 HG01099.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.395+18736G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217702097 | ||||||
| chr1:217702175
|
T | C | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+18814T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217702175 | ||||||
| chr1:217702195
|
T | C | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+18834T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217702195 | ||||||
| chr1:217702371
|
A | G | 27 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(24): Show | 27 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.395+19010A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217702371 | ||||||
| chr1:217702383
|
G | T | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.395+19022G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217702383 | ||||||
| chr1:217702745
|
G | A | 1 | a0001c0001t0008g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.395+19384G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217702745 | ||||||
| chr1:217702810
|
C | A | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.395+19449C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217702810 | ||||||
| chr1:217702811
|
G | A | 1 | a0001c0002t0014g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.395+19450G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217702811 | ||||||
| chr1:217702939
|
A | T | 1 | a0001c0002t0005g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.395+19578A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217702939 | ||||||
| chr1:217702950
|
C | T | 8 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | NA18612.hp1 NA18941.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.395+19589C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217702950 | ||||||
| chr1:217703097
|
A | G | 1 | a0001c0004t0008g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.395+19736A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217703097 | ||||||
| chr1:217703121
|
C | T | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+19760C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217703121 | ||||||
| chr1:217703173
|
C | CATTTTTT others(5): Show |
1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.395+19812_395+1981 others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217703173 | ||||||
| chr1:217703174
|
C | CTTT | 5 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(2): Show | 5 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+19825_395+1982 others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217703174 | |||||
| chr1:217703174
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0209a0001c0001t0006g0201a0001c0001t0006g0202others(1): Show | 4 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.395+19817_395+1982 others(15): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217703174 | |||||
| chr1:217703174
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0006g0096a0001c0001t0006g0203a0001c0001t0006g0204others(2): Show | 5 | HG01981.hp1 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.395+19816_395+1982 others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217703174 | |||||
| chr1:217703174
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0042g0035 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.395+19815_395+1982 others(17): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217703174 | |||||
| chr1:217703174
|
C | CTTTTTTT others(7): Show |
2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.395+19814_395+1982 others(18): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217703174 | |||||
| chr1:217703174
|
C | CTTTTTTT others(8): Show |
31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.395+19827_395+1982 others(19): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217703174 | |||||
| chr1:217703174
|
C | CTTTTTTT others(9): Show |
10 | a0001c0003t0003g0098a0001c0003t0003g0224a0001c0003t0003g0235others(7): Show | 10 | HG01109.hp1 HG01361.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.395+19827_395+1982 others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217703174 | |||||
| chr1:217703174
|
C | CTTTTTTT others(10): Show |
1 | a0001c0003t0003g0226 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.395+19827_395+1982 others(21): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217703174 | |||||
| chr1:217703174
|
C | T | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.395+19813C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217703174 | ||||||
| chr1:217703201
|
C | G | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+19840C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217703201 | ||||||
| chr1:217703423
|
TGGCCTCC others(1071): Show |
T | 1 | a0001c0001t0001g0209 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.395+20095_395+2117 others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217703423 | |||||
| chr1:217703525
|
G | A | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.395+20164G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217703525 | ||||||
| chr1:217703713
|
C | T | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+20352C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217703713 | ||||||
| chr1:217703889
|
C | T | 1 | a0001c0002t0039g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.395+20528C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217703889 | ||||||
| chr1:217704082
|
T | TTTATC | 54 | a0001c0001t0006g0096a0001c0001t0006g0201a0001c0001t0006g0202others(51): Show | 54 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.395+20724_395+2072 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704082 | |||||
| chr1:217704115
|
A | G | 1 | a0001c0002t0001g0112 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.395+20754A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217704115 | ||||||
| chr1:217704196
|
G | GT | 7 | a0001c0003t0003g0214a0001c0003t0003g0217a0001c0003t0003g0223others(4): Show | 7 | HG00609.hp1 HG02165.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+20842dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704196 | |||||
| chr1:217704230
|
C | CT | 44 | a0001c0001t0001g0090a0001c0001t0001g0135a0001c0001t0001g0140others(41): Show | 44 | HG00280.hp1 HG00609.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.395+20900dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704230
|
C | CTT | 31 | a0001c0001t0001g0082a0001c0001t0001g0130a0001c0001t0001g0146others(28): Show | 31 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.395+20899_395+2090 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704230
|
C | CTTT | 16 | a0001c0001t0001g0002a0001c0001t0004g0054a0001c0001t0008g0049others(13): Show | 16 | HG01168.hp1 HG01361.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.395+20898_395+2090 others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704230
|
C | CTTTT | 23 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0021others(20): Show | 23 | HG00140.hp1 HG00738.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.395+20897_395+2090 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704230
|
C | CTTTTT | 32 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(29): Show | 32 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.395+20896_395+2090 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704230
|
C | CTTTTTT | 13 | a0001c0001t0001g0016a0001c0001t0001g0037a0001c0001t0001g0046others(10): Show | 13 | HG00323.hp1 HG00639.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.395+20895_395+2090 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704230
|
C | CTTTTTTT | 7 | a0001c0001t0008g0045a0001c0001t0015g0059a0001c0001t0024g0040others(4): Show | 7 | HG02486.hp2 HG02965.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+20894_395+2090 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704230
|
C | CTTTTTTT others(1): Show |
7 | a0001c0001t0002g0033a0001c0001t0006g0201a0001c0001t0006g0202others(4): Show | 7 | HG00140.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+20893_395+2090 others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704230
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0006g0205 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.395+20891_395+2090 others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704230
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0006g0096 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.395+20890_395+2090 others(15): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704230
|
CT | C | 10 | a0001c0002t0001g0128a0001c0003t0038g0244a0001c0004t0004g0247others(7): Show | 10 | HG02486.hp1 HG02976.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.395+20900delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704230
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0002g0006a0001c0001t0010g0043 | 2 | NA18959.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.395+20891_395+2090 others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704230
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0039 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.395+20888_395+2090 others(17): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704230
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0004t0004g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.395+20880_395+2090 others(25): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217704230 | |||||
| chr1:217704262
|
G | T | 1 | a0001c0004t0053g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.395+20901G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217704262 | ||||||
| chr1:217704283
|
G | A | 1 | a0001c0001t0056g0075 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.395+20922G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217704283 | ||||||
| chr1:217704336
|
C | T | 4 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035others(1): Show | 4 | HG02965.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.395+20975C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217704336 | ||||||
| chr1:217704411
|
C | T | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.395+21050C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217704411 | ||||||
| chr1:217704539
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.395+21178C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217704539 | ||||||
| chr1:217704540
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.395+21179G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217704540 | ||||||
| chr1:217704559
|
A | G | 1 | a0001c0001t0009g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.395+21198A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217704559 | ||||||
| chr1:217704614
|
A | G | 1 | a0001c0001t0002g0181 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.395+21253A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217704614 | ||||||
| chr1:217704671
|
G | T | 1 | a0001c0002t0009g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.395+21310G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217704671 | ||||||
| chr1:217704859
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.395+21498G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217704859 | ||||||
| chr1:217704997
|
C | T | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.395+21636C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217704997 | ||||||
| chr1:217705262
|
C | G | 55 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.395+21901C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217705262 | ||||||
| chr1:217705334
|
TTC | T | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+21974_395+2197 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217705334 | ||||||
| chr1:217705338
|
T | TGCATCTA others(22): Show |
7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+21977_395+2197 others(33): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217705338 | ||||||
| chr1:217705430
|
C | CT | 103 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.395+22097dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217705430 | |||||
| chr1:217705430
|
C | CTT | 24 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0130others(21): Show | 24 | HG00642.hp2 HG01106.hp1 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.395+22096_395+2209 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217705430 | |||||
| chr1:217705430
|
C | CTTT | 20 | a0001c0001t0001g0011a0001c0001t0010g0156a0001c0003t0001g0215others(17): Show | 20 | HG00280.hp2 HG00609.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.395+22095_395+2209 others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217705430 | |||||
| chr1:217705430
|
C | CTTTT | 8 | a0001c0001t0001g0024a0001c0003t0003g0098a0001c0003t0003g0222others(5): Show | 8 | HG01109.hp1 HG01361.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.395+22094_395+2209 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217705430 | |||||
| chr1:217705430
|
C | CTTTTTTT others(3): Show |
2 | a0001c0004t0004g0073a0001c0004t0053g0239 | 2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.395+22088_395+2209 others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217705430 | |||||
| chr1:217705430
|
C | CTTTTTTT others(8): Show |
1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.395+22083_395+2209 others(19): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217705430 | |||||
| chr1:217705430
|
CT | C | 8 | a0001c0001t0001g0123a0001c0001t0006g0201a0001c0001t0016g0172others(5): Show | 8 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(5): Show |
intron_variant | MODIFIER | c.395+22097delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217705430 | |||||
| chr1:217705430
|
CTT | C | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0202others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+22096_395+2209 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217705430 | |||||
| chr1:217705430
|
CTTT | C | 16 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035others(13): Show | 16 | HG02572.hp2 HG02622.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.395+22095_395+2209 others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217705430 | |||||
| chr1:217705472
|
C | T | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+22111C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217705472 | ||||||
| chr1:217705489
|
G | C | 1 | a0001c0002t0001g0128 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.395+22128G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217705489 | ||||||
| chr1:217705490
|
G | C | 4 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035others(1): Show | 4 | HG02965.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.395+22129G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217705490 | ||||||
| chr1:217705788
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.395+22427T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217705788 | ||||||
| chr1:217705809
|
A | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(213): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.395+22448A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217705809 | ||||||
| chr1:217706109
|
T | C | 1 | a0001c0002t0001g0129 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.395+22748T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217706109 | ||||||
| chr1:217706120
|
T | C | 1 | a0001c0002t0010g0125 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.395+22759T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217706120 | ||||||
| chr1:217706514
|
A | G | 2 | a0001c0001t0020g0094a0001c0001t0035g0085 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.395+23153A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217706514 | ||||||
| chr1:217706641
|
A | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.395+23280A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217706641 | ||||||
| chr1:217706651
|
C | T | 30 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.395+23290C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217706651 | ||||||
| chr1:217706723
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.395+23362G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217706723 | ||||||
| chr1:217706872
|
CT | C | 23 | a0001c0001t0005g0084a0001c0001t0008g0045a0001c0001t0008g0049others(20): Show | 23 | HG01433.hp2 HG02055.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.395+23523delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217706872 | |||||
| chr1:217706872
|
CTT | C | 43 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0089others(40): Show | 43 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.395+23522_395+2352 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217706872 | |||||
| chr1:217706960
|
G | A | 5 | a0001c0005t0001g0141a0001c0005t0001g0192a0001c0005t0004g0071others(2): Show | 5 | HG01261.hp1 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+23599G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217706960 | ||||||
| chr1:217707191
|
T | A | 1 | a0001c0002t0012g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.395+23830T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217707191 | ||||||
| chr1:217707192
|
G | C | 1 | a0001c0002t0012g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.395+23831G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217707192 | ||||||
| chr1:217707328
|
G | A | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.395+23967G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217707328 | ||||||
| chr1:217707620
|
A | C | 1 | a0001c0001t0001g0021 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.395+24259A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217707620 | ||||||
| chr1:217708017
|
G | C | 1 | a0001c0001t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.395+24656G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217708017 | ||||||
| chr1:217708111
|
C | T | 7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+24750C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217708111 | ||||||
| chr1:217708397
|
C | T | 2 | a0001c0002t0005g0078a0001c0002t0028g0079 | 2 | HG00140.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.395+25036C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217708397 | ||||||
| chr1:217709031
|
A | G | 1 | a0001c0002t0054g0050 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.395+25670A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217709031 | ||||||
| chr1:217709150
|
C | G | 61 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(58): Show | 61 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.395+25789C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217709150 | ||||||
| chr1:217709190
|
A | G | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+25829A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217709190 | ||||||
| chr1:217709375
|
A | C | 1 | a0001c0004t0004g0252 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.395+26014A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217709375 | ||||||
| chr1:217709546
|
A | G | 15 | a0001c0001t0004g0054a0001c0001t0008g0049a0001c0001t0023g0053others(12): Show | 15 | HG00140.hp2 HG00639.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.395+26185A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217709546 | ||||||
| chr1:217709616
|
A | G | 2 | a0001c0003t0024g0243a0001c0003t0038g0244 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.395+26255A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217709616 | ||||||
| chr1:217709729
|
C | G | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.395+26368C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217709729 | ||||||
| chr1:217710056
|
C | T | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+26695C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217710056 | ||||||
| chr1:217710128
|
T | C | 27 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(24): Show | 27 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.395+26767T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217710128 | ||||||
| chr1:217710461
|
A | G | 55 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.395+27100A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217710461 | ||||||
| chr1:217710705
|
A | G | 1 | a0001c0004t0004g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.395+27344A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217710705 | ||||||
| chr1:217710813
|
TTTATTAG | T | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+27454_395+2746 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217710813 | |||||
| chr1:217710943
|
A | C | 1 | a0001c0002t0039g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.395+27582A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217710943 | ||||||
| chr1:217711067
|
A | G | 1 | a0001c0003t0014g0230 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.395+27706A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217711067 | ||||||
| chr1:217711643
|
C | T | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.395+28282C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217711643 | ||||||
| chr1:217711659
|
G | T | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.395+28298G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217711659 | ||||||
| chr1:217711915
|
T | C | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+28554T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217711915 | ||||||
| chr1:217712033
|
G | A | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.395+28672G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217712033 | ||||||
| chr1:217712059
|
T | C | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.395+28698T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217712059 | ||||||
| chr1:217712128
|
C | CT | 40 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.395+28771dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217712128 | |||||
| chr1:217712128
|
C | CTTTTT | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.395+28771_395+2877 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217712128 | |||||
| chr1:217712128
|
C | CTTTTTT | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.395+28771_395+2877 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217712128 | |||||
| chr1:217712128
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0006g0161 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.395+28771_395+2877 others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217712128 | |||||
| chr1:217712128
|
C | CTTTTTTT others(4): Show |
7 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+28771_395+2877 others(15): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217712128 | |||||
| chr1:217712128
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.395+28771_395+2877 others(19): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217712128 | |||||
| chr1:217712128
|
C | CTTTTTTT others(9): Show |
4 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093others(1): Show | 4 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.395+28771_395+2877 others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217712128 | |||||
| chr1:217712128
|
C | CTTTTTTT others(10): Show |
1 | a0001c0002t0044g0091 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.395+28771_395+2877 others(21): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217712128 | |||||
| chr1:217712128
|
C | CTTTTTTT others(13): Show |
1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.395+28771_395+2877 others(24): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217712128 | |||||
| chr1:217712133
|
G | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.395+28772G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217712133 | ||||||
| chr1:217712148
|
C | T | 5 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035others(2): Show | 5 | HG02258.hp1 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.395+28787C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217712148 | ||||||
| chr1:217712184
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.395+28823T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217712184 | ||||||
| chr1:217712290
|
C | T | 1 | a0001c0003t0003g0224 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.395+28929C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217712290 | ||||||
| chr1:217712333
|
T | C | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.395+28972T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217712333 | ||||||
| chr1:217712391
|
G | T | 2 | a0001c0001t0056g0075a0001c0002t0009g0072 | 2 | HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.395+29030G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217712391 | ||||||
| chr1:217712405
|
C | T | 4 | a0001c0001t0001g0190a0001c0001t0008g0189a0001c0001t0012g0188others(1): Show | 4 | HG03130.hp1 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.395+29044C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217712405 | ||||||
| chr1:217713112
|
T | C | 1 | a0001c0001t0040g0025 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.396-28863T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217713112 | ||||||
| chr1:217713256
|
T | G | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.396-28719T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217713256 | ||||||
| chr1:217713431
|
GTGA | G | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.396-28541_396-2853 others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217713431 | |||||
| chr1:217713473
|
C | G | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.396-28502C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217713473 | ||||||
| chr1:217713708
|
T | C | 18 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(15): Show | 18 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.396-28267T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217713708 | ||||||
| chr1:217713985
|
A | G | 3 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035 | 3 | HG02965.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.396-27990A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217713985 | ||||||
| chr1:217714105
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.396-27870C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217714105 | ||||||
| chr1:217714106
|
G | A | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-27869G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217714106 | ||||||
| chr1:217714160
|
A | G | 62 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.396-27815A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217714160 | ||||||
| chr1:217714203
|
C | T | 1 | a0001c0002t0013g0121 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.396-27772C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217714203 | ||||||
| chr1:217714313
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0002g0019a0001c0001t0002g0023 | 3 | HG00140.hp1 HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.396-27662C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217714313 | ||||||
| chr1:217714321
|
A | G | 62 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.396-27654A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217714321 | ||||||
| chr1:217714488
|
C | CTTTTTTT others(4): Show |
3 | a0001c0004t0004g0073a0001c0004t0032g0186a0001c0004t0053g0239 | 3 | HG01891.hp1 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.396-27483_396-2747 others(15): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217714488 | |||||
| chr1:217714488
|
C | CTTTTTTT others(5): Show |
27 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(24): Show | 27 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.396-27484_396-2747 others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217714488 | |||||
| chr1:217714488
|
C | CTTTTTTT others(6): Show |
5 | a0001c0001t0006g0096a0001c0002t0044g0091a0001c0003t0024g0243others(2): Show | 5 | HG01981.hp1 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-27485_396-2747 others(17): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217714488 | |||||
| chr1:217714488
|
C | CTTTTTTT others(8): Show |
1 | a0001c0003t0014g0230 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.396-27473_396-2747 others(19): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217714488 | |||||
| chr1:217714488
|
C | CTTTTTTT others(9): Show |
16 | a0001c0003t0001g0215a0001c0003t0001g0231a0001c0003t0003g0210others(13): Show | 16 | HG00280.hp2 HG01069.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.396-27473_396-2747 others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217714488 | |||||
| chr1:217714488
|
C | CTTTTTTT others(10): Show |
9 | a0001c0003t0001g0220a0001c0003t0003g0098a0001c0003t0003g0214others(6): Show | 9 | HG00609.hp1 HG01361.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.396-27473_396-2747 others(21): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217714488 | |||||
| chr1:217714488
|
C | CTTTTTTT others(11): Show |
1 | a0001c0003t0003g0097 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.396-27473_396-2747 others(22): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217714488 | |||||
| chr1:217714645
|
G | A | 1 | a0001c0004t0005g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.396-27330G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217714645 | ||||||
| chr1:217714650
|
A | C | 1 | a0002c0006t0003g0014 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.396-27325A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217714650 | ||||||
| chr1:217714675
|
C | T | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.396-27300C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217714675 | ||||||
| chr1:217714774
|
C | T | 1 | a0001c0002t0049g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.396-27201C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217714774 | ||||||
| chr1:217714785
|
G | A | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.396-27190G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217714785 | ||||||
| chr1:217714794
|
G | A | 2 | a0001c0001t0020g0094a0001c0001t0035g0085 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.396-27181G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217714794 | ||||||
| chr1:217714952
|
T | C | 2 | a0001c0001t0008g0045a0001c0001t0042g0035 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.396-27023T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217714952 | ||||||
| chr1:217715009
|
A | G | 30 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.396-26966A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217715009 | ||||||
| chr1:217715218
|
A | T | 1 | a0002c0006t0001g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.396-26757A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217715218 | ||||||
| chr1:217715256
|
T | A | 1 | a0001c0003t0001g0231 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.396-26719T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217715256 | ||||||
| chr1:217715267
|
C | T | 7 | a0001c0003t0003g0214a0001c0003t0003g0217a0001c0003t0003g0223others(4): Show | 7 | HG00609.hp1 HG02165.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-26708C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217715267 | ||||||
| chr1:217715305
|
G | C | 1 | a0001c0001t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.396-26670G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217715305 | ||||||
| chr1:217715343
|
A | C | 1 | a0001c0001t0002g0006 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.396-26632A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217715343 | ||||||
| chr1:217715471
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.396-26504A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217715471 | ||||||
| chr1:217715630
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.396-26345A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217715630 | ||||||
| chr1:217715669
|
C | CA | 7 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0216others(4): Show | 7 | HG01106.hp1 HG02738.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.396-26292dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217715669 | |||||
| chr1:217715669
|
CA | C | 27 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(24): Show | 27 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.396-26292delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217715669 | |||||
| chr1:217715791
|
C | T | 2 | a0001c0001t0015g0058a0001c0001t0015g0059 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.396-26184C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217715791 | ||||||
| chr1:217715828
|
C | T | 1 | a0001c0003t0003g0212 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.396-26147C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217715828 | ||||||
| chr1:217715921
|
A | T | 1 | a0001c0001t0012g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.396-26054A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217715921 | ||||||
| chr1:217716004
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.396-25971A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217716004 | ||||||
| chr1:217716121
|
C | T | 1 | a0003c0007t0009g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.396-25854C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217716121 | ||||||
| chr1:217716458
|
A | G | 42 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(39): Show | 42 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.396-25517A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217716458 | ||||||
| chr1:217716854
|
T | A | 2 | a0001c0001t0015g0058a0001c0001t0015g0059 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.396-25121T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217716854 | ||||||
| chr1:217716948
|
G | A | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.396-25027G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217716948 | ||||||
| chr1:217717109
|
A | T | 251 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.396-24866A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217717109 | ||||||
| chr1:217717211
|
A | AG | 62 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.396-24764_396-2476 others(5): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217717211 | ||||||
| chr1:217717298
|
G | C | 1 | a0001c0008t0051g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.396-24677G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217717298 | ||||||
| chr1:217717462
|
A | G | 1 | a0001c0001t0005g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.396-24513A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217717462 | ||||||
| chr1:217717475
|
G | A | 1 | a0001c0002t0021g0160 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.396-24500G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217717475 | ||||||
| chr1:217717567
|
C | T | 18 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(15): Show | 18 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.396-24408C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217717567 | ||||||
| chr1:217717632
|
T | A | 52 | a0001c0001t0001g0041a0001c0001t0001g0082a0001c0001t0001g0130others(49): Show | 52 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.396-24343T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217717632 | ||||||
| chr1:217717794
|
G | C | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.396-24181G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217717794 | ||||||
| chr1:217717910
|
C | CT | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.396-24064dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217717910 | |||||
| chr1:217717915
|
A | G | 2 | a0001c0001t0002g0026a0001c0001t0002g0032 | 2 | HG02015.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.396-24060A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217717915 | ||||||
| chr1:217718436
|
A | G | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.396-23539A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217718436 | ||||||
| chr1:217718555
|
A | G | 1 | a0002c0006t0018g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.396-23420A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217718555 | ||||||
| chr1:217718872
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.396-23103C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217718872 | ||||||
| chr1:217719548
|
T | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.396-22427T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217719548 | ||||||
| chr1:217719616
|
C | T | 1 | a0001c0002t0001g0132 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.396-22359C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217719616 | ||||||
| chr1:217719828
|
A | T | 62 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.396-22147A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217719828 | ||||||
| chr1:217719961
|
C | T | 62 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.396-22014C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217719961 | ||||||
| chr1:217720162
|
T | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.396-21813T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217720162 | ||||||
| chr1:217720173
|
A | G | 1 | a0001c0012t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.396-21802A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217720173 | ||||||
| chr1:217720260
|
G | C | 1 | a0001c0001t0002g0027 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.396-21715G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217720260 | ||||||
| chr1:217720649
|
A | T | 1 | a0001c0001t0058g0150 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.396-21326A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217720649 | ||||||
| chr1:217720749
|
A | G | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.396-21226A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217720749 | ||||||
| chr1:217720864
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.396-21111G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217720864 | ||||||
| chr1:217720887
|
T | C | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.396-21088T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217720887 | ||||||
| chr1:217721014
|
T | A | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.396-20961T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217721014 | ||||||
| chr1:217721240
|
G | T | 1 | a0001c0001t0046g0153 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.396-20735G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217721240 | ||||||
| chr1:217721460
|
T | G | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.396-20515T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217721460 | ||||||
| chr1:217721495
|
C | T | 11 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(8): Show | 11 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.396-20480C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217721495 | ||||||
| chr1:217721529
|
C | T | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.396-20446C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217721529 | ||||||
| chr1:217721569
|
C | T | 2 | a0001c0001t0008g0045a0001c0001t0042g0035 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.396-20406C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217721569 | ||||||
| chr1:217721609
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.396-20366G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217721609 | ||||||
| chr1:217721623
|
C | A | 1 | a0001c0003t0003g0235 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.396-20352C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217721623 | ||||||
| chr1:217721957
|
T | C | 1 | a0001c0004t0004g0246 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.396-20018T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217721957 | ||||||
| chr1:217721966
|
A | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.396-20009A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217721966 | ||||||
| chr1:217722360
|
A | G | 1 | a0001c0001t0005g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.396-19615A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217722360 | ||||||
| chr1:217722391
|
G | A | 1 | a0001c0002t0049g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.396-19584G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217722391 | ||||||
| chr1:217722509
|
A | G | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.396-19466A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217722509 | ||||||
| chr1:217722610
|
G | T | 1 | a0001c0001t0010g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.396-19365G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217722610 | ||||||
| chr1:217722685
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.396-19290C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217722685 | ||||||
| chr1:217722830
|
C | T | 5 | a0001c0005t0001g0141a0001c0005t0001g0192a0001c0005t0004g0071others(2): Show | 5 | HG01261.hp1 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-19145C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217722830 | ||||||
| chr1:217722831
|
G | A | 3 | a0001c0001t0004g0143a0001c0001t0007g0142a0001c0001t0048g0110 | 3 | HG02109.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.396-19144G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217722831 | ||||||
| chr1:217723060
|
A | G | 1 | a0001c0002t0030g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.396-18915A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217723060 | ||||||
| chr1:217723062
|
G | T | 1 | a0001c0001t0004g0069 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.396-18913G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217723062 | ||||||
| chr1:217723155
|
G | C | 62 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.396-18820G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217723155 | ||||||
| chr1:217723550
|
T | G | 1 | a0001c0002t0009g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.396-18425T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217723550 | ||||||
| chr1:217723743
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.396-18232G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217723743 | ||||||
| chr1:217723860
|
C | T | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.396-18115C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217723860 | ||||||
| chr1:217723933
|
T | G | 2 | a0001c0001t0001g0173a0001c0001t0002g0176 | 2 | HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.396-18042T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217723933 | ||||||
| chr1:217723964
|
G | A | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.396-18011G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217723964 | ||||||
| chr1:217724417
|
G | A | 1 | a0001c0002t0021g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.396-17558G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217724417 | ||||||
| chr1:217724474
|
G | A | 5 | a0001c0005t0001g0141a0001c0005t0001g0192a0001c0005t0004g0071others(2): Show | 5 | HG01261.hp1 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-17501G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217724474 | ||||||
| chr1:217724503
|
A | G | 1 | a0001c0002t0025g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.396-17472A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217724503 | ||||||
| chr1:217724665
|
A | G | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.396-17310A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217724665 | ||||||
| chr1:217724897
|
T | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.396-17078T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217724897 | ||||||
| chr1:217725469
|
T | A | 7 | a0001c0004t0004g0246a0001c0004t0004g0247a0001c0004t0004g0248others(4): Show | 7 | HG02615.hp2 HG02622.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.396-16506T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217725469 | ||||||
| chr1:217725772
|
G | T | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-16203G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217725772 | ||||||
| chr1:217725816
|
G | A | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.396-16159G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217725816 | ||||||
| chr1:217726158
|
G | A | 44 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(41): Show | 44 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.396-15817G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726158 | ||||||
| chr1:217726228
|
C | A | 18 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(15): Show | 18 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.396-15747C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726228 | ||||||
| chr1:217726229
|
C | T | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.396-15746C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726229 | ||||||
| chr1:217726247
|
T | C | 1 | a0001c0004t0053g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.396-15728T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726247 | ||||||
| chr1:217726292
|
A | T | 1 | a0001c0001t0002g0171 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.396-15683A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726292 | ||||||
| chr1:217726364
|
A | G | 1 | a0001c0001t0002g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.396-15611A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726364 | ||||||
| chr1:217726406
|
T | C | 62 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.396-15569T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726406 | ||||||
| chr1:217726507
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.396-15468C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726507 | ||||||
