| geneid | 200162 |
|---|---|
| ensemblid | ENSG00000155761.14 |
| hgncid | 26620 |
| symbol | SPAG17 |
| name | sperm associated antigen 17 |
| refseq_nuc | NM_206996.4 |
| refseq_prot | NP_996879.1 |
| ensembl_nuc | ENST00000336338.10 |
| ensembl_prot | ENSP00000337804.5 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 117953590 |
| end | 118185228 |
| strand | - |
| ver | v1.2 |
| region | chr1:117953590-118185228 |
| region5000 | chr1:117948590-118190228 |
| regionname0 | SPAG17_chr1_117953590_118185228 |
| regionname5000 | SPAG17_chr1_117948590_118190228 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 2223 | 117 | 42 | 22 | 34 | 5 | 13 | 26 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0002 | 0/0 | 2223 | 49 | 0 | 4 | 37 | 0 | 8 | 26 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0003 | 0/1 | 2223 | 33 | 5 | 10 | 7 | 5 | 5 | 2 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0004 | 0/0 | 2223 | 23 | 3 | 2 | 16 | 1 | 1 | 12 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0005 | 0/0 | 2223 | 6 | 0 | 1 | 2 | 0 | 3 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0006 | 0/0 | 2223 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0007 | 0/0 | 2223 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0008 | 0/0 | 2223 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0009 | 0/0 | 2223 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0010 | 0/0 | 2223 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0011 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0012 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0013 | 0/0 | 2223 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0014 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0015 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0016 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0017 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0018 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0019 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0020 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0021 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0022 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0023 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0024 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0025 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0026 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0027 | 0/0 | 2223 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0028 | 0/0 | 2223 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| 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 | 6672 | 57 | 2 | 18 | 25 | 2 | 10 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0002 | 0/0 | 6672 | 46 | 0 | 4 | 34 | 0 | 8 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0003 | 0/1 | 6672 | 32 | 5 | 9 | 7 | 5 | 5 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0004 | 0/0 | 6672 | 26 | 24 | 2 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0005 | 0/0 | 6672 | 23 | 3 | 2 | 16 | 1 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0006 | 1/0 | 6672 | 21 | 8 | 2 | 4 | 3 | 3 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0007 | 0/0 | 6672 | 4 | 0 | 3 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0008 | 0/0 | 6672 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0009 | 0/0 | 6672 | 3 | 3 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0010 | 0/0 | 6672 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0011 | 0/0 | 6672 | 3 | 0 | 1 | 0 | 0 | 2 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0012 | 0/0 | 6672 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0013 | 0/0 | 6672 | 3 | 0 | 3 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0014 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0015 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0016 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0017 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0018 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0019 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0020 | 0/0 | 6672 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0021 | 0/0 | 6672 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0022 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0023 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0024 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0025 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0026 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0027 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0028 | 0/0 | 6672 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0029 | 0/0 | 6672 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0030 | 0/0 | 6672 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0031 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0032 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0033 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0034 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0035 | 0/0 | 6672 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0036 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0037 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0038 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0039 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0040 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0041 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0042 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0043 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| c0044 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 532 | 246 | 54 | 46 | 100 | 12 | 32 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| t0002 | 0/0 | 532 | 17 | 10 | 1 | 4 | 0 | 2 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| t0003 | 0/0 | 532 | 3 | 2 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| 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 | 6672 | 57 | 2 | 18 | 25 | 2 | 10 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0004 | 0/0 | 6672 | 26 | 24 | 2 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0006 | 1/0 | 6672 | 21 | 8 | 2 | 4 | 3 | 3 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0010 | 0/0 | 6672 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0018 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0019 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0025 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0026 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0027 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0032 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0042 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0044 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0002c0002 | 0/0 | 6672 | 46 | 0 | 4 | 34 | 0 | 8 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0002c0008 | 0/0 | 6672 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0003c0003 | 0/1 | 6672 | 32 | 5 | 9 | 7 | 5 | 5 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0003c0029 | 0/0 | 6672 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0004c0005 | 0/0 | 6672 | 23 | 3 | 2 | 16 | 1 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0005c0011 | 0/0 | 6672 | 3 | 0 | 1 | 0 | 0 | 2 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0005c0020 | 0/0 | 6672 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0005c0038 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0006c0007 | 0/0 | 6672 | 4 | 0 | 3 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0007c0017 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0007c0033 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0008c0009 | 0/0 | 6672 | 3 | 3 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0009c0012 | 0/0 | 6672 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0010c0013 | 0/0 | 6672 | 3 | 0 | 3 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0011c0014 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0012c0015 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0013c0021 | 0/0 | 6672 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0014c0016 | 0/0 | 6672 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0015c0022 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0016c0023 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0017c0034 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0018c0031 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0019c0028 | 0/0 | 6672 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0020c0030 | 0/0 | 6672 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0021c0024 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0022c0037 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0023c0043 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0024c0035 | 0/0 | 6672 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0025c0036 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0026c0039 | 0/0 | 6672 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0027c0041 | 0/0 | 6672 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0028c0040 | 0/0 | 6672 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7203 | 57 | 2 | 18 | 25 | 2 | 10 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0004t0001 | 0/0 | 7203 | 25 | 23 | 2 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0004t0003 | 0/0 | 7203 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0006t0001 | 1/0 | 7203 | 21 | 8 | 2 | 4 | 3 | 3 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0010t0001 | 0/0 | 7203 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0018t0001 | 0/0 | 7203 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0019t0001 | 0/0 | 7203 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0025t0001 | 0/0 | 7203 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0026t0001 | 0/0 | 7203 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0027t0001 | 0/0 | 7203 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0032t0001 | 0/0 | 7203 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0042t0001 | 0/0 | 7203 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0001c0044t0001 | 0/0 | 7203 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0002c0002t0001 | 0/0 | 7203 | 46 | 0 | 4 | 34 | 0 | 8 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0002c0008t0001 | 0/0 | 7203 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0003c0003t0001 | 0/1 | 7203 | 31 | 4 | 9 | 7 | 5 | 5 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0003c0003t0003 | 0/0 | 7203 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0003c0029t0001 | 0/0 | 7203 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0004c0005t0001 | 0/0 | 7203 | 23 | 3 | 2 | 16 | 1 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0005c0011t0001 | 0/0 | 7203 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0005c0011t0002 | 0/0 | 7203 | 2 | 0 | 1 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0005c0020t0002 | 0/0 | 7203 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0005c0038t0002 | 0/0 | 7203 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0006c0007t0001 | 0/0 | 7203 | 4 | 0 | 3 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0007c0017t0001 | 0/0 | 7203 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0007c0033t0001 | 0/0 | 7203 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0008c0009t0002 | 0/0 | 7203 | 3 | 3 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0009c0012t0001 | 0/0 | 7203 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0010c0013t0001 | 0/0 | 7203 | 3 | 0 | 3 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0011c0014t0001 | 0/0 | 7203 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0012c0015t0002 | 0/0 | 7203 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0013c0021t0002 | 0/0 | 7203 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0014c0016t0002 | 0/0 | 7203 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0015c0022t0001 | 0/0 | 7203 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0016c0023t0001 | 0/0 | 7203 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0017c0034t0001 | 0/0 | 7203 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0018c0031t0002 | 0/0 | 7203 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0019c0028t0001 | 0/0 | 7203 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0020c0030t0001 | 0/0 | 7203 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0021c0024t0001 | 0/0 | 7203 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0022c0037t0001 | 0/0 | 7203 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0023c0043t0001 | 0/0 | 7203 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0024c0035t0003 | 0/0 | 7203 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0025c0036t0002 | 0/0 | 7203 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0026c0039t0002 | 0/0 | 7203 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0027c0041t0001 | 0/0 | 7203 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| a0028c0040t0001 | 0/0 | 7203 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | copy fasta | chr1 | 117948590 | 118190228 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0004t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0006t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0010t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0010t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0010t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0018t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0018t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0019t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0019t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0025t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0026t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0027t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0032t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0042t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0001c0044t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0008t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0008t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0002c0008t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0003c0029t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0004c0005t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0005c0011t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0005c0011t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0005c0011t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0005c0020t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0005c0020t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0005c0038t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0006c0007t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0006c0007t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0006c0007t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0006c0007t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0007c0017t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0007c0017t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0007c0033t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0008c0009t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0008c0009t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0008c0009t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0009c0012t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0009c0012t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0009c0012t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0010c0013t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0010c0013t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0010c0013t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0011c0014t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0011c0014t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0012c0015t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0012c0015t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0013c0021t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0013c0021t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0014c0016t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0014c0016t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0015c0022t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0016c0023t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0017c0034t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0018c0031t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0019c0028t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0020c0030t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0021c0024t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0022c0037t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0023c0043t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0024c0035t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0025c0036t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0026c0039t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0027c0041t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| a0028c0040t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0006 | t0001 | g0075 | EUR | GBR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0113 | EUR | GBR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00280 | hp1 | a0003 | c0003 | t0001 | g0128 | EUR | FIN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00280 | hp2 | a0001 | c0006 | t0001 | g0153 | EUR | FIN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00323 | hp1 | a0004 | c0005 | t0001 | g0120 | EUR | FIN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00423 | hp1 | a0004 | c0005 | t0001 | g0243 | EAS | CHS | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00438 | hp1 | a0023 | c0043 | t0001 | g0185 | EAS | CHS | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | CHS | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | CHS | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00597 | hp2 | a0004 | c0005 | t0001 | g0248 | EAS | CHS | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00621 | hp1 | a0005 | c0020 | t0002 | g0157 | EAS | CHS | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | CHS | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0108 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00733 | hp2 | a0003 | c0029 | t0001 | g0141 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00738 | hp2 | a0004 | c0005 | t0001 | g0123 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00741 | hp1 | a0001 | c0004 | t0001 | g0230 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG00741 | hp2 | a0004 | c0005 | t0001 | g0119 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01069 | hp2 | a0003 | c0003 | t0001 | g0087 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01070 | hp2 | a0003 | c0003 | t0001 | g0115 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01071 | hp2 | a0003 | c0003 | t0001 | g0089 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0126 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01109 | hp2 | a0001 | c0006 | t0001 | g0103 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0139 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01175 | hp1 | a0024 | c0035 | t0003 | g0207 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01255 | hp1 | a0019 | c0028 | t0001 | g0117 | AMR | CLM | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01346 | hp2 | a0001 | c0006 | t0001 | g0152 | AMR | CLM | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0140 | AMR | CLM | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01358 | hp2 | a0006 | c0007 | t0001 | g0190 | AMR | CLM | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01433 | hp1 | a0006 | c0007 | t0001 | g0188 | AMR | CLM | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01433 | hp2 | a0001 | c0004 | t0001 | g0223 | AMR | CLM | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01496 | hp1 | a0006 | c0007 | t0001 | g0189 | AMR | CLM | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01496 | hp2 | a0010 | c0013 | t0001 | g0121 | AMR | CLM | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | IBS | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0136 | EUR | IBS | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01517 | hp1 | a0003 | c0003 | t0001 | g0137 | EUR | IBS | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01517 | hp2 | a0006 | c0007 | t0001 | g0187 | EUR | IBS | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01928 | hp2 | a0010 | c0013 | t0001 | g0135 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0114 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01952 | hp1 | a0020 | c0030 | t0001 | g0138 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01981 | hp1 | a0003 | c0003 | t0001 | g0088 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02015 | hp1 | a0003 | c0003 | t0001 | g0112 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02027 | hp1 | a0005 | c0020 | t0002 | g0197 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02040 | hp1 | a0004 | c0005 | t0001 | g0249 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02055 | hp1 | a0001 | c0006 | t0001 | g0164 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0250 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0134 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02074 | hp2 | a0003 | c0003 | t0001 | g0101 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02080 | hp1 | a0001 | c0044 | t0001 | g0182 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02080 | hp2 | a0015 | c0022 | t0001 | g0038 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02129 | hp1 | a0001 | c0006 | t0001 | g0071 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02129 | hp2 | a0003 | c0003 | t0001 | g0127 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02135 | hp2 | a0003 | c0003 | t0001 | g0111 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02145 | hp1 | a0001 | c0018 | t0001 | g0148 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0260 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02148 | hp1 | a0010 | c0013 | t0001 | g0132 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | CDX | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02155 | hp2 | a0004 | c0005 | t0001 | g0094 | EAS | CDX | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02257 | hp1 | a0001 | c0006 | t0001 | g0072 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0259 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02258 | hp1 | a0008 | c0009 | t0002 | g0077 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02258 | hp2 | a0012 | c0015 | t0002 | g0102 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02273 | hp1 | a0005 | c0011 | t0002 | g0104 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02280 | hp1 | a0001 | c0004 | t0003 | g0082 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02280 | hp2 | a0001 | c0018 | t0001 | g0229 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02451 | hp1 | a0001 | c0006 | t0001 | g0255 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02451 | hp2 | a0021 | c0024 | t0001 | g0006 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02572 | hp1 | a0011 | c0014 | t0001 | g0009 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0257 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02602 | hp2 | a0016 | c0023 | t0001 | g0068 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0224 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0060 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02622 | hp1 | a0025 | c0036 | t0002 | g0254 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02622 | hp2 | a0001 | c0025 | t0001 | g0063 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0143 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0235 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02647 | hp1 | a0001 | c0006 | t0001 | g0252 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0232 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02683 | hp2 | a0005 | c0011 | t0001 | g0106 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02698 | hp2 | a0005 | c0011 | t0002 | g0202 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0234 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02723 | hp2 | a0001 | c0006 | t0001 | g0253 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02735 | hp1 | a0007 | c0033 | t0001 | g0014 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02735 | hp2 | a0022 | c0037 | t0001 | g0116 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02818 | hp1 | a0014 | c0016 | t0002 | g0085 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0238 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0233 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0078 | AFR | ESN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02922 | hp2 | a0001 | c0032 | t0001 | g0067 | AFR | ESN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02965 | hp1 | a0001 | c0026 | t0001 | g0261 | AFR | ESN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02965 | hp2 | a0012 | c0015 | t0002 | g0079 | AFR | ESN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0231 | AFR | ESN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02976 | hp2 | a0026 | c0039 | t0002 | g0262 | AFR | ESN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0105 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03098 | hp1 | a0004 | c0005 | t0001 | g0084 | AFR | MSL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03098 | hp2 | a0001 | c0027 | t0001 | g0221 | AFR | MSL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03139 | hp1 | a0007 | c0017 | t0001 | g0015 | AFR | ESN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03139 | hp2 | a0011 | c0014 | t0001 | g0008 | AFR | ESN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03195 | hp1 | a0001 | c0006 | t0001 | g0236 | AFR | ESN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03195 | hp2 | a0001 | c0019 | t0001 | g0208 | AFR | ESN | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03225 | hp1 | a0001 | c0006 | t0001 | g0165 | AFR | MSL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03225 | hp2 | a0014 | c0016 | t0002 | g0228 | AFR | MSL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03239 | hp1 | a0004 | c0005 | t0001 | g0125 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03239 | hp2 | a0001 | c0006 | t0001 | g0074 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0061 | AFR | MSL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03453 | hp2 | a0001 | c0004 | t0001 | g0219 | AFR | MSL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0062 | AFR | MSL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03486 | hp2 | a0008 | c0009 | t0002 | g0131 | AFR | MSL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03491 | hp1 | a0005 | c0038 | t0002 | g0212 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03540 | hp1 | a0018 | c0031 | t0002 | g0007 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03540 | hp2 | a0001 | c0019 | t0001 | g0205 | AFR | GWD | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03654 | hp1 | a0003 | c0003 | t0001 | g0109 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0013 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0012 | SAS | STU | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | STU | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0064 | SAS | PJL | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03942 | hp1 | a0001 | c0006 | t0001 | g0073 | SAS | BEB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0055 | SAS | BEB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0130 | SAS | BEB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG04184 | hp2 | a0001 | c0006 | t0001 | g0124 | SAS | BEB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0086 | SAS | STU | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0051 | SAS | STU | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG04204 | hp2 | a0028 | c0040 | t0001 | g0122 | SAS | STU | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | STU | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18522 | hp1 | a0003 | c0003 | t0003 | g0100 | AFR | YRI | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0258 | AFR | YRI | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | CHB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18906 | hp1 | a0001 | c0006 | t0001 | g0193 | AFR | YRI | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0237 | AFR | YRI | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18943 | hp2 | a0004 | c0005 | t0001 | g0090 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18946 | hp1 | a0001 | c0006 | t0001 | g0070 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18948 | hp2 | a0003 | c0003 | t0001 | g0092 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18949 | hp1 | a0009 | c0012 | t0001 | g0245 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18949 | hp2 | a0001 | c0010 | t0001 | g0150 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18963 | hp2 | a0004 | c0005 | t0001 | g0142 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18967 | hp1 | a0004 | c0005 | t0001 | g0242 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18973 | hp1 | a0009 | c0012 | t0001 | g0246 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18979 | hp1 | a0002 | c0008 | t0001 | g0048 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18979 | hp2 | a0001 | c0010 | t0001 | g0156 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18983 | hp2 | a0004 | c0005 | t0001 | g0091 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18990 | hp2 | a0004 | c0005 | t0001 | g0097 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18992 | hp1 | a0002 | c0008 | t0001 | g0046 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19006 | hp1 | a0001 | c0010 | t0001 | g0154 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19012 | hp1 | a0004 | c0005 | t0001 | g0133 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19012 | hp2 | a0013 | c0021 | t0002 | g0158 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19043 | hp1 | a0008 | c0009 | t0002 | g0107 | AFR | LWK | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19043 | hp2 | a0001 | c0004 | t0001 | g0225 | AFR | LWK | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19056 | hp1 | a0009 | c0012 | t0001 | g0247 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19057 | hp1 | a0001 | c0042 | t0001 | g0183 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19057 | hp2 | a0003 | c0003 | t0001 | g0099 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19058 | hp1 | a0004 | c0005 | t0001 | g0004 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19058 | hp2 | a0001 | c0006 | t0001 | g0241 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19065 | hp2 | a0001 | c0006 | t0001 | g0251 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19074 | hp1 | a0013 | c0021 | t0002 | g0155 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19074 | hp2 | a0004 | c0005 | t0001 | g0095 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19079 | hp2 | a0004 | c0005 | t0001 | g0081 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19082 | hp1 | a0027 | c0041 | t0001 | g0093 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19084 | hp1 | a0004 | c0005 | t0001 | g0096 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19086 | hp1 | a0002 | c0008 | t0001 | g0049 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19086 | hp2 | a0004 | c0005 | t0001 | g0244 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19087 | hp2 | a0004 | c0005 | t0001 | g0098 | EAS | JPT | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19240 | hp1 | a0004 | c0005 | t0001 | g0083 | AFR | YRI | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0222 | AFR | YRI | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0227 | AFR | ASW | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0118 | EUR | TSI | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA20805 | hp2 | a0001 | c0006 | t0001 | g0151 | EUR | TSI | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02109 | hp1 | a0007 | c0017 | t0001 | g0016 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0076 | AFR | ACB | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0220 | AFR | USA | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| HG06807 | hp2 | a0003 | c0003 | t0001 | g0256 | AFR | USA | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA20300 | hp1 | a0004 | c0005 | t0001 | g0080 | AFR | USA | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA20300 | hp2 | a0017 | c0034 | t0001 | g0053 | AFR | USA | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0226 | AFR | LWK | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0110 | AFR | LWK | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0129 | REF | REF | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| homoSapiens_grch38 | hp1 | a0001 | c0006 | t0001 | g0206 | REF | REF | SPAG17_chr1_117948590_118190228 | SPAG17 | chr1 | 117948590 | 118190228 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117963799
|
C | T | 1 | a0001 | 1 | HG02080.hp1 | splice_region_variant&stop_retained_variant | LOW | c.6672G>A | p.Ter2224Ter | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/49 | 6743/7203 | 6672/6672 | 2224/2223 | chr1 | 117963799 | ||
| chr1:117963818
|
C | T | 1 | a0028 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.6653G>A | p.Arg2218His | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/49 | 6724/7203 | 6653/6672 | 2218/2223 | chr1 | 117963818 | ||
| chr1:117966661
|
G | T | 3 | a0005a0012a0013 | 10 | HG00621.hp1 HG02027.hp1 HG02258.hp2 others(7): Show |
missense_variant | MODERATE | c.6480C>A | p.His2160Gln | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/49 | 6551/7203 | 6480/6672 | 2160/2223 | chr1 | 117966661 | ||
| chr1:117973459
|
A | T | 9 | a0005a0008a0012others(6): Show | 19 | HG00621.hp1 HG01175.hp1 HG02027.hp1 others(16): Show |
missense_variant | MODERATE | c.6107T>A | p.Leu2036Gln | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/49 | 6178/7203 | 6107/6672 | 2036/2223 | chr1 | 117973459 | ||
| chr1:117973541
|
C | T | 1 | a0023 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.6025G>A | p.Val2009Met | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/49 | 6096/7203 | 6025/6672 | 2009/2223 | chr1 | 117973541 | ||
| chr1:117973558
|
G | C | 5 | a0008a0014a0018others(2): Show | 8 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
missense_variant | MODERATE | c.6008C>G | p.Ala2003Gly | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/49 | 6079/7203 | 6008/6672 | 2003/2223 | chr1 | 117973558 | ||
| chr1:117984716
|
A | T | 1 | a0014 | 2 | HG02818.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.5736T>A | p.Phe1912Leu | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 41/49 | 5807/7203 | 5736/6672 | 1912/2223 | chr1 | 117984716 | ||
| chr1:117988162
|
G | A | 1 | a0020 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.5564C>T | p.Thr1855Met | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 39/49 | 5635/7203 | 5564/6672 | 1855/2223 | chr1 | 117988162 | ||
| chr1:117992569
|
G | A | 1 | a0022 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.5258C>T | p.Pro1753Leu | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/49 | 5329/7203 | 5258/6672 | 1753/2223 | chr1 | 117992569 | ||
| chr1:117992588
|
T | C | 1 | a0006 | 4 | HG01358.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
missense_variant | MODERATE | c.5239A>G | p.Lys1747Glu | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/49 | 5310/7203 | 5239/6672 | 1747/2223 | chr1 | 117992588 | ||
| chr1:117992603
|
G | C | 1 | a0015 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.5224C>G | p.Leu1742Val | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/49 | 5295/7203 | 5224/6672 | 1742/2223 | chr1 | 117992603 | ||
| chr1:117996456
|
C | T | 1 | a0021 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.4967G>A | p.Arg1656Gln | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/49 | 5038/7203 | 4967/6672 | 1656/2223 | chr1 | 117996456 | ||
| chr1:118005421
|
G | T | 1 | a0019 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.4769C>A | p.Thr1590Asn | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/49 | 4840/7203 | 4769/6672 | 1590/2223 | chr1 | 118005421 | ||
| chr1:118005523
|
A | G | 1 | a0017 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.4667T>C | p.Ile1556Thr | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/49 | 4738/7203 | 4667/6672 | 1556/2223 | chr1 | 118005523 | ||
| chr1:118008127
|
T | C | 1 | a0016 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.4504A>G | p.Ile1502Val | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/49 | 4575/7203 | 4504/6672 | 1502/2223 | chr1 | 118008127 | ||
| chr1:118023330
|
G | A | 9 | a0003a0004a0008others(6): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
missense_variant | MODERATE | c.4043C>T | p.Pro1348Leu | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/49 | 4114/7203 | 4043/6672 | 1348/2223 | chr1 | 118023330 | ||