| chr1:217726598
|
G | T | 1 | a0001c0001t0012g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.396-15377G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726598 | ||||||
| chr1:217726668
|
T | C | 4 | a0001c0001t0008g0045a0001c0001t0024g0040a0001c0001t0042g0035others(1): Show | 4 | HG02965.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-15307T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726668 | ||||||
| chr1:217726686
|
G | T | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.396-15289G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726686 | ||||||
| chr1:217726712
|
T | A | 4 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0166others(1): Show | 4 | HG02155.hp1 NA18954.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-15263T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726712 | ||||||
| chr1:217726717
|
G | GT | 63 | a0001c0001t0001g0090a0001c0001t0001g0166a0001c0001t0001g0209others(60): Show | 63 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.396-15248dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217726717 | |||||
| chr1:217726762
|
A | T | 1 | a0001c0001t0005g0052 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.396-15213A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726762 | ||||||
| chr1:217726865
|
T | C | 1 | a0001c0002t0001g0086 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.396-15110T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726865 | ||||||
| chr1:217726959
|
A | C | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.396-15016A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726959 | ||||||
| chr1:217726969
|
G | C | 13 | a0001c0001t0004g0054a0001c0001t0008g0049a0001c0001t0023g0053others(10): Show | 13 | HG00140.hp2 HG00639.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.396-15006G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726969 | ||||||
| chr1:217726983
|
T | C | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.396-14992T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726983 | ||||||
| chr1:217726995
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.396-14980C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217726995 | ||||||
| chr1:217727039
|
G | A | 3 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093 | 3 | HG02559.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.396-14936G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727039 | ||||||
| chr1:217727205
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.396-14770C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727205 | ||||||
| chr1:217727247
|
C | CAAA | 67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 67 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.396-14726_396-1472 others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217727247 | |||||
| chr1:217727247
|
C | CAAAAAT | 17 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0044others(14): Show | 17 | HG00099.hp1 HG00609.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.396-14726_396-1472 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217727247 | |||||
| chr1:217727247
|
C | CAAAAATA others(2): Show |
4 | a0001c0001t0023g0053a0001c0002t0009g0076a0001c0002t0030g0232others(1): Show | 4 | HG01361.hp1 HG01433.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-14726_396-1472 others(13): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217727247 | |||||
| chr1:217727247
|
C | CAAAAATA others(5): Show |
4 | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0033others(1): Show | 4 | HG02004.hp1 HG02015.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-14726_396-1472 others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217727247 | |||||
| chr1:217727247
|
C | CAAAAATA others(8): Show |
1 | a0001c0001t0011g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.396-14726_396-1472 others(19): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217727247 | |||||
| chr1:217727247
|
C | CAAT | 15 | a0001c0001t0001g0082a0001c0001t0001g0140a0001c0001t0001g0154others(12): Show | 15 | HG00438.hp2 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.396-14689_396-1468 others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217727247 | |||||
| chr1:217727247
|
C | CAATAAT | 7 | a0001c0001t0001g0090a0001c0001t0015g0093a0001c0002t0001g0126others(4): Show | 7 | HG00099.hp2 HG00738.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.396-14692_396-1468 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217727247 | |||||
| chr1:217727247
|
CAAT | C | 28 | a0001c0001t0001g0087a0001c0001t0001g0124a0001c0001t0001g0174others(25): Show | 28 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.396-14689_396-1468 others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217727247 | |||||
| chr1:217727247
|
CAATAAT | C | 11 | a0001c0001t0001g0119a0001c0001t0001g0184a0001c0002t0007g0051others(8): Show | 11 | HG01891.hp2 HG02004.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.396-14692_396-1468 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217727247 | |||||
| chr1:217727247
|
CAATAATA others(2): Show |
C | 6 | a0001c0002t0011g0199a0001c0002t0017g0151a0001c0002t0017g0152others(3): Show | 6 | HG01981.hp2 HG02976.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.396-14695_396-1468 others(13): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217727247 | |||||
| chr1:217727247
|
CAATAATA others(8): Show |
C | 2 | a0001c0001t0020g0094a0001c0001t0035g0085 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.396-14701_396-1468 others(19): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217727247 | |||||
| chr1:217727250
|
T | A | 40 | a0001c0001t0001g0065a0001c0001t0006g0201a0001c0001t0006g0202others(37): Show | 40 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.396-14725T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727250 | ||||||
| chr1:217727253
|
T | A | 16 | a0001c0002t0001g0114a0001c0002t0005g0056a0001c0002t0005g0078others(13): Show | 16 | HG00140.hp2 HG00639.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.396-14722T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727253 | ||||||
| chr1:217727256
|
T | A | 8 | a0001c0002t0007g0051a0001c0002t0007g0060a0001c0002t0007g0061others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.396-14719T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727256 | ||||||
| chr1:217727259
|
T | A | 1 | a0001c0003t0038g0244 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.396-14716T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727259 | ||||||
| chr1:217727265
|
T | A | 2 | a0001c0001t0020g0094a0001c0001t0035g0085 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.396-14710T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727265 | ||||||
| chr1:217727266
|
A | G | 4 | a0001c0001t0001g0190a0001c0001t0008g0189a0001c0001t0012g0188others(1): Show | 4 | HG03130.hp1 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-14709A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727266 | ||||||
| chr1:217727268
|
T | C | 3 | a0001c0001t0004g0069a0001c0001t0005g0052a0001c0001t0005g0068 | 3 | HG02055.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.396-14707T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727268 | ||||||
| chr1:217727285
|
A | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.396-14690A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727285 | ||||||
| chr1:217727286
|
T | C | 1 | a0001c0002t0005g0078 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.396-14689T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727286 | ||||||
| chr1:217727528
|
G | T | 3 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093 | 3 | HG02559.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.396-14447G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727528 | ||||||
| chr1:217727529
|
C | T | 62 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.396-14446C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727529 | ||||||
| chr1:217727617
|
A | G | 1 | a0001c0003t0003g0212 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.396-14358A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727617 | ||||||
| chr1:217727812
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.396-14163T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727812 | ||||||
| chr1:217727842
|
T | A | 2 | a0001c0002t0001g0126a0001c0002t0010g0125 | 2 | HG02129.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.396-14133T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217727842 | ||||||
| chr1:217728464
|
T | C | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.396-13511T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217728464 | ||||||
| chr1:217728603
|
T | C | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.396-13372T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217728603 | ||||||
| chr1:217728961
|
G | C | 11 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(8): Show | 11 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.396-13014G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217728961 | ||||||
| chr1:217728981
|
G | A | 49 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(46): Show | 49 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.396-12994G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217728981 | ||||||
| chr1:217728986
|
G | C | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.396-12989G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217728986 | ||||||
| chr1:217729036
|
T | A | 1 | a0001c0001t0001g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.396-12939T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217729036 | ||||||
| chr1:217729242
|
T | C | 62 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.396-12733T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217729242 | ||||||
| chr1:217729248
|
C | T | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.396-12727C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217729248 | ||||||
| chr1:217729280
|
G | C | 62 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.396-12695G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217729280 | ||||||
| chr1:217729458
|
G | C | 49 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(46): Show | 49 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.396-12517G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217729458 | ||||||
| chr1:217729685
|
T | C | 2 | a0001c0001t0015g0058a0001c0001t0015g0059 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.396-12290T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217729685 | ||||||
| chr1:217729818
|
A | T | 10 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(7): Show | 10 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.396-12157A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217729818 | ||||||
| chr1:217729922
|
A | G | 2 | a0001c0001t0006g0204a0001c0001t0006g0205 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.396-12053A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217729922 | ||||||
| chr1:217729946
|
G | A | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.396-12029G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217729946 | ||||||
| chr1:217729984
|
A | G | 1 | a0001c0002t0001g0147 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.396-11991A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217729984 | ||||||
| chr1:217730219
|
A | AT | 12 | a0001c0001t0001g0012a0001c0001t0001g0037a0001c0001t0001g0044others(9): Show | 12 | HG00609.hp1 HG01993.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.396-11740dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217730219 | |||||
| chr1:217730219
|
AT | A | 8 | a0001c0001t0001g0008a0001c0001t0010g0043a0001c0002t0001g0107others(5): Show | 8 | HG01070.hp1 HG01070.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.396-11740delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217730219 | |||||
| chr1:217730275
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.396-11700T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217730275 | ||||||
| chr1:217730308
|
C | T | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.396-11667C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217730308 | ||||||
| chr1:217730309
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.396-11666C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217730309 | ||||||
| chr1:217730310
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.396-11665C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217730310 | ||||||
| chr1:217730798
|
A | T | 1 | a0001c0001t0009g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.396-11177A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217730798 | ||||||
| chr1:217731363
|
A | G | 13 | a0001c0003t0024g0243a0001c0003t0038g0244a0001c0004t0004g0240others(10): Show | 13 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.396-10612A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217731363 | ||||||
| chr1:217731384
|
T | C | 31 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.396-10591T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217731384 | ||||||
| chr1:217731428
|
G | A | 6 | a0001c0002t0001g0144a0001c0002t0001g0149a0001c0002t0001g0179others(3): Show | 6 | HG03831.hp1 NA18946.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.396-10547G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217731428 | ||||||
| chr1:217731498
|
C | T | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.396-10477C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217731498 | ||||||
| chr1:217732067
|
A | C | 49 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(46): Show | 49 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.396-9908A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217732067 | ||||||
| chr1:217732084
|
T | TTCTCTCT others(3): Show |
14 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0089others(11): Show | 14 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.396-9877_396-9868d others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217732084 | |||||
| chr1:217732084
|
T | TTCTCTCT others(5): Show |
2 | a0001c0001t0015g0093a0001c0009t0019g0092 | 2 | HG02896.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.396-9879_396-9868d others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217732084 | |||||
| chr1:217732084
|
T | TTCTCTCT others(7): Show |
1 | a0001c0003t0003g0228 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.396-9881_396-9868d others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217732084 | |||||
| chr1:217732084
|
T | TTCTCTCT others(9): Show |
4 | a0001c0001t0005g0084a0001c0003t0001g0231a0001c0004t0005g0233others(1): Show | 4 | HG01109.hp1 HG02486.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-9883_396-9868d others(18): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217732084 | |||||
| chr1:217732084
|
T | TTCTCTCT others(11): Show |
21 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0003g0097others(18): Show | 21 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.396-9885_396-9868d others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217732084 | |||||
| chr1:217732084
|
T | TTCTCTCT others(13): Show |
3 | a0001c0003t0003g0223a0001c0003t0003g0226a0001c0003t0031g0225 | 3 | HG02165.hp1 NA18990.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.396-9887_396-9868d others(22): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217732084 | |||||
| chr1:217732084
|
T | TTCTCTCT others(15): Show |
2 | a0001c0004t0001g0219a0001c0004t0053g0239 | 2 | HG01074.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.396-9889_396-9868d others(24): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217732084 | |||||
| chr1:217732407
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.396-9568A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217732407 | ||||||
| chr1:217732413
|
G | T | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.396-9562G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217732413 | ||||||
| chr1:217732429
|
A | G | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.396-9546A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217732429 | ||||||
| chr1:217732477
|
A | G | 49 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(46): Show | 49 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.396-9498A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217732477 | ||||||
| chr1:217732718
|
A | T | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.396-9257A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217732718 | ||||||
| chr1:217732787
|
CT | C | 30 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.396-9187delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217732787 | ||||||
| chr1:217732868
|
C | T | 1 | a0001c0004t0055g0242 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.396-9107C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217732868 | ||||||
| chr1:217732965
|
A | G | 1 | a0001c0008t0014g0213 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.396-9010A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217732965 | ||||||
| chr1:217733417
|
C | T | 1 | a0003c0007t0009g0116 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.396-8558C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217733417 | ||||||
| chr1:217733419
|
T | A | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.396-8556T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217733419 | ||||||
| chr1:217733471
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.396-8504C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217733471 | ||||||
| chr1:217733914
|
C | T | 30 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.396-8061C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217733914 | ||||||
| chr1:217733926
|
T | C | 3 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093 | 3 | HG02559.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.396-8049T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217733926 | ||||||
| chr1:217733988
|
C | T | 1 | a0001c0002t0011g0199 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.396-7987C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217733988 | ||||||
| chr1:217734289
|
T | C | 4 | a0001c0002t0005g0078a0001c0002t0012g0077a0001c0002t0012g0080others(1): Show | 4 | HG00140.hp2 HG00639.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-7686T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217734289 | ||||||
| chr1:217734374
|
G | A | 1 | a0001c0002t0028g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.396-7601G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217734374 | ||||||
| chr1:217734374
|
G | T | 62 | a0001c0001t0001g0090a0001c0001t0001g0209a0001c0001t0005g0084others(59): Show | 62 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.396-7601G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217734374 | ||||||
| chr1:217734514
|
T | C | 10 | a0001c0001t0015g0059a0001c0004t0004g0240a0001c0004t0004g0246others(7): Show | 10 | HG02486.hp2 HG02615.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.396-7461T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217734514 | ||||||
| chr1:217734571
|
A | G | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.396-7404A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217734571 | ||||||
| chr1:217734603
|
G | A | 1 | a0001c0001t0006g0161 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.396-7372G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217734603 | ||||||
| chr1:217734622
|
T | A | 2 | a0001c0001t0006g0204a0001c0001t0006g0205 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.396-7353T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217734622 | ||||||
| chr1:217734629
|
T | C | 3 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093 | 3 | HG02559.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.396-7346T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217734629 | ||||||
| chr1:217734874
|
G | C | 1 | a0001c0001t0001g0022 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.396-7101G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217734874 | ||||||
| chr1:217734949
|
C | T | 3 | a0001c0001t0056g0075a0001c0003t0024g0243a0001c0003t0038g0244 | 3 | HG02572.hp2 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.396-7026C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217734949 | ||||||
| chr1:217734990
|
C | G | 6 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(3): Show | 6 | HG01168.hp1 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-6985C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217734990 | ||||||
| chr1:217734991
|
G | A | 1 | a0001c0004t0053g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.396-6984G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217734991 | ||||||
| chr1:217735046
|
T | C | 3 | a0001c0002t0001g0127a0001c0002t0001g0138a0001c0004t0053g0239 | 3 | HG01891.hp1 NA18939.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.396-6929T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217735046 | ||||||
| chr1:217735265
|
C | T | 2 | a0001c0003t0024g0243a0001c0003t0038g0244 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.396-6710C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217735265 | ||||||
| chr1:217735366
|
ATC | A | 5 | a0001c0001t0001g0123a0001c0001t0008g0045a0001c0001t0008g0136others(2): Show | 5 | HG02717.hp1 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-6607_396-6606d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217735366 | |||||
| chr1:217735419
|
A | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.396-6556A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217735419 | ||||||
| chr1:217735717
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.396-6258T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217735717 | ||||||
| chr1:217735877
|
G | A | 1 | a0001c0001t0046g0153 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.396-6098G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217735877 | ||||||
| chr1:217736313
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.396-5662C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217736313 | ||||||
| chr1:217736376
|
G | A | 7 | a0001c0002t0007g0051a0001c0002t0007g0060a0001c0002t0007g0061others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.396-5599G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217736376 | ||||||
| chr1:217736454
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.396-5521C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217736454 | ||||||
| chr1:217736499
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.396-5476A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217736499 | ||||||
| chr1:217736553
|
T | A | 5 | a0001c0001t0001g0123a0001c0001t0008g0045a0001c0001t0008g0136others(2): Show | 5 | HG02717.hp1 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-5422T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217736553 | ||||||
| chr1:217736561
|
AAGATCTT others(1): Show |
A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.396-5411_396-5404d others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217736561 | |||||
| chr1:217736735
|
C | T | 1 | a0001c0001t0043g0155 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.396-5240C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217736735 | ||||||
| chr1:217736779
|
T | C | 1 | a0001c0004t0053g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.396-5196T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217736779 | ||||||
| chr1:217736986
|
G | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.396-4989G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217736986 | ||||||
| chr1:217737004
|
A | G | 6 | a0001c0001t0002g0101a0001c0001t0002g0158a0001c0001t0002g0159others(3): Show | 6 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-4971A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217737004 | ||||||
| chr1:217737123
|
C | T | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.396-4852C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217737123 | ||||||
| chr1:217737189
|
T | C | 9 | a0001c0002t0005g0078a0001c0002t0012g0018a0001c0002t0012g0077others(6): Show | 9 | HG00140.hp2 HG00639.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.396-4786T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217737189 | ||||||
| chr1:217737358
|
G | C | 1 | a0001c0002t0001g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.396-4617G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217737358 | ||||||
| chr1:217737431
|
G | A | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.396-4544G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217737431 | ||||||
| chr1:217737632
|
A | G | 1 | a0001c0004t0004g0247 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.396-4343A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217737632 | ||||||
| chr1:217737675
|
T | C | 74 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0046others(71): Show | 74 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.396-4300T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217737675 | ||||||
| chr1:217737680
|
A | C | 3 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093 | 3 | HG02559.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.396-4295A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217737680 | ||||||
| chr1:217737827
|
C | CT | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.396-4132dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217737827 | |||||
| chr1:217737928
|
G | A | 3 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093 | 3 | HG02559.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.396-4047G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217737928 | ||||||
| chr1:217737934
|
C | T | 1 | a0001c0003t0001g0220 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.396-4041C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217737934 | ||||||
| chr1:217738248
|
A | G | 2 | a0001c0001t0002g0013a0001c0001t0010g0043 | 2 | NA18959.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.396-3727A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217738248 | ||||||
| chr1:217738344
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.396-3631A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217738344 | ||||||
| chr1:217738349
|
G | C | 10 | a0001c0001t0004g0143a0001c0004t0004g0240a0001c0004t0004g0246others(7): Show | 10 | HG01109.hp1 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.396-3626G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217738349 | ||||||
| chr1:217738456
|
C | T | 1 | a0001c0001t0058g0150 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.396-3519C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217738456 | ||||||
| chr1:217738468
|
G | A | 2 | a0001c0001t0015g0058a0001c0001t0015g0059 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.396-3507G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217738468 | ||||||
| chr1:217738586
|
A | T | 13 | a0001c0001t0001g0123a0001c0001t0001g0209a0001c0001t0006g0096others(10): Show | 13 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.396-3389A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217738586 | ||||||
| chr1:217738695
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.396-3280C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217738695 | ||||||
| chr1:217738728
|
G | T | 1 | a0001c0002t0030g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.396-3247G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217738728 | ||||||
| chr1:217738846
|
G | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.396-3129G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217738846 | ||||||
| chr1:217739185
|
CAG | C | 13 | a0001c0001t0001g0123a0001c0001t0001g0209a0001c0001t0006g0096others(10): Show | 13 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.396-2785_396-2784d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217739185 | |||||
| chr1:217739228
|
G | C | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.396-2747G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217739228 | ||||||
| chr1:217739254
|
T | C | 1 | a0001c0001t0040g0025 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.396-2721T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217739254 | ||||||
| chr1:217739474
|
AT | A | 6 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.396-2492delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217739474 | |||||
| chr1:217739563
|
G | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.396-2412G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217739563 | ||||||
| chr1:217739566
|
A | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.396-2409A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217739566 | ||||||
| chr1:217740133
|
G | A | 1 | a0001c0003t0003g0214 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.396-1842G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217740133 | ||||||
| chr1:217740158
|
A | AGGCCTTT others(303): Show |
1 | a0001c0001t0001g0206 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.396-1804_396-1803i others(312): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(306): Show |
1 | a0001c0001t0001g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.396-1804_396-1803i others(315): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(310): Show |
1 | a0001c0001t0001g0236 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.396-1804_396-1803i others(319): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(311): Show |
1 | a0002c0006t0001g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.396-1804_396-1803i others(320): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(315): Show |
1 | a0001c0001t0001g0130 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.396-1804_396-1803i others(324): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(318): Show |
2 | a0001c0001t0001g0166a0001c0001t0046g0153 | 2 | NA18979.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.396-1804_396-1803i others(327): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(332): Show |
12 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0001g0087others(9): Show | 12 | HG00280.hp1 HG02083.hp1 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.396-1804_396-1803i others(341): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(333): Show |
1 | a0001c0001t0001g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.396-1804_396-1803i others(342): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(333): Show |
12 | a0001c0001t0001g0082a0001c0001t0001g0124a0001c0001t0001g0135others(9): Show | 12 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.396-1804_396-1803i others(342): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(334): Show |
11 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0002g0159others(8): Show | 11 | HG00733.hp2 HG01071.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.396-1804_396-1803i others(343): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(335): Show |
4 | a0001c0001t0001g0162a0001c0001t0001g0184a0002c0006t0018g0139others(1): Show | 4 | HG00609.hp2 HG02155.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-1804_396-1803i others(344): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(336): Show |
3 | a0001c0001t0001g0182a0001c0001t0001g0216a0001c0001t0016g0172 | 3 | HG00558.hp2 HG02738.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.396-1804_396-1803i others(345): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(337): Show |
2 | a0001c0001t0001g0164a0002c0006t0018g0137 | 2 | NA19087.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.396-1804_396-1803i others(346): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(339): Show |
2 | a0001c0001t0001g0154a0001c0001t0018g0183 | 2 | NA18612.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.396-1804_396-1803i others(348): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(341): Show |
1 | a0001c0001t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.396-1804_396-1803i others(350): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740158
|
A | AGGCCTTT others(342): Show |
1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.396-1804_396-1803i others(351): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217740158 | |||||
| chr1:217740668
|
G | A | 5 | a0001c0001t0001g0123a0001c0001t0008g0045a0001c0001t0008g0136others(2): Show | 5 | HG02717.hp1 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-1307G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217740668 | ||||||
| chr1:217740774
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.396-1201T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217740774 | ||||||
| chr1:217740878
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.396-1097T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217740878 | ||||||
| chr1:217741047
|
T | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.396-928T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217741047 | ||||||
| chr1:217741141
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.396-834C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217741141 | ||||||
| chr1:217741150
|
T | A | 1 | a0001c0001t0006g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.396-825T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217741150 | ||||||
| chr1:217741206
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.396-769C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217741206 | ||||||
| chr1:217741516
|
G | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.396-459G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217741516 | ||||||
| chr1:217741550
|
G | T | 1 | a0001c0001t0001g0004 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.396-425G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217741550 | ||||||
| chr1:217741638
|
TG | T | 29 | a0001c0002t0001g0064a0001c0002t0001g0083a0001c0002t0001g0103others(26): Show | 29 | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.396-334delG | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 217741638 | |||||
| chr1:217741756
|
A | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0046others(53): Show | 56 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.396-219A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217741756 | ||||||
| chr1:217741802
|
C | T | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.396-173C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 5/10 | chr1 | 217741802 | ||||||
| chr1:217742251
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+153G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217742251 | ||||||
| chr1:217742670
|
A | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0046others(53): Show | 56 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.519+572A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217742670 | ||||||
| chr1:217742688
|
T | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+590T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217742688 | ||||||
| chr1:217742783
|
T | C | 2 | a0001c0002t0009g0072a0001c0002t0013g0121 | 2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.519+685T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217742783 | ||||||
| chr1:217742897
|
G | T | 1 | a0001c0003t0003g0223 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.519+799G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217742897 | ||||||
| chr1:217742907
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+809G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217742907 | ||||||
| chr1:217742919
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+821A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217742919 | ||||||
| chr1:217742941
|
C | T | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+843C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217742941 | ||||||
| chr1:217742949
|
A | AAT | 5 | a0001c0001t0005g0084a0001c0001t0018g0183a0001c0002t0005g0078others(2): Show | 5 | HG00140.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+870_519+871dup others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217742949 | |||||
| chr1:217742949
|
A | AATATAT | 6 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+866_519+871dup others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217742949 | |||||
| chr1:217742949
|
A | AATATATA others(3): Show |
1 | a0001c0001t0035g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.519+862_519+871dup others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217742949 | |||||
| chr1:217742949
|
AAT | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+870_519+871del others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217742949 | |||||
| chr1:217743015
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+917A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217743015 | ||||||
| chr1:217743276
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+1178C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217743276 | ||||||
| chr1:217743324
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+1226G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217743324 | ||||||
| chr1:217743338
|
A | G | 3 | a0001c0001t0001g0090a0001c0001t0005g0089a0001c0001t0015g0093 | 3 | HG02559.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.519+1240A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217743338 | ||||||
| chr1:217743432
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+1334A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217743432 | ||||||
| chr1:217743488
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+1390A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217743488 | ||||||
| chr1:217743756
|
T | C | 179 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.519+1658T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217743756 | ||||||
| chr1:217743800
|
G | A | 8 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+1702G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217743800 | ||||||
| chr1:217743979
|
G | C | 1 | a0001c0001t0008g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.519+1881G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217743979 | ||||||
| chr1:217744018
|
G | GT | 13 | a0001c0001t0001g0123a0001c0001t0001g0209a0001c0001t0006g0096others(10): Show | 13 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.519+1928dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217744018 | |||||
| chr1:217744077
|
C | A | 2 | a0001c0002t0021g0160a0001c0008t0051g0234 | 2 | NA18949.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.519+1979C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744077 | ||||||
| chr1:217744099
|
T | C | 1 | a0001c0002t0013g0121 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.519+2001T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744099 | ||||||
| chr1:217744169
|
CAAAGAAT others(306): Show |
C | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+2083_519+2395d others(2): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217744169 | |||||
| chr1:217744234
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.519+2136G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744234 | ||||||
| chr1:217744253
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.519+2155G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744253 | ||||||
| chr1:217744279
|
G | C | 9 | a0001c0001t0004g0054a0001c0001t0009g0120a0001c0001t0023g0053others(6): Show | 9 | HG01261.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.519+2181G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744279 | ||||||
| chr1:217744355
|
T | C | 3 | a0001c0001t0001g0087a0001c0001t0001g0124a0001c0001t0057g0200 | 3 | HG00639.hp1 HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.519+2257T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744355 | ||||||
| chr1:217744356
|
G | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0124a0001c0001t0057g0200 | 3 | HG00639.hp1 HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.519+2258G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744356 | ||||||
| chr1:217744366
|
G | A | 9 | a0001c0001t0001g0135a0001c0001t0001g0162a0001c0001t0001g0166others(6): Show | 9 | HG00609.hp2 HG02155.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.519+2268G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744366 | ||||||
| chr1:217744384
|
A | G | 2 | a0001c0004t0004g0246a0001c0004t0004g0248 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.519+2286A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744384 | ||||||
| chr1:217744394
|
C | T | 9 | a0001c0001t0004g0054a0001c0001t0009g0120a0001c0001t0023g0053others(6): Show | 9 | HG01261.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.519+2296C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744394 | ||||||
| chr1:217744404
|
A | G | 1 | a0001c0002t0039g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.519+2306A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744404 | ||||||
| chr1:217744438
|
G | A | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.519+2340G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744438 | ||||||
| chr1:217744458
|
G | A | 1 | a0001c0002t0039g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.519+2360G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744458 | ||||||
| chr1:217744462
|
C | CA | 9 | a0001c0002t0001g0106a0001c0002t0001g0127a0001c0002t0005g0078others(6): Show | 9 | HG00140.hp2 HG00639.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.519+2387dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217744462 | |||||
| chr1:217744462
|
C | CAAA | 51 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0046others(48): Show | 51 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.519+2385_519+2387d others(5): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217744462 | |||||
| chr1:217744462
|
C | CAAAA | 19 | a0001c0001t0001g0082a0001c0001t0001g0119a0001c0001t0001g0162others(16): Show | 19 | HG00438.hp2 HG01109.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.519+2384_519+2387d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217744462 | |||||
| chr1:217744462
|
CA | C | 5 | a0001c0001t0056g0075a0001c0002t0013g0121a0001c0002t0044g0091others(2): Show | 5 | HG01168.hp1 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+2387delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217744462 | |||||
| chr1:217744462
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.519+2377_519+2387d others(13): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217744462 | |||||
| chr1:217744462
|
CAAAAAAA others(6): Show |
C | 13 | a0001c0001t0001g0123a0001c0001t0001g0209a0001c0001t0006g0096others(10): Show | 13 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.519+2375_519+2387d others(15): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217744462 | |||||
| chr1:217744591
|
C | T | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+2493C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744591 | ||||||
| chr1:217744628
|
C | T | 1 | a0001c0003t0003g0235 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.519+2530C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744628 | ||||||
| chr1:217744640
|
A | T | 1 | a0001c0001t0008g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.519+2542A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744640 | ||||||
| chr1:217744845
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.519+2747A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744845 | ||||||
| chr1:217744854
|
A | G | 1 | a0001c0001t0003g0168 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.519+2756A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744854 | ||||||
| chr1:217744867
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+2769C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744867 | ||||||
| chr1:217744882
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+2784A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744882 | ||||||
| chr1:217744903
|
T | C | 1 | a0001c0001t0002g0027 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.519+2805T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744903 | ||||||
| chr1:217744909
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+2811G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217744909 | ||||||
| chr1:217745223
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.519+3125G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217745223 | ||||||
| chr1:217745550
|
G | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+3452G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217745550 | ||||||
| chr1:217745561
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+3463A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217745561 | ||||||
| chr1:217745622
|
T | G | 1 | a0001c0002t0001g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.519+3524T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217745622 | ||||||
| chr1:217745674
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+3576G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217745674 | ||||||
| chr1:217745828
|
C | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+3730C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217745828 | ||||||
| chr1:217745879
|
A | G | 1 | a0001c0003t0003g0223 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.519+3781A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217745879 | ||||||
| chr1:217745919
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+3821A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217745919 | ||||||
| chr1:217745940
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.519+3842C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217745940 | ||||||
| chr1:217745969
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+3871G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217745969 | ||||||
| chr1:217746035
|
TTTAC | T | 5 | a0001c0001t0001g0016a0001c0001t0016g0172a0001c0001t0041g0015others(2): Show | 5 | HG00558.hp2 NA18951.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+3941_519+3944d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217746035 | |||||
| chr1:217746077
|
G | A | 3 | a0001c0002t0005g0078a0001c0002t0012g0018a0001c0002t0028g0079 | 3 | HG00140.hp2 HG00639.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.519+3979G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217746077 | ||||||
| chr1:217746168
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+4070G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217746168 | ||||||
| chr1:217746199
|
C | T | 66 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0046others(63): Show | 66 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.519+4101C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217746199 | ||||||
| chr1:217746361
|
A | G | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.519+4263A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217746361 | ||||||
| chr1:217746403
|
T | C | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.519+4305T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217746403 | ||||||
| chr1:217746458
|
GT | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.519+4362delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217746458 | |||||
| chr1:217746545
|
A | T | 1 | a0001c0002t0005g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.519+4447A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217746545 | ||||||
| chr1:217746558
|
T | A | 1 | a0001c0001t0050g0017 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.519+4460T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217746558 | ||||||
| chr1:217746559
|
G | GT | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+4466dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217746559 | |||||
| chr1:217746583
|
C | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.519+4485C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217746583 | ||||||
| chr1:217746616
|
T | C | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.519+4518T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217746616 | ||||||
| chr1:217746908
|
G | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.519+4810G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217746908 | ||||||
| chr1:217746943
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.519+4845A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217746943 | ||||||
| chr1:217747030
|
A | C | 1 | a0001c0001t0001g0236 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.519+4932A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217747030 | ||||||
| chr1:217747141
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.519+5043T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217747141 | ||||||
| chr1:217747204
|
A | G | 13 | a0001c0001t0001g0123a0001c0001t0001g0209a0001c0001t0006g0096others(10): Show | 13 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.519+5106A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217747204 | ||||||
| chr1:217747228
|
T | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0046others(53): Show | 56 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.519+5130T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217747228 | ||||||
| chr1:217747375
|
G | A | 10 | a0001c0002t0009g0076a0001c0002t0013g0099a0001c0002t0013g0193others(7): Show | 10 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.519+5277G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217747375 | ||||||
| chr1:217747459
|
T | C | 1 | a0001c0001t0057g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.519+5361T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217747459 | ||||||
| chr1:217747490
|
A | G | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.519+5392A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217747490 | ||||||
| chr1:217747645
|
G | A | 2 | a0001c0001t0007g0142a0001c0001t0048g0110 | 2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.519+5547G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217747645 | ||||||
| chr1:217747878
|
C | A | 2 | a0001c0001t0001g0028a0001c0001t0002g0171 | 2 | NA18939.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.519+5780C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217747878 | ||||||
| chr1:217748022
|
G | T | 22 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0003g0097others(19): Show | 22 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.519+5924G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217748022 | ||||||
| chr1:217748030
|
G | A | 1 | a0002c0006t0003g0014 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.519+5932G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217748030 | ||||||
| chr1:217748095
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+5997A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217748095 | ||||||
| chr1:217748164
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.519+6066A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217748164 | ||||||
| chr1:217748195
|
C | T | 1 | a0001c0004t0001g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.519+6097C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217748195 | ||||||
| chr1:217748302
|
C | CA | 7 | a0001c0001t0016g0208a0001c0002t0044g0091a0001c0003t0001g0220others(4): Show | 7 | HG02486.hp1 HG02615.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.519+6221dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217748302 | |||||
| chr1:217748302
|
C | CAA | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.519+6220_519+6221d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217748302 | |||||
| chr1:217748339
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.519+6241A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217748339 | ||||||
| chr1:217748400
|
T | G | 1 | a0001c0001t0005g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.519+6302T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217748400 | ||||||
| chr1:217748433
|
G | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.519+6335G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217748433 | ||||||
| chr1:217748495
|
C | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.519+6397C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217748495 | ||||||
| chr1:217748497
|
C | T | 2 | a0001c0002t0001g0147a0001c0002t0001g0191 | 2 | NA18962.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.519+6399C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217748497 | ||||||
| chr1:217748687
|
T | C | 27 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(24): Show | 27 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.519+6589T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217748687 | ||||||
| chr1:217748732
|
A | G | 8 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+6634A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217748732 | ||||||
| chr1:217748743
|
C | CA | 10 | a0001c0001t0001g0123a0001c0001t0008g0045a0001c0001t0008g0136others(7): Show | 10 | HG00438.hp1 HG01168.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.519+6665dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217748743 | |||||
| chr1:217748743
|
CA | C | 11 | a0001c0001t0001g0119a0001c0001t0001g0175a0001c0001t0001g0190others(8): Show | 11 | HG01167.hp2 HG02109.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.519+6665delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217748743 | |||||
| chr1:217748743
|
CAAAA | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.519+6662_519+6665d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217748743 | |||||
| chr1:217748819
|
G | A | 2 | a0001c0001t0015g0058a0001c0001t0015g0059 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.519+6721G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217748819 | ||||||
| chr1:217749012
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.519+6914T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749012 | ||||||
| chr1:217749111
|
A | C | 9 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(6): Show | 9 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.519+7013A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749111 | ||||||
| chr1:217749152
|
G | A | 1 | a0001c0002t0001g0112 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.519+7054G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749152 | ||||||
| chr1:217749304
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.519+7206C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749304 | ||||||
| chr1:217749399
|
G | A | 12 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(9): Show | 12 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.519+7301G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749399 | ||||||
| chr1:217749440
|
T | G | 1 | a0001c0004t0005g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.519+7342T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749440 | ||||||
| chr1:217749461
|
G | GT | 5 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(2): Show | 5 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+7371dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749461 | |||||
| chr1:217749549
|
G | C | 1 | a0001c0002t0054g0050 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.519+7451G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749549 | ||||||
| chr1:217749595
|
G | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.519+7497G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749595 | ||||||
| chr1:217749630
|
T | C | 79 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(76): Show | 79 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.519+7532T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749630 | ||||||
| chr1:217749661
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+7563A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749661 | ||||||
| chr1:217749711
|
A | G | 1 | a0001c0002t0003g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.519+7613A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749711 | ||||||
| chr1:217749824
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.519+7726A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749824 | ||||||
| chr1:217749860
|
A | G | 2 | a0001c0003t0003g0098a0001c0003t0003g0218 | 2 | HG01069.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.519+7762A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749860 | ||||||
| chr1:217749887
|
A | G | 26 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(23): Show | 26 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.519+7789A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749887 | ||||||
| chr1:217749894
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.519+7796G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749894 | ||||||
| chr1:217749943
|
T | TTC | 2 | a0001c0001t0002g0159a0001c0001t0010g0157 | 2 | HG00733.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.519+7887_519+7888d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749943 | |||||
| chr1:217749943
|
T | TTCTC | 4 | a0001c0001t0002g0158a0001c0002t0001g0132a0001c0002t0001g0180others(1): Show | 4 | HG01069.hp2 HG02015.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+7885_519+7888d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749943 | |||||
| chr1:217749943
|
T | TTCTCTC | 2 | a0001c0001t0041g0015a0001c0002t0001g0112 | 2 | HG01070.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.519+7883_519+7888d others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749943 | |||||
| chr1:217749943
|
T | TTCTCTCT others(5): Show |
1 | a0002c0006t0001g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.519+7877_519+7888d others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749943 | |||||
| chr1:217749943
|
TTC | T | 5 | a0001c0001t0001g0148a0001c0001t0012g0188a0001c0002t0001g0144others(2): Show | 5 | HG01168.hp1 HG02258.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+7887_519+7888d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749943 | |||||
| chr1:217749973
|
C | A | 2 | a0001c0002t0001g0128a0001c0002t0012g0080 | 2 | HG03710.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.519+7875C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749973 | ||||||
| chr1:217749973
|
C | CTATATAT others(3): Show |
1 | a0001c0002t0030g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.519+7876_519+7877i others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749973 | |||||
| chr1:217749973
|
C | CTATATAT others(5): Show |
1 | a0001c0002t0013g0121 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.519+7876_519+7877i others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749973 | |||||
| chr1:217749975
|
C | A | 5 | a0001c0001t0008g0049a0001c0002t0001g0128a0001c0002t0012g0080others(2): Show | 5 | HG02451.hp1 HG03041.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+7877C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749975 | ||||||
| chr1:217749975
|
CTCTCTCT others(5): Show |
C | 1 | a0001c0004t0004g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.519+7879_519+7890d others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749975 | |||||
| chr1:217749977
|
C | A | 13 | a0001c0001t0001g0135a0001c0001t0001g0146a0001c0001t0001g0148others(10): Show | 13 | HG01891.hp1 HG02451.hp1 HG03041.hp1 others(10): Show |
intron_variant | MODIFIER | c.519+7879C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749977 | ||||||
| chr1:217749977
|
C | CTATA | 5 | a0001c0001t0001g0041a0001c0001t0024g0040a0001c0002t0028g0079others(2): Show | 5 | HG00639.hp2 HG01109.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+7880_519+7881i others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749977 | |||||
| chr1:217749977
|
C | CTATATAT others(1): Show |
3 | a0001c0002t0001g0108a0001c0002t0022g0194a0001c0005t0001g0141 | 3 | HG02895.hp2 HG02965.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.519+7880_519+7881i others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749977 | |||||
| chr1:217749977
|
C | CTATATAT others(3): Show |
1 | a0001c0002t0001g0127 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.519+7880_519+7881i others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749977 | |||||
| chr1:217749977
|
C | CTATATAT others(7): Show |
3 | a0001c0002t0009g0072a0001c0003t0029g0063a0001c0005t0004g0245 | 3 | HG01261.hp1 HG04204.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.519+7880_519+7881i others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749977 | |||||
| chr1:217749979
|
C | A | 37 | a0001c0001t0001g0041a0001c0001t0001g0130a0001c0001t0001g0135others(34): Show | 37 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.519+7881C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749979 | ||||||
| chr1:217749979
|
C | CTATATA | 3 | a0001c0001t0001g0170a0001c0002t0017g0113a0001c0004t0001g0219 | 3 | HG01074.hp2 HG03710.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.519+7882_519+7883i others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749979 | |||||
| chr1:217749979
|
C | CTATATAT others(1): Show |
4 | a0001c0001t0001g0173a0001c0001t0008g0136a0001c0002t0001g0138others(1): Show | 4 | HG02148.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+7882_519+7883i others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749979 | |||||
| chr1:217749979
|
C | CTATATAT others(3): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0005g0089 | 3 | HG01070.hp2 HG01071.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.519+7882_519+7883i others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749979 | |||||
| chr1:217749979
|
C | CTATATAT others(5): Show |
3 | a0001c0001t0001g0175a0001c0002t0013g0099a0001c0004t0027g0237 | 3 | HG02486.hp1 HG03471.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.519+7882_519+7883i others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749979 | |||||
| chr1:217749979
|
C | CTATATAT others(7): Show |
1 | a0001c0001t0004g0143 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.519+7882_519+7883i others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749979 | |||||
| chr1:217749979
|
C | CTATATAT others(9): Show |
2 | a0001c0002t0049g0055a0003c0007t0009g0117 | 2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.519+7882_519+7883i others(18): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749979 | |||||
| chr1:217749979
|
C | CTATATAT others(11): Show |
2 | a0001c0001t0001g0090a0001c0002t0001g0104 | 2 | HG02559.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.519+7882_519+7883i others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749979 | |||||
| chr1:217749979
|
C | CTATATAT others(13): Show |
1 | a0001c0001t0002g0047 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.519+7882_519+7883i others(22): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749979 | |||||
| chr1:217749981
|
C | A | 65 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0041others(62): Show | 65 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.519+7883C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749981 | ||||||
| chr1:217749981
|
C | CTA | 4 | a0001c0001t0001g0124a0001c0001t0001g0162a0001c0001t0001g0197others(1): Show | 4 | HG00639.hp1 HG02155.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+7884_519+7885i others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749981 | |||||
| chr1:217749981
|
C | CTATA | 5 | a0001c0001t0016g0208a0001c0002t0005g0078a0001c0002t0012g0018others(2): Show | 5 | HG00140.hp2 HG01167.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+7884_519+7885i others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749981 | |||||
| chr1:217749981
|
C | CTATATAT others(1): Show |
4 | a0001c0001t0001g0163a0001c0001t0001g0216a0001c0002t0001g0191others(1): Show | 4 | HG00558.hp1 HG02738.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+7884_519+7885i others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749981 | |||||
| chr1:217749981
|
C | CTATATAT others(5): Show |
4 | a0001c0002t0001g0129a0001c0002t0026g0048a0001c0004t0034g0251others(1): Show | 4 | HG02055.hp1 NA18906.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+7884_519+7885i others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749981 | |||||
| chr1:217749981
|
C | CTATATAT others(7): Show |
1 | a0003c0007t0005g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.519+7884_519+7885i others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749981 | |||||
| chr1:217749981
|
C | CTATATAT others(11): Show |
2 | a0001c0002t0001g0083a0001c0003t0038g0244 | 2 | HG02976.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.519+7884_519+7885i others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749981 | |||||
| chr1:217749983
|
C | A | 90 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0041others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.519+7885C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749983 | ||||||
| chr1:217749983
|
C | CTATATAT others(5): Show |
2 | a0001c0002t0022g0196a0001c0005t0023g0100 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.519+7886_519+7887i others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749983 | |||||
| chr1:217749983
|
C | CTATATAT others(11): Show |
2 | a0001c0001t0001g0140a0001c0003t0003g0221 | 2 | HG00280.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.519+7886_519+7887i others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749983 | |||||
| chr1:217749983
|
C | CTATATAT others(13): Show |
3 | a0001c0001t0002g0013a0001c0001t0015g0059a0001c0003t0003g0210 | 3 | HG02486.hp2 NA18969.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.519+7886_519+7887i others(22): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749983 | |||||
| chr1:217749983
|
C | CTATATAT others(17): Show |
1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.519+7886_519+7887i others(26): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749983 | |||||
| chr1:217749983
|
C | CTATATAT others(23): Show |
1 | a0001c0003t0003g0235 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.519+7886_519+7887i others(32): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749983 | |||||
| chr1:217749985
|
C | A | 106 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0041others(103): Show | 106 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.519+7887C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749985 | ||||||
| chr1:217749985
|
C | CTATA | 3 | a0001c0002t0017g0151a0001c0002t0017g0152a0001c0002t0045g0145 | 3 | NA18962.hp1 NA18975.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.519+7911_519+7914d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTATATA | 4 | a0001c0001t0001g0046a0001c0001t0046g0153a0001c0002t0001g0149others(1): Show | 4 | NA18946.hp1 NA18979.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+7909_519+7914d others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTATATAT others(3): Show |
3 | a0001c0001t0001g0082a0001c0002t0005g0056a0001c0002t0007g0051 | 3 | HG00438.hp2 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.519+7905_519+7914d others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTATATAT others(5): Show |
2 | a0001c0004t0004g0240a0001c0005t0001g0192 | 2 | HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.519+7903_519+7914d others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTATATAT others(7): Show |
3 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0039 | 3 | HG02129.hp1 HG03540.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.519+7901_519+7914d others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTATATAT others(11): Show |
1 | a0003c0007t0009g0116 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.519+7897_519+7914d others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTATATAT others(13): Show |
3 | a0001c0001t0006g0096a0001c0003t0001g0220a0001c0009t0001g0178 | 3 | HG01981.hp1 HG02735.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.519+7895_519+7914d others(22): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTATATAT others(15): Show |
1 | a0001c0001t0004g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.519+7893_519+7914d others(24): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTATATAT others(17): Show |
1 | a0001c0003t0024g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.519+7891_519+7914d others(26): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTATATAT others(19): Show |
1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.519+7889_519+7914d others(28): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTATATAT others(23): Show |
2 | a0001c0001t0002g0023a0001c0003t0003g0224 | 2 | HG00140.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.519+7914_519+7915i others(32): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTATATAT others(31): Show |
1 | a0001c0001t0001g0005 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.519+7914_519+7915i others(40): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTATA | 4 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0111others(1): Show | 4 | NA18951.hp1 NA18979.hp1 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+7888_519+7889i others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTATAT others(3): Show |
1 | a0001c0001t0002g0031 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.519+7888_519+7889i others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTATAT others(5): Show |
2 | a0001c0001t0035g0085a0001c0002t0007g0062 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTATAT others(7): Show |
3 | a0001c0001t0020g0094a0001c0002t0009g0076a0001c0004t0004g0248 | 3 | HG01433.hp2 HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTATAT others(9): Show |
2 | a0001c0001t0006g0203a0001c0003t0003g0229 | 2 | HG04199.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(18): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTATAT others(11): Show |
2 | a0001c0001t0006g0205a0001c0003t0003g0211 | 2 | HG00323.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTATAT others(15): Show |
2 | a0001c0003t0001g0231a0001c0003t0014g0230 | 2 | HG02896.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(24): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTATAT others(19): Show |
1 | a0001c0001t0002g0038 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.519+7888_519+7889i others(28): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTATAT others(21): Show |
2 | a0001c0001t0011g0227a0001c0003t0003g0214 | 2 | HG00609.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(30): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTATAT others(23): Show |
1 | a0001c0001t0002g0032 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.519+7888_519+7889i others(32): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTATAT others(25): Show |
1 | a0001c0001t0002g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(34): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTAT others(5): Show |
3 | a0001c0001t0002g0176a0001c0004t0004g0246a0001c0008t0014g0213 | 3 | HG01952.hp1 HG02886.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTAT others(7): Show |
2 | a0001c0004t0004g0247a0001c0004t0008g0241 | 2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTAT others(9): Show |
2 | a0001c0001t0006g0202a0001c0002t0013g0193 | 2 | HG01074.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(18): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTAT others(11): Show |
1 | a0001c0001t0010g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.519+7888_519+7889i others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTAT others(19): Show |
4 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0002g0019others(1): Show | 4 | HG00738.hp2 HG01168.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+7888_519+7889i others(28): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTAT others(21): Show |
1 | a0001c0003t0003g0223 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(30): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(3): Show |
3 | a0001c0001t0016g0172a0001c0001t0050g0017a0001c0002t0019g0066 | 3 | HG00558.hp2 HG03516.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(5): Show |
2 | a0001c0002t0007g0061a0001c0002t0007g0067 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(7): Show |
1 | a0001c0001t0001g0209 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(9): Show |
6 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0044others(3): Show | 6 | HG01099.hp1 HG01952.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+7888_519+7889i others(18): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(11): Show |
2 | a0001c0001t0002g0006a0001c0001t0048g0110 | 2 | HG03098.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(13): Show |
3 | a0001c0001t0001g0177a0001c0003t0003g0212a0001c0003t0003g0228 | 3 | HG02148.hp1 NA18968.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(22): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(17): Show |
2 | a0001c0001t0002g0001a0001c0001t0002g0030 | 2 | HG01361.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(26): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(19): Show |
1 | a0001c0002t0001g0131 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.519+7888_519+7889i others(28): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(23): Show |
1 | a0001c0001t0001g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.519+7888_519+7889i others(32): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(5): Show |
1 | a0001c0002t0007g0060 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(7): Show |
1 | a0001c0001t0002g0007 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(13): Show |
2 | a0001c0001t0002g0020a0001c0002t0039g0057 | 2 | HG00323.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(22): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(15): Show |
3 | a0001c0001t0001g0037a0001c0001t0010g0043a0001c0003t0003g0226 | 3 | HG03688.hp2 NA18959.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(24): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(17): Show |
1 | a0001c0001t0001g0009 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.519+7888_519+7889i others(26): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(19): Show |
2 | a0001c0001t0001g0011a0001c0002t0001g0064 | 2 | HG02698.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(28): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(5): Show |
1 | a0001c0002t0002g0133 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(11): Show |
1 | a0001c0001t0006g0161 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.519+7888_519+7889i others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(13): Show |
1 | a0001c0001t0001g0065 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(22): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(15): Show |
2 | a0001c0001t0005g0084a0001c0001t0015g0093 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(24): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(17): Show |
2 | a0001c0001t0005g0052a0001c0001t0005g0068 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(26): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(19): Show |
1 | a0001c0001t0001g0012 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(28): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(21): Show |
3 | a0001c0001t0002g0027a0001c0001t0002g0171a0001c0001t0015g0058 | 3 | HG00099.hp1 HG02976.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(30): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(25): Show |
1 | a0001c0003t0003g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.519+7888_519+7889i others(34): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(27): Show |
1 | a0001c0001t0004g0069 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.519+7888_519+7889i others(36): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(29): Show |
1 | a0001c0001t0011g0034 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(38): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(17): Show |
2 | a0001c0001t0056g0075a0001c0003t0001g0215 | 2 | HG02895.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(26): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(19): Show |
1 | a0001c0001t0023g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(28): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(27): Show |
1 | a0001c0003t0003g0218 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(36): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(31): Show |
1 | a0001c0001t0002g0003 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(40): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(13): Show |
1 | a0001c0001t0007g0142 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.519+7888_519+7889i others(22): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(17): Show |
1 | a0001c0003t0003g0222 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.519+7888_519+7889i others(26): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(21): Show |
2 | a0001c0001t0001g0036a0001c0003t0003g0098 | 2 | HG01361.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.519+7888_519+7889i others(30): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(23): Show |
1 | a0001c0003t0031g0225 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(32): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(29): Show |
1 | a0001c0001t0002g0033 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(38): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(35): Show |
1 | a0001c0001t0040g0025 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(44): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(21): Show |
1 | a0001c0003t0003g0097 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(30): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(37): Show |
1 | a0001c0001t0002g0167 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.519+7888_519+7889i others(46): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749985
|
C | CTCTCTCT others(29): Show |
1 | a0001c0001t0001g0028 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.519+7888_519+7889i others(38): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217749985 | |||||
| chr1:217749987
|
A | C | 5 | a0001c0001t0001g0164a0001c0001t0001g0174a0001c0001t0001g0236others(2): Show | 5 | HG00733.hp2 HG01167.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+7889A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749987 | ||||||
| chr1:217749989
|
A | C | 1 | a0001c0001t0001g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.519+7891A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749989 | ||||||
| chr1:217749991
|
A | C | 1 | a0001c0001t0001g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.519+7893A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217749991 | ||||||
| chr1:217750102
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.519+8004G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217750102 | ||||||
| chr1:217750293
|
A | G | 1 | a0001c0003t0001g0220 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.519+8195A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217750293 | ||||||
| chr1:217750501
|
T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.519+8403T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217750501 | ||||||
| chr1:217750601
|
A | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.519+8503A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217750601 | ||||||
| chr1:217750628
|
A | T | 26 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0001g0231others(23): Show | 26 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.519+8530A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217750628 | ||||||
| chr1:217750754
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.519+8656A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217750754 | ||||||
| chr1:217750768
|
C | A | 1 | a0001c0002t0012g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.519+8670C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217750768 | ||||||
| chr1:217750856
|
A | T | 8 | a0001c0002t0005g0078a0001c0002t0012g0018a0001c0002t0012g0077others(5): Show | 8 | HG00140.hp2 HG00639.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+8758A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217750856 | ||||||
| chr1:217750870
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.519+8772G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217750870 | ||||||
| chr1:217750998
|
T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.519+8900T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217750998 | ||||||
| chr1:217751017
|
T | C | 1 | a0001c0012t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+8919T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217751017 | ||||||
| chr1:217751040
|
C | A | 1 | a0001c0001t0008g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.519+8942C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217751040 | ||||||
| chr1:217751147
|
C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.519+9049C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217751147 | ||||||
| chr1:217751242
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.519+9144A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217751242 | ||||||
| chr1:217751415
|
A | C | 5 | a0001c0005t0001g0141a0001c0005t0001g0192a0001c0005t0004g0071others(2): Show | 5 | HG01261.hp1 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+9317A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217751415 | ||||||
| chr1:217751511
|
G | C | 1 | a0001c0002t0014g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.519+9413G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217751511 | ||||||
| chr1:217751704
|
G | A | 2 | a0001c0003t0024g0243a0001c0003t0038g0244 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.519+9606G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217751704 | ||||||
| chr1:217751708
|
T | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.519+9610T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217751708 | ||||||
| chr1:217751801
|
T | C | 3 | a0001c0001t0006g0201a0001c0001t0006g0202a0001c0001t0006g0203 | 3 | HG01074.hp1 HG01099.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.519+9703T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217751801 | ||||||
| chr1:217751812
|
A | G | 2 | a0001c0003t0003g0226a0001c0003t0031g0225 | 2 | NA18990.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.519+9714A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217751812 | ||||||
| chr1:217751878
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.519+9780G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217751878 | ||||||
| chr1:217752274
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.519+10176C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217752274 | ||||||
| chr1:217752330
|
A | T | 84 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(81): Show | 84 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.519+10232A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217752330 | ||||||
| chr1:217752425
|
G | A | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.519+10327G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217752425 | ||||||
| chr1:217752464
|
G | A | 1 | a0001c0003t0001g0220 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.519+10366G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217752464 | ||||||
| chr1:217752705
|
C | T | 1 | a0001c0002t0021g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.519+10607C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217752705 | ||||||
| chr1:217752740
|
C | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.519+10642C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217752740 | ||||||
| chr1:217752853
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.519+10755A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217752853 | ||||||
| chr1:217752870
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.519+10772C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217752870 | ||||||
| chr1:217753152
|
C | T | 1 | a0002c0006t0018g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.519+11054C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217753152 | ||||||
| chr1:217753163
|
T | G | 80 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(77): Show | 80 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.519+11065T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217753163 | ||||||
| chr1:217753192
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.519+11094G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217753192 | ||||||
| chr1:217753334
|
T | G | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.519+11236T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217753334 | ||||||
| chr1:217753379
|
G | A | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.519+11281G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217753379 | ||||||
| chr1:217753441
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.519+11343C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217753441 | ||||||
| chr1:217753452
|
T | C | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.519+11354T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217753452 | ||||||
| chr1:217753473
|
A | T | 7 | a0001c0002t0001g0144a0001c0002t0001g0149a0001c0002t0001g0179others(4): Show | 7 | HG03831.hp1 NA18946.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+11375A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217753473 | ||||||
| chr1:217753580
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.519+11482G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217753580 | ||||||
| chr1:217753950
|
A | G | 1 | a0001c0002t0001g0132 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.519+11852A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217753950 | ||||||
| chr1:217754191
|
C | T | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.519+12093C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217754191 | ||||||
| chr1:217754356
|
A | G | 1 | a0001c0003t0003g0235 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.519+12258A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217754356 | ||||||
| chr1:217754447
|
G | A | 8 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+12349G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217754447 | ||||||
| chr1:217754696
|
T | C | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.519+12598T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217754696 | ||||||
| chr1:217754754
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.519+12656G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217754754 | ||||||
| chr1:217754771
|
C | T | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.519+12673C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217754771 | ||||||
| chr1:217754839
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.519+12741A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217754839 | ||||||
| chr1:217755328
|
T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.519+13230T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217755328 | ||||||
| chr1:217755540
|
C | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.519+13442C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217755540 | ||||||
| chr1:217755601
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0005g0118 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.519+13503T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217755601 | ||||||
| chr1:217755666
|
A | G | 5 | a0001c0002t0001g0104a0001c0002t0001g0108a0001c0002t0001g0127others(2): Show | 5 | NA18939.hp1 NA18942.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+13568A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217755666 | ||||||
| chr1:217755798
|
C | T | 88 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(85): Show | 88 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.519+13700C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217755798 | ||||||
| chr1:217755893
|
G | A | 6 | a0001c0001t0002g0101a0001c0001t0002g0158a0001c0001t0002g0159others(3): Show | 6 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+13795G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217755893 | ||||||
| chr1:217755965
|
C | T | 1 | a0001c0002t0021g0160 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.519+13867C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217755965 | ||||||
| chr1:217755993
|
TA | T | 3 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089 | 3 | HG02559.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.519+13896delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217755993 | ||||||
| chr1:217756323
|
G | GT | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.519+14234dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217756323 | |||||
| chr1:217756350
|
T | A | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.519+14252T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217756350 | ||||||
| chr1:217756372
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.519+14274A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217756372 | ||||||
| chr1:217756388
|
G | T | 5 | a0001c0001t0001g0123a0001c0001t0008g0045a0001c0001t0008g0049others(2): Show | 5 | HG02451.hp1 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+14290G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217756388 | ||||||
| chr1:217756661
|
A | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.519+14563A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217756661 | ||||||
| chr1:217756721
|
G | T | 1 | a0001c0003t0003g0235 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.519+14623G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217756721 | ||||||
| chr1:217756808
|
G | T | 1 | a0001c0002t0025g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.519+14710G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217756808 | ||||||
| chr1:217756880
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.519+14782C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217756880 | ||||||
| chr1:217756947
|
C | T | 1 | a0002c0006t0003g0185 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.519+14849C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217756947 | ||||||
| chr1:217757342
|
T | G | 2 | a0001c0001t0001g0028a0001c0001t0002g0171 | 2 | NA18939.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.519+15244T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217757342 | ||||||
| chr1:217757373
|
C | T | 81 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(78): Show | 81 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.519+15275C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217757373 | ||||||
| chr1:217757642
|
A | G | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.519+15544A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217757642 | ||||||
| chr1:217757674
|
G | A | 3 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089 | 3 | HG02559.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.519+15576G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217757674 | ||||||
| chr1:217757793
|
A | T | 5 | a0001c0002t0001g0104a0001c0002t0001g0108a0001c0002t0001g0127others(2): Show | 5 | NA18939.hp1 NA18942.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+15695A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217757793 | ||||||