| chr1:118031699
|
T | A | 1 | a0018 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.3602A>T | p.Glu1201Val | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/49 | 3673/7203 | 3602/6672 | 1201/2223 | chr1 | 118031699 | ||
| chr1:118041939
|
T | C | 1 | a0011 | 2 | HG02572.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.2918A>G | p.Asp973Gly | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 21/49 | 2989/7203 | 2918/6672 | 973/2223 | chr1 | 118041939 | ||
| chr1:118042020
|
C | A | 1 | a0013 | 2 | NA19012.hp2 NA19074.hp1 |
missense_variant | MODERATE | c.2837G>T | p.Arg946Leu | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 21/49 | 2908/7203 | 2837/6672 | 946/2223 | chr1 | 118042020 | ||
| chr1:118055739
|
A | G | 2 | a0012a0018 | 3 | HG02258.hp2 HG02965.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.2716T>C | p.Ser906Pro | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 19/49 | 2787/7203 | 2716/6672 | 906/2223 | chr1 | 118055739 | ||
| chr1:118086000
|
G | C | 2 | a0007a0017 | 4 | HG02109.hp1 HG02735.hp1 HG03139.hp1 others(1): Show |
missense_variant | MODERATE | c.1684C>G | p.Gln562Glu | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/49 | 1755/7203 | 1684/6672 | 562/2223 | chr1 | 118086000 | ||
| chr1:118086984
|
C | T | 1 | a0011 | 2 | HG02572.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.1384G>A | p.Val462Ile | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 11/49 | 1455/7203 | 1384/6672 | 462/2223 | chr1 | 118086984 | ||
| chr1:118099726
|
T | C | 1 | a0026 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.709A>G | p.Met237Val | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/49 | 780/7203 | 709/6672 | 237/2223 | chr1 | 118099726 | ||
| chr1:118101880
|
T | A | 1 | a0027 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.494A>T | p.Lys165Ile | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 5/49 | 565/7203 | 494/6672 | 165/2223 | chr1 | 118101880 | ||
| chr1:118101901
|
T | A | 5 | a0004a0009a0010others(2): Show | 31 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(28): Show |
missense_variant | MODERATE | c.473A>T | p.Glu158Val | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 5/49 | 544/7203 | 473/6672 | 158/2223 | chr1 | 118101901 | ||
| chr1:118115327
|
G | A | 1 | a0010 | 3 | HG01496.hp2 HG01928.hp2 HG02148.hp1 |
missense_variant | MODERATE | c.430C>T | p.Arg144Trp | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/49 | 501/7203 | 430/6672 | 144/2223 | chr1 | 118115327 | ||
| chr1:118115329
|
C | T | 3 | a0002a0015a0016 | 51 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(48): Show |
missense_variant | MODERATE | c.428G>A | p.Arg143Gln | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/49 | 499/7203 | 428/6672 | 143/2223 | chr1 | 118115329 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117966655
|
G | A | 3 | a0005c0011a0005c0038a0013c0021 | 6 | HG02273.hp1 HG02683.hp2 HG02698.hp2 others(3): Show |
synonymous_variant | LOW | c.6486C>T | p.Ile2162Ile | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/49 | 6557/7203 | 6486/6672 | 2162/2223 | chr1 | 117966655 | ||
| chr1:117970116
|
C | T | 1 | a0001c0026 | 1 | HG02965.hp1 | splice_region_variant&synonymous_variant | LOW | c.6327G>A | p.Arg2109Arg | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/49 | 6398/7203 | 6327/6672 | 2109/2223 | chr1 | 117970116 | ||
| chr1:117987848
|
C | T | 1 | a0011c0014 | 2 | HG02572.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.5655G>A | p.Lys1885Lys | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/49 | 5726/7203 | 5655/6672 | 1885/2223 | chr1 | 117987848 | ||
| chr1:117988173
|
C | T | 12 | a0001c0010a0001c0019a0001c0025others(9): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(58): Show |
synonymous_variant | LOW | c.5553G>A | p.Gln1851Gln | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 39/49 | 5624/7203 | 5553/6672 | 1851/2223 | chr1 | 117988173 | ||
| chr1:117994451
|
A | G | 8 | a0001c0010a0002c0002a0002c0008others(5): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
synonymous_variant | LOW | c.5133T>C | p.Pro1711Pro | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 35/49 | 5204/7203 | 5133/6672 | 1711/2223 | chr1 | 117994451 | ||
| chr1:118008125
|
G | A | 1 | a0005c0038 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.4506C>T | p.Ile1502Ile | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/49 | 4577/7203 | 4506/6672 | 1502/2223 | chr1 | 118008125 | ||
| chr1:118031851
|
A | G | 1 | a0001c0018 | 2 | HG02145.hp1 HG02280.hp2 |
synonymous_variant | LOW | c.3450T>C | p.Asp1150Asp | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/49 | 3521/7203 | 3450/6672 | 1150/2223 | chr1 | 118031851 | ||
| chr1:118040785
|
G | A | 11 | a0001c0027a0003c0003a0003c0029others(8): Show | 68 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
synonymous_variant | LOW | c.3111C>T | p.Tyr1037Tyr | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 22/49 | 3182/7203 | 3111/6672 | 1037/2223 | chr1 | 118040785 | ||
| chr1:118055863
|
T | C | 2 | a0011c0014a0017c0034 | 3 | HG02572.hp1 HG03139.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.2592A>G | p.Glu864Glu | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 19/49 | 2663/7203 | 2592/6672 | 864/2223 | chr1 | 118055863 | ||
| chr1:118081500
|
C | T | 7 | a0002c0002a0002c0008a0007c0017others(4): Show | 56 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(53): Show |
synonymous_variant | LOW | c.1905G>A | p.Pro635Pro | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 14/49 | 1976/7203 | 1905/6672 | 635/2223 | chr1 | 118081500 | ||
| chr1:118086976
|
G | A | 10 | a0001c0032a0002c0002a0002c0008others(7): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
synonymous_variant | LOW | c.1392C>T | p.Pro464Pro | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 11/49 | 1463/7203 | 1392/6672 | 464/2223 | chr1 | 118086976 | ||
| chr1:118101807
|
A | G | 27 | a0001c0004a0001c0025a0001c0026others(24): Show | 162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
synonymous_variant | LOW | c.567T>C | p.Asn189Asn | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 5/49 | 638/7203 | 567/6672 | 189/2223 | chr1 | 118101807 | ||
| chr1:118150594
|
T | C | 5 | a0001c0001a0001c0042a0001c0044others(2): Show | 64 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(61): Show |
synonymous_variant | LOW | c.264A>G | p.Ser88Ser | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/49 | 335/7203 | 264/6672 | 88/2223 | chr1 | 118150594 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117953817
|
T | C | 10 | a0005c0011t0002a0005c0020t0002a0005c0038t0002others(7): Show | 17 | HG00621.hp1 HG02027.hp1 HG02258.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*233A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 49/49 | 9982 | chr1 | 117953817 | |||||
| chr1:117953880
|
C | G | 13 | a0001c0004t0003a0003c0003t0003a0005c0011t0002others(10): Show | 20 | HG00621.hp1 HG01175.hp1 HG02027.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*170G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 49/49 | 9919 | chr1 | 117953880 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117954669
|
G | A | 42 | a0001c0001t0001g0196a0001c0010t0001g0150a0001c0010t0001g0154others(39): Show | 42 | HG00438.hp2 HG01109.hp1 HG02027.hp2 others(39): Show |
intron_variant | MODIFIER | c.*1-620C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117954669 | ||||||
| chr1:117954669
|
G | T | 17 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0020t0002g0157others(14): Show | 17 | HG00621.hp1 HG02027.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.*1-620C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117954669 | ||||||
| chr1:117954731
|
T | C | 1 | a0005c0011t0002g0202 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.*1-682A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117954731 | ||||||
| chr1:117954905
|
T | G | 8 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(5): Show | 8 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.*1-856A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117954905 | ||||||
| chr1:117955246
|
T | C | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.*1-1197A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117955246 | ||||||
| chr1:117955674
|
G | A | 9 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0020t0002g0157others(6): Show | 9 | HG00621.hp1 HG02027.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.*1-1625C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117955674 | ||||||
| chr1:117955740
|
A | G | 1 | a0002c0002t0001g0022 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.*1-1691T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117955740 | ||||||
| chr1:117955763
|
CA | C | 13 | a0002c0002t0001g0023a0003c0003t0001g0064a0005c0020t0002g0157others(10): Show | 13 | HG00621.hp1 HG00621.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.*1-1715delT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117955763 | ||||||
| chr1:117955885
|
T | G | 1 | a0003c0003t0001g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.*1-1836A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117955885 | ||||||
| chr1:117956159
|
T | C | 8 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(5): Show | 8 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.*1-2110A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117956159 | ||||||
| chr1:117956271
|
G | C | 1 | a0004c0005t0001g0244 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.*1-2222C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117956271 | ||||||
| chr1:117956431
|
T | G | 71 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0198others(68): Show | 72 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.*1-2382A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117956431 | ||||||
| chr1:117956578
|
T | G | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.*1-2529A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117956578 | ||||||
| chr1:117956663
|
TACAAAAT others(2): Show |
T | 9 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0020t0002g0157others(6): Show | 9 | HG00621.hp1 HG02027.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.*1-2623_*1-2615del others(9): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117956663 | ||||||
| chr1:117956681
|
A | G | 1 | a0001c0018t0001g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*1-2632T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117956681 | ||||||
| chr1:117956700
|
G | T | 7 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0038t0002g0212others(4): Show | 7 | HG02258.hp2 HG02273.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.*1-2651C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117956700 | ||||||
| chr1:117956773
|
A | G | 1 | a0002c0002t0001g0033 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.*1-2724T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117956773 | ||||||
| chr1:117956954
|
A | T | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.*1-2905T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117956954 | ||||||
| chr1:117957008
|
T | C | 8 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(5): Show | 8 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.*1-2959A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117957008 | ||||||
| chr1:117957146
|
G | A | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.*1-3097C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117957146 | ||||||
| chr1:117957305
|
G | A | 9 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0020t0002g0157others(6): Show | 9 | HG00621.hp1 HG02027.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.*1-3256C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117957305 | ||||||
| chr1:117957318
|
C | T | 3 | a0002c0002t0001g0032a0002c0002t0001g0058a0002c0002t0001g0059 | 3 | NA18973.hp2 NA19079.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.*1-3269G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117957318 | ||||||
| chr1:117957417
|
CATG | C | 8 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(5): Show | 8 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.*1-3371_*1-3369del others(3): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117957417 | ||||||
| chr1:117957493
|
A | G | 8 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(5): Show | 8 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.*1-3444T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117957493 | ||||||
| chr1:117957507
|
A | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.*1-3458T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117957507 | ||||||
| chr1:117957658
|
T | C | 1 | a0001c0004t0001g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.*1-3609A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117957658 | ||||||
| chr1:117958139
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.*1-4090A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117958139 | ||||||
| chr1:117958144
|
A | C | 7 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.*1-4095T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117958144 | ||||||
| chr1:117958399
|
C | T | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.*1-4350G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117958399 | ||||||
| chr1:117958407
|
A | G | 1 | a0022c0037t0001g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.*1-4358T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117958407 | ||||||
| chr1:117958703
|
T | C | 1 | a0002c0002t0001g0023 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.*1-4654A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117958703 | ||||||
| chr1:117958767
|
C | CT | 86 | a0001c0001t0001g0005a0001c0001t0001g0198a0001c0001t0001g0216others(83): Show | 87 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.*1-4719dupA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117958767 | ||||||
| chr1:117958767
|
C | CTT | 14 | a0003c0003t0001g0109a0003c0003t0001g0110a0003c0003t0001g0112others(11): Show | 14 | HG00280.hp1 HG02015.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.*1-4720_*1-4719dup others(2): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117958767 | ||||||
| chr1:117958787
|
C | T | 1 | a0001c0004t0001g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*1-4738G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117958787 | ||||||
| chr1:117959342
|
C | T | 1 | a0001c0026t0001g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.6672+4457G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117959342 | ||||||
| chr1:117959439
|
T | C | 1 | a0003c0003t0001g0256 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6672+4360A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117959439 | ||||||
| chr1:117959481
|
T | G | 2 | a0005c0020t0002g0157a0005c0020t0002g0197 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.6672+4318A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117959481 | ||||||
| chr1:117959539
|
C | T | 6 | a0003c0003t0001g0086a0003c0003t0001g0087a0003c0003t0001g0088others(3): Show | 6 | HG00642.hp1 HG01069.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.6672+4260G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117959539 | ||||||
| chr1:117959803
|
G | A | 2 | a0001c0004t0003g0082a0003c0003t0003g0100 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.6672+3996C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117959803 | ||||||
| chr1:117959933
|
G | C | 9 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0020t0002g0157others(6): Show | 9 | HG00621.hp1 HG02027.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.6672+3866C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117959933 | ||||||
| chr1:117960102
|
A | G | 6 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.6672+3697T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960102 | ||||||
| chr1:117960109
|
C | CGT | 108 | a0001c0001t0001g0003a0001c0001t0001g0065a0001c0001t0001g0066others(105): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.6672+3688_6672+368 others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960109 | ||||||
| chr1:117960109
|
C | CGTGT | 29 | a0001c0001t0001g0002a0001c0001t0001g0147a0001c0001t0001g0163others(26): Show | 30 | HG00597.hp2 HG00642.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.6672+3686_6672+368 others(8): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960109 | ||||||
| chr1:117960109
|
C | CGTGTGT | 11 | a0001c0001t0001g0170a0001c0001t0001g0204a0001c0001t0001g0240others(8): Show | 11 | HG00438.hp1 HG00738.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.6672+3684_6672+368 others(10): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960109 | ||||||
| chr1:117960109
|
C | CGTGTGTG others(3): Show |
1 | a0014c0016t0002g0228 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6672+3689_6672+369 others(14): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960109 | ||||||
| chr1:117960109
|
C | CGTGTGTG others(5): Show |
1 | a0014c0016t0002g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.6672+3689_6672+369 others(16): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960109 | ||||||
| chr1:117960109
|
CGT | C | 13 | a0001c0001t0001g0161a0001c0001t0001g0198a0001c0001t0001g0200others(10): Show | 13 | HG00140.hp2 HG01934.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.6672+3688_6672+368 others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960109 | ||||||
| chr1:117960109
|
CGTGT | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0196a0001c0004t0001g0143others(57): Show | 61 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.6672+3686_6672+368 others(8): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960109 | ||||||
| chr1:117960109
|
CGTGTGTG others(13): Show |
C | 6 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.6672+3670_6672+368 others(24): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960109 | ||||||
| chr1:117960140
|
GTGTGTGT others(1): Show |
G | 3 | a0001c0004t0003g0082a0003c0003t0003g0100a0024c0035t0003g0207 | 3 | HG01175.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.6672+3651_6672+365 others(12): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960140 | ||||||
| chr1:117960142
|
GTGTGTA | G | 7 | a0002c0002t0001g0032a0005c0011t0002g0104a0005c0020t0002g0157others(4): Show | 7 | HG00621.hp1 HG02027.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.6672+3651_6672+365 others(10): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960142 | ||||||
| chr1:117960148
|
A | G | 9 | a0002c0002t0001g0024a0008c0009t0002g0077a0008c0009t0002g0107others(6): Show | 9 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.6672+3651T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960148 | ||||||
| chr1:117960212
|
C | T | 9 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0020t0002g0157others(6): Show | 9 | HG00621.hp1 HG02027.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.6672+3587G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960212 | ||||||
| chr1:117960228
|
C | T | 9 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0020t0002g0157others(6): Show | 9 | HG00621.hp1 HG02027.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.6672+3571G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960228 | ||||||
| chr1:117960577
|
T | C | 2 | a0001c0004t0003g0082a0003c0003t0003g0100 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.6672+3222A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960577 | ||||||
| chr1:117960589
|
G | A | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6672+3210C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960589 | ||||||
| chr1:117960592
|
C | T | 1 | a0003c0003t0001g0092 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.6672+3207G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960592 | ||||||
| chr1:117960613
|
G | T | 6 | a0002c0002t0001g0019a0002c0002t0001g0054a0002c0002t0001g0055others(3): Show | 6 | HG00323.hp1 HG00735.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.6672+3186C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960613 | ||||||
| chr1:117960783
|
CTG | C | 9 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0020t0002g0157others(6): Show | 9 | HG00621.hp1 HG02027.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.6672+3014_6672+301 others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960783 | ||||||
| chr1:117960909
|
T | C | 1 | a0003c0003t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.6672+2890A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117960909 | ||||||
| chr1:117961143
|
C | T | 4 | a0001c0019t0001g0205a0001c0019t0001g0208a0001c0025t0001g0063others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.6672+2656G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117961143 | ||||||
| chr1:117961198
|
A | G | 13 | a0001c0004t0003g0082a0003c0003t0003g0100a0005c0020t0002g0157others(10): Show | 13 | HG00621.hp1 HG01175.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.6672+2601T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117961198 | ||||||
| chr1:117961207
|
C | T | 53 | a0001c0001t0001g0196a0001c0004t0001g0220a0001c0004t0001g0222others(50): Show | 53 | HG00438.hp2 HG01109.hp1 HG01433.hp2 others(50): Show |
intron_variant | MODIFIER | c.6672+2592G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117961207 | ||||||
| chr1:117961214
|
C | T | 8 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(5): Show | 8 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.6672+2585G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117961214 | ||||||
| chr1:117961237
|
A | G | 2 | a0001c0004t0003g0082a0003c0003t0003g0100 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.6672+2562T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117961237 | ||||||
| chr1:117961516
|
A | G | 1 | a0003c0003t0001g0088 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.6672+2283T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117961516 | ||||||
| chr1:117961642
|
T | G | 151 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0196others(148): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.6672+2157A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117961642 | ||||||
| chr1:117961940
|
A | G | 2 | a0005c0020t0002g0157a0005c0020t0002g0197 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.6672+1859T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117961940 | ||||||
| chr1:117961948
|
C | G | 2 | a0003c0003t0001g0139a0003c0003t0001g0140 | 2 | HG01167.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.6672+1851G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117961948 | ||||||
| chr1:117962020
|
C | T | 72 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0198others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.6672+1779G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117962020 | ||||||
| chr1:117962045
|
C | T | 1 | a0001c0006t0001g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.6672+1754G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117962045 | ||||||
| chr1:117962064
|
A | G | 1 | a0002c0008t0001g0049 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.6672+1735T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117962064 | ||||||
| chr1:117962117
|
A | G | 2 | a0005c0020t0002g0157a0005c0020t0002g0197 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.6672+1682T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117962117 | ||||||
| chr1:117962195
|
A | G | 12 | a0001c0004t0003g0082a0003c0003t0003g0100a0005c0011t0002g0104others(9): Show | 12 | HG00621.hp1 HG01175.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.6672+1604T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117962195 | ||||||
| chr1:117962255
|
A | T | 1 | a0002c0002t0001g0017 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.6672+1544T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117962255 | ||||||
| chr1:117962489
|
A | G | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6672+1310T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117962489 | ||||||
| chr1:117962546
|
GA | G | 21 | a0001c0004t0001g0143a0001c0004t0003g0082a0002c0002t0001g0026others(18): Show | 21 | HG01175.hp1 HG02155.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.6672+1252delT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117962546 | ||||||
| chr1:117962578
|
T | C | 1 | a0002c0002t0001g0263 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6672+1221A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117962578 | ||||||
| chr1:117962677
|
G | A | 7 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0038t0002g0212others(4): Show | 7 | HG02258.hp2 HG02273.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.6672+1122C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117962677 | ||||||
| chr1:117962882
|
A | C | 5 | a0001c0001t0001g0003a0006c0007t0001g0187a0006c0007t0001g0188others(2): Show | 6 | HG01358.hp2 HG01433.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.6672+917T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117962882 | ||||||
| chr1:117963395
|
G | A | 8 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(5): Show | 8 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.6672+404C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117963395 | ||||||
| chr1:117963400
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.6672+399C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117963400 | ||||||
| chr1:117963442
|
C | T | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6672+357G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117963442 | ||||||
| chr1:117963450
|
G | A | 1 | a0004c0005t0001g0133 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6672+349C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117963450 | ||||||
| chr1:117963464
|
C | T | 2 | a0005c0020t0002g0157a0005c0020t0002g0197 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.6672+335G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117963464 | ||||||
| chr1:117963513
|
G | A | 1 | a0003c0003t0001g0256 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6672+286C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117963513 | ||||||
| chr1:117963660
|
G | A | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.6672+139C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117963660 | ||||||
| chr1:117963734
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.6672+65G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117963734 | ||||||
| chr1:117963750
|
T | A | 9 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0020t0002g0157others(6): Show | 9 | HG00621.hp1 HG02027.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.6672+49A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 48/48 | chr1 | 117963750 | ||||||
| chr1:117964016
|
A | G | 2 | a0001c0004t0001g0227a0001c0004t0001g0231 | 2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.6533-78T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117964016 | ||||||
| chr1:117964125
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6533-187C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117964125 | ||||||
| chr1:117964236
|
C | CT | 13 | a0001c0001t0001g0240a0001c0027t0001g0221a0004c0005t0001g0084others(10): Show | 13 | HG02027.hp1 HG02258.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.6533-299dupA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117964236 | ||||||
| chr1:117964244
|
T | G | 1 | a0001c0004t0001g0234 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.6533-306A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117964244 | ||||||
| chr1:117964658
|
A | G | 2 | a0005c0020t0002g0157a0005c0020t0002g0197 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.6533-720T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117964658 | ||||||
| chr1:117964752
|
A | G | 3 | a0001c0019t0001g0205a0001c0019t0001g0208a0001c0025t0001g0063 | 3 | HG02622.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.6533-814T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117964752 | ||||||
| chr1:117964994
|
G | A | 17 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0020t0002g0157others(14): Show | 17 | HG00621.hp1 HG02027.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.6533-1056C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117964994 | ||||||
| chr1:117965065
|
T | C | 4 | a0001c0004t0001g0257a0001c0004t0001g0258a0001c0004t0001g0259others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.6533-1127A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117965065 | ||||||
| chr1:117965142
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0176 | 2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.6533-1204A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117965142 | ||||||
| chr1:117965240
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.6533-1302C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117965240 | ||||||
| chr1:117965270
|
T | C | 148 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0196others(145): Show | 149 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.6533-1332A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117965270 | ||||||
| chr1:117965619
|
T | C | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6532+990A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117965619 | ||||||
| chr1:117965632
|
GGCC | G | 7 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0038t0002g0212others(4): Show | 7 | HG02258.hp2 HG02273.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.6532+974_6532+976d others(5): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117965632 | ||||||
| chr1:117965741
|
G | A | 17 | a0005c0011t0002g0104a0005c0011t0002g0202a0005c0020t0002g0157others(14): Show | 17 | HG00621.hp1 HG02027.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.6532+868C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117965741 | ||||||
| chr1:117965894
|
A | G | 5 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(2): Show | 5 | HG02451.hp2 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.6532+715T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117965894 | ||||||
| chr1:117966477
|
G | T | 4 | a0001c0001t0001g0181a0001c0006t0001g0241a0001c0006t0001g0251others(1): Show | 4 | HG01943.hp2 HG01952.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.6532+132C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 47/48 | chr1 | 117966477 | ||||||
| chr1:117966965
|
A | T | 3 | a0001c0019t0001g0205a0001c0019t0001g0208a0001c0025t0001g0063 | 3 | HG02622.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.6388-212T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117966965 | ||||||
| chr1:117967031
|
T | C | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.6388-278A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117967031 | ||||||
| chr1:117967092
|
G | A | 1 | a0004c0005t0001g0091 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.6388-339C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117967092 | ||||||
| chr1:117967237
|
T | G | 18 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(15): Show | 18 | HG00621.hp1 HG02027.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.6388-484A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117967237 | ||||||
| chr1:117967296
|
C | CA | 7 | a0001c0004t0003g0082a0001c0010t0001g0150a0003c0003t0001g0256others(4): Show | 7 | HG02040.hp1 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.6388-544dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117967296 | ||||||
| chr1:117967296
|
CA | C | 71 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0162others(68): Show | 72 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.6388-544delT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117967296 | ||||||
| chr1:117967296
|
CAA | C | 10 | a0003c0003t0001g0136a0003c0029t0001g0141a0005c0011t0001g0106others(7): Show | 10 | HG00733.hp2 HG01515.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.6388-545_6388-544d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117967296 | ||||||
| chr1:117967325
|
C | T | 1 | a0002c0002t0001g0045 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.6388-572G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117967325 | ||||||
| chr1:117967377
|
G | A | 18 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(15): Show | 18 | HG00621.hp1 HG02027.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.6388-624C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117967377 | ||||||
| chr1:117967632
|
T | C | 18 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(15): Show | 18 | HG00621.hp1 HG02027.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.6388-879A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117967632 | ||||||
| chr1:117967663
|
T | TC | 18 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(15): Show | 18 | HG00621.hp1 HG02027.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.6388-911_6388-910i others(3): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117967663 | ||||||
| chr1:117967744
|
G | A | 5 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(2): Show | 5 | HG01433.hp2 HG02647.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.6388-991C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117967744 | ||||||
| chr1:117967849
|
G | A | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6388-1096C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117967849 | ||||||
| chr1:117967975
|
G | A | 1 | a0004c0005t0001g0244 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.6388-1222C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117967975 | ||||||
| chr1:117968161
|
G | A | 146 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0196others(143): Show | 147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.6388-1408C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117968161 | ||||||
| chr1:117968720
|
G | C | 32 | a0001c0001t0001g0196a0001c0042t0001g0183a0002c0002t0001g0011others(29): Show | 32 | HG00438.hp2 HG02027.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.6387+1336C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117968720 | ||||||
| chr1:117968741
|
T | G | 1 | a0001c0004t0001g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6387+1315A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117968741 | ||||||
| chr1:117968806
|
T | G | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6387+1250A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117968806 | ||||||
| chr1:117968868
|
C | T | 1 | a0004c0005t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.6387+1188G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117968868 | ||||||
| chr1:117968935
|
G | T | 18 | a0003c0003t0001g0256a0005c0011t0001g0106a0005c0011t0002g0104others(15): Show | 18 | HG00621.hp1 HG02027.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.6387+1121C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117968935 | ||||||
| chr1:117968961
|
A | C | 1 | a0001c0018t0001g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6387+1095T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117968961 | ||||||
| chr1:117968970
|
G | A | 8 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(5): Show | 8 | HG02258.hp2 HG02273.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.6387+1086C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117968970 | ||||||
| chr1:117968978
|
C | A | 2 | a0007c0017t0001g0015a0007c0017t0001g0016 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.6387+1078G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117968978 | ||||||
| chr1:117969150
|
T | C | 1 | a0003c0003t0001g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.6387+906A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117969150 | ||||||
| chr1:117969164
|
A | ATT | 11 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(8): Show | 11 | HG00621.hp1 HG01175.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.6387+890_6387+891d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117969164 | ||||||
| chr1:117969164
|
A | ATTT | 8 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(5): Show | 8 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.6387+889_6387+891d others(5): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117969164 | ||||||
| chr1:117969306
|
C | T | 1 | a0001c0026t0001g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.6387+750G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117969306 | ||||||
| chr1:117969362
|
A | C | 19 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(16): Show | 19 | HG00621.hp1 HG01175.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.6387+694T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117969362 | ||||||
| chr1:117969376
|
C | T | 1 | a0001c0001t0001g0003 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.6387+680G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117969376 | ||||||