| chr1:217758212
|
T | C | 1 | a0001c0004t0053g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.519+16114T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217758212 | ||||||
| chr1:217758235
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.520-16099A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217758235 | ||||||
| chr1:217758323
|
A | G | 80 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.520-16011A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217758323 | ||||||
| chr1:217758635
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.520-15699A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217758635 | ||||||
| chr1:217758670
|
G | A | 2 | a0001c0002t0009g0072a0001c0002t0013g0121 | 2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.520-15664G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217758670 | ||||||
| chr1:217758746
|
G | A | 1 | a0001c0002t0020g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.520-15588G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217758746 | ||||||
| chr1:217758963
|
T | A | 85 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(82): Show | 85 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.520-15371T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217758963 | ||||||
| chr1:217759088
|
G | T | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.520-15246G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217759088 | ||||||
| chr1:217759124
|
A | G | 1 | a0001c0002t0021g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.520-15210A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217759124 | ||||||
| chr1:217759224
|
C | T | 20 | a0001c0002t0005g0078a0001c0002t0009g0072a0001c0002t0009g0076others(17): Show | 20 | HG00140.hp2 HG00639.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.520-15110C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217759224 | ||||||
| chr1:217759383
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.520-14951C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217759383 | ||||||
| chr1:217759480
|
A | T | 72 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(69): Show | 72 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.520-14854A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217759480 | ||||||
| chr1:217759674
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.520-14660A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217759674 | ||||||
| chr1:217759674
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.520-14660A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217759674 | ||||||
| chr1:217759690
|
G | T | 1 | a0001c0001t0003g0168 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.520-14644G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217759690 | ||||||
| chr1:217759704
|
T | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.520-14630T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217759704 | ||||||
| chr1:217759796
|
G | T | 1 | a0001c0003t0003g0211 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.520-14538G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217759796 | ||||||
| chr1:217759820
|
G | T | 1 | a0001c0002t0039g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.520-14514G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217759820 | ||||||
| chr1:217759886
|
A | G | 8 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-14448A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217759886 | ||||||
| chr1:217760097
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.520-14237T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217760097 | ||||||
| chr1:217760105
|
C | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.520-14229C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217760105 | ||||||
| chr1:217760273
|
C | A | 1 | a0001c0002t0020g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.520-14061C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217760273 | ||||||
| chr1:217760368
|
A | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0033a0001c0001t0002g0167 | 3 | HG01106.hp2 HG02004.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.520-13966A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217760368 | ||||||
| chr1:217760646
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.520-13688G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217760646 | ||||||
| chr1:217761005
|
G | A | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-13329G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217761005 | ||||||
| chr1:217761099
|
T | A | 1 | a0001c0001t0008g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.520-13235T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217761099 | ||||||
| chr1:217761358
|
T | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.520-12976T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217761358 | ||||||
| chr1:217761389
|
A | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(45): Show | 48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.520-12945A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217761389 | ||||||
| chr1:217761413
|
G | A | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-12921G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217761413 | ||||||
| chr1:217761581
|
G | A | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.520-12753G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217761581 | ||||||
| chr1:217761624
|
G | A | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-12710G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217761624 | ||||||
| chr1:217761655
|
A | C | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-12679A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217761655 | ||||||
| chr1:217761725
|
T | A | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-12609T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217761725 | ||||||
| chr1:217761864
|
C | T | 72 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(69): Show | 72 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.520-12470C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217761864 | ||||||
| chr1:217761919
|
C | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.520-12415C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217761919 | ||||||
| chr1:217761998
|
C | T | 1 | a0001c0001t0002g0171 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.520-12336C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217761998 | ||||||
| chr1:217762006
|
T | C | 3 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093 | 3 | HG02486.hp2 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.520-12328T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217762006 | ||||||
| chr1:217762289
|
A | G | 1 | a0001c0004t0004g0247 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.520-12045A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217762289 | ||||||
| chr1:217762430
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.520-11904C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217762430 | ||||||
| chr1:217762448
|
C | G | 8 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-11886C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217762448 | ||||||
| chr1:217762613
|
G | T | 2 | a0001c0001t0001g0173a0001c0001t0002g0176 | 2 | HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.520-11721G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217762613 | ||||||
| chr1:217762666
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.520-11668G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217762666 | ||||||
| chr1:217762713
|
C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.520-11621C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217762713 | ||||||
| chr1:217762734
|
C | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.520-11600C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217762734 | ||||||
| chr1:217763034
|
C | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.520-11300C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217763034 | ||||||
| chr1:217763226
|
A | G | 1 | a0001c0001t0001g0009 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.520-11108A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217763226 | ||||||
| chr1:217763397
|
G | GA | 17 | a0001c0001t0001g0123a0001c0001t0001g0209a0001c0001t0002g0038others(14): Show | 17 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.520-10926dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217763397 | |||||
| chr1:217763397
|
GA | G | 80 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0041others(77): Show | 80 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.520-10926delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217763397 | |||||
| chr1:217763605
|
A | G | 4 | a0001c0001t0001g0190a0001c0001t0008g0189a0001c0001t0012g0188others(1): Show | 4 | HG03130.hp1 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-10729A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217763605 | ||||||
| chr1:217763675
|
G | C | 1 | a0001c0001t0002g0167 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.520-10659G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217763675 | ||||||
| chr1:217763750
|
C | T | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.520-10584C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217763750 | ||||||
| chr1:217763764
|
T | A | 1 | a0001c0005t0001g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.520-10570T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217763764 | ||||||
| chr1:217763926
|
G | T | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.520-10408G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217763926 | ||||||
| chr1:217763988
|
G | A | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-10346G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217763988 | ||||||
| chr1:217764043
|
A | G | 5 | a0001c0001t0001g0123a0001c0001t0008g0045a0001c0001t0008g0049others(2): Show | 5 | HG02451.hp1 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.520-10291A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217764043 | ||||||
| chr1:217764479
|
A | T | 1 | a0001c0002t0044g0091 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.520-9855A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217764479 | ||||||
| chr1:217764576
|
G | A | 1 | a0001c0003t0003g0222 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.520-9758G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217764576 | ||||||
| chr1:217764701
|
T | C | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-9633T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217764701 | ||||||
| chr1:217764819
|
T | C | 2 | a0001c0002t0011g0198a0001c0002t0011g0199 | 2 | HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.520-9515T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217764819 | ||||||
| chr1:217764876
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.520-9458G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217764876 | ||||||
| chr1:217765146
|
T | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.520-9188T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217765146 | ||||||
| chr1:217765159
|
C | CT | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.520-9166dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217765159 | |||||
| chr1:217765159
|
CT | C | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-9166delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217765159 | |||||
| chr1:217765888
|
A | G | 43 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.520-8446A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217765888 | ||||||
| chr1:217766082
|
A | G | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.520-8252A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217766082 | ||||||
| chr1:217766517
|
T | A | 84 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(81): Show | 84 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.520-7817T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217766517 | ||||||
| chr1:217766533
|
A | T | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.520-7801A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217766533 | ||||||
| chr1:217766576
|
G | T | 84 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(81): Show | 84 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.520-7758G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217766576 | ||||||
| chr1:217766681
|
A | T | 62 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(59): Show | 62 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.520-7653A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217766681 | ||||||
| chr1:217766720
|
CT | C | 71 | a0001c0002t0001g0064a0001c0002t0001g0083a0001c0002t0001g0086others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.520-7599delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217766720 | |||||
| chr1:217766720
|
CTT | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.520-7600_520-7599d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217766720 | |||||
| chr1:217766723
|
T | TTC | 72 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(69): Show | 72 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.520-7610_520-7609i others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217766723 | |||||
| chr1:217766724
|
T | TC | 8 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-7610_520-7609i others(3): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217766724 | ||||||
| chr1:217766725
|
T | C | 4 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(1): Show | 4 | HG02559.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-7609T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217766725 | ||||||
| chr1:217766736
|
A | G | 80 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(77): Show | 80 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.520-7598A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217766736 | ||||||
| chr1:217766917
|
G | C | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.520-7417G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217766917 | ||||||
| chr1:217767399
|
GGT | G | 29 | a0001c0002t0001g0064a0001c0002t0001g0083a0001c0002t0001g0103others(26): Show | 29 | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.520-6932_520-6931d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217767399 | |||||
| chr1:217767466
|
T | C | 6 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-6868T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217767466 | ||||||
| chr1:217767560
|
A | T | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.520-6774A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217767560 | ||||||
| chr1:217767665
|
G | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.520-6669G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217767665 | ||||||
| chr1:217767804
|
C | T | 84 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(81): Show | 84 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.520-6530C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217767804 | ||||||
| chr1:217767829
|
T | C | 1 | a0001c0003t0001g0231 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.520-6505T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217767829 | ||||||
| chr1:217767914
|
G | A | 3 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093 | 3 | HG02486.hp2 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.520-6420G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217767914 | ||||||
| chr1:217767970
|
G | A | 2 | a0001c0001t0008g0045a0001c0001t0042g0035 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.520-6364G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217767970 | ||||||
| chr1:217768073
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.520-6261C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217768073 | ||||||
| chr1:217768302
|
G | A | 1 | a0001c0001t0002g0003 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.520-6032G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217768302 | ||||||
| chr1:217768495
|
CT | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0123a0001c0001t0001g0140others(2): Show | 5 | HG00738.hp2 HG02451.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-5825delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217768495 | |||||
| chr1:217768510
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.520-5824A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217768510 | ||||||
| chr1:217768553
|
G | A | 1 | a0001c0001t0006g0096 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.520-5781G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217768553 | ||||||
| chr1:217768576
|
C | T | 1 | a0001c0004t0005g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.520-5758C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217768576 | ||||||
| chr1:217768646
|
C | T | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-5688C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217768646 | ||||||
| chr1:217768788
|
G | A | 3 | a0001c0002t0013g0193a0001c0002t0022g0194a0001c0002t0022g0196 | 3 | HG02630.hp1 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.520-5546G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217768788 | ||||||
| chr1:217768939
|
C | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.520-5395C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217768939 | ||||||
| chr1:217769304
|
C | A | 1 | a0001c0004t0053g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.520-5030C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217769304 | ||||||
| chr1:217769327
|
T | C | 8 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-5007T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217769327 | ||||||
| chr1:217769354
|
C | A | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.520-4980C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217769354 | ||||||
| chr1:217769561
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.520-4773T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217769561 | ||||||
| chr1:217769592
|
G | A | 84 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(81): Show | 84 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.520-4742G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217769592 | ||||||
| chr1:217769874
|
G | A | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.520-4460G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217769874 | ||||||
| chr1:217770082
|
T | C | 22 | a0001c0003t0001g0215a0001c0003t0001g0220a0001c0003t0003g0097others(19): Show | 22 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.520-4252T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770082 | ||||||
| chr1:217770106
|
T | C | 4 | a0001c0002t0001g0108a0001c0002t0001g0127a0001c0002t0001g0128others(1): Show | 4 | NA18939.hp1 NA18942.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-4228T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770106 | ||||||
| chr1:217770265
|
G | T | 3 | a0001c0001t0001g0123a0001c0001t0008g0049a0001c0001t0008g0136 | 3 | HG02451.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.520-4069G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770265 | ||||||
| chr1:217770299
|
C | T | 1 | a0001c0003t0001g0231 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.520-4035C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770299 | ||||||
| chr1:217770456
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.520-3878G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770456 | ||||||
| chr1:217770656
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0041g0015others(1): Show | 4 | NA18951.hp2 NA18984.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-3678G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770656 | ||||||
| chr1:217770918
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.520-3416G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770918 | ||||||
| chr1:217770942
|
T | G | 4 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089others(1): Show | 4 | HG02559.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-3392T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770942 | ||||||
| chr1:217770978
|
A | AATTTTTT | 5 | a0001c0001t0001g0012a0001c0001t0002g0003a0001c0001t0002g0033others(2): Show | 5 | HG01099.hp2 HG01993.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-3356_520-3355i others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770978 | ||||||
| chr1:217770978
|
A | AATTTTTT others(1): Show |
13 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0021others(10): Show | 13 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-3356_520-3355i others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770978 | ||||||
| chr1:217770978
|
A | AATTTTTT others(2): Show |
16 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0024others(13): Show | 16 | HG00099.hp1 HG01168.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.520-3356_520-3355i others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770978 | ||||||
| chr1:217770978
|
A | AATTTTTT others(3): Show |
8 | a0001c0001t0001g0177a0001c0001t0002g0006a0001c0001t0002g0026others(5): Show | 8 | HG02015.hp1 HG02055.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-3356_520-3355i others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770978 | ||||||
| chr1:217770978
|
A | AATTTTTT others(4): Show |
4 | a0001c0001t0001g0065a0001c0001t0002g0001a0001c0001t0002g0032others(1): Show | 4 | HG00733.hp1 HG01361.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-3356_520-3355i others(13): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770978 | ||||||
| chr1:217770978
|
A | AATTTTTT others(5): Show |
1 | a0001c0001t0001g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.520-3356_520-3355i others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770978 | ||||||
| chr1:217770978
|
A | AT | 39 | a0001c0001t0005g0118a0001c0002t0001g0064a0001c0002t0001g0083others(36): Show | 39 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.520-3326dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
A | ATT | 15 | a0001c0001t0001g0236a0001c0001t0002g0181a0001c0002t0001g0108others(12): Show | 15 | HG00639.hp2 HG01167.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.520-3327_520-3326d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
A | ATTTTTTT others(11): Show |
3 | a0001c0001t0024g0040a0001c0004t0004g0240a0001c0004t0004g0247 | 3 | HG02723.hp2 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.520-3343_520-3326d others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
A | ATTTTTTT others(12): Show |
8 | a0001c0001t0001g0010a0001c0001t0001g0164a0001c0001t0002g0159others(5): Show | 8 | HG01071.hp1 HG01071.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-3344_520-3326d others(21): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
A | ATTTTTTT others(13): Show |
13 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0001g0154others(10): Show | 13 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-3345_520-3326d others(22): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
A | ATTTTTTT others(14): Show |
11 | a0001c0001t0001g0041a0001c0001t0001g0124a0001c0001t0001g0130others(8): Show | 11 | HG00558.hp1 HG00558.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-3346_520-3326d others(23): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
A | ATTTTTTT others(15): Show |
10 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0174others(7): Show | 10 | HG00438.hp2 HG00642.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.520-3347_520-3326d others(24): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
A | ATTTTTTT others(18): Show |
2 | a0001c0001t0001g0173a0001c0004t0034g0251 | 2 | HG02148.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.520-3350_520-3326d others(27): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
A | ATTTTTTT others(19): Show |
1 | a0002c0006t0018g0137 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.520-3351_520-3326d others(28): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
AT | A | 8 | a0001c0002t0001g0086a0001c0002t0044g0091a0001c0003t0031g0225others(5): Show | 8 | HG01168.hp1 HG01261.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-3326delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
ATT | A | 5 | a0001c0001t0001g0146a0001c0003t0001g0220a0001c0003t0003g0098others(2): Show | 5 | HG01361.hp1 HG02735.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.520-3327_520-3326d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
ATTT | A | 17 | a0001c0001t0006g0096a0001c0003t0001g0215a0001c0003t0003g0097others(14): Show | 17 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.520-3328_520-3326d others(5): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
ATTTT | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0209others(11): Show | 14 | HG00323.hp2 HG01070.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.520-3329_520-3326d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
ATTTTTT | A | 10 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0162others(7): Show | 10 | HG00609.hp2 HG02155.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.520-3331_520-3326d others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
ATTTTTTT | A | 10 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0005g0089others(7): Show | 10 | HG01109.hp1 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.520-3332_520-3326d others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.520-3335_520-3326d others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770978
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.520-3338_520-3326d others(15): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217770978 | |||||
| chr1:217770980
|
T | A | 1 | a0001c0003t0031g0225 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.520-3354T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770980 | ||||||
| chr1:217770981
|
T | A | 4 | a0001c0003t0001g0220a0001c0003t0003g0098a0001c0003t0003g0212others(1): Show | 4 | HG01361.hp1 HG02735.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-3353T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770981 | ||||||
| chr1:217770982
|
T | A | 16 | a0001c0003t0001g0215a0001c0003t0003g0097a0001c0003t0003g0211others(13): Show | 16 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.520-3352T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770982 | ||||||
| chr1:217770983
|
T | A | 6 | a0001c0001t0001g0044a0001c0003t0001g0231a0001c0003t0003g0210others(3): Show | 6 | HG02572.hp2 HG02896.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-3351T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217770983 | ||||||
| chr1:217771117
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.520-3217G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217771117 | ||||||
| chr1:217771376
|
G | C | 1 | a0001c0002t0001g0114 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.520-2958G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217771376 | ||||||
| chr1:217771380
|
A | G | 1 | a0001c0004t0004g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.520-2954A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217771380 | ||||||
| chr1:217771483
|
T | C | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.520-2851T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217771483 | ||||||
| chr1:217771486
|
T | C | 92 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(89): Show | 92 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.520-2848T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217771486 | ||||||
| chr1:217771643
|
T | C | 1 | a0001c0001t0002g0007 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.520-2691T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217771643 | ||||||
| chr1:217771713
|
A | G | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.520-2621A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217771713 | ||||||
| chr1:217771727
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.520-2607G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217771727 | ||||||
| chr1:217771822
|
A | G | 1 | a0001c0002t0030g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.520-2512A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217771822 | ||||||
| chr1:217771848
|
A | AAGG | 251 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.520-2484_520-2483i others(5): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217771848 | |||||
| chr1:217771928
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.520-2406A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217771928 | ||||||
| chr1:217771946
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0005g0089 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.520-2388T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217771946 | ||||||
| chr1:217771999
|
A | C | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.520-2335A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217771999 | ||||||
| chr1:217772115
|
A | T | 1 | a0001c0001t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.520-2219A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217772115 | ||||||
| chr1:217772118
|
TA | T | 24 | a0001c0001t0001g0087a0001c0001t0001g0124a0001c0001t0001g0154others(21): Show | 24 | HG00639.hp1 HG01109.hp1 HG02083.hp1 others(21): Show |
intron_variant | MODIFIER | c.520-2215delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217772118 | ||||||
| chr1:217772119
|
A | T | 46 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(43): Show | 46 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.520-2215A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217772119 | ||||||
| chr1:217772975
|
G | A | 1 | a0001c0011t0037g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.520-1359G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217772975 | ||||||
| chr1:217773057
|
T | A | 84 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(81): Show | 84 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.520-1277T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217773057 | ||||||
| chr1:217773093
|
C | T | 1 | a0001c0002t0005g0078 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.520-1241C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217773093 | ||||||
| chr1:217773114
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.520-1220G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217773114 | ||||||
| chr1:217773260
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.520-1074G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217773260 | ||||||
| chr1:217773308
|
A | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.520-1026A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217773308 | ||||||
| chr1:217773427
|
T | C | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.520-907T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217773427 | ||||||
| chr1:217773554
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.520-780A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217773554 | ||||||
| chr1:217773705
|
G | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.520-629G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217773705 | ||||||
| chr1:217773760
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.520-574T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217773760 | ||||||
| chr1:217773830
|
G | T | 2 | a0001c0002t0001g0126a0001c0002t0010g0125 | 2 | HG02129.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.520-504G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217773830 | ||||||
| chr1:217773891
|
T | TGAGTACA others(5416): Show |
1 | a0001c0003t0003g0210 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.520-428_520-427ins others(5423): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217773891 | |||||
| chr1:217773891
|
T | TGAGTACA others(5419): Show |
1 | a0001c0003t0003g0211 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.520-428_520-427ins others(5426): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217773891 | |||||
| chr1:217773891
|
T | TGAGTACA others(5420): Show |
1 | a0001c0003t0003g0212 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.520-428_520-427ins others(5427): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 217773891 | |||||
| chr1:217773967
|
C | T | 84 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(81): Show | 84 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.520-367C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217773967 | ||||||
| chr1:217774153
|
G | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.520-181G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 6/10 | chr1 | 217774153 | ||||||
| chr1:217774554
|
T | A | 1 | a0001c0001t0009g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.723+17T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217774554 | ||||||
| chr1:217774638
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.723+101T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217774638 | ||||||
| chr1:217775037
|
G | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.723+500G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217775037 | ||||||
| chr1:217775342
|
T | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.723+805T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217775342 | ||||||
| chr1:217775638
|
G | A | 170 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.723+1101G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217775638 | ||||||
| chr1:217775696
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.723+1159T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217775696 | ||||||
| chr1:217775698
|
T | G | 61 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(58): Show | 61 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.723+1161T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217775698 | ||||||
| chr1:217775700
|
T | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.723+1163T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217775700 | ||||||
| chr1:217775702
|
T | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.723+1165T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217775702 | ||||||
| chr1:217776033
|
A | G | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.723+1496A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217776033 | ||||||
| chr1:217776424
|
C | T | 4 | a0001c0001t0004g0054a0001c0001t0009g0120a0001c0001t0023g0053others(1): Show | 4 | HG02572.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+1887C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217776424 | ||||||
| chr1:217776559
|
T | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.723+2022T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217776559 | ||||||
| chr1:217776676
|
T | TA | 14 | a0001c0001t0001g0123a0001c0001t0001g0146a0001c0001t0001g0190others(11): Show | 14 | HG02015.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.723+2159dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 217776676 | |||||
| chr1:217776676
|
TA | T | 13 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0044others(10): Show | 13 | HG01168.hp1 HG02155.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.723+2159delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 217776676 | |||||
| chr1:217776744
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.723+2207G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217776744 | ||||||
| chr1:217776884
|
T | C | 21 | a0001c0002t0001g0064a0001c0002t0001g0083a0001c0002t0001g0103others(18): Show | 21 | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.723+2347T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217776884 | ||||||
| chr1:217777021
|
C | T | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(70): Show | 73 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.723+2484C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217777021 | ||||||
| chr1:217777042
|
AG | A | 9 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0033others(6): Show | 9 | HG00323.hp1 HG01099.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.723+2507delG | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 217777042 | |||||
| chr1:217777202
|
C | T | 85 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(82): Show | 85 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.723+2665C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217777202 | ||||||
| chr1:217777252
|
C | T | 8 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.723+2715C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217777252 | ||||||
| chr1:217777387
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.723+2850G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217777387 | ||||||
| chr1:217777453
|
G | A | 1 | a0001c0003t0003g0235 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.723+2916G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217777453 | ||||||
| chr1:217777537
|
T | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.723+3000T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217777537 | ||||||
| chr1:217777556
|
C | T | 1 | a0001c0003t0003g0223 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.723+3019C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217777556 | ||||||
| chr1:217777667
|
G | C | 21 | a0001c0003t0001g0215a0001c0003t0003g0097a0001c0003t0003g0098others(18): Show | 21 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.723+3130G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217777667 | ||||||
| chr1:217777814
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.723+3277A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217777814 | ||||||
| chr1:217778024
|
A | G | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+3487A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217778024 | ||||||
| chr1:217778120
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.723+3583T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217778120 | ||||||
| chr1:217778271
|
G | T | 21 | a0001c0003t0001g0215a0001c0003t0003g0097a0001c0003t0003g0098others(18): Show | 21 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.723+3734G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217778271 | ||||||
| chr1:217778307
|
G | T | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.723+3770G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217778307 | ||||||
| chr1:217778319
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.723+3782G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217778319 | ||||||
| chr1:217778327
|
A | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.723+3790A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217778327 | ||||||
| chr1:217778521
|
A | C | 2 | a0001c0001t0001g0090a0001c0001t0005g0089 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.724-3653A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217778521 | ||||||
| chr1:217778547
|
G | A | 1 | a0001c0001t0003g0168 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.724-3627G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217778547 | ||||||
| chr1:217778925
|
C | G | 5 | a0001c0001t0001g0123a0001c0001t0008g0045a0001c0001t0008g0049others(2): Show | 5 | HG02451.hp1 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.724-3249C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217778925 | ||||||
| chr1:217779084
|
G | GAT | 5 | a0001c0001t0001g0123a0001c0001t0008g0045a0001c0001t0008g0049others(2): Show | 5 | HG02451.hp1 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.724-3077_724-3076d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 217779084 | |||||
| chr1:217779144
|
T | TTG | 72 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(69): Show | 72 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.724-3002_724-3001d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 217779144 | |||||
| chr1:217779144
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.724-3010_724-3001d others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 217779144 | |||||
| chr1:217779144
|
TTGTG | T | 10 | a0001c0001t0001g0209a0001c0001t0005g0084a0001c0001t0006g0096others(7): Show | 10 | HG00323.hp2 HG00738.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.724-3004_724-3001d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 217779144 | |||||
| chr1:217779144
|
TTGTGTG | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.724-3006_724-3001d others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 217779144 | |||||
| chr1:217779144
|
TTGTGTGT others(3): Show |
T | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-3010_724-3001d others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 217779144 | |||||
| chr1:217779363
|
G | A | 12 | a0001c0002t0009g0072a0001c0002t0009g0076a0001c0002t0013g0099others(9): Show | 12 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.724-2811G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217779363 | ||||||
| chr1:217779534
|
G | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.724-2640G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217779534 | ||||||
| chr1:217779798
|
T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.724-2376T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217779798 | ||||||
| chr1:217779853
|
G | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.724-2321G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217779853 | ||||||
| chr1:217779999
|
C | G | 1 | a0001c0002t0009g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.724-2175C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217779999 | ||||||
| chr1:217780336
|
T | TAA | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.724-1836_724-1835d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 217780336 | |||||
| chr1:217780397
|
G | A | 21 | a0001c0003t0001g0215a0001c0003t0003g0097a0001c0003t0003g0098others(18): Show | 21 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.724-1777G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217780397 | ||||||
| chr1:217780465
|
G | A | 1 | a0001c0001t0008g0189 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.724-1709G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217780465 | ||||||
| chr1:217780511
|
A | C | 1 | a0001c0002t0025g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.724-1663A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217780511 | ||||||
| chr1:217780672
|
C | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0001g0163others(3): Show | 6 | HG00558.hp1 NA18951.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.724-1502C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217780672 | ||||||
| chr1:217780726
|
A | G | 1 | a0001c0004t0004g0240 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.724-1448A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217780726 | ||||||
| chr1:217780803
|
G | A | 1 | a0001c0002t0013g0193 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.724-1371G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217780803 | ||||||
| chr1:217780972
|
T | C | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.724-1202T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217780972 | ||||||
| chr1:217781036
|
G | A | 93 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.724-1138G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217781036 | ||||||
| chr1:217781093
|
T | C | 1 | a0001c0002t0003g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.724-1081T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217781093 | ||||||
| chr1:217781126
|
C | T | 1 | a0001c0001t0048g0110 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.724-1048C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217781126 | ||||||
| chr1:217781181
|
G | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.724-993G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217781181 | ||||||
| chr1:217781190
|
A | G | 10 | a0001c0002t0009g0076a0001c0002t0013g0099a0001c0002t0013g0193others(7): Show | 10 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.724-984A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217781190 | ||||||
| chr1:217781284
|
C | G | 1 | a0001c0004t0004g0248 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.724-890C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217781284 | ||||||
| chr1:217781443
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0005g0118 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.724-731C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217781443 | ||||||
| chr1:217781545
|
A | T | 1 | a0001c0001t0018g0183 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.724-629A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217781545 | ||||||
| chr1:217781631
|
A | G | 1 | a0001c0003t0003g0097 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.724-543A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217781631 | ||||||
| chr1:217781678
|
G | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.724-496G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | chr1 | 217781678 | ||||||
| chr1:217782013
|
ATAT | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.724-157_724-155del others(3): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 217782013 | |||||
| chr1:217782589
|
A | C | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.872+267A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217782589 | ||||||
| chr1:217782705
|
A | G | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.872+383A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217782705 | ||||||
| chr1:217782823
|
A | AT | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.872+509dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217782823 | |||||
| chr1:217782852
|
T | C | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.872+530T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217782852 | ||||||
| chr1:217783182
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.872+860G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217783182 | ||||||
| chr1:217783287
|
T | C | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+965T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217783287 | ||||||
| chr1:217783365
|
C | A | 25 | a0001c0003t0001g0215a0001c0003t0001g0231a0001c0003t0003g0097others(22): Show | 25 | HG00280.hp2 HG00609.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.872+1043C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217783365 | ||||||
| chr1:217783402
|
A | C | 3 | a0003c0007t0005g0115a0003c0007t0009g0116a0003c0007t0009g0117 | 3 | HG02257.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.872+1080A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217783402 | ||||||
| chr1:217783656
|
GCAAAGGT others(3): Show |
G | 1 | a0001c0002t0012g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.872+1339_872+1348d others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217783656 | |||||
| chr1:217783917
|
T | G | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.872+1595T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217783917 | ||||||
| chr1:217784013
|
T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.872+1691T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217784013 | ||||||
| chr1:217784052
|
A | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.872+1730A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217784052 | ||||||
| chr1:217784089
|
A | AT | 6 | a0001c0005t0001g0141a0001c0005t0001g0192a0001c0005t0004g0071others(3): Show | 6 | HG01261.hp1 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.872+1775dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217784089 | |||||
| chr1:217784120
|
T | A | 1 | a0001c0003t0003g0212 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.872+1798T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217784120 | ||||||
| chr1:217784240
|
T | A | 3 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093 | 3 | HG02486.hp2 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.872+1918T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217784240 | ||||||
| chr1:217784260
|
G | A | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(70): Show | 73 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.872+1938G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217784260 | ||||||
| chr1:217784264
|
C | T | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.872+1942C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217784264 | ||||||
| chr1:217784290
|
T | C | 1 | a0001c0012t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.872+1968T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217784290 | ||||||
| chr1:217784452
|
A | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.872+2130A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217784452 | ||||||
| chr1:217784587
|
A | G | 1 | a0002c0006t0018g0137 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.872+2265A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217784587 | ||||||
| chr1:217784682
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.872+2360A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217784682 | ||||||
| chr1:217785052
|
T | C | 6 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+2730T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217785052 | ||||||
| chr1:217785328
|
C | T | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.872+3006C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217785328 | ||||||
| chr1:217785399
|
C | G | 1 | a0001c0001t0005g0052 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.872+3077C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217785399 | ||||||
| chr1:217785546
|
G | A | 1 | a0001c0001t0011g0227 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.872+3224G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217785546 | ||||||
| chr1:217785558
|
C | T | 2 | a0001c0003t0024g0243a0001c0003t0038g0244 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.872+3236C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217785558 | ||||||
| chr1:217785669
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.872+3347G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217785669 | ||||||
| chr1:217785734
|
A | C | 2 | a0001c0004t0004g0246a0001c0004t0004g0248 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.872+3412A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217785734 | ||||||
| chr1:217785829
|
C | A | 1 | a0001c0001t0001g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.872+3507C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217785829 | ||||||
| chr1:217785869
|
C | T | 1 | a0001c0002t0001g0104 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.872+3547C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217785869 | ||||||
| chr1:217785875
|
T | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.872+3553T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217785875 | ||||||
| chr1:217786025
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.872+3703T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786025 | ||||||
| chr1:217786051
|
G | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.872+3729G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786051 | ||||||
| chr1:217786112
|
T | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.872+3790T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786112 | ||||||
| chr1:217786306
|
T | C | 1 | a0001c0002t0001g0132 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.872+3984T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786306 | ||||||
| chr1:217786372
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.872+4050G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786372 | ||||||
| chr1:217786390
|
G | A | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.872+4068G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786390 | ||||||
| chr1:217786478
|
T | G | 1 | a0001c0001t0002g0030 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.872+4156T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786478 | ||||||
| chr1:217786630
|
A | C | 8 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.872+4308A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786630 | ||||||
| chr1:217786670
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.872+4348A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786670 | ||||||
| chr1:217786749
|
C | CCTTCTTC others(5): Show |
1 | a0001c0002t0001g0111 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.872+4427_872+4428i others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786749 | ||||||
| chr1:217786749
|
C | CCTTCTTC others(8): Show |
1 | a0001c0002t0001g0134 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.872+4427_872+4428i others(17): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786749 | ||||||
| chr1:217786749
|
C | CCTTCTTC others(14): Show |
1 | a0001c0002t0001g0107 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.872+4427_872+4428i others(23): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786749 | ||||||
| chr1:217786750
|
T | C | 3 | a0001c0002t0001g0107a0001c0002t0001g0111a0001c0002t0001g0134 | 3 | NA18979.hp1 NA19087.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.872+4428T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786750 | ||||||
| chr1:217786750
|
T | TTCTTCTT others(4): Show |
1 | a0001c0002t0045g0145 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.872+4429_872+4430i others(13): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
T | TTCTTCTT others(10): Show |
1 | a0001c0002t0017g0113 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.872+4429_872+4430i others(19): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
T | TTTC | 13 | a0001c0001t0002g0020a0001c0001t0002g0030a0001c0001t0004g0069others(10): Show | 13 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.872+4489_872+4491d others(5): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
T | TTTCTTC | 26 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0002g0023others(23): Show | 26 | HG00140.hp1 HG00642.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.872+4486_872+4491d others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
T | TTTCTTCC others(8): Show |
1 | a0001c0003t0029g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.872+4434_872+4435i others(17): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
T | TTTCTTCT others(2): Show |
22 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0037others(19): Show | 22 | HG00280.hp2 HG01106.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.872+4483_872+4491d others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
T | TTTCTTCT others(5): Show |
24 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0081others(21): Show | 24 | HG01069.hp1 HG01361.hp2 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.872+4480_872+4491d others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
T | TTTCTTCT others(8): Show |
22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0044others(19): Show | 22 | HG00099.hp1 HG00733.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.872+4477_872+4491d others(17): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
T | TTTCTTCT others(11): Show |
10 | a0001c0001t0001g0011a0001c0002t0001g0083a0001c0002t0001g0103others(7): Show | 10 | HG00438.hp1 HG01981.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.872+4474_872+4491d others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
T | TTTCTTCT others(14): Show |
8 | a0001c0001t0001g0009a0001c0001t0002g0013a0001c0002t0001g0114others(5): Show | 8 | HG00099.hp2 HG00738.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.872+4471_872+4491d others(23): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
T | TTTCTTCT others(17): Show |
7 | a0001c0001t0002g0171a0001c0001t0010g0043a0001c0002t0001g0147others(4): Show | 7 | HG02004.hp2 NA18939.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.872+4468_872+4491d others(26): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
T | TTTCTTCT others(20): Show |
2 | a0001c0003t0003g0235a0001c0008t0014g0213 | 2 | NA18941.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.872+4465_872+4491d others(29): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
T | TTTCTTCT others(23): Show |
1 | a0001c0003t0003g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.872+4462_872+4491d others(32): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
TTTC | T | 24 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0046others(21): Show | 24 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.872+4489_872+4491d others(5): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
TTTCTTC | T | 28 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0123others(25): Show | 28 | HG00558.hp2 HG00642.hp2 HG01981.hp1 others(25): Show |
intron_variant | MODIFIER | c.872+4486_872+4491d others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
TTTCTTCT others(2): Show |
T | 11 | a0001c0001t0001g0036a0001c0001t0001g0170a0001c0001t0001g0173others(8): Show | 11 | HG00280.hp1 HG01167.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.872+4483_872+4491d others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
TTTCTTCT others(8): Show |
T | 9 | a0001c0001t0001g0119a0001c0001t0001g0148a0001c0001t0001g0190others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.872+4477_872+4491d others(17): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786750
|
TTTCTTCT others(11): Show |
T | 3 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089 | 3 | HG02559.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.872+4474_872+4491d others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786750 | |||||
| chr1:217786751
|
T | TTCTTCTT others(5): Show |
2 | a0001c0001t0020g0094a0001c0001t0035g0085 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.872+4440_872+4441i others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786751 | |||||
| chr1:217786757
|
T | TTCTTCC | 4 | a0001c0001t0003g0168a0001c0001t0004g0054a0001c0001t0018g0183others(1): Show | 4 | HG02886.hp1 NA18747.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+4440_872+4441i others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786757 | |||||
| chr1:217786760
|
T | TTCC | 5 | a0001c0001t0001g0082a0001c0001t0023g0053a0001c0004t0005g0233others(2): Show | 5 | HG00438.hp2 HG01109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.872+4440_872+4441i others(5): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217786760 | |||||
| chr1:217786763
|
T | C | 11 | a0001c0001t0001g0146a0001c0001t0001g0166a0001c0001t0001g0197others(8): Show | 11 | HG00609.hp2 HG01261.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.872+4441T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786763 | ||||||
| chr1:217786766
|
T | C | 20 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0046others(17): Show | 20 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.872+4444T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786766 | ||||||
| chr1:217786769
|
T | C | 23 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0130others(20): Show | 23 | HG00558.hp2 HG00642.hp2 HG02083.hp1 others(20): Show |
intron_variant | MODIFIER | c.872+4447T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786769 | ||||||
| chr1:217786772
|
T | C | 9 | a0001c0001t0001g0170a0001c0001t0001g0173a0001c0001t0001g0216others(6): Show | 9 | HG00280.hp1 HG01167.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.872+4450T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786772 | ||||||
| chr1:217786778
|
T | C | 8 | a0001c0001t0001g0119a0001c0001t0001g0148a0001c0001t0001g0190others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.872+4456T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786778 | ||||||
| chr1:217786781
|
T | C | 3 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089 | 3 | HG02559.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.872+4459T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786781 | ||||||
| chr1:217786798
|
C | A | 1 | a0005c0010t0001g0169 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.872+4476C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786798 | ||||||
| chr1:217786876
|
A | G | 3 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212 | 3 | NA18942.hp1 NA18969.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.872+4554A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786876 | ||||||
| chr1:217786879
|
A | T | 1 | a0001c0002t0003g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.872+4557A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786879 | ||||||
| chr1:217786940
|
A | G | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+4618A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786940 | ||||||
| chr1:217786956
|
C | T | 85 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(82): Show | 85 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.872+4634C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217786956 | ||||||
| chr1:217787088
|
A | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0010 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.872+4766A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217787088 | ||||||
| chr1:217787221
|
A | T | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(70): Show | 73 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.872+4899A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217787221 | ||||||
| chr1:217787335
|
C | T | 1 | a0001c0002t0054g0050 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.872+5013C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217787335 | ||||||
| chr1:217787662
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.872+5340G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217787662 | ||||||
| chr1:217787880
|
G | C | 2 | a0001c0001t0008g0045a0001c0001t0042g0035 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.872+5558G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217787880 | ||||||
| chr1:217787894
|
T | C | 5 | a0001c0002t0001g0104a0001c0002t0001g0108a0001c0002t0001g0127others(2): Show | 5 | NA18939.hp1 NA18942.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.872+5572T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217787894 | ||||||
| chr1:217788108
|
G | A | 2 | a0001c0001t0008g0045a0001c0001t0042g0035 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.872+5786G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217788108 | ||||||
| chr1:217788132
|
G | A | 1 | a0001c0001t0036g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.872+5810G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217788132 | ||||||
| chr1:217788345
|
TTC | T | 81 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(78): Show | 81 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.872+6025_872+6026d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217788345 | |||||
| chr1:217788376
|
C | T | 1 | a0001c0002t0001g0107 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.872+6054C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217788376 | ||||||
| chr1:217788390
|
A | G | 1 | a0001c0002t0012g0018 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.872+6068A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217788390 | ||||||
| chr1:217788473
|
G | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.872+6151G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217788473 | ||||||
| chr1:217788514
|
C | T | 87 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(84): Show | 87 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.872+6192C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217788514 | ||||||
| chr1:217788545
|
A | G | 85 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(82): Show | 85 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.872+6223A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217788545 | ||||||
| chr1:217788578
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.872+6256C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217788578 | ||||||
| chr1:217788755
|
G | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0033a0001c0001t0002g0167others(1): Show | 4 | HG01106.hp2 HG02004.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+6433G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217788755 | ||||||
| chr1:217788856
|
C | T | 5 | a0001c0001t0001g0123a0001c0001t0008g0045a0001c0001t0008g0049others(2): Show | 5 | HG02451.hp1 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+6534C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217788856 | ||||||
| chr1:217788984
|
C | T | 1 | a0001c0001t0004g0143 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.872+6662C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217788984 | ||||||
| chr1:217789117
|
T | C | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.872+6795T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217789117 | ||||||
| chr1:217789731
|
CTT | C | 5 | a0001c0001t0001g0123a0001c0001t0008g0045a0001c0001t0008g0049others(2): Show | 5 | HG02451.hp1 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+7412_872+7413d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217789731 | |||||
| chr1:217789809
|
T | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.872+7487T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217789809 | ||||||
| chr1:217789853
|
A | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 180 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.872+7531A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217789853 | ||||||
| chr1:217789951
|
C | T | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.872+7629C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217789951 | ||||||
| chr1:217789952
|
G | A | 4 | a0001c0001t0001g0154a0001c0001t0001g0165a0001c0001t0001g0216others(1): Show | 4 | HG02735.hp2 HG02738.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.872+7630G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217789952 | ||||||
| chr1:217789968
|
C | T | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.872+7646C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217789968 | ||||||
| chr1:217789969
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.872+7647G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217789969 | ||||||
| chr1:217789992
|
G | A | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.872+7670G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217789992 | ||||||
| chr1:217790001
|
CA | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.872+7681delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217790001 | |||||
| chr1:217790642
|
G | T | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+8320G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217790642 | ||||||
| chr1:217790660
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.872+8338C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217790660 | ||||||
| chr1:217790720
|
G | A | 1 | a0001c0003t0003g0226 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.872+8398G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217790720 | ||||||
| chr1:217790738
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0001t0005g0089 | 3 | HG02559.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.872+8416C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217790738 | ||||||
| chr1:217790873
|
C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.872+8551C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217790873 | ||||||
| chr1:217790903
|
A | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.872+8581A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217790903 | ||||||
| chr1:217790924
|
T | G | 2 | a0001c0001t0008g0045a0001c0001t0042g0035 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.872+8602T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217790924 | ||||||
| chr1:217791031
|
A | G | 73 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(70): Show | 73 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.872+8709A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217791031 | ||||||
| chr1:217791162
|
A | G | 4 | a0001c0001t0004g0054a0001c0001t0009g0120a0001c0001t0023g0053others(1): Show | 4 | HG02572.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+8840A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217791162 | ||||||
| chr1:217791318
|
A | G | 1 | a0001c0003t0031g0225 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.872+8996A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217791318 | ||||||
| chr1:217791610
|
C | A | 4 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0053g0239others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+9288C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217791610 | ||||||
| chr1:217791659
|
T | C | 1 | a0001c0002t0021g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.872+9337T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217791659 | ||||||
| chr1:217791674
|
T | C | 85 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(82): Show | 85 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.872+9352T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217791674 | ||||||
| chr1:217791679
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.872+9357T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217791679 | ||||||
| chr1:217791834
|
A | G | 2 | a0001c0002t0007g0051a0001c0009t0019g0092 | 2 | HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.872+9512A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217791834 | ||||||
| chr1:217791954
|
T | C | 5 | a0001c0001t0001g0123a0001c0001t0008g0045a0001c0001t0008g0049others(2): Show | 5 | HG02451.hp1 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.872+9632T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217791954 | ||||||
| chr1:217792134
|
G | T | 1 | a0001c0001t0001g0004 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.873-9584G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217792134 | ||||||
| chr1:217792329
|
G | C | 6 | a0001c0001t0001g0123a0001c0001t0008g0045a0001c0001t0008g0049others(3): Show | 6 | HG02451.hp1 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.873-9389G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217792329 | ||||||
| chr1:217792585
|
G | T | 1 | a0001c0001t0006g0096 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.873-9133G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217792585 | ||||||
| chr1:217792727
|
A | G | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.873-8991A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217792727 | ||||||
| chr1:217792749
|
G | A | 1 | a0001c0002t0012g0077 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.873-8969G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217792749 | ||||||
| chr1:217792783
|
T | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-8935T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217792783 | ||||||
| chr1:217792955
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0065 | 2 | HG00733.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.873-8763A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217792955 | ||||||
| chr1:217793067
|
G | A | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.873-8651G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793067 | ||||||
| chr1:217793215
|
G | GT | 35 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(32): Show | 35 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.873-8498dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217793215 | |||||
| chr1:217793215
|
G | GTT | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(55): Show | 58 | HG00280.hp1 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.873-8499_873-8498d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217793215 | |||||
| chr1:217793215
|
G | GTTT | 21 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0123others(18): Show | 21 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.873-8500_873-8498d others(5): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217793215 | |||||
| chr1:217793215
|
G | GTTTT | 9 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(6): Show | 9 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.873-8501_873-8498d others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217793215 | |||||
| chr1:217793220
|
TG | T | 9 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.873-8497delG | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793220 | ||||||
| chr1:217793221
|
G | GT | 13 | a0001c0002t0001g0107a0001c0002t0001g0114a0001c0002t0001g0128others(10): Show | 13 | HG00140.hp2 HG00639.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.873-8480dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217793221 | |||||
| chr1:217793221
|
G | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.873-8497G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793221 | ||||||
| chr1:217793224
|
T | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-8494T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793224 | ||||||
| chr1:217793228
|
T | G | 9 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(6): Show | 9 | HG00099.hp2 HG00323.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.873-8490T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793228 | ||||||
| chr1:217793288
|
T | A | 77 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(74): Show | 77 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.873-8430T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793288 | ||||||
| chr1:217793314
|
G | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-8404G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793314 | ||||||
| chr1:217793333
|
G | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-8385G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793333 | ||||||
| chr1:217793351
|
G | T | 10 | a0001c0001t0004g0143a0001c0004t0004g0240a0001c0004t0004g0246others(7): Show | 10 | HG01109.hp1 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.873-8367G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793351 | ||||||
| chr1:217793410
|
C | T | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.873-8308C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793410 | ||||||
| chr1:217793441
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.873-8277C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793441 | ||||||
| chr1:217793463
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.873-8255G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793463 | ||||||
| chr1:217793495
|
C | T | 3 | a0003c0007t0005g0115a0003c0007t0009g0116a0003c0007t0009g0117 | 3 | HG02257.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.873-8223C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793495 | ||||||
| chr1:217793644
|
C | T | 1 | a0001c0003t0001g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.873-8074C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793644 | ||||||
| chr1:217793669
|
G | C | 8 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.873-8049G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793669 | ||||||
| chr1:217793752
|
T | C | 75 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(72): Show | 75 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.873-7966T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793752 | ||||||
| chr1:217793841
|
T | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-7877T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793841 | ||||||
| chr1:217793999
|
C | T | 8 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.873-7719C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217793999 | ||||||
| chr1:217794015
|
G | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.873-7703G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217794015 | ||||||
| chr1:217794017
|
A | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.873-7701A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217794017 | ||||||
| chr1:217794115
|
C | CA | 7 | a0001c0001t0001g0009a0001c0001t0010g0043a0001c0002t0001g0134others(4): Show | 7 | HG02615.hp2 HG03225.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.873-7587dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217794115 | |||||
| chr1:217794115
|
CA | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-7587delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217794115 | |||||
| chr1:217794226
|
T | C | 1 | a0001c0002t0049g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.873-7492T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217794226 | ||||||
| chr1:217794427
|
T | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-7291T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217794427 | ||||||
| chr1:217794577
|
G | T | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.873-7141G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217794577 | ||||||
| chr1:217794687
|
T | A | 10 | a0001c0001t0004g0143a0001c0004t0004g0240a0001c0004t0004g0246others(7): Show | 10 | HG01109.hp1 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.873-7031T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217794687 | ||||||
| chr1:217795036
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.873-6682A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217795036 | ||||||
| chr1:217795362
|
C | CT | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.873-6332dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217795362 | |||||
| chr1:217795362
|
C | CTT | 8 | a0001c0001t0001g0177a0001c0001t0002g0001a0001c0001t0002g0101others(5): Show | 8 | HG00642.hp2 HG01106.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.873-6333_873-6332d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217795362 | |||||
| chr1:217795386
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.873-6332T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217795386 | ||||||
| chr1:217795439
|
G | A | 2 | a0001c0001t0001g0123a0001c0003t0001g0231 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.873-6279G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217795439 | ||||||
| chr1:217795443
|
C | T | 4 | a0001c0005t0001g0141a0001c0005t0001g0192a0001c0005t0004g0071others(1): Show | 4 | HG02280.hp2 HG02895.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.873-6275C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217795443 | ||||||
| chr1:217795456
|
G | A | 2 | a0001c0001t0007g0142a0001c0001t0048g0110 | 2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.873-6262G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217795456 | ||||||
| chr1:217795622
|
G | A | 67 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(64): Show | 67 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.873-6096G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217795622 | ||||||
| chr1:217795732
|
C | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-5986C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217795732 | ||||||
| chr1:217795880
|
C | T | 1 | a0001c0001t0048g0110 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.873-5838C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217795880 | ||||||
| chr1:217796101
|
T | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-5617T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217796101 | ||||||
| chr1:217796297
|
A | G | 4 | a0001c0001t0008g0045a0001c0001t0008g0049a0001c0001t0008g0136others(1): Show | 4 | HG02451.hp1 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.873-5421A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217796297 | ||||||
| chr1:217796652
|
C | T | 2 | a0001c0004t0004g0240a0001c0004t0008g0241 | 2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.873-5066C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217796652 | ||||||
| chr1:217796912
|
A | G | 3 | a0001c0001t0006g0201a0001c0001t0006g0202a0001c0001t0006g0203 | 3 | HG01074.hp1 HG01099.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.873-4806A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217796912 | ||||||
| chr1:217796986
|
G | A | 1 | a0001c0002t0013g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.873-4732G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217796986 | ||||||
| chr1:217797251
|
CT | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(161): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.873-4451delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217797251 | |||||
| chr1:217797318
|
C | T | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.873-4400C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217797318 | ||||||
| chr1:217797543
|
C | A | 1 | a0001c0002t0030g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.873-4175C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217797543 | ||||||
| chr1:217797602
|
T | C | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.873-4116T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217797602 | ||||||
| chr1:217797619
|
G | A | 4 | a0001c0002t0005g0078a0001c0002t0012g0018a0001c0002t0012g0077others(1): Show | 4 | HG00140.hp2 HG01167.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.873-4099G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217797619 | ||||||
| chr1:217797676
|
T | C | 14 | a0001c0001t0001g0209a0001c0001t0005g0084a0001c0001t0006g0096others(11): Show | 14 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.873-4042T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217797676 | ||||||
| chr1:217797700
|
T | G | 3 | a0001c0001t0001g0123a0001c0003t0001g0231a0001c0004t0005g0233 | 3 | HG01109.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.873-4018T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217797700 | ||||||
| chr1:217797840
|
C | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.873-3878C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217797840 | ||||||
| chr1:217798101
|
G | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-3617G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798101 | ||||||
| chr1:217798145
|
T | G | 1 | a0001c0004t0004g0247 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.873-3573T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798145 | ||||||
| chr1:217798275
|
T | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-3443T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798275 | ||||||
| chr1:217798382
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.873-3336T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798382 | ||||||
| chr1:217798547
|
G | A | 50 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(47): Show | 50 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.873-3171G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798547 | ||||||
| chr1:217798581
|
CAG | C | 10 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0118others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.873-3134_873-3133d others(4): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217798581 | |||||
| chr1:217798638
|
C | T | 120 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(117): Show | 120 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.873-3080C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798638 | ||||||
| chr1:217798651
|
A | G | 130 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.873-3067A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798651 | ||||||
| chr1:217798664
|
C | G | 11 | a0001c0001t0004g0143a0001c0004t0004g0240a0001c0004t0004g0246others(8): Show | 11 | HG01109.hp1 HG01261.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.873-3054C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798664 | ||||||
| chr1:217798769
|
A | T | 1 | a0001c0005t0004g0245 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.873-2949A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798769 | ||||||
| chr1:217798783
|
A | G | 7 | a0001c0001t0001g0119a0001c0001t0005g0118a0001c0004t0004g0073others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.873-2935A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798783 | ||||||
| chr1:217798815
|
TTGACC | T | 120 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(117): Show | 120 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.873-2900_873-2896d others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217798815 | |||||
| chr1:217798874
|
C | CT | 5 | a0001c0001t0001g0024a0001c0001t0005g0052a0001c0002t0001g0107others(2): Show | 5 | HG01952.hp2 HG02280.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.873-2827dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217798874 | |||||
| chr1:217798874
|
CT | C | 9 | a0001c0001t0001g0119a0001c0001t0005g0084a0001c0001t0005g0118others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.873-2827delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217798874 | |||||
| chr1:217798891
|
T | C | 84 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(81): Show | 84 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.873-2827T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798891 | ||||||
| chr1:217798898
|
C | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(46): Show | 49 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.873-2820C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798898 | ||||||
| chr1:217798954
|
G | A | 2 | a0001c0002t0022g0194a0001c0002t0022g0196 | 2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.873-2764G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798954 | ||||||
| chr1:217798959
|
A | G | 6 | a0001c0001t0002g0101a0001c0001t0002g0158a0001c0001t0002g0159others(3): Show | 6 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.873-2759A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798959 | ||||||
| chr1:217798971
|
T | C | 29 | a0001c0001t0006g0096a0001c0001t0008g0045a0001c0001t0008g0049others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.873-2747T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798971 | ||||||
| chr1:217798994
|
G | A | 7 | a0001c0001t0001g0119a0001c0001t0005g0118a0001c0004t0004g0073others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.873-2724G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217798994 | ||||||
| chr1:217799173
|
T | A | 1 | a0001c0002t0001g0129 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.873-2545T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217799173 | ||||||
| chr1:217799300
|
G | A | 7 | a0001c0001t0001g0209a0001c0001t0006g0161a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.873-2418G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217799300 | ||||||
| chr1:217799318
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.873-2400G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217799318 | ||||||
| chr1:217799339
|
A | G | 16 | a0001c0001t0007g0142a0001c0001t0015g0058a0001c0001t0015g0059others(13): Show | 16 | HG01168.hp1 HG01891.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.873-2379A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217799339 | ||||||
| chr1:217799543
|
C | T | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.873-2175C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217799543 | ||||||
| chr1:217799628
|
T | A | 2 | a0001c0002t0001g0083a0001c0008t0014g0213 | 2 | NA18941.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.873-2090T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217799628 | ||||||
| chr1:217799630
|
T | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-2088T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217799630 | ||||||
| chr1:217800004
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0005g0118 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.873-1714T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217800004 | ||||||
| chr1:217800029
|
A | G | 2 | a0001c0001t0006g0204a0001c0001t0006g0205 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.873-1689A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217800029 | ||||||
| chr1:217800256
|
C | G | 1 | a0001c0012t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.873-1462C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217800256 | ||||||
| chr1:217800265
|
CA | C | 68 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(65): Show | 68 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.873-1449delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217800265 | |||||
| chr1:217800393
|
G | GAAAGAGT others(7514): Show |
1 | a0001c0004t0004g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.873-1309_873-1308i others(7523): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217800393 | |||||
| chr1:217800393
|
G | GAAAGAGT others(7515): Show |
1 | a0001c0005t0004g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.873-1309_873-1308i others(7524): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 217800393 | |||||
| chr1:217800466
|
G | A | 28 | a0001c0001t0008g0045a0001c0001t0008g0049a0001c0001t0008g0136others(25): Show | 28 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.873-1252G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217800466 | ||||||
| chr1:217800470
|
G | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-1248G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217800470 | ||||||
| chr1:217800498
|
G | T | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.873-1220G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217800498 | ||||||
| chr1:217800542
|
G | A | 1 | a0001c0009t0019g0092 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.873-1176G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217800542 | ||||||
| chr1:217800687
|
T | C | 1 | a0001c0001t0005g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.873-1031T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217800687 | ||||||
| chr1:217800826
|
T | C | 1 | a0001c0005t0023g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.873-892T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217800826 | ||||||
| chr1:217801062
|
G | A | 3 | a0001c0001t0001g0190a0001c0001t0012g0188a0001c0001t0036g0187 | 3 | HG03130.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.873-656G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217801062 | ||||||
| chr1:217801263
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0005g0118 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.873-455C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217801263 | ||||||
| chr1:217801406
|
G | A | 7 | a0001c0001t0001g0209a0001c0001t0006g0161a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.873-312G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217801406 | ||||||
| chr1:217801461
|
T | C | 3 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0055g0242 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.873-257T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217801461 | ||||||
| chr1:217801479
|
G | C | 5 | a0001c0001t0020g0094a0001c0002t0044g0091a0001c0005t0001g0141others(2): Show | 5 | HG01168.hp1 HG02895.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.873-239G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217801479 | ||||||
| chr1:217801493
|
C | A | 1 | a0002c0006t0003g0185 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.873-225C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217801493 | ||||||
| chr1:217801639
|
T | G | 11 | a0001c0002t0009g0072a0001c0002t0009g0076a0001c0002t0013g0099others(8): Show | 11 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.873-79T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217801639 | ||||||
| chr1:217801656
|