| chr1:117969505
|
G | GGAGGCAG others(10): Show |
2 | a0001c0004t0001g0225a0001c0004t0001g0237 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.6387+534_6387+550d others(19): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117969505 | ||||||
| chr1:117969613
|
TATG | T | 6 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.6387+440_6387+442d others(5): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 46/48 | chr1 | 117969613 | ||||||
| chr1:117970618
|
A | G | 4 | a0001c0001t0001g0198a0002c0002t0001g0022a0003c0003t0001g0111others(1): Show | 4 | HG02135.hp2 HG02735.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.6327-502T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 45/48 | chr1 | 117970618 | ||||||
| chr1:117970703
|
G | A | 7 | a0001c0001t0001g0174a0001c0001t0001g0181a0001c0006t0001g0152others(4): Show | 7 | HG00280.hp2 HG01346.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.6327-587C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 45/48 | chr1 | 117970703 | ||||||
| chr1:117970861
|
C | T | 168 | a0001c0001t0001g0005a0001c0001t0001g0146a0001c0001t0001g0161others(165): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.6327-745G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 45/48 | chr1 | 117970861 | ||||||
| chr1:117971243
|
G | A | 8 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(5): Show | 8 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.6326+620C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 45/48 | chr1 | 117971243 | ||||||
| chr1:117971277
|
A | C | 2 | a0001c0004t0003g0082a0003c0003t0003g0100 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.6326+586T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 45/48 | chr1 | 117971277 | ||||||
| chr1:117971284
|
A | G | 2 | a0005c0020t0002g0157a0005c0020t0002g0197 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.6326+579T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 45/48 | chr1 | 117971284 | ||||||
| chr1:117971373
|
C | G | 2 | a0001c0004t0003g0082a0003c0003t0003g0100 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.6326+490G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 45/48 | chr1 | 117971373 | ||||||
| chr1:117971553
|
CTT | C | 21 | a0001c0004t0003g0082a0003c0003t0003g0100a0005c0011t0001g0106others(18): Show | 21 | HG00621.hp1 HG01175.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.6326+308_6326+309d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 45/48 | chr1 | 117971553 | ||||||
| chr1:117971626
|
AATG | A | 17 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(14): Show | 17 | HG01175.hp1 HG02258.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.6326+234_6326+236d others(5): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 45/48 | chr1 | 117971626 | ||||||
| chr1:117971769
|
C | T | 1 | a0003c0003t0001g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6326+94G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 45/48 | chr1 | 117971769 | ||||||
| chr1:117972054
|
A | G | 8 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(5): Show | 8 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.6142-7T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117972054 | ||||||
| chr1:117972105
|
A | T | 8 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(5): Show | 8 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.6142-58T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117972105 | ||||||
| chr1:117972361
|
G | A | 40 | a0001c0001t0001g0196a0001c0010t0001g0150a0001c0010t0001g0154others(37): Show | 40 | HG00438.hp2 HG01109.hp1 HG02027.hp2 others(37): Show |
intron_variant | MODIFIER | c.6142-314C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117972361 | ||||||
| chr1:117972453
|
G | A | 1 | a0004c0005t0001g0004 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.6142-406C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117972453 | ||||||
| chr1:117972638
|
T | C | 1 | a0003c0003t0001g0256 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6142-591A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117972638 | ||||||
| chr1:117972712
|
A | T | 1 | a0001c0001t0001g0195 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.6142-665T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117972712 | ||||||
| chr1:117972739
|
A | C | 1 | a0001c0001t0001g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6141+686T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117972739 | ||||||
| chr1:117972776
|
GA | G | 157 | a0001c0001t0001g0005a0001c0001t0001g0146a0001c0001t0001g0161others(154): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.6141+648delT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117972776 | ||||||
| chr1:117972873
|
C | G | 22 | a0002c0002t0001g0001a0002c0002t0001g0020a0003c0029t0001g0141others(19): Show | 23 | HG00621.hp1 HG00733.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.6141+552G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117972873 | ||||||
| chr1:117972968
|
C | A | 3 | a0001c0019t0001g0205a0001c0019t0001g0208a0001c0025t0001g0063 | 3 | HG02622.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.6141+457G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117972968 | ||||||
| chr1:117973001
|
A | C | 3 | a0002c0008t0001g0046a0002c0008t0001g0048a0002c0008t0001g0049 | 3 | NA18979.hp1 NA18992.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.6141+424T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117973001 | ||||||
| chr1:117973120
|
C | A | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6141+305G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117973120 | ||||||
| chr1:117973121
|
A | G | 2 | a0005c0020t0002g0157a0005c0020t0002g0197 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.6141+304T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117973121 | ||||||
| chr1:117973272
|
C | T | 2 | a0002c0002t0001g0043a0002c0002t0001g0044 | 2 | NA18971.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.6141+153G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117973272 | ||||||
| chr1:117973362
|
AAAAT | A | 19 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(16): Show | 19 | HG00621.hp1 HG01175.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.6141+59_6141+62del others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117973362 | ||||||
| chr1:117973366
|
T | A | 1 | a0016c0023t0001g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6141+59A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117973366 | ||||||
| chr1:117973381
|
A | G | 1 | a0004c0005t0001g0243 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.6141+44T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 44/48 | chr1 | 117973381 | ||||||
| chr1:117973631
|
A | G | 15 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(12): Show | 15 | HG00621.hp1 HG01175.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.6005-70T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117973631 | ||||||
| chr1:117973651
|
A | G | 3 | a0001c0004t0001g0226a0001c0004t0001g0227a0001c0004t0001g0231 | 3 | HG02976.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.6005-90T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117973651 | ||||||
| chr1:117973801
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6005-240T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117973801 | ||||||
| chr1:117973904
|
G | C | 19 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(16): Show | 19 | HG00621.hp1 HG01175.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.6005-343C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117973904 | ||||||
| chr1:117973945
|
T | G | 19 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(16): Show | 19 | HG00621.hp1 HG01175.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.6005-384A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117973945 | ||||||
| chr1:117974017
|
A | G | 1 | a0002c0002t0001g0022 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.6005-456T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117974017 | ||||||
| chr1:117974112
|
T | C | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6005-551A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117974112 | ||||||
| chr1:117974150
|
T | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.6005-589A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117974150 | ||||||
| chr1:117974206
|
T | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6005-645A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117974206 | ||||||
| chr1:117974338
|
T | C | 2 | a0005c0020t0002g0157a0005c0020t0002g0197 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.6005-777A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117974338 | ||||||
| chr1:117974456
|
G | A | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6005-895C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117974456 | ||||||
| chr1:117974487
|
C | T | 9 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(6): Show | 9 | HG01175.hp1 HG02258.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.6005-926G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117974487 | ||||||
| chr1:117974521
|
CTAA | C | 8 | a0005c0011t0001g0106a0005c0011t0002g0104a0005c0011t0002g0202others(5): Show | 8 | HG02258.hp2 HG02273.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.6005-963_6005-961d others(5): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117974521 | ||||||
| chr1:117974529
|
T | TA | 6 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.6005-969dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117974529 | ||||||
| chr1:117974529
|
T | TAA | 42 | a0001c0001t0001g0196a0001c0010t0001g0150a0001c0010t0001g0154others(39): Show | 42 | HG00438.hp2 HG01109.hp1 HG02027.hp2 others(39): Show |
intron_variant | MODIFIER | c.6005-970_6005-969d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117974529 | ||||||
| chr1:117974572
|
T | G | 52 | a0001c0001t0001g0196a0001c0004t0001g0220a0001c0004t0001g0222others(49): Show | 52 | HG00438.hp2 HG01109.hp1 HG01433.hp2 others(49): Show |
intron_variant | MODIFIER | c.6005-1011A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117974572 | ||||||
| chr1:117974801
|
A | T | 1 | a0001c0018t0001g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6005-1240T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117974801 | ||||||
| chr1:117974882
|
C | T | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6005-1321G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117974882 | ||||||
| chr1:117975020
|
A | G | 6 | a0001c0004t0001g0257a0001c0006t0001g0164a0001c0006t0001g0165others(3): Show | 6 | HG00621.hp1 HG02027.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.6005-1459T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117975020 | ||||||
| chr1:117975199
|
G | C | 9 | a0001c0001t0001g0204a0001c0004t0001g0060a0001c0004t0001g0061others(6): Show | 9 | HG00621.hp1 HG01934.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.6005-1638C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117975199 | ||||||
| chr1:117975221
|
G | T | 1 | a0011c0014t0001g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.6005-1660C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117975221 | ||||||
| chr1:117975274
|
T | C | 1 | a0001c0004t0001g0224 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6005-1713A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117975274 | ||||||
| chr1:117975387
|
G | C | 50 | a0001c0001t0001g0196a0001c0004t0001g0220a0001c0004t0001g0222others(47): Show | 50 | HG00438.hp2 HG01109.hp1 HG01433.hp2 others(47): Show |
intron_variant | MODIFIER | c.6005-1826C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117975387 | ||||||
| chr1:117975569
|
C | T | 6 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.6005-2008G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117975569 | ||||||
| chr1:117975686
|
A | G | 8 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(5): Show | 8 | HG01175.hp1 HG02258.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.6005-2125T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117975686 | ||||||
| chr1:117975694
|
C | T | 6 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.6005-2133G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117975694 | ||||||
| chr1:117975747
|
G | A | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6005-2186C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117975747 | ||||||
| chr1:117975841
|
G | A | 1 | a0004c0005t0001g0248 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.6005-2280C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117975841 | ||||||
| chr1:117975841
|
G | T | 138 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0198others(135): Show | 139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.6005-2280C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117975841 | ||||||
| chr1:117975877
|
C | T | 1 | a0004c0005t0001g0248 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.6005-2316G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117975877 | ||||||
| chr1:117976004
|
A | G | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG00140.hp1 HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.6005-2443T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117976004 | ||||||
| chr1:117976062
|
G | C | 2 | a0001c0018t0001g0148a0001c0018t0001g0229 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.6005-2501C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117976062 | ||||||
| chr1:117976092
|
G | T | 8 | a0001c0006t0001g0152a0001c0006t0001g0153a0005c0011t0001g0106others(5): Show | 8 | HG00280.hp2 HG01346.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.6005-2531C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117976092 | ||||||
| chr1:117976119
|
G | A | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6005-2558C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117976119 | ||||||
| chr1:117976250
|
T | C | 1 | a0002c0002t0001g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.6005-2689A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117976250 | ||||||
| chr1:117976312
|
G | A | 6 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.6005-2751C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117976312 | ||||||
| chr1:117976485
|
T | C | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.6005-2924A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117976485 | ||||||
| chr1:117976636
|
C | T | 129 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0198others(126): Show | 130 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.6005-3075G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117976636 | ||||||
| chr1:117977068
|
G | T | 1 | a0024c0035t0003g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6005-3507C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117977068 | ||||||
| chr1:117977155
|
CA | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0065others(128): Show | 133 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.6005-3595delT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117977155 | ||||||
| chr1:117977159
|
A | G | 58 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0198others(55): Show | 59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.6005-3598T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117977159 | ||||||
| chr1:117977160
|
A | G | 1 | a0003c0003t0001g0129 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.6005-3599T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117977160 | ||||||
| chr1:117977193
|
T | C | 11 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(8): Show | 11 | HG01175.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.6005-3632A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117977193 | ||||||
| chr1:117977316
|
C | A | 1 | a0001c0006t0001g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6005-3755G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117977316 | ||||||
| chr1:117977349
|
C | A | 1 | a0001c0001t0001g0210 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.6005-3788G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117977349 | ||||||
| chr1:117977419
|
C | T | 129 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0198others(126): Show | 130 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.6004+3851G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117977419 | ||||||
| chr1:117977625
|
A | G | 59 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0198others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.6004+3645T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117977625 | ||||||
| chr1:117977936
|
T | C | 1 | a0024c0035t0003g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6004+3334A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117977936 | ||||||
| chr1:117978230
|
A | C | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6004+3040T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117978230 | ||||||
| chr1:117978359
|
T | C | 1 | a0001c0006t0001g0253 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6004+2911A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117978359 | ||||||
| chr1:117978362
|
A | G | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6004+2908T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117978362 | ||||||
| chr1:117978648
|
A | G | 4 | a0001c0001t0001g0198a0002c0002t0001g0022a0003c0003t0001g0111others(1): Show | 4 | HG02135.hp2 HG02735.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.6004+2622T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117978648 | ||||||
| chr1:117978685
|
C | T | 2 | a0001c0004t0001g0225a0001c0004t0001g0237 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.6004+2585G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117978685 | ||||||
| chr1:117978727
|
C | T | 80 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0198others(77): Show | 81 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.6004+2543G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117978727 | ||||||
| chr1:117978869
|
C | CTT | 11 | a0008c0009t0002g0077a0008c0009t0002g0107a0008c0009t0002g0131others(8): Show | 11 | HG01175.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.6004+2399_6004+240 others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117978869 | ||||||
| chr1:117978869
|
CT | C | 65 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0198others(62): Show | 66 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.6004+2400delA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117978869 | ||||||
| chr1:117978961
|
T | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.6004+2309A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117978961 | ||||||
| chr1:117978992
|
T | C | 1 | a0001c0004t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6004+2278A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117978992 | ||||||
| chr1:117979022
|
C | T | 1 | a0001c0004t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6004+2248G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117979022 | ||||||
| chr1:117979028
|
T | C | 1 | a0001c0004t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6004+2242A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117979028 | ||||||
| chr1:117979029
|
G | A | 1 | a0001c0004t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6004+2241C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117979029 | ||||||
| chr1:117979067
|
G | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0065others(143): Show | 148 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.6004+2203C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117979067 | ||||||
| chr1:117979151
|
G | A | 4 | a0001c0004t0001g0062a0001c0019t0001g0205a0001c0019t0001g0208others(1): Show | 4 | HG02622.hp2 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.6004+2119C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117979151 | ||||||
| chr1:117979323
|
C | T | 9 | a0001c0001t0001g0174a0003c0003t0001g0076a0003c0003t0001g0078others(6): Show | 9 | HG01175.hp1 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.6004+1947G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117979323 | ||||||
| chr1:117979361
|
T | C | 1 | a0002c0002t0001g0031 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.6004+1909A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117979361 | ||||||
| chr1:117979402
|
T | G | 8 | a0001c0004t0001g0226a0001c0004t0001g0227a0001c0004t0001g0231others(5): Show | 8 | HG02109.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.6004+1868A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117979402 | ||||||
| chr1:117979431
|
T | C | 1 | a0002c0002t0001g0030 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.6004+1839A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117979431 | ||||||
| chr1:117979454
|
T | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6004+1816A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117979454 | ||||||
| chr1:117979797
|
T | C | 1 | a0003c0003t0001g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.6004+1473A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117979797 | ||||||
| chr1:117979922
|
G | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0065others(145): Show | 150 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.6004+1348C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117979922 | ||||||
| chr1:117980381
|
G | A | 1 | a0005c0011t0002g0202 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.6004+889C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117980381 | ||||||
| chr1:117980385
|
C | A | 1 | a0001c0001t0001g0239 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.6004+885G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117980385 | ||||||
| chr1:117980526
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6004+744G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117980526 | ||||||
| chr1:117980766
|
T | C | 1 | a0002c0002t0001g0040 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.6004+504A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117980766 | ||||||
| chr1:117980787
|
T | C | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6004+483A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117980787 | ||||||
| chr1:117980826
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6004+444A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 43/48 | chr1 | 117980826 | ||||||
| chr1:117981482
|
T | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5873-81A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117981482 | ||||||
| chr1:117981651
|
G | A | 1 | a0001c0026t0001g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5873-250C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117981651 | ||||||
| chr1:117981747
|
G | A | 53 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(50): Show | 53 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.5873-346C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117981747 | ||||||
| chr1:117981902
|
C | T | 16 | a0001c0042t0001g0183a0002c0002t0001g0024a0002c0002t0001g0032others(13): Show | 16 | HG00438.hp2 HG02080.hp2 NA18946.hp2 others(13): Show |
intron_variant | MODIFIER | c.5873-501G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117981902 | ||||||
| chr1:117982040
|
G | T | 27 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0222others(24): Show | 27 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.5873-639C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117982040 | ||||||
| chr1:117982095
|
C | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0065others(131): Show | 136 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.5873-694G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117982095 | ||||||
| chr1:117982124
|
C | A | 1 | a0024c0035t0003g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.5873-723G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117982124 | ||||||
| chr1:117982241
|
A | AT | 57 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0004t0001g0060others(54): Show | 58 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.5873-841dupA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117982241 | ||||||
| chr1:117982241
|
A | ATT | 8 | a0003c0003t0001g0113a0004c0005t0001g0080a0004c0005t0001g0123others(5): Show | 8 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(5): Show |
intron_variant | MODIFIER | c.5873-842_5873-841d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117982241 | ||||||
| chr1:117982241
|
AT | A | 15 | a0001c0006t0001g0151a0001c0006t0001g0152a0001c0006t0001g0153others(12): Show | 15 | HG00280.hp2 HG01175.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.5873-841delA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117982241 | ||||||
| chr1:117982244
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5873-843A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117982244 | ||||||
| chr1:117982247
|
T | A | 1 | a0005c0038t0002g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.5873-846A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117982247 | ||||||
| chr1:117982307
|
T | C | 3 | a0002c0002t0001g0022a0002c0002t0001g0023a0007c0033t0001g0014 | 3 | HG00621.hp2 HG02735.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.5873-906A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117982307 | ||||||
| chr1:117982476
|
C | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5873-1075G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117982476 | ||||||
| chr1:117982785
|
C | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5872+1026G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117982785 | ||||||
| chr1:117982922
|
C | T | 2 | a0001c0004t0001g0219a0001c0004t0001g0233 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.5872+889G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117982922 | ||||||
| chr1:117982941
|
C | A | 1 | a0001c0006t0001g0241 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.5872+870G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117982941 | ||||||
| chr1:117983110
|
A | ACCTC | 3 | a0012c0015t0002g0079a0012c0015t0002g0102a0018c0031t0002g0007 | 3 | HG02258.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.5872+700_5872+701i others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117983110 | ||||||
| chr1:117983111
|
A | T | 3 | a0012c0015t0002g0079a0012c0015t0002g0102a0018c0031t0002g0007 | 3 | HG02258.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.5872+700T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117983111 | ||||||
| chr1:117983192
|
A | G | 1 | a0001c0006t0001g0071 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5872+619T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117983192 | ||||||
| chr1:117983430
|
T | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5872+381A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117983430 | ||||||
| chr1:117983706
|
T | G | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5872+105A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 42/48 | chr1 | 117983706 | ||||||
| chr1:117983921
|
G | GA | 4 | a0001c0001t0001g0002a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 5 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.5770-9dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 41/48 | chr1 | 117983921 | ||||||
| chr1:117983969
|
G | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.5770-56C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 41/48 | chr1 | 117983969 | ||||||
| chr1:117984242
|
C | T | 1 | a0003c0003t0001g0256 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5770-329G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 41/48 | chr1 | 117984242 | ||||||
| chr1:117984254
|
G | A | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5770-341C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 41/48 | chr1 | 117984254 | ||||||
| chr1:117984553
|
A | G | 1 | a0001c0004t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5769+130T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 41/48 | chr1 | 117984553 | ||||||
| chr1:117984657
|
G | T | 1 | a0005c0011t0002g0202 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.5769+26C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 41/48 | chr1 | 117984657 | ||||||
| chr1:117985169
|
T | C | 1 | a0001c0027t0001g0221 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5670-387A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985169 | ||||||
| chr1:117985323
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.5670-541G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985323 | ||||||
| chr1:117985325
|
A | C | 1 | a0004c0005t0001g0244 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.5670-543T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985325 | ||||||
| chr1:117985659
|
G | A | 50 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(47): Show | 51 | HG00438.hp2 HG00597.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.5670-877C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985659 | ||||||
| chr1:117985694
|
C | G | 64 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(61): Show | 65 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.5670-912G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985694 | ||||||
| chr1:117985903
|
A | G | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5670-1121T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985903 | ||||||
| chr1:117985940
|
G | A | 1 | a0008c0009t0002g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5670-1158C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985940 | ||||||
| chr1:117985958
|
G | C | 1 | a0002c0002t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.5670-1176C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985958 | ||||||
| chr1:117985969
|
G | T | 1 | a0002c0002t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.5670-1187C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985969 | ||||||
| chr1:117985970
|
A | C | 1 | a0002c0002t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.5670-1188T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985970 | ||||||
| chr1:117985971
|
C | G | 1 | a0002c0002t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.5670-1189G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985971 | ||||||
| chr1:117985973
|
T | G | 1 | a0002c0002t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.5670-1191A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985973 | ||||||
| chr1:117985975
|
A | G | 1 | a0002c0002t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.5670-1193T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985975 | ||||||
| chr1:117985976
|
G | T | 1 | a0002c0002t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.5670-1194C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985976 | ||||||
| chr1:117985977
|
A | T | 1 | a0002c0002t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.5670-1195T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117985977 | ||||||
| chr1:117986069
|
T | C | 1 | a0001c0004t0001g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5670-1287A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117986069 | ||||||
| chr1:117986206
|
G | T | 1 | a0002c0002t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.5670-1424C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117986206 | ||||||
| chr1:117986242
|
C | T | 1 | a0003c0003t0001g0256 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5670-1460G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117986242 | ||||||
| chr1:117986249
|
C | T | 60 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(57): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.5670-1467G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117986249 | ||||||
| chr1:117986434
|
T | C | 1 | a0004c0005t0001g0133 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.5669+1400A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117986434 | ||||||
| chr1:117986436
|
C | T | 2 | a0003c0003t0001g0092a0003c0003t0001g0099 | 2 | NA18948.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.5669+1398G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117986436 | ||||||
| chr1:117986572
|
G | A | 60 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(57): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.5669+1262C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117986572 | ||||||
| chr1:117986576
|
G | T | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.5669+1258C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117986576 | ||||||
| chr1:117986939
|
TGAAATAC others(6): Show |
T | 6 | a0001c0019t0001g0205a0001c0019t0001g0208a0001c0025t0001g0063others(3): Show | 6 | HG00621.hp2 HG02622.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.5669+882_5669+894d others(15): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117986939 | ||||||
| chr1:117987185
|
T | C | 3 | a0001c0006t0001g0164a0001c0006t0001g0165a0001c0006t0001g0193 | 3 | HG02055.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5669+649A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117987185 | ||||||
| chr1:117987324
|
T | A | 1 | a0003c0003t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5669+510A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117987324 | ||||||
| chr1:117987373
|
T | A | 1 | a0004c0005t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5669+461A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117987373 | ||||||
| chr1:117987442
|
T | C | 57 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.5669+392A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117987442 | ||||||
| chr1:117987473
|
C | G | 57 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.5669+361G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117987473 | ||||||
| chr1:117987501
|
C | T | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.5669+333G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117987501 | ||||||
| chr1:117987586
|
T | A | 60 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(57): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.5669+248A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117987586 | ||||||
| chr1:117987636
|
A | T | 1 | a0008c0009t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5669+198T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117987636 | ||||||
| chr1:117987758
|
A | G | 3 | a0012c0015t0002g0079a0012c0015t0002g0102a0018c0031t0002g0007 | 3 | HG02258.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.5669+76T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117987758 | ||||||
| chr1:117987827
|
T | C | 1 | a0004c0005t0001g0249 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.5669+7A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117987827 | ||||||
| chr1:117987828
|
A | C | 1 | a0003c0003t0001g0105 | 1 | HG03017.hp2 | splice_region_variant&intron_variant | LOW | c.5669+6T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 40/48 | chr1 | 117987828 | ||||||
| chr1:117988250
|
G | C | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.5522-46C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117988250 | ||||||
| chr1:117988266
|
T | C | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5522-62A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117988266 | ||||||
| chr1:117988450
|
A | G | 1 | a0003c0003t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5522-246T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117988450 | ||||||
| chr1:117988656
|
A | G | 3 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156 | 3 | NA18949.hp2 NA18979.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.5522-452T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117988656 | ||||||
| chr1:117988716
|
G | A | 2 | a0001c0004t0001g0225a0001c0004t0001g0237 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.5522-512C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117988716 | ||||||
| chr1:117988789
|
GACTC | G | 50 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(47): Show | 51 | HG00438.hp2 HG00597.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.5522-589_5522-586d others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117988789 | ||||||
| chr1:117988954
|
T | C | 1 | a0003c0003t0001g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.5522-750A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117988954 | ||||||
| chr1:117988986
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.5522-782C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117988986 | ||||||
| chr1:117989104
|
C | G | 1 | a0003c0003t0001g0256 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5522-900G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989104 | ||||||
| chr1:117989214
|
G | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(203): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.5522-1010C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989214 | ||||||