A | T | 7 | a0001c0001t0001g0209a0001c0001t0006g0161a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.873-62A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 8/10 | chr1 | 217801656 | ||||||
| chr1:217801947
|
C | T | 29 | a0001c0001t0006g0096a0001c0001t0008g0045a0001c0001t0008g0049others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1005+97C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217801947 | ||||||
| chr1:217802012
|
AT | A | 12 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0001g0209others(9): Show | 12 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1005+173delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217802012 | |||||
| chr1:217802085
|
A | G | 1 | a0001c0001t0036g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1005+235A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217802085 | ||||||
| chr1:217802198
|
A | C | 1 | a0001c0012t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1005+348A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217802198 | ||||||
| chr1:217802291
|
C | G | 7 | a0001c0001t0001g0209a0001c0001t0006g0161a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+441C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217802291 | ||||||
| chr1:217802488
|
C | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(173): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1005+638C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217802488 | ||||||
| chr1:217802634
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1005+784G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217802634 | ||||||
| chr1:217802671
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+821A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217802671 | ||||||
| chr1:217802757
|
T | C | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1005+907T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217802757 | ||||||
| chr1:217802892
|
G | A | 1 | a0001c0002t0039g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1005+1042G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217802892 | ||||||
| chr1:217803120
|
G | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(53): Show | 56 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1005+1270G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217803120 | ||||||
| chr1:217803147
|
G | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(171): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1005+1297G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217803147 | ||||||
| chr1:217803209
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1005+1359G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217803209 | ||||||
| chr1:217803243
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+1393A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217803243 | ||||||
| chr1:217803282
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0041g0015others(1): Show | 4 | NA18951.hp2 NA18984.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+1432A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217803282 | ||||||
| chr1:217803411
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1005+1561G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217803411 | ||||||
| chr1:217803813
|
T | C | 1 | a0001c0001t0016g0172 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1005+1963T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217803813 | ||||||
| chr1:217803876
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+2026G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217803876 | ||||||
| chr1:217803937
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+2087A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217803937 | ||||||
| chr1:217803940
|
C | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+2090C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217803940 | ||||||
| chr1:217804057
|
C | A | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+2207C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217804057 | ||||||
| chr1:217804072
|
C | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(46): Show | 49 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1005+2222C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217804072 | ||||||
| chr1:217804259
|
T | C | 1 | a0001c0001t0048g0110 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1005+2409T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217804259 | ||||||
| chr1:217804307
|
G | C | 1 | a0001c0001t0015g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1005+2457G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217804307 | ||||||
| chr1:217804308
|
G | A | 2 | a0001c0003t0024g0243a0001c0003t0038g0244 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1005+2458G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217804308 | ||||||
| chr1:217804407
|
A | G | 1 | a0001c0002t0039g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1005+2557A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217804407 | ||||||
| chr1:217804609
|
G | A | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1005+2759G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217804609 | ||||||
| chr1:217804616
|
GA | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+2774delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217804616 | |||||
| chr1:217804652
|
A | C | 1 | a0001c0001t0056g0075 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1005+2802A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217804652 | ||||||
| chr1:217804831
|
C | T | 1 | a0002c0006t0001g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1005+2981C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217804831 | ||||||
| chr1:217805329
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1005+3479T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217805329 | ||||||
| chr1:217805363
|
C | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+3513C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217805363 | ||||||
| chr1:217805368
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+3518A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217805368 | ||||||
| chr1:217805386
|
G | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(46): Show | 49 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1005+3536G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217805386 | ||||||
| chr1:217805389
|
G | T | 56 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(53): Show | 56 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1005+3539G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217805389 | ||||||
| chr1:217805623
|
G | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1005+3773G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217805623 | ||||||
| chr1:217805676
|
C | A | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+3826C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217805676 | ||||||
| chr1:217805903
|
T | C | 16 | a0001c0001t0007g0142a0001c0001t0015g0058a0001c0001t0015g0059others(13): Show | 16 | HG01168.hp1 HG01891.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1005+4053T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217805903 | ||||||
| chr1:217805976
|
A | T | 79 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(76): Show | 79 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1005+4126A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217805976 | ||||||
| chr1:217806364
|
T | C | 2 | a0001c0002t0001g0083a0001c0008t0014g0213 | 2 | NA18941.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1005+4514T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217806364 | ||||||
| chr1:217806458
|
C | T | 12 | a0001c0001t0007g0142a0001c0001t0020g0094a0001c0002t0007g0051others(9): Show | 12 | HG01168.hp1 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1005+4608C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217806458 | ||||||
| chr1:217806647
|
C | G | 7 | a0001c0001t0001g0209a0001c0001t0006g0161a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+4797C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217806647 | ||||||
| chr1:217806742
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+4892G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217806742 | ||||||
| chr1:217807101
|
A | G | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1005+5251A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217807101 | ||||||
| chr1:217807505
|
A | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1005+5655A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217807505 | ||||||
| chr1:217807691
|
G | A | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+5841G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217807691 | ||||||
| chr1:217807740
|
C | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+5890C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217807740 | ||||||
| chr1:217807797
|
T | C | 3 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0055g0242 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1005+5947T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217807797 | ||||||
| chr1:217807982
|
C | A | 2 | a0001c0001t0001g0123a0001c0003t0001g0231 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1005+6132C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217807982 | ||||||
| chr1:217808333
|
A | G | 12 | a0001c0001t0007g0142a0001c0001t0020g0094a0001c0002t0007g0051others(9): Show | 12 | HG01168.hp1 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1005+6483A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217808333 | ||||||
| chr1:217808346
|
T | TAC | 27 | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0166others(24): Show | 27 | HG01109.hp2 HG01168.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.1005+6531_1005+653 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217808346 | |||||
| chr1:217808346
|
T | TACAC | 3 | a0001c0001t0001g0170a0001c0002t0049g0055a0001c0004t0005g0233 | 3 | HG01109.hp1 HG02622.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1005+6529_1005+653 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217808346 | |||||
| chr1:217808346
|
TAC | T | 4 | a0001c0001t0048g0110a0001c0002t0005g0078a0001c0002t0012g0018others(1): Show | 4 | HG00140.hp2 HG01167.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+6531_1005+653 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217808346 | |||||
| chr1:217808369
|
ACACACAC others(9): Show |
A | 1 | a0001c0002t0022g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1005+6521_1005+653 others(20): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217808369 | |||||
| chr1:217808373
|
ACACACAC others(5): Show |
A | 29 | a0001c0001t0008g0045a0001c0001t0008g0049a0001c0001t0008g0136others(26): Show | 29 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1005+6525_1005+653 others(16): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217808373 | |||||
| chr1:217808375
|
ACACACAC others(3): Show |
A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+6527_1005+653 others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217808375 | |||||
| chr1:217808377
|
ACACACCC others(1): Show |
A | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+6529_1005+653 others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217808377 | |||||
| chr1:217808381
|
ACC | A | 12 | a0001c0001t0001g0190a0001c0001t0001g0197a0001c0001t0012g0188others(9): Show | 12 | HG02486.hp2 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1005+6536_1005+653 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217808381 | |||||
| chr1:217808381
|
ACCCC | A | 34 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(31): Show | 34 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1005+6534_1005+653 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217808381 | |||||
| chr1:217808383
|
C | A | 95 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0041others(92): Show | 95 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1005+6533C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217808383 | ||||||
| chr1:217808385
|
C | A | 9 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0005g0089others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1005+6535C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217808385 | ||||||
| chr1:217808588
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1005+6738C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217808588 | ||||||
| chr1:217808758
|
G | A | 3 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0055g0242 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1005+6908G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217808758 | ||||||
| chr1:217808765
|
G | C | 1 | a0005c0010t0001g0169 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1005+6915G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217808765 | ||||||
| chr1:217808779
|
T | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1005+6929T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217808779 | ||||||
| chr1:217808853
|
C | CA | 5 | a0001c0001t0001g0011a0001c0001t0002g0003a0001c0001t0002g0033others(2): Show | 5 | HG01106.hp1 HG01981.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1005+7018dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217808853 | |||||
| chr1:217808853
|
CA | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0041others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1005+7018delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217808853 | |||||
| chr1:217809008
|
A | G | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+7158A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217809008 | ||||||
| chr1:217809074
|
A | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+7224A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217809074 | ||||||
| chr1:217809168
|
G | A | 2 | a0001c0001t0008g0045a0001c0001t0042g0035 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1005+7318G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217809168 | ||||||
| chr1:217809554
|
T | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.1005+7704T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217809554 | ||||||
| chr1:217809578
|
TTATAATA | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0041others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1005+7729_1005+773 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217809578 | ||||||
| chr1:217809588
|
A | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1005+7738A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217809588 | ||||||
| chr1:217809781
|
C | T | 1 | a0001c0003t0003g0097 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1005+7931C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217809781 | ||||||
| chr1:217809895
|
TTATC | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0041others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1005+8048_1005+805 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217809895 | |||||
| chr1:217809899
|
C | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+8049C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217809899 | ||||||
| chr1:217810140
|
A | G | 1 | a0001c0002t0009g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1005+8290A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217810140 | ||||||
| chr1:217810239
|
G | T | 2 | a0001c0001t0015g0058a0001c0001t0015g0059 | 2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1005+8389G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217810239 | ||||||
| chr1:217810294
|
G | A | 1 | a0001c0003t0014g0230 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1005+8444G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217810294 | ||||||
| chr1:217810420
|
G | A | 1 | a0001c0004t0004g0248 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1005+8570G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217810420 | ||||||
| chr1:217810495
|
AC | A | 32 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(29): Show | 32 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1005+8647delC | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217810495 | |||||
| chr1:217810517
|
G | A | 3 | a0001c0001t0020g0094a0001c0005t0001g0141a0001c0005t0001g0192 | 3 | HG02895.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1005+8667G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217810517 | ||||||
| chr1:217810551
|
G | A | 30 | a0001c0001t0008g0045a0001c0001t0008g0049a0001c0001t0008g0136others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1005+8701G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217810551 | ||||||
| chr1:217810617
|
C | CA | 7 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(4): Show | 7 | HG00280.hp2 HG02486.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1005+8777dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217810617 | |||||
| chr1:217810709
|
C | T | 30 | a0001c0001t0008g0045a0001c0001t0008g0049a0001c0001t0008g0136others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1005+8859C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217810709 | ||||||
| chr1:217810722
|
G | T | 12 | a0001c0001t0007g0142a0001c0001t0020g0094a0001c0002t0007g0051others(9): Show | 12 | HG01168.hp1 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1005+8872G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217810722 | ||||||
| chr1:217810838
|
A | G | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1005+8988A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217810838 | ||||||
| chr1:217810874
|
A | G | 30 | a0001c0001t0008g0045a0001c0001t0008g0049a0001c0001t0008g0136others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1005+9024A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217810874 | ||||||
| chr1:217810937
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1005+9087T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217810937 | ||||||
| chr1:217811141
|
C | T | 72 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0041others(69): Show | 72 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1005+9291C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217811141 | ||||||
| chr1:217811211
|
T | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0041others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1005+9361T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217811211 | ||||||
| chr1:217811254
|
G | C | 3 | a0001c0001t0001g0190a0001c0001t0012g0188a0001c0001t0036g0187 | 3 | HG03130.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1005+9404G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217811254 | ||||||
| chr1:217811259
|
C | G | 30 | a0001c0001t0008g0045a0001c0001t0008g0049a0001c0001t0008g0136others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1005+9409C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217811259 | ||||||
| chr1:217811579
|
G | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+9729G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217811579 | ||||||
| chr1:217811618
|
G | C | 13 | a0001c0001t0001g0216a0001c0002t0001g0086a0001c0002t0001g0112others(10): Show | 13 | HG00738.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1005+9768G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217811618 | ||||||
| chr1:217811695
|
G | GA | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.1005+9860dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217811695 | |||||
| chr1:217811695
|
GA | G | 33 | a0001c0001t0008g0045a0001c0001t0008g0049a0001c0001t0008g0136others(30): Show | 33 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1005+9860delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217811695 | |||||
| chr1:217811924
|
A | C | 1 | a0001c0012t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1005+10074A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217811924 | ||||||
| chr1:217812086
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+10236T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217812086 | ||||||
| chr1:217812299
|
C | T | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+10449C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217812299 | ||||||
| chr1:217812534
|
T | A | 1 | a0004c0013t0033g0095 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1005+10684T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217812534 | ||||||
| chr1:217812744
|
A | G | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+10894A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217812744 | ||||||
| chr1:217812909
|
A | G | 16 | a0001c0001t0001g0119a0001c0001t0005g0089a0001c0001t0005g0118others(13): Show | 16 | HG01109.hp2 HG01168.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1005+11059A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217812909 | ||||||
| chr1:217812980
|
A | G | 11 | a0001c0001t0004g0143a0001c0004t0004g0240a0001c0004t0004g0246others(8): Show | 11 | HG01109.hp1 HG01261.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1005+11130A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217812980 | ||||||
| chr1:217812981
|
C | G | 11 | a0001c0001t0004g0143a0001c0004t0004g0240a0001c0004t0004g0246others(8): Show | 11 | HG01109.hp1 HG01261.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1005+11131C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217812981 | ||||||
| chr1:217813125
|
A | G | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+11275A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217813125 | ||||||
| chr1:217813619
|
G | A | 29 | a0001c0001t0008g0045a0001c0001t0008g0049a0001c0001t0008g0136others(26): Show | 29 | HG00609.hp1 HG00639.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1005+11769G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217813619 | ||||||
| chr1:217813769
|
T | G | 28 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(25): Show | 28 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1005+11919T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217813769 | ||||||
| chr1:217813812
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(22): Show | 25 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1005+11962G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217813812 | ||||||
| chr1:217813875
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1005+12025G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217813875 | ||||||
| chr1:217813977
|
T | A | 1 | a0001c0002t0039g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1005+12127T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217813977 | ||||||
| chr1:217814096
|
G | A | 7 | a0001c0001t0001g0209a0001c0001t0006g0161a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+12246G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217814096 | ||||||
| chr1:217814097
|
C | A | 7 | a0001c0001t0001g0209a0001c0001t0006g0161a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+12247C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217814097 | ||||||
| chr1:217814215
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1005+12365T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217814215 | ||||||
| chr1:217814355
|
A | T | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+12505A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217814355 | ||||||
| chr1:217814483
|
T | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+12633T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217814483 | ||||||
| chr1:217814571
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1005+12721G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217814571 | ||||||
| chr1:217814659
|
G | A | 3 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0055g0242 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1005+12809G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217814659 | ||||||
| chr1:217814783
|
G | A | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1005+12933G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217814783 | ||||||
| chr1:217814847
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0002g0030 | 2 | HG02083.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1005+12997C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217814847 | ||||||
| chr1:217814933
|
G | A | 1 | a0001c0002t0014g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1005+13083G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217814933 | ||||||
| chr1:217814947
|
A | G | 1 | a0001c0003t0029g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1005+13097A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217814947 | ||||||
| chr1:217815091
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1005+13241C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217815091 | ||||||
| chr1:217815195
|
G | A | 2 | a0001c0002t0016g0074a0001c0002t0049g0055 | 2 | HG02622.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1005+13345G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217815195 | ||||||
| chr1:217815247
|
C | G | 17 | a0001c0002t0005g0078a0001c0002t0009g0072a0001c0002t0009g0076others(14): Show | 17 | HG00140.hp2 HG01167.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1005+13397C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217815247 | ||||||
| chr1:217815277
|
A | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+13427A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217815277 | ||||||
| chr1:217815430
|
A | G | 88 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(85): Show | 88 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.1005+13580A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217815430 | ||||||
| chr1:217815609
|
C | T | 72 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(69): Show | 72 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.1005+13759C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217815609 | ||||||
| chr1:217815629
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+13779G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217815629 | ||||||
| chr1:217815642
|
A | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1005+13792A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217815642 | ||||||
| chr1:217815694
|
G | A | 1 | a0001c0012t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1005+13844G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217815694 | ||||||
| chr1:217815792
|
T | A | 41 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0216others(38): Show | 41 | HG00140.hp2 HG00738.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1005+13942T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217815792 | ||||||
| chr1:217815804
|
G | T | 1 | a0002c0006t0001g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1005+13954G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217815804 | ||||||
| chr1:217815979
|
A | G | 1 | a0001c0004t0032g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1005+14129A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217815979 | ||||||
| chr1:217816067
|
GT | G | 7 | a0001c0001t0001g0123a0001c0002t0022g0194a0001c0002t0022g0196others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+14222delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217816067 | |||||
| chr1:217816095
|
C | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1005+14245C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217816095 | ||||||
| chr1:217816175
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+14325T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217816175 | ||||||
| chr1:217816251
|
G | A | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+14401G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217816251 | ||||||
| chr1:217816423
|
A | G | 1 | a0001c0002t0054g0050 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1005+14573A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217816423 | ||||||
| chr1:217816603
|
G | T | 1 | a0002c0006t0018g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1005+14753G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217816603 | ||||||
| chr1:217816624
|
A | T | 1 | a0001c0002t0022g0196 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1005+14774A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217816624 | ||||||
| chr1:217816871
|
T | G | 1 | a0001c0001t0056g0075 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1005+15021T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217816871 | ||||||
| chr1:217816955
|
T | C | 2 | a0001c0002t0011g0198a0001c0002t0011g0199 | 2 | HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1005+15105T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217816955 | ||||||
| chr1:217816965
|
T | A | 2 | a0001c0002t0005g0078a0001c0002t0012g0018 | 2 | HG00140.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1005+15115T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217816965 | ||||||
| chr1:217817199
|
C | T | 88 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(85): Show | 88 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.1005+15349C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217817199 | ||||||
| chr1:217817239
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1005+15389G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217817239 | ||||||
| chr1:217817283
|
A | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1005+15433A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217817283 | ||||||
| chr1:217817283
|
A | T | 28 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(25): Show | 28 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1005+15433A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217817283 | ||||||
| chr1:217817366
|
A | C | 31 | a0001c0001t0006g0096a0001c0001t0008g0045a0001c0001t0008g0049others(28): Show | 31 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1005+15516A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217817366 | ||||||
| chr1:217817386
|
C | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+15536C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217817386 | ||||||
| chr1:217817545
|
G | A | 11 | a0001c0002t0009g0072a0001c0002t0009g0076a0001c0002t0013g0099others(8): Show | 11 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1005+15695G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217817545 | ||||||
| chr1:217817576
|
A | G | 62 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0041others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1005+15726A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217817576 | ||||||
| chr1:217817696
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1005+15846G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217817696 | ||||||
| chr1:217817777
|
G | C | 30 | a0001c0001t0008g0045a0001c0001t0008g0049a0001c0001t0008g0136others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1005+15927G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217817777 | ||||||
| chr1:217817794
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0002g0171a0001c0005t0001g0141 | 3 | HG02895.hp2 NA18939.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1005+15944G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217817794 | ||||||
| chr1:217817813
|
A | G | 1 | a0001c0002t0026g0048 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1005+15963A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217817813 | ||||||
| chr1:217818115
|
A | G | 1 | a0001c0002t0030g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1005+16265A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217818115 | ||||||
| chr1:217818196
|
A | G | 2 | a0001c0001t0001g0090a0001c0004t0053g0239 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1005+16346A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217818196 | ||||||
| chr1:217818328
|
A | G | 1 | a0002c0006t0018g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1005+16478A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217818328 | ||||||
| chr1:217818384
|
G | A | 41 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0216others(38): Show | 41 | HG00140.hp2 HG00738.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1005+16534G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217818384 | ||||||
| chr1:217818431
|
A | G | 41 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0216others(38): Show | 41 | HG00140.hp2 HG00738.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1005+16581A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217818431 | ||||||
| chr1:217818769
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1005+16919A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217818769 | ||||||
| chr1:217818769
|
A | T | 7 | a0001c0001t0001g0123a0001c0002t0022g0194a0001c0002t0022g0196others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+16919A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217818769 | ||||||
| chr1:217818882
|
C | CT | 102 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1005+17047dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217818882 | |||||
| chr1:217818882
|
C | CTT | 15 | a0001c0001t0001g0216a0001c0001t0040g0025a0001c0002t0001g0086others(12): Show | 15 | HG00738.hp1 HG01070.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1005+17046_1005+17 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217818882 | |||||
| chr1:217818882
|
CT | C | 16 | a0001c0001t0004g0143a0001c0001t0008g0045a0001c0001t0018g0183others(13): Show | 16 | HG01109.hp1 HG01261.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1005+17047delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217818882 | |||||
| chr1:217818989
|
A | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+17139A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217818989 | ||||||
| chr1:217819193
|
A | G | 1 | a0001c0002t0028g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1005+17343A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217819193 | ||||||
| chr1:217819193
|
A | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+17343A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217819193 | ||||||
| chr1:217819228
|
T | C | 13 | a0001c0001t0001g0216a0001c0002t0001g0086a0001c0002t0001g0112others(10): Show | 13 | HG00738.hp1 HG01070.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1005+17378T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217819228 | ||||||
| chr1:217819362
|
G | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(25): Show | 28 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1005+17512G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217819362 | ||||||
| chr1:217819362
|
G | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+17512G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217819362 | ||||||
| chr1:217819392
|
T | G | 1 | a0001c0001t0001g0119 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1005+17542T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217819392 | ||||||
| chr1:217819402
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(22): Show | 25 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1005+17552G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217819402 | ||||||
| chr1:217819687
|
T | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+17837T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217819687 | ||||||
| chr1:217819970
|
T | C | 4 | a0001c0001t0002g0019a0001c0001t0002g0023a0001c0001t0002g0027others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005+18120T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217819970 | ||||||
| chr1:217819984
|
A | T | 2 | a0001c0004t0004g0246a0001c0004t0004g0248 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1005+18134A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217819984 | ||||||
| chr1:217820000
|
G | C | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+18150G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217820000 | ||||||
| chr1:217820001
|
A | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+18151A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217820001 | ||||||
| chr1:217820095
|
C | G | 44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1005+18245C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217820095 | ||||||
| chr1:217820166
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0012g0188 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1005+18316G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217820166 | ||||||
| chr1:217820185
|
G | T | 2 | a0001c0004t0052g0238a0001c0004t0055g0242 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1005+18335G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217820185 | ||||||
| chr1:217820187
|
A | G | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1005+18337A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217820187 | ||||||
| chr1:217820349
|
A | C | 2 | a0001c0001t0001g0090a0001c0004t0053g0239 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1005+18499A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217820349 | ||||||
| chr1:217820589
|
A | G | 250 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1005+18739A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217820589 | ||||||
| chr1:217820796
|
C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1005+18946C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217820796 | ||||||
| chr1:217820847
|
C | T | 1 | a0001c0004t0055g0242 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1005+18997C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217820847 | ||||||
| chr1:217820847
|
CG | C | 7 | a0001c0001t0001g0123a0001c0002t0022g0194a0001c0002t0022g0196others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+19000delG | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217820847 | |||||
| chr1:217821005
|
A | C | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+19155A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217821005 | ||||||
| chr1:217821009
|
T | C | 133 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(130): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1005+19159T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217821009 | ||||||
| chr1:217821094
|
G | A | 1 | a0001c0001t0006g0096 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1005+19244G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217821094 | ||||||
| chr1:217821111
|
A | T | 1 | a0001c0001t0040g0025 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1005+19261A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217821111 | ||||||
| chr1:217821222
|
A | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+19372A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217821222 | ||||||
| chr1:217821235
|
C | T | 1 | a0001c0002t0001g0131 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1005+19385C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217821235 | ||||||
| chr1:217821450
|
G | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1005+19600G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217821450 | ||||||
| chr1:217821529
|
G | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1005+19679G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217821529 | ||||||
| chr1:217821623
|
T | C | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+19773T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217821623 | ||||||
| chr1:217821685
|
AT | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+19841delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217821685 | |||||
| chr1:217821807
|
C | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+19957C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217821807 | ||||||
| chr1:217821831
|
T | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+19981T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217821831 | ||||||
| chr1:217821905
|
T | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+20055T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217821905 | ||||||
| chr1:217821995
|
C | A | 11 | a0001c0002t0009g0072a0001c0002t0009g0076a0001c0002t0013g0099others(8): Show | 11 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1005+20145C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217821995 | ||||||
| chr1:217822078
|
A | G | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+20228A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217822078 | ||||||
| chr1:217822243
|
ATTT | A | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+20397_1005+20 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217822243 | |||||
| chr1:217822368
|
TG | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(22): Show | 25 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1005+20519delG | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217822368 | ||||||
| chr1:217822403
|
C | T | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1005+20553C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217822403 | ||||||
| chr1:217822404
|
G | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(25): Show | 28 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1005+20554G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217822404 | ||||||
| chr1:217822541
|
T | C | 2 | a0001c0002t0011g0198a0001c0002t0011g0199 | 2 | HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1005+20691T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217822541 | ||||||
| chr1:217822634
|
CTA | C | 16 | a0001c0001t0001g0190a0001c0001t0001g0209a0001c0001t0006g0096others(13): Show | 16 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1005+20797_1005+20 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217822634 | |||||
| chr1:217822754
|
A | G | 3 | a0001c0001t0001g0190a0001c0001t0012g0188a0001c0001t0036g0187 | 3 | HG03130.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1005+20904A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217822754 | ||||||
| chr1:217822785
|
AT | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(43): Show | 46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.1005+20943delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217822785 | |||||
| chr1:217822898
|
A | G | 1 | a0001c0001t0002g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1005+21048A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217822898 | ||||||
| chr1:217822975
|
T | G | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+21125T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217822975 | ||||||
| chr1:217823218
|
G | A | 1 | a0001c0002t0028g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1005+21368G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217823218 | ||||||
| chr1:217823265
|
AG | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+21417delG | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217823265 | |||||
| chr1:217823463
|
AT | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+21614delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217823463 | ||||||
| chr1:217823513
|
G | T | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+21663G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217823513 | ||||||
| chr1:217823787
|
T | A | 34 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0005g0084others(31): Show | 34 | HG00140.hp2 HG00738.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1005+21937T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217823787 | ||||||
| chr1:217823949
|
G | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+22099G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217823949 | ||||||
| chr1:217824020
|
T | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(175): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1005+22170T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217824020 | ||||||
| chr1:217824535
|
A | G | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+22685A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217824535 | ||||||
| chr1:217824576
|
G | T | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1005+22726G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217824576 | ||||||
| chr1:217824812
|
T | C | 2 | a0001c0004t0004g0240a0001c0004t0008g0241 | 2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1005+22962T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217824812 | ||||||
| chr1:217824842
|
A | G | 1 | a0001c0001t0002g0039 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1005+22992A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217824842 | ||||||
| chr1:217824853
|
G | C | 1 | a0001c0002t0022g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1005+23003G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217824853 | ||||||
| chr1:217824877
|
A | C | 34 | a0001c0001t0008g0045a0001c0001t0008g0049a0001c0001t0008g0136others(31): Show | 34 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1005+23027A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217824877 | ||||||
| chr1:217824927
|
T | G | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+23077T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217824927 | ||||||
| chr1:217824994
|
T | C | 1 | a0001c0002t0001g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1005+23144T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217824994 | ||||||
| chr1:217825054
|
T | TTG | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1005+23205_1005+23 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217825054 | |||||
| chr1:217825095
|
T | C | 3 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0055g0242 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1005+23245T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217825095 | ||||||
| chr1:217825115
|
C | A | 1 | a0001c0001t0002g0001 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1005+23265C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217825115 | ||||||
| chr1:217825155
|