| chr1:117989294
|
G | A | 3 | a0012c0015t0002g0079a0012c0015t0002g0102a0018c0031t0002g0007 | 3 | HG02258.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.5522-1090C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989294 | ||||||
| chr1:117989316
|
C | A | 6 | a0001c0004t0001g0226a0001c0004t0001g0227a0001c0004t0001g0230others(3): Show | 6 | HG00741.hp1 HG02630.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.5522-1112G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989316 | ||||||
| chr1:117989351
|
G | C | 4 | a0002c0002t0001g0035a0002c0002t0001g0036a0002c0002t0001g0039others(1): Show | 4 | HG00438.hp2 HG02080.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.5522-1147C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989351 | ||||||
| chr1:117989357
|
C | T | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(191): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.5522-1153G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989357 | ||||||
| chr1:117989402
|
A | C | 1 | a0001c0010t0001g0154 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.5522-1198T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989402 | ||||||
| chr1:117989483
|
G | T | 53 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.5522-1279C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989483 | ||||||
| chr1:117989547
|
C | T | 50 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(47): Show | 51 | HG00438.hp2 HG00597.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.5521+1314G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989547 | ||||||
| chr1:117989574
|
T | C | 2 | a0003c0003t0001g0092a0003c0003t0001g0099 | 2 | NA18948.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.5521+1287A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989574 | ||||||
| chr1:117989672
|
C | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5521+1189G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989672 | ||||||
| chr1:117989673
|
G | A | 2 | a0001c0004t0001g0220a0001c0004t0001g0222 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5521+1188C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989673 | ||||||
| chr1:117989690
|
C | T | 2 | a0003c0003t0001g0092a0003c0003t0001g0099 | 2 | NA18948.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.5521+1171G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989690 | ||||||
| chr1:117989726
|
C | T | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5521+1135G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117989726 | ||||||
| chr1:117990271
|
C | T | 54 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.5521+590G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117990271 | ||||||
| chr1:117990326
|
C | T | 27 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0222others(24): Show | 27 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.5521+535G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117990326 | ||||||
| chr1:117990367
|
C | T | 27 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0222others(24): Show | 27 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.5521+494G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117990367 | ||||||
| chr1:117990622
|
G | T | 50 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(47): Show | 51 | HG00438.hp2 HG00597.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.5521+239C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117990622 | ||||||
| chr1:117990735
|
G | A | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5521+126C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 38/48 | chr1 | 117990735 | ||||||
| chr1:117990991
|
T | C | 1 | a0004c0005t0001g0133 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.5476-85A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 37/48 | chr1 | 117990991 | ||||||
| chr1:117991012
|
G | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5476-106C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 37/48 | chr1 | 117991012 | ||||||
| chr1:117991231
|
C | T | 1 | a0004c0005t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5475+184G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 37/48 | chr1 | 117991231 | ||||||
| chr1:117991669
|
C | T | 2 | a0003c0003t0001g0092a0003c0003t0001g0099 | 2 | NA18948.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.5362-141G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/48 | chr1 | 117991669 | ||||||
| chr1:117991715
|
G | A | 59 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(56): Show | 60 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.5362-187C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/48 | chr1 | 117991715 | ||||||
| chr1:117991727
|
C | T | 1 | a0025c0036t0002g0254 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5362-199G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/48 | chr1 | 117991727 | ||||||
| chr1:117991775
|
G | A | 54 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.5362-247C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/48 | chr1 | 117991775 | ||||||
| chr1:117991857
|
G | A | 5 | a0011c0014t0001g0008a0011c0014t0001g0009a0012c0015t0002g0079others(2): Show | 5 | HG02258.hp2 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.5362-329C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/48 | chr1 | 117991857 | ||||||
| chr1:117991991
|
G | A | 3 | a0001c0006t0001g0164a0001c0006t0001g0165a0001c0006t0001g0193 | 3 | HG02055.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5362-463C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/48 | chr1 | 117991991 | ||||||
| chr1:117992096
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.5361+370G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/48 | chr1 | 117992096 | ||||||
| chr1:117992109
|
C | G | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5361+357G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/48 | chr1 | 117992109 | ||||||
| chr1:117992110
|
G | A | 26 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0222others(23): Show | 26 | HG01433.hp2 HG02055.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.5361+356C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/48 | chr1 | 117992110 | ||||||
| chr1:117992205
|
G | A | 3 | a0012c0015t0002g0079a0012c0015t0002g0102a0018c0031t0002g0007 | 3 | HG02258.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.5361+261C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/48 | chr1 | 117992205 | ||||||
| chr1:117992353
|
T | C | 62 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(59): Show | 63 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.5361+113A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/48 | chr1 | 117992353 | ||||||
| chr1:117992449
|
C | T | 4 | a0011c0014t0001g0008a0011c0014t0001g0009a0017c0034t0001g0053others(1): Show | 4 | HG02572.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.5361+17G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 36/48 | chr1 | 117992449 | ||||||
| chr1:117993095
|
G | A | 1 | a0002c0002t0001g0025 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5179-447C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 35/48 | chr1 | 117993095 | ||||||
| chr1:117993109
|
C | T | 81 | a0001c0001t0001g0144a0001c0001t0001g0239a0001c0001t0001g0240others(78): Show | 82 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.5179-461G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 35/48 | chr1 | 117993109 | ||||||
| chr1:117993795
|
C | T | 15 | a0001c0006t0001g0151a0001c0006t0001g0152a0001c0006t0001g0153others(12): Show | 15 | HG00280.hp2 HG00621.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.5178+611G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 35/48 | chr1 | 117993795 | ||||||
| chr1:117993869
|
A | T | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5178+537T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 35/48 | chr1 | 117993869 | ||||||
| chr1:117993962
|
G | A | 160 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(157): Show | 161 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.5178+444C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 35/48 | chr1 | 117993962 | ||||||
| chr1:117994021
|
G | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.5178+385C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 35/48 | chr1 | 117994021 | ||||||
| chr1:117994108
|
G | C | 1 | a0001c0004t0001g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5178+298C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 35/48 | chr1 | 117994108 | ||||||
| chr1:117994749
|
G | A | 1 | a0003c0003t0001g0108 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5054-219C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117994749 | ||||||
| chr1:117994892
|
A | G | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.5054-362T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117994892 | ||||||
| chr1:117994927
|
T | G | 57 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.5054-397A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117994927 | ||||||
| chr1:117994942
|
A | G | 4 | a0001c0001t0001g0174a0001c0001t0001g0181a0001c0006t0001g0241others(1): Show | 4 | HG01952.hp2 HG02818.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.5054-412T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117994942 | ||||||
| chr1:117995017
|
G | A | 1 | a0001c0006t0001g0193 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5054-487C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995017 | ||||||
| chr1:117995455
|
T | C | 166 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(163): Show | 167 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.5053+915A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995455 | ||||||
| chr1:117995684
|
A | G | 3 | a0001c0006t0001g0164a0001c0006t0001g0165a0001c0006t0001g0193 | 3 | HG02055.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5053+686T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995684 | ||||||
| chr1:117995695
|
A | AAC | 6 | a0001c0001t0001g0214a0001c0006t0001g0073a0001c0006t0001g0074others(3): Show | 6 | HG00140.hp1 HG01346.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.5053+673_5053+674d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995695 | ||||||
| chr1:117995695
|
AAC | A | 101 | a0001c0001t0001g0149a0001c0001t0001g0175a0001c0001t0001g0200others(98): Show | 101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.5053+673_5053+674d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995695 | ||||||
| chr1:117995695
|
AACAC | A | 11 | a0001c0001t0001g0003a0001c0032t0001g0067a0003c0003t0001g0108others(8): Show | 12 | HG00642.hp1 HG01496.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.5053+671_5053+674d others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995695 | ||||||
| chr1:117995695
|
AACACAC | A | 5 | a0001c0006t0001g0193a0003c0003t0001g0114a0003c0003t0001g0115others(2): Show | 5 | HG01070.hp2 HG01943.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.5053+669_5053+674d others(8): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995695 | ||||||
| chr1:117995735
|
C | CACACACA others(3): Show |
4 | a0002c0002t0001g0001a0002c0002t0001g0019a0002c0002t0001g0020others(1): Show | 5 | HG01346.hp1 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.5053+634_5053+635i others(12): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995735 | ||||||
| chr1:117995735
|
C | CACACACA others(1): Show |
3 | a0002c0002t0001g0040a0002c0002t0001g0054a0002c0002t0001g0056 | 3 | HG00735.hp2 HG01934.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.5053+634_5053+635i others(10): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995735 | ||||||
| chr1:117995735
|
C | CACACAT | 11 | a0001c0010t0001g0154a0002c0002t0001g0013a0002c0002t0001g0028others(8): Show | 11 | HG00438.hp2 HG02074.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.5053+634_5053+635i others(8): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995735 | ||||||
| chr1:117995735
|
C | CACAT | 30 | a0001c0010t0001g0150a0001c0010t0001g0156a0002c0002t0001g0010others(27): Show | 30 | HG00597.hp1 HG00621.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.5053+634_5053+635i others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995735 | ||||||
| chr1:117995735
|
C | CAT | 9 | a0002c0002t0001g0011a0002c0002t0001g0025a0002c0002t0001g0026others(6): Show | 9 | HG02071.hp1 HG02135.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.5053+634_5053+635i others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995735 | ||||||
| chr1:117995735
|
C | T | 105 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(102): Show | 105 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.5053+635G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995735 | ||||||
| chr1:117995818
|
T | C | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5053+552A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995818 | ||||||
| chr1:117995926
|
G | C | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.5053+444C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995926 | ||||||
| chr1:117995964
|
T | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5053+406A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117995964 | ||||||
| chr1:117996138
|
G | A | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5053+232C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 34/48 | chr1 | 117996138 | ||||||
| chr1:117996522
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4923-22A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 33/48 | chr1 | 117996522 | ||||||
| chr1:117996588
|
A | G | 5 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(2): Show | 5 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+10T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 33/48 | chr1 | 117996588 | ||||||
| chr1:117996760
|
G | A | 1 | a0005c0011t0001g0106 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4777-17C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117996760 | ||||||
| chr1:117997019
|
T | C | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.4777-276A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117997019 | ||||||
| chr1:117997039
|
G | C | 1 | a0002c0002t0001g0023 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4777-296C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117997039 | ||||||
| chr1:117997093
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0191 | 2 | HG01255.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.4777-350T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117997093 | ||||||
| chr1:117997122
|
G | A | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4777-379C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117997122 | ||||||
| chr1:117997171
|
T | A | 18 | a0001c0004t0001g0219a0001c0004t0001g0225a0001c0004t0001g0226others(15): Show | 18 | HG00741.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.4777-428A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117997171 | ||||||
| chr1:117997244
|
C | T | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4777-501G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117997244 | ||||||
| chr1:117997351
|
T | C | 57 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.4777-608A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117997351 | ||||||
| chr1:117997523
|
T | C | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.4777-780A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117997523 | ||||||
| chr1:117997566
|
T | TA | 95 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(92): Show | 95 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.4777-824dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117997566 | ||||||
| chr1:117997566
|
TA | T | 68 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(65): Show | 69 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.4777-824delT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117997566 | ||||||
| chr1:117997683
|
A | G | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4777-940T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117997683 | ||||||
| chr1:117997946
|
G | A | 57 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.4777-1203C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117997946 | ||||||
| chr1:117997948
|
G | A | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4777-1205C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117997948 | ||||||
| chr1:117998036
|
C | A | 1 | a0001c0004t0001g0226 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4777-1293G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117998036 | ||||||
| chr1:117998037
|
T | G | 1 | a0001c0004t0001g0226 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4777-1294A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117998037 | ||||||
| chr1:117998236
|
G | A | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4777-1493C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117998236 | ||||||
| chr1:117998266
|
T | C | 95 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0222others(92): Show | 95 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.4777-1523A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117998266 | ||||||
| chr1:117998375
|
C | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4777-1632G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117998375 | ||||||
| chr1:117998461
|
T | G | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4777-1718A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117998461 | ||||||
| chr1:117998540
|
C | CT | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4777-1798dupA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117998540 | ||||||
| chr1:117998577
|
T | C | 2 | a0002c0002t0001g0058a0002c0002t0001g0059 | 2 | NA18973.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.4777-1834A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117998577 | ||||||
| chr1:117998583
|
T | G | 1 | a0003c0003t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4777-1840A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117998583 | ||||||
| chr1:117998668
|
T | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG02015.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.4777-1925A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117998668 | ||||||
| chr1:117998735
|
C | T | 1 | a0004c0005t0001g0004 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4777-1992G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117998735 | ||||||
| chr1:117998960
|
T | C | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4777-2217A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117998960 | ||||||
| chr1:117998994
|
C | T | 1 | a0004c0005t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4777-2251G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117998994 | ||||||
| chr1:117999022
|
G | A | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.4777-2279C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117999022 | ||||||
| chr1:117999105
|
T | C | 1 | a0003c0003t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4777-2362A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117999105 | ||||||
| chr1:117999125
|
C | T | 3 | a0001c0006t0001g0103a0001c0006t0001g0124a0022c0037t0001g0116 | 3 | HG01109.hp2 HG02735.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.4777-2382G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117999125 | ||||||
| chr1:117999196
|
A | G | 2 | a0001c0004t0001g0219a0001c0004t0001g0233 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4777-2453T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117999196 | ||||||
| chr1:117999277
|
C | T | 53 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.4777-2534G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117999277 | ||||||
| chr1:117999370
|
T | G | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4777-2627A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117999370 | ||||||
| chr1:117999401
|
C | G | 1 | a0002c0002t0001g0010 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4777-2658G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117999401 | ||||||
| chr1:117999606
|
T | C | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162 | 3 | HG01167.hp2 HG01928.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.4777-2863A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117999606 | ||||||
| chr1:117999609
|
G | C | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4777-2866C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117999609 | ||||||
| chr1:117999641
|
G | C | 57 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.4777-2898C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117999641 | ||||||
| chr1:117999652
|
G | T | 2 | a0001c0004t0001g0225a0001c0004t0001g0237 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4777-2909C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117999652 | ||||||
| chr1:117999737
|
G | A | 6 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(3): Show | 6 | HG01433.hp2 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.4777-2994C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117999737 | ||||||
| chr1:117999815
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4777-3072G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 117999815 | ||||||
| chr1:118000022
|
A | C | 67 | a0003c0003t0001g0064a0003c0003t0001g0076a0003c0003t0001g0078others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.4777-3279T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000022 | ||||||
| chr1:118000134
|
G | A | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4777-3391C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000134 | ||||||
| chr1:118000272
|
G | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4777-3529C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000272 | ||||||
| chr1:118000303
|
T | C | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4777-3560A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000303 | ||||||
| chr1:118000438
|
A | T | 5 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(2): Show | 5 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4777-3695T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000438 | ||||||
| chr1:118000619
|
C | T | 5 | a0003c0003t0001g0136a0003c0003t0001g0137a0003c0003t0001g0139others(2): Show | 5 | HG01167.hp1 HG01358.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.4777-3876G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000619 | ||||||
| chr1:118000653
|
G | T | 2 | a0002c0002t0001g0043a0002c0002t0001g0044 | 2 | NA18971.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.4777-3910C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000653 | ||||||
| chr1:118000658
|
T | C | 1 | a0001c0004t0001g0227 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4777-3915A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000658 | ||||||
| chr1:118000805
|
C | T | 25 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0222others(22): Show | 25 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.4777-4062G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000805 | ||||||
| chr1:118000854
|
C | G | 53 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.4777-4111G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000854 | ||||||
| chr1:118000900
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4777-4157C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000900 | ||||||
| chr1:118000919
|
T | G | 1 | a0023c0043t0001g0185 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4777-4176A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000919 | ||||||
| chr1:118000946
|
T | C | 1 | a0004c0005t0001g0125 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4777-4203A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000946 | ||||||
| chr1:118000998
|
T | C | 60 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(57): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.4777-4255A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118000998 | ||||||
| chr1:118001047
|
G | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4777-4304C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118001047 | ||||||
| chr1:118001187
|
G | A | 6 | a0001c0006t0001g0070a0001c0006t0001g0071a0001c0006t0001g0072others(3): Show | 6 | HG00140.hp1 HG02129.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.4776+4227C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118001187 | ||||||
| chr1:118001351
|
G | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4776+4063C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118001351 | ||||||
| chr1:118001364
|
T | A | 1 | a0004c0005t0001g0081 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4776+4050A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118001364 | ||||||
| chr1:118001653
|
T | G | 60 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(57): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.4776+3761A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118001653 | ||||||
| chr1:118001813
|
G | A | 1 | a0001c0004t0003g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4776+3601C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118001813 | ||||||
| chr1:118001943
|
T | A | 1 | a0004c0005t0001g0081 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4776+3471A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118001943 | ||||||
| chr1:118002213
|
A | T | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4776+3201T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002213 | ||||||
| chr1:118002258
|
T | C | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4776+3156A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002258 | ||||||
| chr1:118002296
|
T | C | 1 | a0003c0003t0001g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4776+3118A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002296 | ||||||
| chr1:118002354
|
C | T | 1 | a0001c0006t0001g0070 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.4776+3060G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002354 | ||||||
| chr1:118002474
|
C | G | 3 | a0011c0014t0001g0008a0011c0014t0001g0009a0021c0024t0001g0006 | 3 | HG02451.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4776+2940G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002474 | ||||||
| chr1:118002512
|
T | C | 1 | a0006c0007t0001g0189 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4776+2902A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002512 | ||||||
| chr1:118002524
|
A | G | 57 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.4776+2890T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002524 | ||||||
| chr1:118002652
|
T | C | 1 | a0001c0006t0001g0152 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4776+2762A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002652 | ||||||
| chr1:118002688
|
C | T | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4776+2726G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002688 | ||||||
| chr1:118002732
|
A | G | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4776+2682T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002732 | ||||||
| chr1:118002765
|
G | A | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4776+2649C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002765 | ||||||
| chr1:118002818
|
C | T | 3 | a0011c0014t0001g0008a0011c0014t0001g0009a0021c0024t0001g0006 | 3 | HG02451.hp2 HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4776+2596G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002818 | ||||||
| chr1:118002824
|
C | T | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4776+2590G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002824 | ||||||
| chr1:118002987
|
T | G | 1 | a0005c0020t0002g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4776+2427A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002987 | ||||||
| chr1:118002996
|
C | T | 57 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.4776+2418G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118002996 | ||||||
| chr1:118003249
|
C | T | 2 | a0004c0005t0001g0083a0004c0005t0001g0084 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4776+2165G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118003249 | ||||||
| chr1:118003251
|
A | G | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4776+2163T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118003251 | ||||||
| chr1:118003494
|
T | C | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4776+1920A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118003494 | ||||||
| chr1:118003722
|
T | C | 1 | a0011c0014t0001g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4776+1692A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118003722 | ||||||
| chr1:118003746
|
C | T | 1 | a0005c0038t0002g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4776+1668G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118003746 | ||||||
| chr1:118003747
|
G | A | 3 | a0009c0012t0001g0245a0009c0012t0001g0246a0009c0012t0001g0247 | 3 | NA18949.hp1 NA18973.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.4776+1667C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118003747 | ||||||
| chr1:118003781
|
G | T | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.4776+1633C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118003781 | ||||||
| chr1:118003947
|
G | A | 53 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.4776+1467C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118003947 | ||||||
| chr1:118003991
|
A | G | 160 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(157): Show | 161 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.4776+1423T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118003991 | ||||||
| chr1:118004014
|
T | G | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4776+1400A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004014 | ||||||
| chr1:118004022
|
C | T | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4776+1392G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004022 | ||||||
| chr1:118004129
|
C | T | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4776+1285G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004129 | ||||||
| chr1:118004209
|
C | T | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4776+1205G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004209 | ||||||
| chr1:118004242
|
G | T | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4776+1172C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004242 | ||||||
| chr1:118004305
|
C | T | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4776+1109G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004305 | ||||||
| chr1:118004354
|
T | C | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4776+1060A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004354 | ||||||
| chr1:118004457
|
T | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(253): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.4776+957A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004457 | ||||||
| chr1:118004458
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4776+956C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004458 | ||||||
| chr1:118004462
|
G | A | 1 | a0002c0002t0001g0057 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4776+952C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004462 | ||||||
| chr1:118004560
|
T | C | 162 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(159): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.4776+854A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004560 | ||||||
| chr1:118004561
|
G | A | 1 | a0002c0002t0001g0011 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4776+853C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004561 | ||||||
| chr1:118004578
|
T | C | 1 | a0001c0001t0001g0217 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4776+836A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004578 | ||||||
| chr1:118004602
|
C | T | 57 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.4776+812G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004602 | ||||||
| chr1:118004810
|
G | A | 3 | a0001c0006t0001g0151a0001c0006t0001g0152a0001c0006t0001g0153 | 3 | HG00280.hp2 HG01346.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.4776+604C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004810 | ||||||
| chr1:118004833
|
T | C | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4776+581A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118004833 | ||||||
| chr1:118005211
|
C | T | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4776+203G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118005211 | ||||||
| chr1:118005293
|
C | T | 1 | a0003c0003t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4776+121G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118005293 | ||||||
| chr1:118005354
|
T | C | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4776+60A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 32/48 | chr1 | 118005354 | ||||||
| chr1:118005691
|
C | T | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4588-89G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118005691 | ||||||
| chr1:118005842
|
T | C | 1 | a0001c0001t0001g0217 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4588-240A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118005842 | ||||||
| chr1:118005860
|
G | C | 53 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.4588-258C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118005860 | ||||||
| chr1:118006106
|
C | T | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4588-504G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118006106 | ||||||
| chr1:118006263
|
C | T | 3 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156 | 3 | NA18949.hp2 NA18979.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.4588-661G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118006263 | ||||||
| chr1:118006494
|
G | A | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4588-892C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118006494 | ||||||
| chr1:118006508
|
T | C | 1 | a0001c0006t0001g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4588-906A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118006508 | ||||||
| chr1:118006555
|
T | C | 1 | a0003c0003t0001g0113 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4588-953A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118006555 | ||||||
| chr1:118006646
|
T | C | 1 | a0004c0005t0001g0142 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4588-1044A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118006646 | ||||||
| chr1:118007099
|
T | G | 25 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0222others(22): Show | 25 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.4587+945A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118007099 | ||||||
| chr1:118007171
|
A | C | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4587+873T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118007171 | ||||||
| chr1:118007669
|
G | A | 1 | a0028c0040t0001g0122 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4587+375C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118007669 | ||||||
| chr1:118007821
|
C | T | 67 | a0003c0003t0001g0064a0003c0003t0001g0076a0003c0003t0001g0078others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.4587+223G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118007821 | ||||||
| chr1:118007929
|
G | GA | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4587+114dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118007929 | ||||||
| chr1:118007932
|
T | G | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4587+112A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118007932 | ||||||
| chr1:118007934
|
A | C | 1 | a0001c0001t0001g0065 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4587+110T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118007934 | ||||||
| chr1:118007946
|
G | A | 7 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(4): Show | 7 | HG01433.hp2 HG02055.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.4587+98C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118007946 | ||||||
| chr1:118007971
|
C | A | 53 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.4587+73G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118007971 | ||||||
| chr1:118008033
|
C | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4587+11G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 31/48 | chr1 | 118008033 | ||||||
| chr1:118008313
|
C | T | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4433-115G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118008313 | ||||||
| chr1:118008547
|
T | G | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4433-349A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118008547 | ||||||
| chr1:118008569
|
A | C | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4433-371T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118008569 | ||||||
| chr1:118008986
|
C | T | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4433-788G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118008986 | ||||||
| chr1:118009076
|
C | A | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4433-878G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009076 | ||||||
| chr1:118009164
|
T | C | 67 | a0003c0003t0001g0064a0003c0003t0001g0076a0003c0003t0001g0078others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.4433-966A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009164 | ||||||
| chr1:118009181
|
A | G | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4433-983T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009181 | ||||||
| chr1:118009248
|
A | AAC | 32 | a0001c0001t0001g0002a0001c0001t0001g0161a0001c0001t0001g0166others(29): Show | 33 | HG00738.hp1 HG00741.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.4433-1052_4433-105 others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009248 | ||||||
| chr1:118009248
|
A | AACAC | 14 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0001g0203others(11): Show | 14 | HG00642.hp2 HG01175.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.4433-1054_4433-105 others(8): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009248 | ||||||
| chr1:118009248
|
A | AACACAC | 5 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0234others(2): Show | 5 | HG02615.hp2 HG02698.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4433-1056_4433-105 others(10): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009248 | ||||||
| chr1:118009248
|
AAC | A | 74 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(71): Show | 74 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.4433-1052_4433-105 others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009248 | ||||||
| chr1:118009248
|
AACAC | A | 52 | a0001c0001t0001g0174a0001c0004t0001g0224a0001c0010t0001g0150others(49): Show | 53 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.4433-1054_4433-105 others(8): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009248 | ||||||
| chr1:118009248
|
AACACAC | A | 5 | a0004c0005t0001g0125a0004c0005t0001g0242a0004c0005t0001g0248others(2): Show | 5 | HG00597.hp2 HG02258.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4433-1056_4433-105 others(10): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009248 | ||||||
| chr1:118009248
|
AACACACA others(9): Show |
A | 1 | a0002c0002t0001g0057 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4433-1066_4433-105 others(20): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009248 | ||||||
| chr1:118009555
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.4433-1357T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009555 | ||||||
| chr1:118009628
|
C | T | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4433-1430G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009628 | ||||||
| chr1:118009722
|
T | C | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.4433-1524A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009722 | ||||||
| chr1:118009856
|
GGAAAATA others(2): Show |
G | 62 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(59): Show | 63 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.4433-1667_4433-165 others(13): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009856 | ||||||
| chr1:118009908
|
T | G | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.4433-1710A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009908 | ||||||
| chr1:118009947
|
T | G | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4433-1749A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009947 | ||||||
| chr1:118009980
|
A | G | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4433-1782T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118009980 | ||||||
| chr1:118010275
|
CAACCGT | C | 60 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(57): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.4432+1947_4432+195 others(10): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118010275 | ||||||
| chr1:118010286
|
G | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4432+1942C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118010286 | ||||||
| chr1:118010303
|
G | A | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4432+1925C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118010303 | ||||||
| chr1:118010550
|
T | C | 2 | a0001c0004t0001g0238a0001c0032t0001g0067 | 2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.4432+1678A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118010550 | ||||||
| chr1:118010624
|
T | C | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.4432+1604A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118010624 | ||||||
| chr1:118010779
|
C | G | 25 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0222others(22): Show | 25 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.4432+1449G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118010779 | ||||||
| chr1:118010873
|
G | A | 58 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4432+1355C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118010873 | ||||||
| chr1:118011166
|
T | C | 60 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(57): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.4432+1062A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011166 | ||||||
| chr1:118011327
|
C | T | 55 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(52): Show | 56 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.4432+901G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011327 | ||||||
| chr1:118011334
|
G | A | 60 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(57): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.4432+894C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011334 | ||||||
| chr1:118011375
|
G | A | 67 | a0003c0003t0001g0064a0003c0003t0001g0076a0003c0003t0001g0078others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.4432+853C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011375 | ||||||
| chr1:118011428
|
G | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4432+800C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011428 | ||||||
| chr1:118011652
|
G | A | 59 | a0003c0003t0001g0064a0003c0003t0001g0086a0003c0003t0001g0087others(56): Show | 59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.4432+576C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011652 | ||||||
| chr1:118011659
|
C | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4432+569G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011659 | ||||||
| chr1:118011697
|
T | C | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4432+531A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011697 | ||||||
| chr1:118011702
|
C | A | 1 | a0001c0001t0001g0144 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.4432+526G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011702 | ||||||
| chr1:118011743
|
A | AAC | 4 | a0003c0003t0001g0086a0003c0003t0001g0087a0003c0003t0001g0088others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.4432+483_4432+484d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011743 | ||||||
| chr1:118011759
|
G | GAC | 3 | a0001c0001t0001g0002a0001c0001t0001g0172a0001c0001t0001g0173 | 4 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.4432+467_4432+468d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011759 | ||||||
| chr1:118011900
|
C | T | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4432+328G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011900 | ||||||
| chr1:118011920
|
T | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4432+308A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011920 | ||||||
| chr1:118011963
|
TTA | T | 3 | a0014c0016t0002g0085a0014c0016t0002g0228a0017c0034t0001g0053 | 3 | HG02818.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4432+263_4432+264d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011963 | ||||||
| chr1:118011976
|
T | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0176a0005c0020t0002g0157 | 3 | HG00423.hp2 HG00621.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.4432+252A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011976 | ||||||
| chr1:118011990
|
C | T | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4432+238G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118011990 | ||||||
| chr1:118012054
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.4432+174T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118012054 | ||||||
| chr1:118012066
|
C | A | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4432+162G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118012066 | ||||||
| chr1:118012075
|
C | A | 1 | a0002c0002t0001g0050 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.4432+153G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118012075 | ||||||
| chr1:118012088
|
G | T | 162 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(159): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.4432+140C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118012088 | ||||||
| chr1:118012179
|
C | T | 2 | a0001c0004t0001g0238a0001c0032t0001g0067 | 2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.4432+49G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118012179 | ||||||
| chr1:118012205
|
T | C | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4432+23A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118012205 | ||||||
| chr1:118012206
|
G | A | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4432+22C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 30/48 | chr1 | 118012206 | ||||||
| chr1:118012402
|
T | G | 1 | a0001c0004t0001g0234 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4288-30A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118012402 | ||||||
| chr1:118012549
|
AT | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0172a0001c0001t0001g0173 | 4 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.4288-178delA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118012549 | ||||||
| chr1:118012783
|
C | T | 1 | a0001c0004t0001g0232 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4288-411G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118012783 | ||||||
| chr1:118012883
|
A | G | 59 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(56): Show | 60 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.4288-511T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118012883 | ||||||
| chr1:118013102
|
C | T | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.4288-730G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118013102 | ||||||
| chr1:118013403
|
T | C | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4288-1031A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118013403 | ||||||
| chr1:118013410
|
T | C | 59 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(56): Show | 60 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.4288-1038A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118013410 | ||||||
| chr1:118013495
|
G | C | 1 | a0001c0044t0001g0182 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4288-1123C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118013495 | ||||||
| chr1:118013622
|
G | A | 2 | a0002c0002t0001g0058a0002c0002t0001g0059 | 2 | NA18973.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.4288-1250C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118013622 | ||||||
| chr1:118013679
|
C | T | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.4288-1307G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118013679 | ||||||
| chr1:118013738
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.4288-1366C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118013738 | ||||||
| chr1:118014232
|
G | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4287+1733C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118014232 | ||||||
| chr1:118014264
|
T | C | 4 | a0001c0019t0001g0205a0001c0019t0001g0208a0001c0025t0001g0063others(1): Show | 4 | HG01175.hp1 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4287+1701A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118014264 | ||||||
| chr1:118014387
|
T | C | 1 | a0003c0003t0001g0111 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4287+1578A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118014387 | ||||||
| chr1:118014688
|
G | A | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.4287+1277C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118014688 | ||||||
| chr1:118014934
|
C | T | 4 | a0001c0004t0001g0226a0001c0004t0001g0227a0001c0004t0001g0231others(1): Show | 4 | HG02630.hp2 HG02976.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.4287+1031G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118014934 | ||||||
| chr1:118015012
|
T | C | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4287+953A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118015012 | ||||||
| chr1:118015055
|
C | T | 53 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.4287+910G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118015055 | ||||||
| chr1:118015130
|
C | T | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4287+835G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118015130 | ||||||
| chr1:118015142
|
G | A | 1 | a0003c0003t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4287+823C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118015142 | ||||||
| chr1:118015165
|
A | G | 3 | a0003c0003t0001g0108a0003c0003t0001g0114a0003c0003t0001g0115 | 3 | HG00642.hp1 HG01070.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.4287+800T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118015165 | ||||||
| chr1:118015271
|
C | CA | 61 | a0001c0001t0001g0210a0001c0001t0001g0217a0001c0001t0001g0239others(58): Show | 62 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.4287+693dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118015271 | ||||||
| chr1:118015271
|
CA | C | 13 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(10): Show | 13 | HG01069.hp2 HG01167.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.4287+693delT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118015271 | ||||||
| chr1:118015400
|
A | C | 3 | a0009c0012t0001g0245a0009c0012t0001g0246a0009c0012t0001g0247 | 3 | NA18949.hp1 NA18973.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.4287+565T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118015400 | ||||||
| chr1:118015672
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4287+293A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 29/48 | chr1 | 118015672 | ||||||
| chr1:118016362
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4070-180C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118016362 | ||||||
| chr1:118016431
|
C | A | 1 | a0004c0005t0001g0249 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4070-249G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118016431 | ||||||
| chr1:118016523
|
G | T | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.4070-341C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118016523 | ||||||
| chr1:118016989
|
G | T | 1 | a0007c0033t0001g0014 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4070-807C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118016989 | ||||||
| chr1:118017064
|
G | A | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.4070-882C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118017064 | ||||||
| chr1:118017124
|
C | A | 11 | a0001c0006t0001g0151a0001c0006t0001g0152a0001c0006t0001g0153others(8): Show | 11 | HG00280.hp2 HG00621.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.4070-942G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118017124 | ||||||
| chr1:118017276
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4070-1094G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118017276 | ||||||
| chr1:118017424
|
G | A | 67 | a0003c0003t0001g0064a0003c0003t0001g0076a0003c0003t0001g0078others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.4070-1242C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118017424 | ||||||
| chr1:118017469
|
G | A | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4070-1287C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118017469 | ||||||
| chr1:118017783
|
A | G | 3 | a0004c0005t0001g0096a0004c0005t0001g0097a0004c0005t0001g0098 | 3 | NA18990.hp2 NA19084.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.4070-1601T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118017783 | ||||||
| chr1:118017859
|
A | C | 2 | a0001c0004t0001g0219a0001c0004t0001g0233 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4070-1677T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118017859 | ||||||
| chr1:118018193
|
C | T | 67 | a0003c0003t0001g0064a0003c0003t0001g0076a0003c0003t0001g0078others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.4070-2011G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118018193 | ||||||
| chr1:118018260
|
G | A | 62 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(59): Show | 63 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.4070-2078C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118018260 | ||||||
| chr1:118018281
|
G | A | 1 | a0003c0003t0001g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4070-2099C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118018281 | ||||||
| chr1:118018346
|
C | T | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.4070-2164G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118018346 | ||||||
| chr1:118018572
|
C | T | 6 | a0002c0002t0001g0035a0002c0002t0001g0036a0002c0002t0001g0039others(3): Show | 6 | HG00438.hp2 HG02080.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.4070-2390G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118018572 | ||||||
| chr1:118018688
|
G | A | 53 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.4070-2506C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118018688 | ||||||
| chr1:118018701
|
G | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4070-2519C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118018701 | ||||||
| chr1:118018895
|
A | T | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4070-2713T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118018895 | ||||||
| chr1:118018930
|
G | C | 67 | a0003c0003t0001g0064a0003c0003t0001g0076a0003c0003t0001g0078others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.4070-2748C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118018930 | ||||||
| chr1:118018931
|
T | A | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(253): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.4070-2749A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118018931 | ||||||
| chr1:118019028
|
T | C | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4070-2846A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019028 | ||||||
| chr1:118019033
|
C | CA | 30 | a0001c0001t0001g0168a0001c0001t0001g0174a0001c0001t0001g0177others(27): Show | 30 | HG01175.hp1 HG01175.hp2 HG01952.hp2 others(27): Show |
intron_variant | MODIFIER | c.4070-2852dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019033 | ||||||
| chr1:118019033
|
C | CAA | 56 | a0001c0001t0001g0163a0001c0004t0001g0060a0001c0004t0001g0061others(53): Show | 56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.4070-2853_4070-285 others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019033 | ||||||
| chr1:118019033
|
C | CAAA | 35 | a0001c0004t0001g0062a0001c0004t0001g0143a0001c0004t0001g0219others(32): Show | 35 | HG00741.hp1 HG01167.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.4070-2854_4070-285 others(7): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019033 | ||||||
| chr1:118019033
|
CA | C | 10 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(7): Show | 10 | HG01167.hp2 HG01928.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.4070-2852delT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019033 | ||||||
| chr1:118019138
|
G | A | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4070-2956C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019138 | ||||||
| chr1:118019293
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4070-3111T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019293 | ||||||
| chr1:118019348
|
T | A | 1 | a0002c0002t0001g0057 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4070-3166A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019348 | ||||||
| chr1:118019354
|
T | G | 1 | a0001c0001t0001g0149 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.4070-3172A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019354 | ||||||
| chr1:118019422
|
G | A | 1 | a0004c0005t0001g0125 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4070-3240C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019422 | ||||||
| chr1:118019471
|
A | T | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.4070-3289T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019471 | ||||||
| chr1:118019492
|
C | T | 1 | a0002c0002t0001g0057 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4070-3310G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019492 | ||||||
| chr1:118019527
|
G | A | 4 | a0001c0019t0001g0205a0001c0019t0001g0208a0001c0025t0001g0063others(1): Show | 4 | HG01175.hp1 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4070-3345C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019527 | ||||||
| chr1:118019593
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4070-3411G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019593 | ||||||
| chr1:118019766
|
C | A | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4069+3538G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118019766 | ||||||
| chr1:118020131
|
G | C | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4069+3173C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118020131 | ||||||
| chr1:118020271
|
C | A | 62 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(59): Show | 63 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.4069+3033G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118020271 | ||||||
| chr1:118020342
|
G | A | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4069+2962C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118020342 | ||||||
| chr1:118020347
|
T | C | 1 | a0001c0004t0003g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4069+2957A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118020347 | ||||||
| chr1:118020370
|
G | T | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4069+2934C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118020370 | ||||||
| chr1:118020635
|
CA | C | 4 | a0002c0002t0001g0033a0002c0002t0001g0034a0002c0002t0001g0052others(1): Show | 4 | NA18946.hp2 NA18948.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.4069+2668delT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118020635 | ||||||
| chr1:118021202
|
A | G | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4069+2102T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118021202 | ||||||
| chr1:118021524
|
A | G | 3 | a0002c0002t0001g0033a0002c0002t0001g0034a0002c0002t0001g0052 | 3 | NA18946.hp2 NA18948.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.4069+1780T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118021524 | ||||||
| chr1:118021583
|
T | A | 177 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(174): Show | 178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.4069+1721A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118021583 | ||||||
| chr1:118021917
|
C | T | 1 | a0001c0004t0001g0227 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4069+1387G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118021917 | ||||||
| chr1:118021935
|
T | C | 1 | a0001c0006t0001g0153 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4069+1369A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118021935 | ||||||
| chr1:118021937
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4069+1367G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118021937 | ||||||
| chr1:118022048
|
G | T | 59 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(56): Show | 60 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.4069+1256C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118022048 | ||||||
| chr1:118022128
|
C | A | 1 | a0001c0001t0001g0191 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4069+1176G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118022128 | ||||||
| chr1:118022370
|
A | G | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4069+934T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118022370 | ||||||
| chr1:118022432
|
A | AAAAC | 181 | a0001c0001t0001g0174a0001c0001t0001g0181a0001c0004t0001g0060others(178): Show | 182 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.4069+868_4069+871d others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118022432 | ||||||
| chr1:118022516
|
T | C | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.4069+788A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118022516 | ||||||
| chr1:118022577
|
G | T | 1 | a0001c0004t0003g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4069+727C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118022577 | ||||||
| chr1:118022591
|
G | A | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4069+713C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118022591 | ||||||
| chr1:118022809
|
C | T | 5 | a0001c0004t0001g0257a0001c0004t0001g0258a0001c0004t0001g0259others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.4069+495G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118022809 | ||||||
| chr1:118023136
|
G | A | 1 | a0001c0018t0001g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4069+168C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 28/48 | chr1 | 118023136 | ||||||
| chr1:118023994
|
C | G | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3910-531G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 27/48 | chr1 | 118023994 | ||||||
| chr1:118024269
|
C | G | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.3910-806G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 27/48 | chr1 | 118024269 | ||||||
| chr1:118024306
|
C | T | 2 | a0002c0002t0001g0024a0002c0002t0001g0037 | 2 | NA18972.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.3910-843G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 27/48 | chr1 | 118024306 | ||||||
| chr1:118024350
|
C | T | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3910-887G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 27/48 | chr1 | 118024350 | ||||||
| chr1:118024405
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3909+833T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 27/48 | chr1 | 118024405 | ||||||
| chr1:118024500
|
C | T | 4 | a0001c0019t0001g0205a0001c0019t0001g0208a0001c0025t0001g0063others(1): Show | 4 | HG01175.hp1 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3909+738G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 27/48 | chr1 | 118024500 | ||||||
| chr1:118024516
|
T | C | 1 | a0002c0002t0001g0011 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3909+722A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 27/48 | chr1 | 118024516 | ||||||
| chr1:118024694
|
T | C | 62 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(59): Show | 63 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.3909+544A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 27/48 | chr1 | 118024694 | ||||||
| chr1:118024783
|
G | A | 1 | a0003c0003t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3909+455C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 27/48 | chr1 | 118024783 | ||||||
| chr1:118024801
|
A | T | 1 | a0001c0026t0001g0261 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3909+437T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 27/48 | chr1 | 118024801 | ||||||
| chr1:118024863
|
G | C | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3909+375C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 27/48 | chr1 | 118024863 | ||||||
| chr1:118025031
|
T | C | 59 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(56): Show | 60 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.3909+207A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 27/48 | chr1 | 118025031 | ||||||
| chr1:118025161
|
A | C | 1 | a0006c0007t0001g0187 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3909+77T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 27/48 | chr1 | 118025161 | ||||||
| chr1:118025631
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3731-215G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118025631 | ||||||
| chr1:118025641
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3731-225G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118025641 | ||||||
| chr1:118025804
|
C | A | 5 | a0003c0003t0001g0256a0003c0003t0003g0100a0008c0009t0002g0077others(2): Show | 5 | HG02258.hp1 HG03486.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.3731-388G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118025804 | ||||||
| chr1:118026037
|
C | T | 1 | a0001c0004t0001g0234 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3731-621G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118026037 | ||||||
| chr1:118026133
|
AC | A | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3731-718delG | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118026133 | ||||||
| chr1:118026237
|
T | A | 67 | a0003c0003t0001g0064a0003c0003t0001g0076a0003c0003t0001g0078others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.3731-821A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118026237 | ||||||
| chr1:118026359
|
T | A | 1 | a0022c0037t0001g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3731-943A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118026359 | ||||||
| chr1:118026532
|
T | C | 3 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156 | 3 | NA18949.hp2 NA18979.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.3731-1116A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118026532 | ||||||
| chr1:118026975
|
A | G | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3730+1299T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118026975 | ||||||
| chr1:118027420
|
T | C | 1 | a0001c0006t0001g0251 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3730+854A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118027420 | ||||||
| chr1:118027604
|
G | A | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3730+670C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118027604 | ||||||
| chr1:118027660
|
C | A | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3730+614G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118027660 | ||||||
| chr1:118027772
|
T | C | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3730+502A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118027772 | ||||||
| chr1:118027821
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0201 | 2 | NA18941.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.3730+453G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118027821 | ||||||
| chr1:118028204
|
T | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3730+70A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118028204 | ||||||
| chr1:118028213
|
TC | T | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3730+60delG | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118028213 | ||||||
| chr1:118028214
|
C | T | 1 | a0002c0002t0001g0017 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3730+60G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 26/48 | chr1 | 118028214 | ||||||
| chr1:118028466
|
C | A | 62 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(59): Show | 63 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.3610-72G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118028466 | ||||||
| chr1:118028824
|
C | A | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3610-430G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118028824 | ||||||
| chr1:118028989
|
G | A | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3610-595C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118028989 | ||||||
| chr1:118029198
|
T | C | 2 | a0002c0002t0001g0017a0002c0002t0001g0018 | 2 | HG02027.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.3610-804A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118029198 | ||||||
| chr1:118029231
|
T | C | 18 | a0001c0001t0001g0002a0001c0001t0001g0146a0001c0001t0001g0167others(15): Show | 19 | HG00423.hp2 HG00642.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.3610-837A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118029231 | ||||||
| chr1:118029755
|
A | G | 59 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(56): Show | 60 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.3610-1361T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118029755 | ||||||
| chr1:118029780
|
C | T | 3 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0057 | 3 | HG02027.hp2 HG02056.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.3610-1386G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118029780 | ||||||
| chr1:118029795
|
T | C | 1 | a0003c0003t0001g0140 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3610-1401A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118029795 | ||||||
| chr1:118029801
|
T | C | 2 | a0001c0004t0001g0238a0001c0032t0001g0067 | 2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3610-1407A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118029801 | ||||||
| chr1:118029867
|
G | A | 1 | a0008c0009t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3610-1473C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118029867 | ||||||
| chr1:118029887
|
G | A | 5 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(2): Show | 5 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3610-1493C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118029887 | ||||||
| chr1:118030142
|
G | A | 47 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(44): Show | 47 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.3609+1550C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118030142 | ||||||
| chr1:118030416
|
T | C | 3 | a0011c0014t0001g0008a0011c0014t0001g0009a0017c0034t0001g0053 | 3 | HG02572.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3609+1276A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118030416 | ||||||
| chr1:118030420
|
A | G | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3609+1272T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118030420 | ||||||
| chr1:118030531
|
G | A | 2 | a0003c0003t0001g0087a0003c0003t0001g0089 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3609+1161C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118030531 | ||||||
| chr1:118030599
|
A | T | 2 | a0005c0020t0002g0157a0005c0020t0002g0197 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.3609+1093T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118030599 | ||||||
| chr1:118030676
|
A | G | 196 | a0001c0001t0001g0174a0001c0001t0001g0181a0001c0004t0001g0060others(193): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.3609+1016T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118030676 | ||||||
| chr1:118030805
|
T | C | 2 | a0001c0006t0001g0151a0001c0006t0001g0152 | 2 | HG01346.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3609+887A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118030805 | ||||||
| chr1:118031076
|
C | T | 1 | a0010c0013t0001g0132 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3609+616G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118031076 | ||||||
| chr1:118031119
|
A | AGT | 6 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0004t0001g0060others(3): Show | 6 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.3609+571_3609+572d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118031119 | ||||||
| chr1:118031177
|
C | CT | 31 | a0001c0001t0001g0210a0001c0001t0001g0214a0001c0004t0001g0219others(28): Show | 31 | HG00735.hp2 HG00741.hp1 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.3609+514dupA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118031177 | ||||||
| chr1:118031177
|
CT | C | 31 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162others(28): Show | 31 | HG00323.hp1 HG00438.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.3609+514delA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118031177 | ||||||
| chr1:118031313
|
A | G | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3609+379T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118031313 | ||||||
| chr1:118031452
|