A | G | 2 | a0001c0001t0006g0204a0001c0001t0006g0205 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1005+23305A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217825155 | ||||||
| chr1:217825383
|
C | G | 1 | a0001c0001t0040g0025 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1005+23533C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217825383 | ||||||
| chr1:217825558
|
G | A | 30 | a0001c0001t0008g0045a0001c0001t0008g0049a0001c0001t0008g0136others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1005+23708G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217825558 | ||||||
| chr1:217825592
|
A | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+23742A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217825592 | ||||||
| chr1:217825636
|
T | C | 10 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(7): Show | 10 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1005+23786T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217825636 | ||||||
| chr1:217825816
|
A | G | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+23966A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217825816 | ||||||
| chr1:217825893
|
T | C | 1 | a0001c0001t0057g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1005+24043T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217825893 | ||||||
| chr1:217825962
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1005+24112G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217825962 | ||||||
| chr1:217825999
|
A | G | 55 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0041others(52): Show | 55 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1005+24149A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217825999 | ||||||
| chr1:217826045
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1005+24195T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217826045 | ||||||
| chr1:217826150
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+24300G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217826150 | ||||||
| chr1:217826336
|
G | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+24486G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217826336 | ||||||
| chr1:217826895
|
C | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+25045C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217826895 | ||||||
| chr1:217826958
|
T | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1005+25108T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217826958 | ||||||
| chr1:217827035
|
G | C | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+25185G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217827035 | ||||||
| chr1:217827178
|
T | C | 41 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0216others(38): Show | 41 | HG00140.hp2 HG00738.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1005+25328T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217827178 | ||||||
| chr1:217827242
|
A | G | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+25392A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217827242 | ||||||
| chr1:217827411
|
CT | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+25565delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217827411 | |||||
| chr1:217827531
|
G | A | 7 | a0001c0001t0001g0123a0001c0002t0022g0194a0001c0002t0022g0196others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+25681G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217827531 | ||||||
| chr1:217827536
|
A | G | 16 | a0001c0001t0001g0119a0001c0001t0005g0089a0001c0001t0005g0118others(13): Show | 16 | HG01109.hp2 HG01168.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1005+25686A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217827536 | ||||||
| chr1:217827638
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1005+25788C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217827638 | ||||||
| chr1:217827656
|
G | A | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1005+25806G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217827656 | ||||||
| chr1:217827668
|
G | A | 1 | a0001c0002t0005g0056 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1005+25818G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217827668 | ||||||
| chr1:217827675
|
A | G | 1 | a0001c0002t0054g0050 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1005+25825A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217827675 | ||||||
| chr1:217827695
|
T | C | 30 | a0001c0001t0008g0045a0001c0001t0008g0049a0001c0001t0008g0136others(27): Show | 30 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1005+25845T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217827695 | ||||||
| chr1:217827941
|
T | C | 1 | a0001c0001t0011g0227 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1005+26091T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217827941 | ||||||
| chr1:217828021
|
C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1005+26171C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217828021 | ||||||
| chr1:217828023
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1005+26173T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217828023 | ||||||
| chr1:217828027
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1005+26177T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217828027 | ||||||
| chr1:217828053
|
A | G | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+26203A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217828053 | ||||||
| chr1:217828093
|
A | G | 1 | a0001c0001t0058g0150 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1005+26243A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217828093 | ||||||
| chr1:217828125
|
G | A | 1 | a0001c0005t0023g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1005+26275G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217828125 | ||||||
| chr1:217828275
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0004t0001g0219 | 3 | HG01070.hp2 HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1005+26425A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217828275 | ||||||
| chr1:217828344
|
A | T | 3 | a0001c0001t0001g0190a0001c0001t0012g0188a0001c0001t0036g0187 | 3 | HG03130.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1005+26494A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217828344 | ||||||
| chr1:217828404
|
T | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1005+26554T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217828404 | ||||||
| chr1:217828483
|
A | ATATAGGT others(318): Show |
1 | a0001c0001t0010g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1005+26651_1005+26 others(331): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217828483 | |||||
| chr1:217828483
|
A | ATATAGGT others(319): Show |
1 | a0001c0001t0002g0006 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1005+26651_1005+26 others(332): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217828483 | |||||
| chr1:217828483
|
A | ATATAGGT others(319): Show |
31 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1005+26651_1005+26 others(332): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217828483 | |||||
| chr1:217828483
|
A | ATATAGGT others(320): Show |
1 | a0001c0001t0002g0007 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1005+26651_1005+26 others(333): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217828483 | |||||
| chr1:217828483
|
A | ATATAGGT others(320): Show |
10 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0002g0001others(7): Show | 10 | HG01071.hp2 HG01106.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1005+26651_1005+26 others(333): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217828483 | |||||
| chr1:217828483
|
A | ATGTAGGT others(319): Show |
1 | a0001c0001t0001g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1005+26634_1005+26 others(332): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217828483 | |||||
| chr1:217828539
|
C | CA | 157 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(154): Show | 157 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1005+26699dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217828539 | |||||
| chr1:217828539
|
C | CAA | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1005+26698_1005+26 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217828539 | |||||
| chr1:217828702
|
A | G | 28 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(25): Show | 28 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1005+26852A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217828702 | ||||||
| chr1:217828960
|
T | C | 1 | a0001c0003t0003g0098 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1005+27110T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217828960 | ||||||
| chr1:217829016
|
A | T | 7 | a0001c0001t0007g0142a0001c0002t0007g0051a0001c0002t0007g0060others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1005+27166A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217829016 | ||||||
| chr1:217829221
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+27371A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217829221 | ||||||
| chr1:217829431
|
C | A | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+27581C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217829431 | ||||||
| chr1:217829491
|
G | T | 4 | a0001c0001t0001g0119a0001c0001t0005g0089a0001c0001t0005g0118others(1): Show | 4 | HG01109.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005+27641G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217829491 | ||||||
| chr1:217829614
|
C | T | 17 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0005g0084others(14): Show | 17 | HG00738.hp1 HG01070.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.1005+27764C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217829614 | ||||||
| chr1:217829627
|
C | CA | 61 | a0001c0001t0001g0005a0001c0001t0001g0041a0001c0001t0001g0046others(58): Show | 61 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1005+27804dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217829627 | |||||
| chr1:217829627
|
C | CAA | 19 | a0001c0001t0001g0016a0001c0001t0001g0123a0001c0001t0001g0148others(16): Show | 19 | HG00558.hp1 HG02630.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.1005+27803_1005+27 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217829627 | |||||
| chr1:217829627
|
C | CAAA | 10 | a0001c0001t0001g0175a0001c0001t0001g0190a0001c0001t0012g0188others(7): Show | 10 | HG02486.hp1 HG02486.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1005+27802_1005+27 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217829627 | |||||
| chr1:217829627
|
C | CAAAA | 5 | a0001c0001t0001g0119a0001c0001t0005g0089a0001c0002t0001g0147others(2): Show | 5 | HG02109.hp1 HG02615.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1005+27801_1005+27 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217829627 | |||||
| chr1:217829627
|
C | CAAAAA | 16 | a0001c0001t0001g0022a0001c0001t0005g0118a0001c0001t0008g0049others(13): Show | 16 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1005+27800_1005+27 others(11): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217829627 | |||||
| chr1:217829627
|
C | CAAAAAA | 29 | a0001c0001t0001g0024a0001c0001t0001g0081a0001c0001t0006g0161others(26): Show | 29 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1005+27799_1005+27 others(12): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217829627 | |||||
| chr1:217829627
|
C | CAAAAAAA | 16 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0209others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1005+27798_1005+27 others(13): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217829627 | |||||
| chr1:217829627
|
C | CAAAAAAA others(1): Show |
8 | a0001c0001t0006g0201a0001c0001t0006g0202a0001c0001t0006g0203others(5): Show | 8 | HG01074.hp1 HG01099.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1005+27797_1005+27 others(14): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217829627 | |||||
| chr1:217829627
|
CA | C | 22 | a0001c0001t0001g0037a0001c0001t0001g0177a0001c0001t0002g0038others(19): Show | 22 | HG00140.hp2 HG01261.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1005+27804delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217829627 | |||||
| chr1:217829627
|
CAA | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1005+27803_1005+27 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217829627 | |||||
| chr1:217829635
|
A | G | 3 | a0003c0007t0005g0115a0003c0007t0009g0116a0003c0007t0009g0117 | 3 | HG02257.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1005+27785A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217829635 | ||||||
| chr1:217829802
|
G | A | 2 | a0001c0001t0008g0049a0001c0001t0008g0136 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1005+27952G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217829802 | ||||||
| chr1:217829845
|
C | T | 1 | a0001c0004t0055g0242 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1005+27995C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217829845 | ||||||
| chr1:217829963
|
A | T | 1 | a0001c0001t0048g0110 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1005+28113A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217829963 | ||||||
| chr1:217830019
|
C | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1005+28169C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217830019 | ||||||
| chr1:217830049
|
A | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+28199A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217830049 | ||||||
| chr1:217830262
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1005+28412G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217830262 | ||||||
| chr1:217830471
|
C | A | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+28621C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217830471 | ||||||
| chr1:217830819
|
A | T | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+28969A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217830819 | ||||||
| chr1:217830871
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0012g0188a0001c0001t0036g0187 | 3 | HG03130.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1005+29021C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217830871 | ||||||
| chr1:217831173
|
A | C | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+29323A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217831173 | ||||||
| chr1:217831178
|
A | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+29328A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217831178 | ||||||
| chr1:217831234
|
C | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+29384C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217831234 | ||||||
| chr1:217831239
|
G | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+29389G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217831239 | ||||||
| chr1:217831351
|
G | A | 4 | a0001c0001t0004g0054a0001c0001t0009g0120a0001c0001t0023g0053others(1): Show | 4 | HG02572.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+29501G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217831351 | ||||||
| chr1:217831586
|
G | T | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1005+29736G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217831586 | ||||||
| chr1:217831669
|
G | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1005+29819G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217831669 | ||||||
| chr1:217831703
|
A | G | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+29853A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217831703 | ||||||
| chr1:217831918
|
T | C | 2 | a0001c0002t0030g0232a0001c0005t0023g0100 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1005+30068T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217831918 | ||||||
| chr1:217832015
|
T | A | 34 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0005g0084others(31): Show | 34 | HG00140.hp2 HG00738.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1005+30165T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217832015 | ||||||
| chr1:217832038
|
A | G | 250 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1005+30188A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217832038 | ||||||
| chr1:217832317
|
G | A | 2 | a0001c0002t0011g0198a0001c0002t0011g0199 | 2 | HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1006-30457G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217832317 | ||||||
| chr1:217832338
|
G | A | 1 | a0001c0001t0009g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1006-30436G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217832338 | ||||||
| chr1:217832477
|
T | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(25): Show | 28 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1006-30297T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217832477 | ||||||
| chr1:217832515
|
G | A | 17 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(14): Show | 17 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1006-30259G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217832515 | ||||||
| chr1:217832543
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1006-30231C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217832543 | ||||||
| chr1:217832647
|
T | A | 1 | a0001c0005t0004g0245 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1006-30127T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217832647 | ||||||
| chr1:217832679
|
A | G | 25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(22): Show | 25 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1006-30095A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217832679 | ||||||
| chr1:217832709
|
G | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(43): Show | 46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.1006-30065G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217832709 | ||||||
| chr1:217832860
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1006-29914C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217832860 | ||||||
| chr1:217833088
|
A | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1006-29686A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217833088 | ||||||
| chr1:217833180
|
T | C | 1 | a0001c0002t0001g0179 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1006-29594T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217833180 | ||||||
| chr1:217833185
|
A | G | 16 | a0001c0001t0001g0119a0001c0001t0005g0089a0001c0001t0005g0118others(13): Show | 16 | HG01109.hp2 HG01168.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006-29589A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217833185 | ||||||
| chr1:217833332
|
G | T | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-29442G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217833332 | ||||||
| chr1:217833335
|
C | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-29439C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217833335 | ||||||
| chr1:217833382
|
T | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-29392T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217833382 | ||||||
| chr1:217833508
|
A | C | 72 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(69): Show | 72 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.1006-29266A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217833508 | ||||||
| chr1:217833562
|
G | A | 1 | a0001c0002t0020g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1006-29212G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217833562 | ||||||
| chr1:217833595
|
G | A | 1 | a0001c0002t0001g0112 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1006-29179G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217833595 | ||||||
| chr1:217833707
|
A | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1006-29067A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217833707 | ||||||
| chr1:217833711
|
A | T | 1 | a0001c0001t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1006-29063A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217833711 | ||||||
| chr1:217833855
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1006-28919A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217833855 | ||||||
| chr1:217833879
|
A | T | 1 | a0001c0002t0001g0207 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1006-28895A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217833879 | ||||||
| chr1:217834088
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-28686A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834088 | ||||||
| chr1:217834094
|
T | C | 72 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(69): Show | 72 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.1006-28680T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834094 | ||||||
| chr1:217834179
|
C | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(22): Show | 25 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1006-28595C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834179 | ||||||
| chr1:217834195
|
C | T | 74 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(71): Show | 74 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.1006-28579C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834195 | ||||||
| chr1:217834226
|
C | T | 1 | a0001c0002t0013g0193 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1006-28548C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834226 | ||||||
| chr1:217834312
|
C | T | 7 | a0001c0001t0001g0123a0001c0002t0022g0194a0001c0002t0022g0196others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006-28462C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834312 | ||||||
| chr1:217834321
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1006-28453C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834321 | ||||||
| chr1:217834408
|
C | T | 62 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0041others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1006-28366C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834408 | ||||||
| chr1:217834479
|
T | C | 28 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(25): Show | 28 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1006-28295T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834479 | ||||||
| chr1:217834497
|
T | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(25): Show | 28 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1006-28277T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834497 | ||||||
| chr1:217834539
|
A | G | 11 | a0001c0001t0004g0143a0001c0004t0004g0240a0001c0004t0004g0246others(8): Show | 11 | HG01109.hp1 HG01261.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1006-28235A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834539 | ||||||
| chr1:217834634
|
A | C | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-28140A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834634 | ||||||
| chr1:217834660
|
G | A | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1006-28114G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834660 | ||||||
| chr1:217834859
|
C | T | 1 | a0001c0002t0014g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1006-27915C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834859 | ||||||
| chr1:217834995
|
G | A | 44 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0190others(41): Show | 44 | HG00140.hp2 HG00738.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.1006-27779G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217834995 | ||||||
| chr1:217835257
|
T | C | 2 | a0001c0004t0004g0240a0001c0004t0008g0241 | 2 | HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1006-27517T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217835257 | ||||||
| chr1:217835313
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-27461A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217835313 | ||||||
| chr1:217835388
|
T | C | 2 | a0001c0001t0008g0045a0001c0001t0042g0035 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1006-27386T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217835388 | ||||||
| chr1:217835446
|
G | A | 133 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(130): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1006-27328G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217835446 | ||||||
| chr1:217835526
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0020g0094 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1006-27248C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217835526 | ||||||
| chr1:217835684
|
G | C | 12 | a0001c0001t0001g0216a0001c0002t0001g0086a0001c0002t0001g0112others(9): Show | 12 | HG00738.hp1 HG01070.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.1006-27090G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217835684 | ||||||
| chr1:217835713
|
G | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-27061G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217835713 | ||||||
| chr1:217835728
|
CT | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-27045delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217835728 | ||||||
| chr1:217835950
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(22): Show | 25 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1006-26824G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217835950 | ||||||
| chr1:217836029
|
C | T | 16 | a0001c0001t0001g0119a0001c0001t0005g0089a0001c0001t0005g0118others(13): Show | 16 | HG01109.hp2 HG01168.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006-26745C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217836029 | ||||||
| chr1:217836093
|
C | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1006-26681C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217836093 | ||||||
| chr1:217836154
|
T | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1006-26620T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217836154 | ||||||
| chr1:217836432
|
G | A | 42 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.1006-26342G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217836432 | ||||||
| chr1:217836457
|
G | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1006-26317G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217836457 | ||||||
| chr1:217836563
|
C | T | 78 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(75): Show | 78 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.1006-26211C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217836563 | ||||||
| chr1:217836570
|
C | T | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-26204C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217836570 | ||||||
| chr1:217836620
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1006-26154T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217836620 | ||||||
| chr1:217836726
|
G | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1006-26048G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217836726 | ||||||
| chr1:217836830
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1006-25944C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217836830 | ||||||
| chr1:217837039
|
A | T | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-25735A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217837039 | ||||||
| chr1:217837093
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1006-25681C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217837093 | ||||||
| chr1:217837099
|
C | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1006-25675C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217837099 | ||||||
| chr1:217837249
|
A | C | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-25525A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217837249 | ||||||
| chr1:217837431
|
G | A | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-25343G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217837431 | ||||||
| chr1:217837736
|
T | C | 2 | a0001c0001t0005g0089a0001c0004t0005g0250 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1006-25038T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217837736 | ||||||
| chr1:217837923
|
G | C | 16 | a0001c0001t0001g0119a0001c0001t0005g0089a0001c0001t0005g0118others(13): Show | 16 | HG01109.hp2 HG01168.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006-24851G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217837923 | ||||||
| chr1:217837931
|
A | G | 250 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1006-24843A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217837931 | ||||||
| chr1:217838727
|
T | C | 2 | a0001c0001t0005g0084a0001c0002t0005g0056 | 2 | HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1006-24047T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217838727 | ||||||
| chr1:217838777
|
C | A | 1 | a0001c0003t0003g0222 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1006-23997C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217838777 | ||||||
| chr1:217838883
|
A | G | 4 | a0001c0001t0001g0090a0001c0001t0005g0084a0001c0002t0005g0056others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-23891A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217838883 | ||||||
| chr1:217838894
|
A | G | 3 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0055g0242 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1006-23880A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217838894 | ||||||
| chr1:217839164
|
A | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-23610A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217839164 | ||||||
| chr1:217839346
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(22): Show | 25 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1006-23428G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217839346 | ||||||
| chr1:217839357
|
C | T | 1 | a0001c0003t0003g0229 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1006-23417C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217839357 | ||||||
| chr1:217839378
|
T | C | 2 | a0001c0001t0010g0156a0001c0002t0002g0133 | 2 | HG00642.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1006-23396T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217839378 | ||||||
| chr1:217839503
|
G | T | 1 | a0001c0002t0001g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1006-23271G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217839503 | ||||||
| chr1:217839540
|
T | G | 1 | a0001c0002t0013g0121 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1006-23234T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217839540 | ||||||
| chr1:217839706
|
C | CT | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-23058dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217839706 | |||||
| chr1:217839706
|
CT | C | 37 | a0001c0001t0001g0190a0001c0001t0008g0045a0001c0001t0008g0049others(34): Show | 37 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1006-23058delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217839706 | |||||
| chr1:217839930
|
A | G | 68 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(65): Show | 68 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1006-22844A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217839930 | ||||||
| chr1:217839950
|
C | T | 7 | a0001c0001t0001g0123a0001c0002t0022g0194a0001c0002t0022g0196others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006-22824C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217839950 | ||||||
| chr1:217840001
|
T | C | 24 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0216others(21): Show | 24 | HG00738.hp1 HG01070.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1006-22773T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217840001 | ||||||
| chr1:217840008
|
G | GA | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1006-22759dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217840008 | |||||
| chr1:217840224
|
T | C | 3 | a0001c0001t0001g0190a0001c0001t0012g0188a0001c0001t0036g0187 | 3 | HG03130.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1006-22550T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217840224 | ||||||
| chr1:217840406
|
C | A | 2 | a0001c0001t0001g0036a0001c0001t0002g0030 | 2 | HG02083.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1006-22368C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217840406 | ||||||
| chr1:217840435
|
T | G | 2 | a0001c0001t0001g0123a0001c0003t0001g0231 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1006-22339T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217840435 | ||||||
| chr1:217840468
|
C | A | 2 | a0001c0001t0001g0123a0001c0003t0001g0231 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1006-22306C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217840468 | ||||||
| chr1:217840495
|
T | C | 2 | a0001c0002t0022g0194a0001c0002t0022g0196 | 2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1006-22279T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217840495 | ||||||
| chr1:217840579
|
G | A | 25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(22): Show | 25 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1006-22195G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217840579 | ||||||
| chr1:217840704
|
C | T | 1 | a0002c0006t0003g0014 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1006-22070C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217840704 | ||||||
| chr1:217840822
|
G | A | 17 | a0001c0002t0005g0078a0001c0002t0009g0072a0001c0002t0009g0076others(14): Show | 17 | HG00140.hp2 HG01167.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1006-21952G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217840822 | ||||||
| chr1:217840860
|
A | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0124a0001c0001t0057g0200 | 3 | HG00639.hp1 HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1006-21914A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217840860 | ||||||
| chr1:217840930
|
T | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-21844T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217840930 | ||||||
| chr1:217841023
|
C | CT | 16 | a0001c0001t0001g0119a0001c0001t0005g0089a0001c0001t0005g0118others(13): Show | 16 | HG01109.hp2 HG01168.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006-21748dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217841023 | |||||
| chr1:217841212
|
A | G | 1 | a0001c0001t0043g0155 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1006-21562A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217841212 | ||||||
| chr1:217841606
|
ATTC | A | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-21161_1006-21 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217841606 | |||||
| chr1:217841650
|
C | T | 1 | a0001c0001t0004g0069 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1006-21124C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217841650 | ||||||
| chr1:217841805
|
TAA | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(22): Show | 25 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1006-20967_1006-20 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217841805 | |||||
| chr1:217841844
|
C | T | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1006-20930C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217841844 | ||||||
| chr1:217841971
|
C | T | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-20803C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217841971 | ||||||
| chr1:217842010
|
C | T | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1006-20764C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217842010 | ||||||
| chr1:217842345
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0012g0188a0001c0001t0036g0187 | 3 | HG03130.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1006-20429C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217842345 | ||||||
| chr1:217842659
|
G | A | 1 | a0001c0009t0001g0178 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1006-20115G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217842659 | ||||||
| chr1:217842875
|
A | C | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-19899A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217842875 | ||||||
| chr1:217842953
|
CT | C | 34 | a0001c0001t0001g0148a0001c0001t0008g0045a0001c0001t0008g0049others(31): Show | 34 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1006-19811delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217842953 | |||||
| chr1:217843218
|
C | A | 250 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1006-19556C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217843218 | ||||||
| chr1:217843266
|
T | C | 68 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(65): Show | 68 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1006-19508T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217843266 | ||||||
| chr1:217843344
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0012g0188a0001c0001t0036g0187 | 3 | HG03130.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1006-19430C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217843344 | ||||||
| chr1:217843485
|
A | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1006-19289A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217843485 | ||||||
| chr1:217843573
|
C | A | 17 | a0001c0002t0005g0078a0001c0002t0009g0072a0001c0002t0009g0076others(14): Show | 17 | HG00140.hp2 HG01167.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1006-19201C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217843573 | ||||||
| chr1:217843606
|
G | T | 16 | a0001c0001t0001g0119a0001c0001t0005g0089a0001c0001t0005g0118others(13): Show | 16 | HG01109.hp2 HG01168.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006-19168G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217843606 | ||||||
| chr1:217843766
|
C | G | 1 | a0001c0001t0006g0161 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1006-19008C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217843766 | ||||||
| chr1:217843902
|
T | C | 1 | a0001c0002t0039g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1006-18872T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217843902 | ||||||
| chr1:217844162
|
G | A | 7 | a0001c0001t0002g0101a0001c0001t0002g0158a0001c0001t0002g0159others(4): Show | 7 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006-18612G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217844162 | ||||||
| chr1:217844322
|
C | G | 1 | a0001c0001t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1006-18452C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217844322 | ||||||
| chr1:217844526
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1006-18248G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217844526 | ||||||
| chr1:217844532
|
T | C | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1006-18242T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217844532 | ||||||
| chr1:217844747
|
T | C | 37 | a0001c0001t0001g0190a0001c0001t0008g0045a0001c0001t0008g0049others(34): Show | 37 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1006-18027T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217844747 | ||||||
| chr1:217844849
|
A | G | 3 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0055g0242 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1006-17925A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217844849 | ||||||
| chr1:217844935
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-17839A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217844935 | ||||||
| chr1:217844980
|
G | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1006-17794G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217844980 | ||||||
| chr1:217845380
|
A | C | 3 | a0001c0001t0004g0069a0001c0001t0005g0052a0001c0001t0005g0068 | 3 | HG02055.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1006-17394A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217845380 | ||||||
| chr1:217845525
|
C | T | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1006-17249C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217845525 | ||||||
| chr1:217845614
|
C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(174): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1006-17160C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217845614 | ||||||
| chr1:217845950
|
G | A | 17 | a0001c0002t0005g0078a0001c0002t0009g0072a0001c0002t0009g0076others(14): Show | 17 | HG00140.hp2 HG01167.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1006-16824G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217845950 | ||||||
| chr1:217845968
|
G | C | 19 | a0001c0002t0005g0078a0001c0002t0009g0072a0001c0002t0009g0076others(16): Show | 19 | HG00140.hp2 HG01167.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.1006-16806G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217845968 | ||||||
| chr1:217846091
|
G | A | 1 | a0001c0002t0028g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1006-16683G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217846091 | ||||||
| chr1:217846284
|
A | G | 1 | a0001c0002t0028g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1006-16490A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217846284 | ||||||
| chr1:217846292
|
A | G | 25 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0216others(22): Show | 25 | HG00738.hp1 HG01070.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.1006-16482A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217846292 | ||||||
| chr1:217846434
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1006-16340T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217846434 | ||||||
| chr1:217846483
|
T | C | 1 | a0001c0001t0005g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1006-16291T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217846483 | ||||||
| chr1:217846676
|
G | A | 3 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0055g0242 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1006-16098G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217846676 | ||||||
| chr1:217846741
|
A | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.1006-16033A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217846741 | ||||||
| chr1:217846792
|
A | C | 24 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0216others(21): Show | 24 | HG00738.hp1 HG01070.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1006-15982A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217846792 | ||||||
| chr1:217846945
|
C | T | 1 | a0001c0003t0003g0235 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1006-15829C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217846945 | ||||||
| chr1:217846971
|
T | G | 40 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(37): Show | 40 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1006-15803T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217846971 | ||||||
| chr1:217847093
|
C | G | 1 | a0001c0001t0020g0094 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1006-15681C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217847093 | ||||||
| chr1:217847146
|
A | G | 8 | a0001c0001t0001g0209a0001c0001t0006g0096a0001c0001t0006g0161others(5): Show | 8 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1006-15628A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217847146 | ||||||
| chr1:217847292
|
G | T | 4 | a0001c0001t0004g0054a0001c0001t0009g0120a0001c0001t0023g0053others(1): Show | 4 | HG02572.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-15482G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217847292 | ||||||
| chr1:217847362
|
T | C | 1 | a0001c0002t0021g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1006-15412T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217847362 | ||||||
| chr1:217847421
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0012g0188 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1006-15353T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217847421 | ||||||
| chr1:217847471
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1006-15303T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217847471 | ||||||
| chr1:217847795
|
C | T | 142 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(139): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1006-14979C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217847795 | ||||||
| chr1:217847914
|
C | A | 7 | a0001c0001t0001g0123a0001c0002t0022g0194a0001c0002t0022g0196others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006-14860C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217847914 | ||||||
| chr1:217847927
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1006-14847G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217847927 | ||||||
| chr1:217847933
|
G | A | 16 | a0001c0001t0001g0090a0001c0001t0001g0216a0001c0001t0005g0084others(13): Show | 16 | HG01070.hp1 HG01123.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1006-14841G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217847933 | ||||||
| chr1:217847948
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1006-14826T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217847948 | ||||||
| chr1:217847965
|
G | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1006-14809G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217847965 | ||||||
| chr1:217847974
|
G | C | 3 | a0003c0007t0005g0115a0003c0007t0009g0116a0003c0007t0009g0117 | 3 | HG02257.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1006-14800G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217847974 | ||||||
| chr1:217848019
|
G | C | 19 | a0001c0002t0005g0078a0001c0002t0009g0072a0001c0002t0009g0076others(16): Show | 19 | HG00140.hp2 HG01167.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.1006-14755G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217848019 | ||||||