A | G | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3609+240T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118031452 | ||||||
| chr1:118031586
|
T | G | 1 | a0001c0004t0003g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3609+106A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 25/48 | chr1 | 118031586 | ||||||
| chr1:118031926
|
G | A | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3434-59C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118031926 | ||||||
| chr1:118031990
|
A | G | 1 | a0004c0005t0001g0244 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.3434-123T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118031990 | ||||||
| chr1:118032479
|
T | C | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3434-612A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118032479 | ||||||
| chr1:118032554
|
C | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(63): Show | 68 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.3434-687G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118032554 | ||||||
| chr1:118032716
|
T | C | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3434-849A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118032716 | ||||||
| chr1:118032782
|
C | T | 3 | a0011c0014t0001g0008a0011c0014t0001g0009a0017c0034t0001g0053 | 3 | HG02572.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3434-915G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118032782 | ||||||
| chr1:118032837
|
G | A | 6 | a0001c0001t0001g0003a0002c0002t0001g0026a0006c0007t0001g0187others(3): Show | 7 | HG01358.hp2 HG01433.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.3434-970C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118032837 | ||||||
| chr1:118032930
|
G | T | 1 | a0004c0005t0001g0091 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3434-1063C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118032930 | ||||||
| chr1:118033105
|
A | G | 1 | a0003c0029t0001g0141 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3434-1238T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118033105 | ||||||
| chr1:118033134
|
T | C | 162 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(159): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.3434-1267A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118033134 | ||||||
| chr1:118033636
|
T | G | 1 | a0001c0001t0001g0196 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3434-1769A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118033636 | ||||||
| chr1:118033733
|
C | T | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3434-1866G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118033733 | ||||||
| chr1:118033750
|
C | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3434-1883G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118033750 | ||||||
| chr1:118033915
|
T | C | 1 | a0004c0005t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3434-2048A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118033915 | ||||||
| chr1:118034004
|
A | T | 67 | a0003c0003t0001g0064a0003c0003t0001g0076a0003c0003t0001g0078others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.3434-2137T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118034004 | ||||||
| chr1:118034021
|
G | A | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.3434-2154C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118034021 | ||||||
| chr1:118034207
|
T | C | 7 | a0002c0002t0001g0025a0002c0002t0001g0026a0002c0002t0001g0027others(4): Show | 7 | HG02071.hp1 HG02135.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.3434-2340A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118034207 | ||||||
| chr1:118034444
|
G | T | 162 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(159): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.3433+2326C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118034444 | ||||||
| chr1:118034504
|
A | C | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3433+2266T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118034504 | ||||||
| chr1:118034608
|
G | T | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3433+2162C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118034608 | ||||||
| chr1:118034621
|
C | G | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3433+2149G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118034621 | ||||||
| chr1:118034692
|
C | G | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3433+2078G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118034692 | ||||||
| chr1:118034792
|
T | C | 1 | a0006c0007t0001g0190 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3433+1978A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118034792 | ||||||
| chr1:118034812
|
G | C | 2 | a0001c0004t0001g0225a0001c0004t0001g0237 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3433+1958C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118034812 | ||||||
| chr1:118034968
|
A | T | 1 | a0002c0002t0001g0055 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3433+1802T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118034968 | ||||||
| chr1:118035091
|
A | G | 18 | a0001c0004t0001g0219a0001c0004t0001g0225a0001c0004t0001g0226others(15): Show | 18 | HG00741.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.3433+1679T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118035091 | ||||||
| chr1:118035220
|
C | T | 1 | a0010c0013t0001g0135 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3433+1550G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118035220 | ||||||
| chr1:118035232
|
T | C | 1 | a0004c0005t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3433+1538A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118035232 | ||||||
| chr1:118035322
|
A | G | 3 | a0009c0012t0001g0245a0009c0012t0001g0246a0009c0012t0001g0247 | 3 | NA18949.hp1 NA18973.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.3433+1448T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118035322 | ||||||
| chr1:118035336
|
T | C | 1 | a0008c0009t0002g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3433+1434A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118035336 | ||||||
| chr1:118035518
|
A | C | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3433+1252T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118035518 | ||||||
| chr1:118035803
|
G | A | 1 | a0019c0028t0001g0117 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3433+967C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118035803 | ||||||
| chr1:118035822
|
T | C | 1 | a0020c0030t0001g0138 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3433+948A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118035822 | ||||||
| chr1:118035886
|
T | C | 3 | a0011c0014t0001g0008a0011c0014t0001g0009a0017c0034t0001g0053 | 3 | HG02572.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3433+884A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118035886 | ||||||
| chr1:118035925
|
G | C | 3 | a0011c0014t0001g0008a0011c0014t0001g0009a0017c0034t0001g0053 | 3 | HG02572.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3433+845C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118035925 | ||||||
| chr1:118035982
|
C | T | 1 | a0001c0004t0003g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3433+788G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118035982 | ||||||
| chr1:118036252
|
G | A | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3433+518C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118036252 | ||||||
| chr1:118036319
|
C | T | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.3433+451G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118036319 | ||||||
| chr1:118036352
|
G | A | 3 | a0011c0014t0001g0008a0011c0014t0001g0009a0017c0034t0001g0053 | 3 | HG02572.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3433+418C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118036352 | ||||||
| chr1:118036364
|
A | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3433+406T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118036364 | ||||||
| chr1:118036368
|
T | TA | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3433+401dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118036368 | ||||||
| chr1:118036470
|
T | C | 2 | a0001c0004t0001g0225a0001c0004t0001g0237 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3433+300A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118036470 | ||||||
| chr1:118036539
|
T | G | 2 | a0014c0016t0002g0085a0014c0016t0002g0228 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3433+231A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118036539 | ||||||
| chr1:118036547
|
T | TTGTA | 160 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(157): Show | 161 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.3433+219_3433+222d others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118036547 | ||||||
| chr1:118036567
|
T | TTA | 2 | a0001c0001t0001g0169a0001c0026t0001g0261 | 2 | HG02071.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3433+201_3433+202d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118036567 | ||||||
| chr1:118036601
|
G | GAC | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(67): Show | 72 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.3433+167_3433+168d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 24/48 | chr1 | 118036601 | ||||||
| chr1:118037022
|
A | T | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.3320-139T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118037022 | ||||||
| chr1:118037161
|
A | G | 1 | a0001c0010t0001g0150 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3320-278T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118037161 | ||||||
| chr1:118037232
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3320-349A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118037232 | ||||||
| chr1:118037233
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3320-350G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118037233 | ||||||
| chr1:118037360
|
A | G | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3320-477T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118037360 | ||||||
| chr1:118037432
|
C | T | 3 | a0011c0014t0001g0008a0011c0014t0001g0009a0017c0034t0001g0053 | 3 | HG02572.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3320-549G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118037432 | ||||||
| chr1:118037506
|
C | T | 1 | a0004c0005t0001g0243 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3320-623G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118037506 | ||||||
| chr1:118037682
|
T | G | 6 | a0001c0004t0001g0226a0001c0004t0001g0227a0001c0004t0001g0230others(3): Show | 6 | HG00741.hp1 HG02630.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3320-799A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118037682 | ||||||
| chr1:118037688
|
G | A | 2 | a0003c0003t0001g0105a0019c0028t0001g0117 | 2 | HG01255.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.3320-805C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118037688 | ||||||
| chr1:118037742
|
A | G | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3320-859T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118037742 | ||||||
| chr1:118038012
|
A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(255): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.3320-1129T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118038012 | ||||||
| chr1:118038120
|
T | C | 4 | a0001c0006t0001g0252a0001c0006t0001g0253a0001c0006t0001g0255others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3319+1172A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118038120 | ||||||
| chr1:118038264
|
T | A | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3319+1028A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118038264 | ||||||
| chr1:118038344
|
A | G | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3319+948T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118038344 | ||||||
| chr1:118038484
|
C | A | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3319+808G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118038484 | ||||||
| chr1:118038509
|
G | C | 11 | a0001c0006t0001g0151a0001c0006t0001g0152a0001c0006t0001g0153others(8): Show | 11 | HG00280.hp2 HG00621.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.3319+783C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118038509 | ||||||
| chr1:118038756
|
C | T | 162 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(159): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.3319+536G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118038756 | ||||||
| chr1:118038858
|
A | G | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3319+434T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118038858 | ||||||
| chr1:118038994
|
A | G | 162 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(159): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.3319+298T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118038994 | ||||||
| chr1:118039013
|
G | A | 67 | a0003c0003t0001g0064a0003c0003t0001g0076a0003c0003t0001g0078others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.3319+279C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118039013 | ||||||
| chr1:118039027
|
G | A | 2 | a0002c0002t0001g0012a0002c0002t0001g0013 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.3319+265C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118039027 | ||||||
| chr1:118039214
|
G | A | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3319+78C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 23/48 | chr1 | 118039214 | ||||||
| chr1:118039563
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3167-119G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 22/48 | chr1 | 118039563 | ||||||
| chr1:118039673
|
C | A | 1 | a0003c0003t0001g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3167-229G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 22/48 | chr1 | 118039673 | ||||||
| chr1:118039681
|
C | T | 1 | a0001c0004t0001g0230 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3167-237G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 22/48 | chr1 | 118039681 | ||||||
| chr1:118039803
|
A | C | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.3167-359T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 22/48 | chr1 | 118039803 | ||||||
| chr1:118039860
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3167-416G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 22/48 | chr1 | 118039860 | ||||||
| chr1:118039923
|
G | A | 67 | a0003c0003t0001g0064a0003c0003t0001g0076a0003c0003t0001g0078others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.3167-479C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 22/48 | chr1 | 118039923 | ||||||
| chr1:118040641
|
G | A | 5 | a0001c0001t0001g0149a0001c0001t0001g0201a0009c0012t0001g0245others(2): Show | 5 | NA18941.hp1 NA18949.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.3166+89C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 22/48 | chr1 | 118040641 | ||||||
| chr1:118040862
|
C | T | 1 | a0002c0002t0001g0028 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3055-21G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 21/48 | chr1 | 118040862 | ||||||
| chr1:118041231
|
T | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3055-390A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 21/48 | chr1 | 118041231 | ||||||
| chr1:118041291
|
T | G | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3055-450A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 21/48 | chr1 | 118041291 | ||||||
| chr1:118041370
|
G | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3054+433C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 21/48 | chr1 | 118041370 | ||||||
| chr1:118041462
|
C | T | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3054+341G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 21/48 | chr1 | 118041462 | ||||||
| chr1:118041713
|
T | A | 1 | a0001c0001t0001g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3054+90A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 21/48 | chr1 | 118041713 | ||||||
| chr1:118042209
|
T | G | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2815-167A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118042209 | ||||||
| chr1:118042606
|
G | A | 4 | a0001c0004t0001g0257a0001c0004t0001g0258a0001c0004t0001g0259others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2815-564C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118042606 | ||||||
| chr1:118042756
|
T | C | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2815-714A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118042756 | ||||||
| chr1:118043133
|
T | TTAAAAGC others(1912): Show |
1 | a0003c0003t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2815-1092_2815-109 others(1923): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118043133 | ||||||
| chr1:118043222
|
G | C | 1 | a0001c0004t0001g0235 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2815-1180C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118043222 | ||||||
| chr1:118043233
|
A | G | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2815-1191T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118043233 | ||||||
| chr1:118043337
|
C | T | 4 | a0001c0006t0001g0252a0001c0006t0001g0253a0001c0006t0001g0255others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2815-1295G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118043337 | ||||||
| chr1:118043341
|
G | C | 1 | a0008c0009t0002g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2815-1299C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118043341 | ||||||
| chr1:118043523
|
A | G | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2815-1481T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118043523 | ||||||
| chr1:118043560
|
C | T | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2815-1518G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118043560 | ||||||
| chr1:118043680
|
C | T | 2 | a0003c0003t0001g0112a0003c0003t0001g0118 | 2 | HG02015.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2815-1638G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118043680 | ||||||
| chr1:118043726
|
A | G | 5 | a0003c0003t0001g0256a0003c0003t0003g0100a0008c0009t0002g0077others(2): Show | 5 | HG02258.hp1 HG03486.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2815-1684T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118043726 | ||||||
| chr1:118043781
|
G | A | 1 | a0003c0003t0001g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2815-1739C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118043781 | ||||||
| chr1:118043832
|
A | C | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2815-1790T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118043832 | ||||||
| chr1:118043880
|
T | C | 1 | a0001c0001t0001g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2815-1838A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118043880 | ||||||
| chr1:118044134
|
G | T | 1 | a0003c0003t0001g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2815-2092C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118044134 | ||||||
| chr1:118044206
|
T | G | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2815-2164A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118044206 | ||||||
| chr1:118044282
|
C | T | 70 | a0003c0003t0001g0064a0003c0003t0001g0076a0003c0003t0001g0078others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.2815-2240G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118044282 | ||||||
| chr1:118044433
|
C | T | 1 | a0003c0003t0001g0140 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2815-2391G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118044433 | ||||||
| chr1:118044509
|
A | G | 2 | a0003c0003t0001g0076a0003c0003t0001g0078 | 2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2815-2467T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118044509 | ||||||
| chr1:118044996
|
A | G | 4 | a0002c0002t0001g0033a0002c0002t0001g0034a0002c0002t0001g0052others(1): Show | 4 | NA18946.hp2 NA18948.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.2815-2954T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118044996 | ||||||
| chr1:118045014
|
G | A | 1 | a0028c0040t0001g0122 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2815-2972C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118045014 | ||||||
| chr1:118045256
|
T | A | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2815-3214A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118045256 | ||||||
| chr1:118045376
|
C | A | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2815-3334G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118045376 | ||||||
| chr1:118045726
|
T | C | 70 | a0003c0003t0001g0064a0003c0003t0001g0076a0003c0003t0001g0078others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.2815-3684A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118045726 | ||||||
| chr1:118045814
|
T | G | 1 | a0001c0001t0001g0199 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2815-3772A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118045814 | ||||||
| chr1:118046030
|
T | C | 53 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2815-3988A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118046030 | ||||||
| chr1:118046168
|
CT | C | 7 | a0004c0005t0001g0242a0004c0005t0001g0243a0004c0005t0001g0244others(4): Show | 7 | HG00423.hp1 HG00597.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.2815-4127delA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118046168 | ||||||
| chr1:118046475
|
T | C | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2815-4433A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118046475 | ||||||
| chr1:118046607
|
A | C | 2 | a0001c0018t0001g0148a0001c0018t0001g0229 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2815-4565T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118046607 | ||||||
| chr1:118046651
|
A | G | 26 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(23): Show | 26 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.2815-4609T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118046651 | ||||||
| chr1:118046677
|
G | A | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2815-4635C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118046677 | ||||||
| chr1:118046768
|
C | A | 1 | a0005c0038t0002g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2815-4726G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118046768 | ||||||
| chr1:118046829
|
A | G | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2815-4787T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118046829 | ||||||
| chr1:118047210
|
A | C | 1 | a0003c0003t0001g0129 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2815-5168T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118047210 | ||||||
| chr1:118047214
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2815-5172G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118047214 | ||||||
| chr1:118048554
|
C | T | 59 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(56): Show | 60 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.2814+5448G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118048554 | ||||||
| chr1:118048582
|
C | A | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2814+5420G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118048582 | ||||||
| chr1:118048619
|
C | T | 1 | a0003c0003t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2814+5383G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118048619 | ||||||
| chr1:118048685
|
C | T | 1 | a0002c0002t0001g0010 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2814+5317G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118048685 | ||||||
| chr1:118048694
|
G | A | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2814+5308C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118048694 | ||||||
| chr1:118048778
|
T | A | 1 | a0003c0003t0001g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2814+5224A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118048778 | ||||||
| chr1:118048942
|
C | T | 4 | a0001c0004t0001g0226a0001c0004t0001g0227a0001c0004t0001g0231others(1): Show | 4 | HG02630.hp2 HG02976.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2814+5060G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118048942 | ||||||
| chr1:118048975
|
C | T | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2814+5027G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118048975 | ||||||
| chr1:118049061
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2814+4941T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118049061 | ||||||
| chr1:118049328
|
A | G | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2814+4674T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118049328 | ||||||
| chr1:118049476
|
T | C | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2814+4526A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118049476 | ||||||
| chr1:118049507
|
C | T | 2 | a0001c0001t0001g0171a0018c0031t0002g0007 | 2 | HG03017.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2814+4495G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118049507 | ||||||
| chr1:118049543
|
C | T | 25 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(22): Show | 25 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2814+4459G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118049543 | ||||||
| chr1:118049553
|
G | A | 1 | a0002c0002t0001g0057 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2814+4449C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118049553 | ||||||
| chr1:118049604
|
G | A | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2814+4398C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118049604 | ||||||
| chr1:118049620
|
A | G | 1 | a0002c0002t0001g0020 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2814+4382T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118049620 | ||||||
| chr1:118049670
|
G | A | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(255): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.2814+4332C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118049670 | ||||||
| chr1:118049882
|
G | A | 60 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(57): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2814+4120C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118049882 | ||||||
| chr1:118049964
|
C | T | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2814+4038G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118049964 | ||||||
| chr1:118050078
|
C | T | 4 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(1): Show | 4 | HG01433.hp2 HG03098.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2814+3924G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050078 | ||||||
| chr1:118050114
|
T | C | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2814+3888A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050114 | ||||||
| chr1:118050538
|
G | A | 1 | a0004c0005t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2814+3464C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050538 | ||||||
| chr1:118050539
|
G | C | 1 | a0004c0005t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2814+3463C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050539 | ||||||
| chr1:118050540
|
C | A | 1 | a0004c0005t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2814+3462G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050540 | ||||||
| chr1:118050541
|
A | C | 1 | a0004c0005t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2814+3461T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050541 | ||||||
| chr1:118050544
|
A | G | 1 | a0004c0005t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2814+3458T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050544 | ||||||
| chr1:118050546
|
C | T | 1 | a0004c0005t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2814+3456G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050546 | ||||||
| chr1:118050547
|
A | C | 1 | a0004c0005t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2814+3455T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050547 | ||||||
| chr1:118050548
|
C | G | 1 | a0004c0005t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2814+3454G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050548 | ||||||
| chr1:118050549
|
A | C | 1 | a0004c0005t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2814+3453T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050549 | ||||||
| chr1:118050551
|
A | T | 1 | a0004c0005t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2814+3451T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050551 | ||||||
| chr1:118050553
|
A | T | 1 | a0004c0005t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2814+3449T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050553 | ||||||
| chr1:118050759
|
A | T | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2814+3243T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050759 | ||||||
| chr1:118050787
|
CTTACTAG others(168): Show |
C | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2814+3040_2814+321 others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050787 | ||||||
| chr1:118050894
|
G | A | 2 | a0014c0016t0002g0085a0014c0016t0002g0228 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2814+3108C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118050894 | ||||||
| chr1:118051065
|
T | C | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2814+2937A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051065 | ||||||
| chr1:118051170
|
A | G | 6 | a0002c0002t0001g0001a0002c0002t0001g0019a0002c0002t0001g0020others(3): Show | 7 | HG00735.hp2 HG01346.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2814+2832T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051170 | ||||||
| chr1:118051219
|
C | T | 2 | a0003c0003t0001g0101a0003c0003t0001g0134 | 2 | HG02056.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.2814+2783G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051219 | ||||||
| chr1:118051318
|
T | C | 3 | a0011c0014t0001g0008a0011c0014t0001g0009a0017c0034t0001g0053 | 3 | HG02572.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2814+2684A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051318 | ||||||
| chr1:118051359
|
A | C | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2814+2643T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051359 | ||||||
| chr1:118051360
|
T | C | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2814+2642A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051360 | ||||||
| chr1:118051544
|
T | TACACACA others(1): Show |
161 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(158): Show | 162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2814+2450_2814+245 others(12): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051544 | ||||||
| chr1:118051544
|
T | TACACACA others(3): Show |
5 | a0003c0003t0001g0064a0007c0017t0001g0015a0007c0017t0001g0016others(2): Show | 5 | HG02109.hp1 HG02572.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2814+2448_2814+245 others(14): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051544 | ||||||
| chr1:118051544
|
T | TACACACA others(5): Show |
1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2814+2446_2814+245 others(16): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051544 | ||||||
| chr1:118051595
|
A | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG00735.hp1 HG03490.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2814+2407T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051595 | ||||||
| chr1:118051692
|
GTATGTAT others(5): Show |
G | 1 | a0004c0005t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2814+2298_2814+230 others(16): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051692 | ||||||
| chr1:118051702
|
TTATAA | T | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2814+2295_2814+229 others(9): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051702 | ||||||
| chr1:118051714
|
G | A | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2814+2288C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051714 | ||||||
| chr1:118051715
|
T | G | 1 | a0004c0005t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2814+2287A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051715 | ||||||
| chr1:118051785
|
AATATATA others(336): Show |
A | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2814+1874_2814+221 others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051785 | ||||||
| chr1:118051915
|
A | G | 2 | a0001c0004t0001g0225a0001c0004t0001g0237 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2814+2087T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051915 | ||||||
| chr1:118051925
|
TTATAA | T | 2 | a0001c0018t0001g0148a0001c0018t0001g0229 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2814+2072_2814+207 others(9): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051925 | ||||||
| chr1:118051941
|
A | T | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2814+2061T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118051941 | ||||||
| chr1:118052122
|
T | C | 1 | a0019c0028t0001g0117 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2814+1880A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118052122 | ||||||
| chr1:118052138
|
C | G | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2814+1864G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118052138 | ||||||
| chr1:118052201
|
T | G | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2814+1801A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118052201 | ||||||
| chr1:118052271
|
C | A | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2814+1731G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118052271 | ||||||
| chr1:118052636
|
C | T | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2814+1366G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118052636 | ||||||
| chr1:118052667
|
A | G | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2814+1335T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118052667 | ||||||
| chr1:118052816
|
C | A | 2 | a0007c0017t0001g0015a0007c0017t0001g0016 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2814+1186G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118052816 | ||||||
| chr1:118053432
|
A | G | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2814+570T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118053432 | ||||||
| chr1:118053599
|
T | C | 2 | a0002c0002t0001g0041a0002c0002t0001g0042 | 2 | NA19064.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2814+403A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118053599 | ||||||
| chr1:118053648
|
A | G | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2814+354T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118053648 | ||||||
| chr1:118053669
|
A | C | 3 | a0002c0002t0001g0032a0002c0002t0001g0058a0002c0002t0001g0059 | 3 | NA18973.hp2 NA19079.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2814+333T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118053669 | ||||||
| chr1:118053869
|
C | G | 3 | a0011c0014t0001g0008a0011c0014t0001g0009a0017c0034t0001g0053 | 3 | HG02572.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2814+133G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 20/48 | chr1 | 118053869 | ||||||
| chr1:118054145
|
A | G | 2 | a0001c0004t0001g0225a0001c0004t0001g0237 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2723-52T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 19/48 | chr1 | 118054145 | ||||||
| chr1:118054353
|
G | GTC | 25 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(22): Show | 25 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2723-262_2723-261d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 19/48 | chr1 | 118054353 | ||||||
| chr1:118054498
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2723-405G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 19/48 | chr1 | 118054498 | ||||||
| chr1:118054615
|
G | T | 2 | a0002c0002t0001g0012a0002c0002t0001g0013 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2723-522C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 19/48 | chr1 | 118054615 | ||||||
| chr1:118054698
|
T | A | 4 | a0003c0003t0001g0129a0011c0014t0001g0008a0011c0014t0001g0009others(1): Show | 4 | HG02572.hp1 HG03139.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.2723-605A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 19/48 | chr1 | 118054698 | ||||||
| chr1:118054931
|
C | T | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2722+802G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 19/48 | chr1 | 118054931 | ||||||
| chr1:118054932
|
G | A | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2722+801C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 19/48 | chr1 | 118054932 | ||||||
| chr1:118055003
|
C | T | 60 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(57): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2722+730G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 19/48 | chr1 | 118055003 | ||||||
| chr1:118055054
|
A | T | 60 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(57): Show | 61 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2722+679T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 19/48 | chr1 | 118055054 | ||||||
| chr1:118055451
|
G | A | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2722+282C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 19/48 | chr1 | 118055451 | ||||||
| chr1:118056115
|
C | T | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2541-201G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118056115 | ||||||
| chr1:118056178
|
A | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2541-264T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118056178 | ||||||
| chr1:118056278
|
T | C | 1 | a0002c0002t0001g0054 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2541-364A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118056278 | ||||||
| chr1:118056327
|
T | C | 29 | a0001c0001t0001g0178a0001c0004t0003g0082a0003c0003t0001g0064others(26): Show | 29 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.2541-413A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118056327 | ||||||
| chr1:118056341
|
A | G | 1 | a0003c0003t0001g0140 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2541-427T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118056341 | ||||||
| chr1:118056498
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2541-584A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118056498 | ||||||
| chr1:118056503
|
C | T | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2541-589G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118056503 | ||||||
| chr1:118056514
|
T | A | 25 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(22): Show | 25 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2541-600A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118056514 | ||||||
| chr1:118056695
|
T | C | 2 | a0001c0018t0001g0148a0001c0018t0001g0229 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2541-781A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118056695 | ||||||
| chr1:118056920
|
A | G | 72 | a0001c0001t0001g0178a0001c0004t0003g0082a0003c0003t0001g0064others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.2541-1006T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118056920 | ||||||
| chr1:118056980
|
C | CT | 5 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(2): Show | 5 | HG02615.hp2 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2541-1067dupA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118056980 | ||||||
| chr1:118057062
|
C | T | 3 | a0002c0002t0001g0033a0002c0002t0001g0034a0002c0002t0001g0052 | 3 | NA18946.hp2 NA18948.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.2541-1148G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118057062 | ||||||
| chr1:118057383
|
T | C | 63 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(60): Show | 64 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.2541-1469A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118057383 | ||||||
| chr1:118057470
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2541-1556C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118057470 | ||||||
| chr1:118057844
|
AT | A | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2541-1931delA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118057844 | ||||||
| chr1:118057939
|
C | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2541-2025G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118057939 | ||||||
| chr1:118058119
|
G | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2541-2205C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118058119 | ||||||
| chr1:118058160
|
T | C | 1 | a0005c0011t0002g0202 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2541-2246A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118058160 | ||||||
| chr1:118058281
|
C | T | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2541-2367G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118058281 | ||||||
| chr1:118058397
|
A | C | 1 | a0001c0001t0001g0168 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2541-2483T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118058397 | ||||||
| chr1:118058482
|
TAGGCATG others(11): Show |
T | 2 | a0007c0017t0001g0015a0007c0017t0001g0016 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2541-2586_2541-256 others(22): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118058482 | ||||||
| chr1:118058744
|
C | T | 2 | a0001c0004t0001g0225a0001c0004t0001g0237 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2541-2830G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118058744 | ||||||
| chr1:118058795
|
G | A | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2541-2881C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118058795 | ||||||
| chr1:118059074
|
G | A | 1 | a0002c0002t0001g0030 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2541-3160C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118059074 | ||||||
| chr1:118059395
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2541-3481A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118059395 | ||||||
| chr1:118059464
|
A | G | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2541-3550T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118059464 | ||||||
| chr1:118059570
|
T | C | 75 | a0001c0004t0003g0082a0003c0003t0001g0064a0003c0003t0001g0076others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.2541-3656A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118059570 | ||||||
| chr1:118059611
|
G | T | 1 | a0004c0005t0001g0096 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2541-3697C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118059611 | ||||||
| chr1:118059669
|
T | C | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2541-3755A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118059669 | ||||||
| chr1:118059859
|
A | C | 1 | a0005c0011t0002g0202 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2541-3945T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118059859 | ||||||
| chr1:118059881
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2541-3967A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118059881 | ||||||
| chr1:118060095
|
T | C | 1 | a0004c0005t0001g0249 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2541-4181A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118060095 | ||||||
| chr1:118060663
|
T | C | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2541-4749A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118060663 | ||||||
| chr1:118060738
|
G | A | 1 | a0002c0002t0001g0050 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2541-4824C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118060738 | ||||||
| chr1:118060874
|
T | G | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2541-4960A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118060874 | ||||||
| chr1:118060986
|
A | G | 1 | a0003c0003t0001g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2541-5072T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118060986 | ||||||
| chr1:118061131
|
G | A | 1 | a0003c0003t0001g0113 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2541-5217C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118061131 | ||||||
| chr1:118061209
|
G | A | 63 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(60): Show | 64 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.2541-5295C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118061209 | ||||||
| chr1:118061303
|
A | C | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2541-5389T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118061303 | ||||||
| chr1:118061316
|
T | C | 2 | a0003c0003t0001g0092a0003c0003t0001g0099 | 2 | NA18948.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2541-5402A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118061316 | ||||||
| chr1:118061378
|
C | T | 23 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(20): Show | 23 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2540+5367G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118061378 | ||||||
| chr1:118061625
|
T | C | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2540+5120A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118061625 | ||||||
| chr1:118061712
|
A | G | 1 | a0002c0002t0001g0010 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2540+5033T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118061712 | ||||||
| chr1:118061931
|
A | C | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2540+4814T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118061931 | ||||||
| chr1:118061935
|
G | T | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2540+4810C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118061935 | ||||||
| chr1:118062005
|
T | A | 25 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(22): Show | 25 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2540+4740A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062005 | ||||||
| chr1:118062097
|
GT | G | 6 | a0002c0002t0001g0001a0002c0002t0001g0019a0002c0002t0001g0020others(3): Show | 7 | HG00735.hp2 HG01346.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2540+4647delA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062097 | ||||||
| chr1:118062292
|
G | A | 1 | a0004c0005t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2540+4453C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062292 | ||||||
| chr1:118062337
|
A | G | 56 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2540+4408T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062337 | ||||||
| chr1:118062340
|
C | T | 1 | a0001c0004t0001g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2540+4405G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062340 | ||||||
| chr1:118062347
|
A | G | 3 | a0011c0014t0001g0008a0011c0014t0001g0009a0017c0034t0001g0053 | 3 | HG02572.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2540+4398T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062347 | ||||||
| chr1:118062361
|
C | T | 1 | a0004c0005t0001g0119 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2540+4384G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062361 | ||||||
| chr1:118062362
|
A | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(256): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.2540+4383T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062362 | ||||||
| chr1:118062366
|
C | CA | 8 | a0001c0001t0001g0174a0001c0001t0001g0195a0001c0001t0001g0203others(5): Show | 8 | HG00621.hp1 HG01175.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2540+4378dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062366 | ||||||
| chr1:118062366
|
C | CAAAAAAA others(1): Show |
43 | a0001c0010t0001g0156a0002c0002t0001g0010a0002c0002t0001g0011others(40): Show | 43 | HG00597.hp1 HG00597.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2540+4371_2540+437 others(12): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062366 | ||||||
| chr1:118062366
|
C | CAAAAAAA others(2): Show |
61 | a0001c0004t0001g0060a0001c0004t0003g0082a0001c0010t0001g0150others(58): Show | 61 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.2540+4370_2540+437 others(13): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062366 | ||||||
| chr1:118062366
|
C | CAAAAAAA others(3): Show |
22 | a0001c0004t0001g0061a0001c0004t0001g0234a0002c0002t0001g0001others(19): Show | 23 | HG00733.hp2 HG01099.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.2540+4369_2540+437 others(14): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062366 | ||||||
| chr1:118062366
|
C | CAAAAAAA others(4): Show |
8 | a0001c0004t0001g0062a0001c0004t0001g0219a0001c0004t0001g0233others(5): Show | 8 | HG00323.hp1 HG00741.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2540+4368_2540+437 others(15): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062366 | ||||||
| chr1:118062366
|
C | CAAAAAAA others(5): Show |
13 | a0001c0004t0001g0143a0001c0004t0001g0223a0001c0004t0001g0225others(10): Show | 13 | HG00741.hp1 HG01433.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2540+4367_2540+437 others(16): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062366 | ||||||
| chr1:118062366
|
C | CAAAAAAA others(6): Show |
11 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0232others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2540+4366_2540+437 others(17): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062366 | ||||||
| chr1:118062366
|
C | CAAAAAAA others(7): Show |
3 | a0001c0004t0001g0224a0001c0006t0001g0236a0001c0027t0001g0221 | 3 | HG02615.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2540+4365_2540+437 others(18): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062366 | ||||||
| chr1:118062366
|
C | CAAAAAAA others(12): Show |
1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2540+4360_2540+437 others(23): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062366 | ||||||
| chr1:118062728
|
C | T | 14 | a0001c0001t0001g0145a0001c0001t0001g0159a0001c0001t0001g0160others(11): Show | 14 | HG00323.hp2 HG00438.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.2540+4017G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062728 | ||||||
| chr1:118062770
|
C | T | 2 | a0007c0017t0001g0015a0007c0017t0001g0016 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2540+3975G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062770 | ||||||
| chr1:118062771
|
A | C | 165 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(162): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.2540+3974T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062771 | ||||||
| chr1:118062775
|
C | T | 1 | a0003c0003t0001g0115 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2540+3970G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118062775 | ||||||
| chr1:118063054
|
A | C | 1 | a0004c0005t0001g0243 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2540+3691T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118063054 | ||||||
| chr1:118063277
|
G | A | 3 | a0011c0014t0001g0008a0011c0014t0001g0009a0017c0034t0001g0053 | 3 | HG02572.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2540+3468C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118063277 | ||||||
| chr1:118063306
|
G | A | 2 | a0001c0025t0001g0063a0021c0024t0001g0006 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2540+3439C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118063306 | ||||||
| chr1:118063386
|
G | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2540+3359C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118063386 | ||||||
| chr1:118064063
|
C | G | 3 | a0011c0014t0001g0008a0011c0014t0001g0009a0017c0034t0001g0053 | 3 | HG02572.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2540+2682G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118064063 | ||||||
| chr1:118064189
|
G | A | 1 | a0003c0003t0001g0115 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2540+2556C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118064189 | ||||||
| chr1:118064287
|
G | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2540+2458C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118064287 | ||||||
| chr1:118064300
|
G | A | 4 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2540+2445C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118064300 | ||||||
| chr1:118064417
|
A | T | 1 | a0002c0002t0001g0019 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2540+2328T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118064417 | ||||||
| chr1:118064491
|
G | A | 63 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(60): Show | 64 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.2540+2254C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118064491 | ||||||
| chr1:118064601
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0203 | 2 | HG01175.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2540+2144C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118064601 | ||||||
| chr1:118064749
|
AAAAATAA others(3): Show |
A | 1 | a0002c0002t0001g0011 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2540+1986_2540+199 others(14): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118064749 | ||||||
| chr1:118064823
|
A | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0167a0001c0001t0001g0170others(11): Show | 15 | HG00642.hp2 HG00738.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.2540+1922T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118064823 | ||||||
| chr1:118065026
|
A | C | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2540+1719T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118065026 | ||||||
| chr1:118065029
|
A | C | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2540+1716T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118065029 | ||||||
| chr1:118065127
|
C | T | 7 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(4): Show | 7 | HG01433.hp2 HG02055.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2540+1618G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118065127 | ||||||
| chr1:118065147
|
C | T | 1 | a0004c0005t0001g0244 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2540+1598G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118065147 | ||||||
| chr1:118065310
|
C | T | 2 | a0014c0016t0002g0085a0014c0016t0002g0228 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2540+1435G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118065310 | ||||||
| chr1:118065437
|
A | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2540+1308T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118065437 | ||||||
| chr1:118065731
|
C | A | 2 | a0001c0004t0001g0060a0001c0004t0001g0061 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2540+1014G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118065731 | ||||||
| chr1:118065772
|
C | T | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2540+973G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118065772 | ||||||
| chr1:118065808
|
A | G | 2 | a0001c0025t0001g0063a0021c0024t0001g0006 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2540+937T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118065808 | ||||||
| chr1:118065811
|
T | C | 2 | a0004c0005t0001g0119a0004c0005t0001g0120 | 2 | HG00323.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.2540+934A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118065811 | ||||||
| chr1:118065950
|
T | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2540+795A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118065950 | ||||||
| chr1:118066095
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2540+650G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118066095 | ||||||
| chr1:118066209
|
AAT | A | 53 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2540+534_2540+535d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118066209 | ||||||
| chr1:118066442
|
T | C | 2 | a0001c0018t0001g0148a0001c0018t0001g0229 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2540+303A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118066442 | ||||||
| chr1:118066583
|
A | G | 57 | a0001c0001t0001g0176a0001c0010t0001g0150a0001c0010t0001g0154others(54): Show | 58 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2540+162T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 18/48 | chr1 | 118066583 | ||||||
| chr1:118066930
|
C | A | 3 | a0010c0013t0001g0121a0010c0013t0001g0132a0010c0013t0001g0135 | 3 | HG01496.hp2 HG01928.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2386-31G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118066930 | ||||||
| chr1:118067138
|
C | A | 61 | a0001c0001t0001g0176a0001c0010t0001g0150a0001c0010t0001g0154others(58): Show | 62 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.2386-239G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118067138 | ||||||
| chr1:118067169
|
T | G | 4 | a0001c0032t0001g0067a0012c0015t0002g0079a0012c0015t0002g0102others(1): Show | 4 | HG02258.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2386-270A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118067169 | ||||||
| chr1:118067231
|
C | T | 163 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(160): Show | 164 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.2386-332G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118067231 | ||||||
| chr1:118067288
|
G | T | 2 | a0001c0032t0001g0067a0018c0031t0002g0007 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2386-389C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118067288 | ||||||
| chr1:118067363
|
A | G | 9 | a0001c0025t0001g0063a0001c0032t0001g0067a0011c0014t0001g0008others(6): Show | 9 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2386-464T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118067363 | ||||||
| chr1:118067402
|
A | G | 1 | a0001c0025t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2386-503T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118067402 | ||||||
| chr1:118067514
|
C | T | 3 | a0012c0015t0002g0079a0012c0015t0002g0102a0018c0031t0002g0007 | 3 | HG02258.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2386-615G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118067514 | ||||||
| chr1:118067733
|
A | G | 4 | a0001c0032t0001g0067a0012c0015t0002g0079a0012c0015t0002g0102others(1): Show | 4 | HG02258.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2386-834T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118067733 | ||||||
| chr1:118067744
|
G | A | 1 | a0003c0003t0001g0129 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2386-845C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118067744 | ||||||
| chr1:118067950
|
C | T | 1 | a0001c0006t0001g0153 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2386-1051G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118067950 | ||||||
| chr1:118068000
|
T | C | 101 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(98): Show | 101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.2386-1101A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118068000 | ||||||
| chr1:118068150
|
T | A | 1 | a0016c0023t0001g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2386-1251A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118068150 | ||||||
| chr1:118068151
|
A | AAT | 3 | a0001c0001t0001g0144a0001c0025t0001g0063a0021c0024t0001g0006 | 3 | HG02451.hp2 HG02622.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.2386-1254_2386-125 others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118068151 | ||||||
| chr1:118068151
|
A | T | 1 | a0016c0023t0001g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2386-1252T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118068151 | ||||||
| chr1:118068158
|
A | G | 1 | a0001c0004t0003g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2386-1259T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118068158 | ||||||
| chr1:118068368
|
T | C | 3 | a0002c0002t0001g0043a0002c0002t0001g0044a0002c0002t0001g0045 | 3 | NA18971.hp2 NA19056.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2386-1469A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118068368 | ||||||
| chr1:118068448
|
G | A | 3 | a0004c0005t0001g0242a0004c0005t0001g0248a0014c0016t0002g0228 | 3 | HG00597.hp2 HG03225.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.2386-1549C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118068448 | ||||||
| chr1:118068657
|
C | T | 50 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(47): Show | 51 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.2386-1758G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118068657 | ||||||
| chr1:118068658
|
G | T | 50 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(47): Show | 51 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.2386-1759C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118068658 | ||||||
| chr1:118068773
|
T | A | 73 | a0001c0004t0003g0082a0003c0003t0001g0064a0003c0003t0001g0076others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.2386-1874A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118068773 | ||||||
| chr1:118068983
|
G | T | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2386-2084C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118068983 | ||||||
| chr1:118069109
|
T | G | 57 | a0001c0032t0001g0067a0002c0002t0001g0001a0002c0002t0001g0010others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.2386-2210A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069109 | ||||||
| chr1:118069189
|
C | T | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2386-2290G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069189 | ||||||
| chr1:118069342
|
C | A | 1 | a0002c0002t0001g0028 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2386-2443G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069342 | ||||||
| chr1:118069344
|
C | CAAAAAAA others(6): Show |
47 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(44): Show | 47 | HG00621.hp2 HG00735.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.2386-2458_2386-244 others(17): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069344 | ||||||
| chr1:118069344
|
C | CAAAAAAA others(7): Show |
8 | a0001c0004t0001g0225a0001c0004t0001g0237a0002c0002t0001g0001others(5): Show | 9 | HG00438.hp2 HG02698.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.2386-2459_2386-244 others(18): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069344 | ||||||
| chr1:118069344
|
C | CAAAAAAA others(8): Show |
19 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(16): Show | 19 | HG00597.hp1 HG01433.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2386-2446_2386-244 others(19): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069344 | ||||||
| chr1:118069344
|
C | CAAAAAAA others(9): Show |
14 | a0001c0004t0001g0143a0001c0004t0001g0226a0001c0004t0001g0227others(11): Show | 14 | HG00597.hp2 HG00741.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.2386-2446_2386-244 others(20): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069344 | ||||||
| chr1:118069344
|
C | CAAAAAAA others(10): Show |
46 | a0001c0004t0003g0082a0003c0003t0001g0064a0003c0003t0001g0086others(43): Show | 46 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.2386-2446_2386-244 others(21): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069344 | ||||||
| chr1:118069344
|
C | CAAAAAAA others(11): Show |
20 | a0001c0025t0001g0063a0003c0003t0001g0076a0003c0003t0001g0078others(17): Show | 20 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.2386-2446_2386-244 others(22): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069344 | ||||||
| chr1:118069344
|
C | CAAAAAAA others(12): Show |
6 | a0003c0003t0001g0118a0003c0003t0001g0129a0003c0003t0001g0130others(3): Show | 6 | HG00423.hp1 HG04184.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.2386-2446_2386-244 others(23): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069344 | ||||||
| chr1:118069413
|
T | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2386-2514A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069413 | ||||||
| chr1:118069633
|
T | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2386-2734A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069633 | ||||||
| chr1:118069704
|
T | C | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2386-2805A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069704 | ||||||
| chr1:118069920
|
G | A | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2386-3021C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118069920 | ||||||
| chr1:118070073
|
T | C | 2 | a0001c0025t0001g0063a0021c0024t0001g0006 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2386-3174A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118070073 | ||||||
| chr1:118070784
|
A | C | 2 | a0001c0025t0001g0063a0021c0024t0001g0006 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2385+3070T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118070784 | ||||||
| chr1:118070983
|
A | T | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2385+2871T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118070983 | ||||||
| chr1:118071096
|
A | C | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2385+2758T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118071096 | ||||||
| chr1:118071154
|
C | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2385+2700G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118071154 | ||||||
| chr1:118071194
|
A | C | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2385+2660T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118071194 | ||||||
| chr1:118071463
|
A | G | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2385+2391T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118071463 | ||||||
| chr1:118071596
|
G | A | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2385+2258C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118071596 | ||||||
| chr1:118071893
|
G | A | 2 | a0001c0018t0001g0148a0001c0018t0001g0229 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2385+1961C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118071893 | ||||||
| chr1:118071901
|
A | T | 1 | a0001c0001t0001g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2385+1953T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118071901 | ||||||
| chr1:118071945
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2385+1909G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118071945 | ||||||
| chr1:118071982
|
A | G | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2385+1872T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118071982 | ||||||
| chr1:118072011
|
T | G | 5 | a0001c0001t0001g0003a0006c0007t0001g0187a0006c0007t0001g0188others(2): Show | 6 | HG01358.hp2 HG01433.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.2385+1843A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118072011 | ||||||
| chr1:118072032
|
T | C | 2 | a0001c0019t0001g0205a0001c0019t0001g0208 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2385+1822A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118072032 | ||||||
| chr1:118072312
|
A | G | 1 | a0001c0004t0001g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2385+1542T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118072312 | ||||||
| chr1:118072383
|
A | G | 4 | a0006c0007t0001g0187a0006c0007t0001g0188a0006c0007t0001g0189others(1): Show | 4 | HG01358.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.2385+1471T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118072383 | ||||||
| chr1:118072424
|
G | A | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2385+1430C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118072424 | ||||||
| chr1:118072592
|
T | TA | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2385+1261dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118072592 | ||||||
| chr1:118072814
|
G | C | 53 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2385+1040C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118072814 | ||||||
| chr1:118072836
|
G | A | 2 | a0002c0002t0001g0058a0002c0002t0001g0059 | 2 | NA18973.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2385+1018C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118072836 | ||||||
| chr1:118072872
|
C | T | 1 | a0001c0044t0001g0182 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2385+982G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118072872 | ||||||
| chr1:118073000
|
G | T | 1 | a0001c0001t0001g0194 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2385+854C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118073000 | ||||||
| chr1:118073175
|
G | T | 1 | a0007c0033t0001g0014 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2385+679C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118073175 | ||||||
| chr1:118073210
|
T | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2385+644A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118073210 | ||||||
| chr1:118073255
|
CTAGCTTC others(5): Show |
C | 1 | a0001c0001t0001g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2385+587_2385+598d others(14): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118073255 | ||||||
| chr1:118073281
|
A | C | 3 | a0001c0004t0001g0234a0014c0016t0002g0085a0014c0016t0002g0228 | 3 | HG02723.hp1 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2385+573T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118073281 | ||||||
| chr1:118073613
|
CT | C | 3 | a0002c0002t0001g0054a0002c0002t0001g0055a0002c0002t0001g0056 | 3 | HG00735.hp2 HG01934.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2385+240delA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 17/48 | chr1 | 118073613 | ||||||
| chr1:118074041
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2272-74T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 16/48 | chr1 | 118074041 | ||||||
| chr1:118074064
|
A | G | 1 | a0003c0003t0001g0111 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2272-97T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 16/48 | chr1 | 118074064 | ||||||
| chr1:118074202
|
A | C | 1 | a0001c0025t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2272-235T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 16/48 | chr1 | 118074202 | ||||||
| chr1:118074216
|
T | C | 3 | a0002c0002t0001g0032a0002c0002t0001g0058a0002c0002t0001g0059 | 3 | NA18973.hp2 NA19079.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2272-249A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 16/48 | chr1 | 118074216 | ||||||
| chr1:118074349
|
C | T | 2 | a0001c0025t0001g0063a0021c0024t0001g0006 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2271+190G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 16/48 | chr1 | 118074349 | ||||||
| chr1:118074377
|
C | T | 1 | a0019c0028t0001g0117 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2271+162G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 16/48 | chr1 | 118074377 | ||||||
| chr1:118074402
|
C | T | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2271+137G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 16/48 | chr1 | 118074402 | ||||||
| chr1:118074651
|
C | T | 103 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(100): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.2210-51G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118074651 | ||||||
| chr1:118074749
|
G | A | 6 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0001t0001g0178others(3): Show | 6 | HG00733.hp1 HG01099.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.2210-149C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118074749 | ||||||
| chr1:118074802
|
C | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2210-202G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118074802 | ||||||
| chr1:118075049
|
G | A | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2210-449C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118075049 | ||||||
| chr1:118075082
|
C | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2210-482G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118075082 | ||||||
| chr1:118075094
|
G | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0199a0001c0001t0001g0209 | 3 | NA18971.hp1 NA19081.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2210-494C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118075094 | ||||||
| chr1:118075267
|
C | A | 5 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2210-667G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118075267 | ||||||
| chr1:118075461
|
C | T | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2210-861G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118075461 | ||||||
| chr1:118075517
|
C | T | 2 | a0001c0004t0001g0225a0001c0004t0001g0237 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2210-917G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118075517 | ||||||
| chr1:118075619
|
T | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2210-1019A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118075619 | ||||||
| chr1:118075944
|
C | G | 1 | a0001c0006t0001g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2210-1344G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118075944 | ||||||
| chr1:118076147
|
G | C | 1 | a0002c0002t0001g0037 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2210-1547C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118076147 | ||||||
| chr1:118076177
|