| chr1:217848079
|
A | G | 16 | a0001c0001t0001g0119a0001c0001t0005g0089a0001c0001t0005g0118others(13): Show | 16 | HG01109.hp2 HG01168.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006-14695A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217848079 | ||||||
| chr1:217848184
|
A | G | 7 | a0001c0001t0001g0123a0001c0002t0022g0194a0001c0002t0022g0196others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006-14590A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217848184 | ||||||
| chr1:217848236
|
C | T | 1 | a0001c0001t0002g0006 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1006-14538C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217848236 | ||||||
| chr1:217848320
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.1006-14454A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217848320 | ||||||
| chr1:217848503
|
T | G | 1 | a0001c0001t0020g0094 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1006-14271T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217848503 | ||||||
| chr1:217848623
|
G | C | 1 | a0001c0003t0003g0097 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1006-14151G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217848623 | ||||||
| chr1:217848704
|
T | G | 1 | a0001c0003t0003g0224 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1006-14070T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217848704 | ||||||
| chr1:217848864
|
A | G | 3 | a0001c0004t0032g0186a0001c0004t0052g0238a0001c0004t0055g0242 | 3 | HG02630.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1006-13910A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217848864 | ||||||
| chr1:217849034
|
C | A | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1006-13740C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217849034 | ||||||
| chr1:217849289
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1006-13485A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217849289 | ||||||
| chr1:217849308
|
C | A | 3 | a0001c0001t0001g0190a0001c0001t0012g0188a0001c0001t0036g0187 | 3 | HG03130.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1006-13466C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217849308 | ||||||
| chr1:217849393
|
T | G | 1 | a0001c0001t0048g0110 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1006-13381T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217849393 | ||||||
| chr1:217849489
|
G | T | 1 | a0001c0003t0014g0230 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1006-13285G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217849489 | ||||||
| chr1:217849521
|
A | AAT | 11 | a0001c0002t0009g0072a0001c0002t0009g0076a0001c0002t0013g0099others(8): Show | 11 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1006-13245_1006-13 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217849521 | |||||
| chr1:217849588
|
T | C | 1 | a0001c0002t0054g0050 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1006-13186T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217849588 | ||||||
| chr1:217849726
|
T | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1006-13048T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217849726 | ||||||
| chr1:217849875
|
C | G | 250 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1006-12899C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217849875 | ||||||
| chr1:217849936
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1006-12838G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217849936 | ||||||
| chr1:217849986
|
C | T | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1006-12788C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217849986 | ||||||
| chr1:217850104
|
T | A | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-12670T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217850104 | ||||||
| chr1:217850264
|
T | A | 2 | a0001c0001t0002g0013a0001c0001t0010g0043 | 2 | NA18959.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1006-12510T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217850264 | ||||||
| chr1:217850478
|
C | CA | 251 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(248): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1006-12296_1006-12 others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217850478 | ||||||
| chr1:217850570
|
T | C | 7 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006-12204T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217850570 | ||||||
| chr1:217850643
|
T | C | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1006-12131T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217850643 | ||||||
| chr1:217850665
|
G | A | 7 | a0001c0001t0001g0022a0001c0001t0006g0096a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006-12109G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217850665 | ||||||
| chr1:217850755
|
T | G | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1006-12019T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217850755 | ||||||
| chr1:217850772
|
T | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0046others(11): Show | 14 | HG01168.hp1 HG01433.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1006-12002T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217850772 | ||||||
| chr1:217850774
|
T | C | 2 | a0001c0002t0022g0194a0001c0002t0022g0196 | 2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1006-12000T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217850774 | ||||||
| chr1:217850889
|
C | T | 1 | a0001c0001t0015g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1006-11885C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217850889 | ||||||
| chr1:217850948
|
T | C | 4 | a0001c0002t0054g0050a0001c0004t0052g0238a0001c0004t0055g0242others(1): Show | 4 | HG02258.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-11826T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217850948 | ||||||
| chr1:217850966
|
G | A | 35 | a0001c0001t0001g0022a0001c0001t0001g0119a0001c0001t0001g0124others(32): Show | 35 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1006-11808G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217850966 | ||||||
| chr1:217851020
|
T | A | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1006-11754T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217851020 | ||||||
| chr1:217851161
|
A | G | 30 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0216others(27): Show | 30 | HG00280.hp1 HG00280.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1006-11613A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217851161 | ||||||
| chr1:217851183
|
C | G | 14 | a0001c0001t0009g0120a0001c0001t0024g0040a0001c0002t0009g0072others(11): Show | 14 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1006-11591C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217851183 | ||||||
| chr1:217851279
|
G | A | 1 | a0004c0013t0033g0095 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1006-11495G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217851279 | ||||||
| chr1:217851280
|
T | G | 1 | a0004c0013t0033g0095 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1006-11494T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217851280 | ||||||
| chr1:217851873
|
G | A | 7 | a0001c0001t0006g0096a0001c0001t0006g0161a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006-10901G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217851873 | ||||||
| chr1:217851895
|
A | G | 3 | a0001c0001t0020g0094a0001c0002t0020g0070a0001c0011t0037g0249 | 3 | HG02615.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1006-10879A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217851895 | ||||||
| chr1:217851993
|
C | T | 8 | a0001c0001t0002g0101a0001c0001t0002g0158a0001c0001t0002g0159others(5): Show | 8 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006-10781C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217851993 | ||||||
| chr1:217852028
|
A | C | 1 | a0001c0001t0023g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1006-10746A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217852028 | ||||||
| chr1:217852057
|
A | G | 3 | a0001c0002t0054g0050a0001c0004t0052g0238a0001c0004t0055g0242 | 3 | HG02258.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1006-10717A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217852057 | ||||||
| chr1:217852164
|
C | A | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1006-10610C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217852164 | ||||||
| chr1:217852430
|
T | C | 55 | a0001c0001t0001g0022a0001c0001t0002g0001a0001c0001t0002g0003others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1006-10344T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217852430 | ||||||
| chr1:217852462
|
A | G | 1 | a0001c0002t0001g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1006-10312A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217852462 | ||||||
| chr1:217852469
|
C | T | 1 | a0001c0001t0004g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1006-10305C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217852469 | ||||||
| chr1:217852550
|
G | T | 1 | a0001c0001t0005g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1006-10224G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217852550 | ||||||
| chr1:217852554
|
T | C | 1 | a0001c0002t0002g0133 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1006-10220T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217852554 | ||||||
| chr1:217852607
|
A | T | 8 | a0001c0001t0007g0142a0001c0002t0007g0051a0001c0002t0007g0060others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006-10167A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217852607 | ||||||
| chr1:217852655
|
G | A | 3 | a0001c0002t0054g0050a0001c0004t0052g0238a0001c0004t0055g0242 | 3 | HG02258.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1006-10119G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217852655 | ||||||
| chr1:217852693
|
T | C | 3 | a0001c0001t0020g0094a0001c0002t0020g0070a0001c0011t0037g0249 | 3 | HG02615.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1006-10081T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217852693 | ||||||
| chr1:217852709
|
A | G | 4 | a0001c0001t0001g0135a0001c0001t0001g0148a0001c0001t0001g0166others(1): Show | 4 | NA18944.hp2 NA18969.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006-10065A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217852709 | ||||||
| chr1:217853006
|
G | A | 1 | a0003c0007t0005g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1006-9768G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217853006 | ||||||
| chr1:217853235
|
A | C | 81 | a0001c0001t0001g0022a0001c0001t0002g0001a0001c0001t0002g0003others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.1006-9539A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217853235 | ||||||
| chr1:217853250
|
C | T | 8 | a0001c0001t0007g0142a0001c0002t0007g0051a0001c0002t0007g0060others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006-9524C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217853250 | ||||||
| chr1:217853318
|
C | G | 3 | a0001c0001t0004g0054a0001c0001t0004g0069a0001c0001t0056g0075 | 3 | HG02055.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1006-9456C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217853318 | ||||||
| chr1:217853357
|
T | C | 1 | a0001c0002t0007g0051 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1006-9417T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217853357 | ||||||
| chr1:217853626
|
T | A | 7 | a0001c0001t0006g0096a0001c0001t0006g0161a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006-9148T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217853626 | ||||||
| chr1:217853635
|
G | A | 11 | a0001c0001t0009g0120a0001c0001t0024g0040a0001c0002t0009g0072others(8): Show | 11 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1006-9139G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217853635 | ||||||
| chr1:217853674
|
C | T | 1 | a0001c0002t0001g0126 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1006-9100C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217853674 | ||||||
| chr1:217853710
|
C | T | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1006-9064C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217853710 | ||||||
| chr1:217853785
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 65 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1006-8989G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217853785 | ||||||
| chr1:217853847
|
T | C | 1 | a0001c0002t0001g0086 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1006-8927T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217853847 | ||||||
| chr1:217853962
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1006-8812C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217853962 | ||||||
| chr1:217853968
|
G | A | 2 | a0001c0001t0006g0204a0001c0001t0006g0205 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1006-8806G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217853968 | ||||||
| chr1:217854212
|
C | A | 1 | a0001c0003t0024g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1006-8562C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217854212 | ||||||
| chr1:217854408
|
C | G | 47 | a0001c0001t0001g0022a0001c0001t0002g0001a0001c0001t0002g0003others(44): Show | 47 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1006-8366C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217854408 | ||||||
| chr1:217854452
|
T | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 65 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1006-8322T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217854452 | ||||||
| chr1:217854465
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1006-8309A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217854465 | ||||||
| chr1:217854662
|
A | G | 6 | a0001c0001t0012g0188a0001c0002t0005g0078a0001c0002t0012g0018others(3): Show | 6 | HG00140.hp2 HG01167.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006-8112A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217854662 | ||||||
| chr1:217854699
|
G | GA | 10 | a0001c0001t0009g0120a0001c0002t0009g0072a0001c0002t0009g0076others(7): Show | 10 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1006-8066dupA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217854699 | |||||
| chr1:217854705
|
A | T | 47 | a0001c0001t0001g0022a0001c0001t0002g0001a0001c0001t0002g0003others(44): Show | 47 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1006-8069A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217854705 | ||||||
| chr1:217854753
|
G | A | 1 | a0002c0006t0001g0105 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1006-8021G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217854753 | ||||||
| chr1:217854792
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1006-7982A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217854792 | ||||||
| chr1:217854831
|
A | C | 3 | a0001c0002t0054g0050a0001c0004t0052g0238a0001c0004t0055g0242 | 3 | HG02258.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1006-7943A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217854831 | ||||||
| chr1:217854855
|
C | T | 1 | a0001c0001t0048g0110 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1006-7919C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217854855 | ||||||
| chr1:217855012
|
T | C | 1 | a0001c0002t0002g0133 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1006-7762T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217855012 | ||||||
| chr1:217855032
|
T | G | 1 | a0001c0001t0002g0033 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1006-7742T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217855032 | ||||||
| chr1:217855185
|
G | A | 1 | a0001c0002t0009g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1006-7589G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217855185 | ||||||
| chr1:217855380
|
C | T | 9 | a0001c0001t0005g0084a0001c0001t0005g0118a0001c0001t0048g0110others(6): Show | 9 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006-7394C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217855380 | ||||||
| chr1:217855425
|
G | C | 11 | a0001c0001t0009g0120a0001c0001t0024g0040a0001c0002t0009g0072others(8): Show | 11 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1006-7349G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217855425 | ||||||
| chr1:217855538
|
C | T | 77 | a0001c0001t0001g0022a0001c0001t0002g0001a0001c0001t0002g0003others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.1006-7236C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217855538 | ||||||
| chr1:217855595
|
C | A | 1 | a0001c0001t0001g0004 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1006-7179C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217855595 | ||||||
| chr1:217855606
|
T | A | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1006-7168T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217855606 | ||||||
| chr1:217855729
|
A | AT | 39 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(36): Show | 39 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1006-7029dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217855729 | |||||
| chr1:217855729
|
A | ATT | 47 | a0001c0001t0001g0011a0001c0001t0003g0168a0001c0001t0007g0142others(44): Show | 47 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1006-7030_1006-702 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217855729 | |||||
| chr1:217855729
|
A | ATTT | 35 | a0001c0001t0004g0143a0001c0001t0005g0084a0001c0001t0005g0118others(32): Show | 35 | HG00140.hp2 HG00323.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1006-7031_1006-702 others(7): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217855729 | |||||
| chr1:217855729
|
A | ATTTT | 33 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0037others(30): Show | 33 | HG01070.hp1 HG01106.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.1006-7032_1006-702 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217855729 | |||||
| chr1:217855729
|
A | ATTTTT | 85 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0016others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1006-7033_1006-702 others(9): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217855729 | |||||
| chr1:217855729
|
A | ATTTTTT | 9 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0177others(6): Show | 9 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006-7034_1006-702 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217855729 | |||||
| chr1:217855759
|
G | T | 1 | a0001c0011t0037g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1006-7015G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217855759 | ||||||
| chr1:217855766
|
C | T | 1 | a0001c0002t0001g0129 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1006-7008C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217855766 | ||||||
| chr1:217855812
|
C | T | 2 | a0001c0004t0004g0073a0001c0005t0004g0071 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1006-6962C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217855812 | ||||||
| chr1:217855960
|
C | T | 1 | a0001c0003t0003g0210 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1006-6814C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217855960 | ||||||
| chr1:217856074
|
A | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(62): Show | 65 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1006-6700A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217856074 | ||||||
| chr1:217856142
|
G | A | 1 | a0001c0001t0009g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1006-6632G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217856142 | ||||||
| chr1:217856322
|
A | G | 1 | a0001c0001t0040g0025 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1006-6452A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217856322 | ||||||
| chr1:217856426
|
A | G | 1 | a0001c0001t0036g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1006-6348A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217856426 | ||||||
| chr1:217856616
|
C | T | 8 | a0001c0001t0005g0084a0001c0001t0005g0118a0001c0002t0005g0056others(5): Show | 8 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006-6158C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217856616 | ||||||
| chr1:217856829
|
A | G | 15 | a0001c0001t0004g0054a0001c0001t0004g0069a0001c0001t0004g0143others(12): Show | 15 | HG01261.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1006-5945A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217856829 | ||||||
| chr1:217856864
|
G | A | 1 | a0001c0001t0004g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1006-5910G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217856864 | ||||||
| chr1:217857174
|
G | A | 1 | a0001c0002t0028g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1006-5600G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217857174 | ||||||
| chr1:217857242
|
G | T | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.1006-5532G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217857242 | ||||||
| chr1:217857424
|
A | G | 1 | a0001c0003t0003g0098 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1006-5350A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217857424 | ||||||
| chr1:217857587
|
G | C | 39 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.1006-5187G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217857587 | ||||||
| chr1:217857677
|
A | G | 76 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.1006-5097A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217857677 | ||||||
| chr1:217857683
|
G | A | 7 | a0001c0001t0006g0096a0001c0001t0006g0161a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006-5091G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217857683 | ||||||
| chr1:217858082
|
T | C | 3 | a0001c0002t0005g0078a0001c0002t0012g0018a0001c0002t0012g0080 | 3 | HG00140.hp2 HG01167.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1006-4692T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217858082 | ||||||
| chr1:217858221
|
G | A | 100 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.1006-4553G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217858221 | ||||||
| chr1:217858271
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(5): Show | 8 | HG02738.hp1 HG03017.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006-4503A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217858271 | ||||||
| chr1:217858522
|
T | C | 1 | a0001c0001t0006g0202 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1006-4252T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217858522 | ||||||
| chr1:217858701
|
G | A | 1 | a0001c0001t0005g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1006-4073G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217858701 | ||||||
| chr1:217858708
|
CA | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(63): Show | 66 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1006-4064delA | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217858708 | |||||
| chr1:217858811
|
C | T | 39 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.1006-3963C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217858811 | ||||||
| chr1:217858888
|
C | T | 15 | a0001c0001t0004g0054a0001c0001t0004g0069a0001c0001t0004g0143others(12): Show | 15 | HG01261.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1006-3886C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217858888 | ||||||
| chr1:217858889
|
G | A | 12 | a0001c0001t0005g0052a0001c0001t0005g0068a0001c0001t0005g0089others(9): Show | 12 | HG00140.hp2 HG01109.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1006-3885G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217858889 | ||||||
| chr1:217859098
|
G | T | 1 | a0002c0006t0003g0014 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1006-3676G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859098 | ||||||
| chr1:217859099
|
A | G | 1 | a0002c0006t0003g0014 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1006-3675A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859099 | ||||||
| chr1:217859100
|
G | T | 1 | a0002c0006t0003g0014 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1006-3674G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859100 | ||||||
| chr1:217859132
|
ATAAT | A | 37 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(34): Show | 37 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1006-3638_1006-363 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217859132 | |||||
| chr1:217859205
|
A | G | 1 | a0002c0006t0018g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1006-3569A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859205 | ||||||
| chr1:217859284
|
A | G | 3 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093 | 3 | HG02486.hp2 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1006-3490A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859284 | ||||||
| chr1:217859401
|
G | A | 1 | a0001c0011t0037g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1006-3373G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859401 | ||||||
| chr1:217859411
|
G | A | 1 | a0001c0001t0015g0093 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1006-3363G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859411 | ||||||
| chr1:217859411
|
G | GTA | 8 | a0001c0001t0007g0142a0001c0002t0007g0051a0001c0002t0007g0060others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006-3354_1006-335 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217859411 | |||||
| chr1:217859433
|
C | T | 1 | a0002c0006t0018g0137 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1006-3341C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859433 | ||||||
| chr1:217859543
|
G | A | 1 | a0001c0001t0036g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1006-3231G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859543 | ||||||
| chr1:217859661
|
C | T | 2 | a0001c0003t0024g0243a0001c0003t0038g0244 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1006-3113C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859661 | ||||||
| chr1:217859681
|
T | C | 1 | a0001c0011t0037g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1006-3093T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859681 | ||||||
| chr1:217859700
|
C | G | 11 | a0001c0001t0009g0120a0001c0001t0024g0040a0001c0002t0009g0072others(8): Show | 11 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1006-3074C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859700 | ||||||
| chr1:217859715
|
A | G | 7 | a0001c0002t0009g0076a0001c0002t0013g0099a0001c0002t0013g0193others(4): Show | 7 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006-3059A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859715 | ||||||
| chr1:217859925
|
T | C | 1 | a0001c0001t0036g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1006-2849T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217859925 | ||||||
| chr1:217860001
|
C | T | 1 | a0001c0002t0001g0064 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1006-2773C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217860001 | ||||||
| chr1:217860095
|
G | C | 6 | a0001c0001t0005g0052a0001c0001t0005g0068a0001c0001t0005g0089others(3): Show | 6 | HG01109.hp1 HG02615.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1006-2679G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217860095 | ||||||
| chr1:217860196
|
C | T | 7 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(4): Show | 7 | HG01168.hp1 HG02486.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006-2578C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217860196 | ||||||
| chr1:217860266
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0173a0001c0001t0001g0175 | 3 | HG01952.hp2 HG02148.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1006-2508G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217860266 | ||||||
| chr1:217860416
|
G | A | 1 | a0001c0011t0037g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1006-2358G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217860416 | ||||||
| chr1:217860469
|
G | T | 4 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(1): Show | 4 | NA18941.hp1 NA18942.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-2305G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217860469 | ||||||
| chr1:217860521
|
T | C | 79 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.1006-2253T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217860521 | ||||||
| chr1:217860565
|
A | T | 1 | a0001c0001t0002g0001 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1006-2209A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217860565 | ||||||
| chr1:217860600
|
T | C | 1 | a0001c0003t0003g0212 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1006-2174T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217860600 | ||||||
| chr1:217860872
|
C | G | 3 | a0001c0001t0018g0183a0002c0006t0018g0137a0002c0006t0018g0139 | 3 | NA18959.hp1 NA19077.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1006-1902C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217860872 | ||||||
| chr1:217860972
|
A | G | 8 | a0001c0001t0007g0142a0001c0002t0007g0051a0001c0002t0007g0060others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006-1802A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217860972 | ||||||
| chr1:217861033
|
G | A | 1 | a0001c0002t0013g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1006-1741G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861033 | ||||||
| chr1:217861042
|
C | T | 2 | a0001c0001t0002g0033a0001c0001t0002g0167 | 2 | HG01106.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1006-1732C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861042 | ||||||
| chr1:217861078
|
A | G | 1 | a0001c0001t0002g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1006-1696A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861078 | ||||||
| chr1:217861104
|
C | T | 4 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006-1670C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861104 | ||||||
| chr1:217861157
|
G | A | 7 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(4): Show | 7 | HG01168.hp1 HG02486.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006-1617G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861157 | ||||||
| chr1:217861171
|
G | A | 7 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093others(4): Show | 7 | HG01168.hp1 HG02486.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006-1603G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861171 | ||||||
| chr1:217861387
|
T | TTA | 24 | a0001c0001t0001g0090a0001c0001t0006g0096a0001c0001t0006g0161others(21): Show | 24 | HG00323.hp2 HG01070.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1006-1371_1006-137 others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217861387 | |||||
| chr1:217861387
|
T | TTATA | 47 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(44): Show | 47 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1006-1373_1006-137 others(8): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217861387 | |||||
| chr1:217861387
|
T | TTATATA | 7 | a0001c0001t0002g0020a0001c0001t0002g0027a0001c0001t0018g0183others(4): Show | 7 | HG00099.hp1 HG00323.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006-1375_1006-137 others(10): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 217861387 | |||||
| chr1:217861405
|
T | A | 1 | a0001c0004t0053g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1006-1369T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861405 | ||||||
| chr1:217861645
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1006-1129A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861645 | ||||||
| chr1:217861689
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1006-1085A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861689 | ||||||
| chr1:217861695
|
G | T | 1 | a0001c0001t0001g0090 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1006-1079G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861695 | ||||||
| chr1:217861709
|
A | T | 1 | a0001c0004t0053g0239 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1006-1065A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861709 | ||||||
| chr1:217861800
|
A | G | 1 | a0001c0001t0036g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1006-974A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861800 | ||||||
| chr1:217861806
|
C | A | 1 | a0001c0002t0013g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1006-968C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861806 | ||||||
| chr1:217861850
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1006-924A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861850 | ||||||
| chr1:217861933
|
C | T | 3 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093 | 3 | HG02486.hp2 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1006-841C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861933 | ||||||
| chr1:217861937
|
A | C | 7 | a0001c0001t0006g0096a0001c0001t0006g0161a0001c0001t0006g0201others(4): Show | 7 | HG00323.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006-837A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217861937 | ||||||
| chr1:217862030
|
C | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1006-744C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217862030 | ||||||
| chr1:217862225
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1006-549A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217862225 | ||||||
| chr1:217862439
|
A | T | 1 | a0004c0013t0033g0095 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1006-335A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217862439 | ||||||
| chr1:217862490
|
A | G | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1006-284A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 9/10 | chr1 | 217862490 | ||||||
| chr1:217862895
|
T | G | 46 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(43): Show | 46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.*2+39T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217862895 | ||||||
| chr1:217863070
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0173a0001c0001t0001g0175 | 3 | HG01952.hp2 HG02148.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.*2+214G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217863070 | ||||||
| chr1:217863119
|
C | CT | 45 | a0001c0001t0001g0190a0001c0001t0002g0001a0001c0001t0002g0003others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.*2+284dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 217863119 | |||||
| chr1:217863119
|
CT | C | 24 | a0001c0001t0001g0154a0001c0001t0006g0096a0001c0001t0006g0161others(21): Show | 24 | HG01070.hp1 HG01074.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.*2+284delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 217863119 | |||||
| chr1:217863119
|
CTT | C | 15 | a0001c0001t0005g0052a0001c0001t0005g0068a0001c0001t0005g0089others(12): Show | 15 | HG00140.hp2 HG00323.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.*2+283_*2+284delTT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 217863119 | |||||
| chr1:217863123
|
T | C | 1 | a0001c0002t0028g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.*2+267T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217863123 | ||||||
| chr1:217863184
|
G | A | 1 | a0001c0001t0046g0153 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.*2+328G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217863184 | ||||||
| chr1:217863474
|
C | T | 1 | a0001c0001t0024g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*2+618C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217863474 | ||||||
| chr1:217863475
|
G | A | 15 | a0001c0001t0005g0052a0001c0001t0005g0068a0001c0001t0005g0089others(12): Show | 15 | HG00140.hp2 HG01109.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.*2+619G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217863475 | ||||||
| chr1:217863835
|
G | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(63): Show | 66 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.*2+979G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217863835 | ||||||
| chr1:217863879
|
C | A | 1 | a0001c0001t0002g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.*2+1023C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217863879 | ||||||
| chr1:217864099
|
T | C | 3 | a0001c0001t0018g0183a0002c0006t0018g0137a0002c0006t0018g0139 | 3 | NA18959.hp1 NA19077.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.*2+1243T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864099 | ||||||
| chr1:217864105
|
G | A | 137 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.*2+1249G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864105 | ||||||
| chr1:217864210
|
A | G | 1 | a0001c0002t0001g0147 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.*2+1354A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864210 | ||||||
| chr1:217864264
|
A | G | 1 | a0001c0003t0003g0222 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.*2+1408A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864264 | ||||||
| chr1:217864515
|
G | A | 1 | a0001c0001t0036g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.*2+1659G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864515 | ||||||
| chr1:217864563
|
C | T | 18 | a0001c0001t0005g0052a0001c0001t0005g0068a0001c0001t0005g0084others(15): Show | 18 | HG00140.hp2 HG01109.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.*2+1707C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864563 | ||||||
| chr1:217864578
|
A | G | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.*2+1722A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864578 | ||||||
| chr1:217864626
|
A | T | 15 | a0001c0001t0005g0052a0001c0001t0005g0068a0001c0001t0005g0084others(12): Show | 15 | HG00140.hp2 HG01109.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.*2+1770A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864626 | ||||||
| chr1:217864635
|
T | C | 1 | a0001c0004t0004g0252 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*2+1779T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864635 | ||||||
| chr1:217864639
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0041g0015a0001c0001t0050g0017 | 3 | NA18951.hp2 NA18984.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.*2+1783G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864639 | ||||||
| chr1:217864640
|
A | T | 3 | a0001c0001t0001g0016a0001c0001t0041g0015a0001c0001t0050g0017 | 3 | NA18951.hp2 NA18984.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.*2+1784A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864640 | ||||||
| chr1:217864641
|
G | C | 3 | a0001c0001t0001g0016a0001c0001t0041g0015a0001c0001t0050g0017 | 3 | NA18951.hp2 NA18984.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.*2+1785G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864641 | ||||||
| chr1:217864642
|
A | T | 3 | a0001c0001t0001g0016a0001c0001t0041g0015a0001c0001t0050g0017 | 3 | NA18951.hp2 NA18984.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.*2+1786A>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864642 | ||||||
| chr1:217864645
|
A | C | 3 | a0001c0001t0001g0016a0001c0001t0041g0015a0001c0001t0050g0017 | 3 | NA18951.hp2 NA18984.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.*2+1789A>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864645 | ||||||
| chr1:217864647
|
G | GTGGGAT | 3 | a0001c0001t0001g0016a0001c0001t0041g0015a0001c0001t0050g0017 | 3 | NA18951.hp2 NA18984.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.*2+1791_*2+1792ins others(6): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864647 | ||||||
| chr1:217864651
|
A | AT | 3 | a0001c0001t0001g0016a0001c0001t0041g0015a0001c0001t0050g0017 | 3 | NA18951.hp2 NA18984.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.*2+1795_*2+1796ins others(1): Show |
SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864651 | ||||||
| chr1:217864685
|
T | G | 1 | a0001c0002t0017g0113 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.*2+1829T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864685 | ||||||
| chr1:217864709
|
G | A | 1 | a0001c0002t0044g0091 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.*2+1853G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864709 | ||||||
| chr1:217864714
|
C | A | 1 | a0001c0002t0005g0078 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.*2+1858C>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864714 | ||||||
| chr1:217864795
|
T | G | 5 | a0001c0001t0048g0110a0001c0002t0054g0050a0001c0004t0052g0238others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.*2+1939T>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864795 | ||||||
| chr1:217864904
|
T | C | 3 | a0001c0001t0015g0058a0001c0001t0015g0059a0001c0001t0015g0093 | 3 | HG02486.hp2 HG02896.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.*2+2048T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864904 | ||||||
| chr1:217864934
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.*2+2078G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217864934 | ||||||
| chr1:217865023
|
G | A | 19 | a0001c0001t0005g0052a0001c0001t0005g0068a0001c0001t0005g0084others(16): Show | 19 | HG00140.hp2 HG01109.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.*3-1999G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217865023 | ||||||
| chr1:217865137
|
A | G | 37 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.*3-1885A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217865137 | ||||||
| chr1:217865271
|
A | G | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.*3-1751A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217865271 | ||||||
| chr1:217865570
|
A | G | 1 | a0001c0004t0027g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.*3-1452A>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217865570 | ||||||
| chr1:217865636
|
C | G | 40 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.*3-1386C>G | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217865636 | ||||||
| chr1:217865876
|
G | T | 1 | a0001c0003t0003g0224 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.*3-1146G>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217865876 | ||||||
| chr1:217865879
|
C | T | 35 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.*3-1143C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217865879 | ||||||
| chr1:217865963
|
G | A | 1 | a0001c0001t0009g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.*3-1059G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217865963 | ||||||
| chr1:217866034
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.*3-988G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217866034 | ||||||
| chr1:217866048
|
C | T | 4 | a0001c0001t0018g0183a0001c0004t0053g0239a0002c0006t0018g0137others(1): Show | 4 | HG01891.hp1 NA18959.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3-974C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217866048 | ||||||
| chr1:217866075
|
T | C | 1 | a0001c0003t0003g0097 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.*3-947T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217866075 | ||||||
| chr1:217866259
|
G | C | 1 | a0001c0004t0005g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*3-763G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217866259 | ||||||
| chr1:217866333
|
C | T | 2 | a0001c0002t0044g0091a0004c0013t0033g0095 | 2 | HG01168.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.*3-689C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217866333 | ||||||
| chr1:217866343
|
G | A | 39 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0006others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.*3-679G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217866343 | ||||||
| chr1:217866437
|
T | C | 1 | a0001c0002t0001g0131 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.*3-585T>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217866437 | ||||||
| chr1:217866619
|
C | T | 5 | a0001c0002t0005g0078a0001c0002t0012g0018a0001c0002t0012g0077others(2): Show | 5 | HG00140.hp2 HG01167.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.*3-403C>T | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217866619 | ||||||
| chr1:217866715
|
G | A | 1 | a0001c0001t0005g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.*3-307G>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217866715 | ||||||
| chr1:217866741
|
G | C | 18 | a0001c0001t0005g0052a0001c0001t0005g0068a0001c0001t0005g0084others(15): Show | 18 | HG00140.hp2 HG01109.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.*3-281G>C | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217866741 | ||||||
| chr1:217866816
|
T | A | 1 | a0001c0002t0012g0077 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*3-206T>A | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | chr1 | 217866816 | ||||||
| chr1:217866840
|
C | CT | 5 | a0001c0001t0001g0082a0001c0002t0054g0050a0001c0004t0052g0238others(2): Show | 5 | HG00438.hp2 HG01891.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.*3-167dupT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 217866840 | |||||
| chr1:217866840
|
CT | C | 6 | a0001c0001t0001g0041a0001c0001t0002g0026a0001c0001t0008g0045others(3): Show | 6 | HG02015.hp1 HG02630.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.*3-167delT | SPATA17 | ENSG00000162814.11 | transcript | ENST00000366933.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 217866840 |