A | G | 1 | a0004c0005t0001g0081 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2210-1577T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118076177 | ||||||
| chr1:118076644
|
T | G | 1 | a0001c0001t0001g0196 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2210-2044A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118076644 | ||||||
| chr1:118076733
|
AT | A | 25 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(22): Show | 25 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2210-2134delA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118076733 | ||||||
| chr1:118077093
|
T | C | 3 | a0001c0006t0001g0164a0001c0006t0001g0165a0001c0006t0001g0193 | 3 | HG02055.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2210-2493A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118077093 | ||||||
| chr1:118077329
|
G | A | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2210-2729C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118077329 | ||||||
| chr1:118077369
|
C | T | 1 | a0005c0038t0002g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2210-2769G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118077369 | ||||||
| chr1:118077688
|
A | T | 25 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(22): Show | 25 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.2210-3088T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118077688 | ||||||
| chr1:118077792
|
A | T | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2210-3192T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118077792 | ||||||
| chr1:118077960
|
C | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2209+3141G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118077960 | ||||||
| chr1:118078464
|
T | A | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2209+2637A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118078464 | ||||||
| chr1:118078981
|
T | A | 1 | a0001c0006t0001g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2209+2120A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118078981 | ||||||
| chr1:118078996
|
G | A | 1 | a0016c0023t0001g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2209+2105C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118078996 | ||||||
| chr1:118079153
|
T | C | 2 | a0001c0025t0001g0063a0021c0024t0001g0006 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2209+1948A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118079153 | ||||||
| chr1:118079170
|
G | A | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2209+1931C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118079170 | ||||||
| chr1:118079348
|
T | G | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG00621.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2209+1753A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118079348 | ||||||
| chr1:118079452
|
G | A | 54 | a0001c0032t0001g0067a0002c0002t0001g0001a0002c0002t0001g0010others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.2209+1649C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118079452 | ||||||
| chr1:118079580
|
A | T | 3 | a0004c0005t0001g0096a0004c0005t0001g0097a0004c0005t0001g0098 | 3 | NA18990.hp2 NA19084.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2209+1521T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118079580 | ||||||
| chr1:118079864
|
GTGTTAAA others(17): Show |
G | 2 | a0002c0002t0001g0012a0002c0002t0001g0013 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2209+1213_2209+123 others(28): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118079864 | ||||||
| chr1:118079865
|
T | G | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2209+1236A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118079865 | ||||||
| chr1:118079881
|
G | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2209+1220C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118079881 | ||||||
| chr1:118080432
|
A | G | 26 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(23): Show | 26 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.2209+669T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118080432 | ||||||
| chr1:118080458
|
G | A | 53 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2209+643C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118080458 | ||||||
| chr1:118080760
|
C | G | 100 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(97): Show | 100 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.2209+341G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118080760 | ||||||
| chr1:118080807
|
T | C | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2209+294A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118080807 | ||||||
| chr1:118080898
|
T | C | 53 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2209+203A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118080898 | ||||||
| chr1:118081058
|
T | TAC | 13 | a0001c0001t0001g0163a0001c0001t0001g0168a0001c0001t0001g0171others(10): Show | 13 | HG00733.hp1 HG01099.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2209+41_2209+42dup others(2): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118081058 | ||||||
| chr1:118081058
|
T | TACAC | 4 | a0001c0006t0001g0252a0001c0006t0001g0253a0001c0006t0001g0255others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2209+39_2209+42dup others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118081058 | ||||||
| chr1:118081058
|
TAC | T | 10 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(7): Show | 10 | HG01346.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2209+41_2209+42del others(2): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118081058 | ||||||
| chr1:118081058
|
TACAC | T | 53 | a0001c0001t0001g0192a0001c0004t0001g0219a0001c0032t0001g0067others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2209+39_2209+42del others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118081058 | ||||||
| chr1:118081058
|
TACACAC | T | 95 | a0001c0004t0001g0143a0001c0004t0001g0220a0001c0004t0001g0222others(92): Show | 95 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.2209+37_2209+42del others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118081058 | ||||||
| chr1:118081058
|
TACACACA others(3): Show |
T | 2 | a0001c0025t0001g0063a0021c0024t0001g0006 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2209+33_2209+42del others(10): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 15/48 | chr1 | 118081058 | ||||||
| chr1:118081713
|
T | C | 57 | a0001c0032t0001g0067a0002c0002t0001g0001a0002c0002t0001g0010others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1763-71A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118081713 | ||||||
| chr1:118081791
|
C | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1763-149G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118081791 | ||||||
| chr1:118082289
|
G | C | 53 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1763-647C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118082289 | ||||||
| chr1:118082491
|
A | G | 1 | a0004c0005t0001g0249 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1763-849T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118082491 | ||||||
| chr1:118082594
|
A | G | 1 | a0002c0002t0001g0028 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1763-952T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118082594 | ||||||
| chr1:118083007
|
C | T | 161 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(158): Show | 162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1763-1365G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118083007 | ||||||
| chr1:118083119
|
G | A | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1763-1477C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118083119 | ||||||
| chr1:118083131
|
A | G | 3 | a0004c0005t0001g0096a0004c0005t0001g0097a0004c0005t0001g0098 | 3 | NA18990.hp2 NA19084.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1763-1489T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118083131 | ||||||
| chr1:118083514
|
C | T | 53 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1763-1872G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118083514 | ||||||
| chr1:118083550
|
A | G | 161 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(158): Show | 162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1763-1908T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118083550 | ||||||
| chr1:118083968
|
C | G | 44 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0012others(41): Show | 44 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1762+1954G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118083968 | ||||||
| chr1:118083980
|
A | G | 3 | a0002c0002t0001g0001a0002c0002t0001g0019a0002c0002t0001g0020 | 4 | HG01346.hp1 HG02698.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762+1942T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118083980 | ||||||
| chr1:118084041
|
G | C | 57 | a0001c0032t0001g0067a0002c0002t0001g0001a0002c0002t0001g0010others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1762+1881C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118084041 | ||||||
| chr1:118084320
|
C | T | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1762+1602G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118084320 | ||||||
| chr1:118084411
|
T | C | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1762+1511A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118084411 | ||||||
| chr1:118084520
|
C | T | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1762+1402G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118084520 | ||||||
| chr1:118084693
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG00735.hp1 HG03490.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1762+1229C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118084693 | ||||||
| chr1:118084732
|
G | A | 1 | a0001c0006t0001g0071 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1762+1190C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118084732 | ||||||
| chr1:118084810
|
CT | C | 5 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1762+1111delA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118084810 | ||||||
| chr1:118084826
|
C | T | 56 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1762+1096G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118084826 | ||||||
| chr1:118085125
|
C | T | 2 | a0001c0025t0001g0063a0021c0024t0001g0006 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1762+797G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118085125 | ||||||
| chr1:118085510
|
A | ATGCGTGC others(11): Show |
53 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(50): Show | 54 | HG00438.hp2 HG00621.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1762+394_1762+411d others(20): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118085510 | ||||||
| chr1:118085529
|
T | TGC | 3 | a0001c0004t0001g0060a0011c0014t0001g0008a0011c0014t0001g0009 | 3 | HG02572.hp1 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1762+391_1762+392d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118085529 | ||||||
| chr1:118085529
|
T | TGCGTGCG others(13): Show |
1 | a0002c0002t0001g0021 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1762+392_1762+393i others(22): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118085529 | ||||||
| chr1:118085538
|
G | A | 1 | a0002c0002t0001g0021 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1762+384C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118085538 | ||||||
| chr1:118085538
|
G | GCA | 5 | a0001c0001t0001g0196a0001c0004t0001g0224a0001c0026t0001g0261others(2): Show | 5 | HG02615.hp1 HG02698.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762+382_1762+383d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118085538 | ||||||
| chr1:118085540
|
A | G | 2 | a0001c0004t0001g0061a0001c0004t0001g0062 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1762+382T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118085540 | ||||||
| chr1:118085612
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1762+310G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 13/48 | chr1 | 118085612 | ||||||
| chr1:118086142
|
G | A | 2 | a0014c0016t0002g0085a0014c0016t0002g0228 | 2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1612-70C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 12/48 | chr1 | 118086142 | ||||||
| chr1:118086178
|
A | C | 1 | a0019c0028t0001g0117 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1612-106T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 12/48 | chr1 | 118086178 | ||||||
| chr1:118086231
|
G | A | 25 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(22): Show | 25 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1612-159C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 12/48 | chr1 | 118086231 | ||||||
| chr1:118086251
|
T | C | 1 | a0008c0009t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1612-179A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 12/48 | chr1 | 118086251 | ||||||
| chr1:118086284
|
T | G | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1612-212A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 12/48 | chr1 | 118086284 | ||||||
| chr1:118086297
|
A | G | 5 | a0001c0004t0001g0257a0001c0004t0001g0258a0001c0004t0001g0259others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1612-225T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 12/48 | chr1 | 118086297 | ||||||
| chr1:118086359
|
C | T | 3 | a0001c0001t0001g0163a0001c0001t0001g0171a0001c0001t0001g0198 | 3 | HG02602.hp1 HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1612-287G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 12/48 | chr1 | 118086359 | ||||||
| chr1:118086502
|
T | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(256): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1611+169A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 12/48 | chr1 | 118086502 | ||||||
| chr1:118086651
|
G | A | 4 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014others(1): Show | 4 | HG02109.hp1 HG02735.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1611+20C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 12/48 | chr1 | 118086651 | ||||||
| chr1:118086800
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1498-16G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 11/48 | chr1 | 118086800 | ||||||
| chr1:118087115
|
G | A | 54 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1360-107C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118087115 | ||||||
| chr1:118087141
|
A | G | 1 | a0003c0003t0001g0092 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1360-133T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118087141 | ||||||
| chr1:118087217
|
T | C | 11 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156others(8): Show | 11 | HG00621.hp1 HG02027.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1360-209A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118087217 | ||||||
| chr1:118087872
|
T | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1360-864A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118087872 | ||||||
| chr1:118088297
|
G | A | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1360-1289C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118088297 | ||||||
| chr1:118088454
|
A | T | 54 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1360-1446T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118088454 | ||||||
| chr1:118088690
|
G | T | 58 | a0001c0032t0001g0067a0002c0002t0001g0001a0002c0002t0001g0010others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1360-1682C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118088690 | ||||||
| chr1:118089025
|
G | C | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1360-2017C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089025 | ||||||
| chr1:118089066
|
A | G | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1360-2058T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089066 | ||||||
| chr1:118089332
|
C | CGTGTGTG others(7): Show |
3 | a0001c0025t0001g0063a0003c0003t0001g0109a0021c0024t0001g0006 | 3 | HG02451.hp2 HG02622.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1359+2260_1359+227 others(18): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089332 | ||||||
| chr1:118089332
|
C | CGTGTGTG others(9): Show |
3 | a0001c0004t0001g0220a0003c0029t0001g0141a0004c0005t0001g0123 | 3 | HG00733.hp2 HG00738.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1359+2258_1359+227 others(20): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089332 | ||||||
| chr1:118089332
|
C | CGTGTGTG others(11): Show |
64 | a0001c0004t0001g0143a0001c0004t0001g0231a0001c0004t0001g0238others(61): Show | 64 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1359+2256_1359+227 others(22): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089332 | ||||||
| chr1:118089332
|
C | CGTGTGTG others(13): Show |
18 | a0001c0004t0001g0222a0001c0004t0001g0223a0001c0004t0001g0224others(15): Show | 18 | HG00140.hp2 HG00323.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.1359+2254_1359+227 others(24): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089332 | ||||||
| chr1:118089332
|
C | CGTGTGTG others(15): Show |
11 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(8): Show | 11 | HG02615.hp2 HG02630.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1359+2252_1359+227 others(26): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089332 | ||||||
| chr1:118089332
|
C | CGTGTGTG others(17): Show |
4 | a0001c0004t0001g0219a0001c0004t0001g0226a0001c0004t0001g0230others(1): Show | 4 | HG00741.hp1 HG02723.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1359+2273_1359+227 others(28): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089332 | ||||||
| chr1:118089354
|
T | TGTGTGTG others(11): Show |
1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1359+2251_1359+225 others(22): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089354 | ||||||
| chr1:118089354
|
T | TGTGTGTG others(17): Show |
3 | a0007c0017t0001g0015a0007c0017t0001g0016a0017c0034t0001g0053 | 3 | HG02109.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1359+2251_1359+225 others(28): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089354 | ||||||
| chr1:118089354
|
T | TGTGTGTG others(19): Show |
4 | a0002c0002t0001g0018a0007c0033t0001g0014a0011c0014t0001g0008others(1): Show | 4 | HG02027.hp2 HG02572.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1359+2251_1359+225 others(30): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089354 | ||||||
| chr1:118089354
|
T | TGTGTGTG others(21): Show |
1 | a0016c0023t0001g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1359+2251_1359+225 others(32): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089354 | ||||||
| chr1:118089354
|
T | TGTGTGTG others(23): Show |
11 | a0002c0002t0001g0001a0002c0002t0001g0013a0002c0002t0001g0020others(8): Show | 12 | HG00735.hp2 HG01109.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1359+2251_1359+225 others(34): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089354 | ||||||
| chr1:118089354
|
T | TGTGTGTG others(25): Show |
14 | a0002c0002t0001g0010a0002c0002t0001g0012a0002c0002t0001g0017others(11): Show | 14 | HG02698.hp1 HG03688.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.1359+2251_1359+225 others(36): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089354 | ||||||
| chr1:118089354
|
T | TGTGTGTG others(27): Show |
15 | a0002c0002t0001g0011a0002c0002t0001g0021a0002c0002t0001g0024others(12): Show | 15 | HG00597.hp1 HG02080.hp2 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.1359+2251_1359+225 others(38): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089354 | ||||||
| chr1:118089354
|
T | TGTGTGTG others(29): Show |
4 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0050others(1): Show | 4 | HG00621.hp2 NA18979.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1359+2251_1359+225 others(40): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089354 | ||||||
| chr1:118089354
|
T | TGTGTGTG others(31): Show |
2 | a0002c0002t0001g0028a0002c0002t0001g0035 | 2 | HG00438.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.1359+2251_1359+225 others(42): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089354 | ||||||
| chr1:118089354
|
T | TGTGTGTG others(33): Show |
2 | a0002c0002t0001g0041a0002c0002t0001g0042 | 2 | NA19064.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1359+2251_1359+225 others(44): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089354 | ||||||
| chr1:118089693
|
A | G | 26 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(23): Show | 26 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.1359+1913T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089693 | ||||||
| chr1:118089854
|
T | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(256): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1359+1752A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089854 | ||||||
| chr1:118089899
|
A | C | 2 | a0001c0004t0001g0219a0001c0004t0001g0233 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1359+1707T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118089899 | ||||||
| chr1:118090130
|
C | G | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1359+1476G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118090130 | ||||||
| chr1:118090219
|
G | T | 1 | a0002c0002t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1359+1387C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118090219 | ||||||
| chr1:118090660
|
G | T | 1 | a0003c0003t0001g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1359+946C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118090660 | ||||||
| chr1:118090676
|
G | A | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1359+930C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118090676 | ||||||
| chr1:118090696
|
C | G | 1 | a0002c0002t0001g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1359+910G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118090696 | ||||||
| chr1:118090761
|
C | T | 1 | a0004c0005t0001g0004 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1359+845G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118090761 | ||||||
| chr1:118090994
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1359+612A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118090994 | ||||||
| chr1:118091013
|
A | G | 1 | a0003c0003t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1359+593T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118091013 | ||||||
| chr1:118091167
|
A | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(256): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1359+439T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118091167 | ||||||
| chr1:118091353
|
A | C | 1 | a0001c0006t0001g0070 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1359+253T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118091353 | ||||||
| chr1:118091560
|
T | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1359+46A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 10/48 | chr1 | 118091560 | ||||||
| chr1:118092189
|
G | T | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG00140.hp1 HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1174-187C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 8/48 | chr1 | 118092189 | ||||||
| chr1:118092378
|
A | G | 1 | a0001c0004t0001g0235 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1174-376T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 8/48 | chr1 | 118092378 | ||||||
| chr1:118092955
|
G | T | 1 | a0028c0040t0001g0122 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1173+201C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 8/48 | chr1 | 118092955 | ||||||
| chr1:118093696
|
T | C | 1 | a0003c0003t0001g0076 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1012-379A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118093696 | ||||||
| chr1:118093935
|
T | G | 54 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1012-618A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118093935 | ||||||
| chr1:118094023
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1012-706C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118094023 | ||||||
| chr1:118094132
|
G | T | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1012-815C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118094132 | ||||||
| chr1:118094176
|
A | G | 1 | a0004c0005t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1012-859T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118094176 | ||||||
| chr1:118094261
|
G | C | 1 | a0014c0016t0002g0228 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1012-944C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118094261 | ||||||
| chr1:118094421
|
A | G | 56 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1012-1104T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118094421 | ||||||
| chr1:118094687
|
G | T | 1 | a0001c0001t0001g0217 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1012-1370C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118094687 | ||||||
| chr1:118096032
|
C | T | 56 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1011+1638G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118096032 | ||||||
| chr1:118096090
|
T | A | 1 | a0005c0020t0002g0157 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1011+1580A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118096090 | ||||||
| chr1:118096280
|
C | T | 6 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0001t0001g0178others(3): Show | 6 | HG00733.hp1 HG01099.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1011+1390G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118096280 | ||||||
| chr1:118096320
|
G | A | 1 | a0003c0003t0001g0076 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1011+1350C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118096320 | ||||||
| chr1:118096353
|
C | CT | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(94): Show | 99 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1011+1316dupA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118096353 | ||||||
| chr1:118096394
|
G | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1011+1276C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118096394 | ||||||
| chr1:118096535
|
G | A | 1 | a0001c0006t0001g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1011+1135C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118096535 | ||||||
| chr1:118096554
|
A | G | 54 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1011+1116T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118096554 | ||||||
| chr1:118096721
|
T | C | 1 | a0002c0002t0001g0054 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1011+949A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118096721 | ||||||
| chr1:118096775
|
G | T | 2 | a0001c0025t0001g0063a0021c0024t0001g0006 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1011+895C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118096775 | ||||||
| chr1:118096833
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1011+837A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118096833 | ||||||
| chr1:118096851
|
A | G | 3 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156 | 3 | NA18949.hp2 NA18979.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1011+819T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118096851 | ||||||
| chr1:118096992
|
C | T | 74 | a0001c0004t0003g0082a0001c0025t0001g0063a0003c0003t0001g0064others(71): Show | 74 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1011+678G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118096992 | ||||||
| chr1:118097032
|
C | T | 3 | a0001c0010t0001g0150a0001c0010t0001g0154a0001c0010t0001g0156 | 3 | NA18949.hp2 NA18979.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1011+638G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118097032 | ||||||
| chr1:118097135
|
T | C | 1 | a0002c0002t0001g0011 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1011+535A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118097135 | ||||||
| chr1:118097171
|
G | T | 1 | a0001c0004t0003g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1011+499C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118097171 | ||||||
| chr1:118097227
|
CA | C | 72 | a0001c0004t0003g0082a0002c0002t0001g0050a0003c0003t0001g0064others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1011+442delT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118097227 | ||||||
| chr1:118097240
|
A | G | 2 | a0001c0006t0001g0071a0004c0005t0001g0080 | 2 | HG02129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1011+430T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118097240 | ||||||
| chr1:118097439
|
C | T | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1011+231G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118097439 | ||||||
| chr1:118097576
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1011+94C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 7/48 | chr1 | 118097576 | ||||||
| chr1:118097868
|
G | A | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.830-17C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/48 | chr1 | 118097868 | ||||||
| chr1:118097955
|
A | T | 2 | a0001c0004t0001g0219a0001c0004t0001g0233 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.830-104T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/48 | chr1 | 118097955 | ||||||
| chr1:118098004
|
G | A | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.830-153C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/48 | chr1 | 118098004 | ||||||
| chr1:118098074
|
C | T | 50 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(47): Show | 51 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.830-223G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/48 | chr1 | 118098074 | ||||||
| chr1:118098195
|
T | A | 58 | a0001c0032t0001g0067a0002c0002t0001g0001a0002c0002t0001g0010others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.830-344A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/48 | chr1 | 118098195 | ||||||
| chr1:118098655
|
T | C | 2 | a0002c0002t0001g0017a0002c0002t0001g0018 | 2 | HG02027.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.830-804A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/48 | chr1 | 118098655 | ||||||
| chr1:118098963
|
A | T | 1 | a0001c0001t0001g0149 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.829+643T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/48 | chr1 | 118098963 | ||||||
| chr1:118099083
|
T | C | 54 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.829+523A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/48 | chr1 | 118099083 | ||||||
| chr1:118099105
|
G | A | 1 | a0001c0006t0001g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.829+501C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/48 | chr1 | 118099105 | ||||||
| chr1:118099287
|
G | A | 1 | a0004c0005t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.829+319C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/48 | chr1 | 118099287 | ||||||
| chr1:118099332
|
A | G | 3 | a0001c0001t0001g0181a0001c0006t0001g0241a0001c0006t0001g0251 | 3 | HG01952.hp2 NA19058.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.829+274T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/48 | chr1 | 118099332 | ||||||
| chr1:118099350
|
T | C | 24 | a0003c0003t0001g0086a0003c0003t0001g0087a0003c0003t0001g0088others(21): Show | 24 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.829+256A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/48 | chr1 | 118099350 | ||||||
| chr1:118099563
|
G | A | 1 | a0013c0021t0002g0158 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.829+43C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 6/48 | chr1 | 118099563 | ||||||
| chr1:118099990
|
G | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18988.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.635-190C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 5/48 | chr1 | 118099990 | ||||||
| chr1:118100450
|
C | T | 1 | a0002c0002t0001g0017 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.635-650G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 5/48 | chr1 | 118100450 | ||||||
| chr1:118100542
|
A | G | 2 | a0001c0025t0001g0063a0021c0024t0001g0006 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.635-742T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 5/48 | chr1 | 118100542 | ||||||
| chr1:118100882
|
G | C | 3 | a0003c0003t0001g0108a0003c0003t0001g0114a0003c0003t0001g0115 | 3 | HG00642.hp1 HG01070.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.634+858C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 5/48 | chr1 | 118100882 | ||||||
| chr1:118101005
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.634+735G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 5/48 | chr1 | 118101005 | ||||||
| chr1:118101007
|
T | C | 1 | a0022c0037t0001g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.634+733A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 5/48 | chr1 | 118101007 | ||||||
| chr1:118101060
|
C | T | 1 | a0001c0004t0001g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.634+680G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 5/48 | chr1 | 118101060 | ||||||
| chr1:118101307
|
T | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.634+433A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 5/48 | chr1 | 118101307 | ||||||
| chr1:118101454
|
C | A | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.634+286G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 5/48 | chr1 | 118101454 | ||||||
| chr1:118102047
|
T | G | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.448-121A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118102047 | ||||||
| chr1:118102194
|
C | T | 4 | a0003c0003t0001g0086a0003c0003t0001g0087a0003c0003t0001g0088others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.448-268G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118102194 | ||||||
| chr1:118102215
|
C | T | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.448-289G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118102215 | ||||||
| chr1:118102346
|
A | AAAAAC | 58 | a0001c0032t0001g0067a0002c0002t0001g0001a0002c0002t0001g0010others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.448-425_448-421dup others(5): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118102346 | ||||||
| chr1:118102501
|
T | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.448-575A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118102501 | ||||||
| chr1:118102516
|
A | C | 1 | a0003c0003t0001g0111 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.448-590T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118102516 | ||||||
| chr1:118102611
|
G | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.448-685C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118102611 | ||||||
| chr1:118103044
|
G | C | 26 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(23): Show | 26 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.448-1118C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103044 | ||||||
| chr1:118103100
|
C | G | 1 | a0001c0004t0001g0234 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.448-1174G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103100 | ||||||
| chr1:118103383
|
A | G | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.448-1457T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103383 | ||||||
| chr1:118103528
|
G | A | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.448-1602C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103528 | ||||||
| chr1:118103560
|
T | G | 1 | a0001c0001t0001g0184 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.448-1634A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103560 | ||||||
| chr1:118103599
|
C | T | 2 | a0012c0015t0002g0079a0012c0015t0002g0102 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.448-1673G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103599 | ||||||
| chr1:118103840
|
A | AGTGT | 6 | a0001c0004t0001g0061a0001c0006t0001g0151a0001c0006t0001g0152others(3): Show | 6 | HG00280.hp2 HG01346.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-1918_448-1915d others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103840 | ||||||
| chr1:118103840
|
A | AGTGTGT | 6 | a0001c0004t0001g0060a0001c0004t0001g0062a0005c0011t0001g0106others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.448-1920_448-1915d others(8): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103840 | ||||||
| chr1:118103840
|
A | AGTGTGTG others(1): Show |
11 | a0001c0001t0001g0211a0001c0004t0001g0143a0001c0010t0001g0150others(8): Show | 11 | HG00621.hp1 HG02027.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.448-1922_448-1915d others(10): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103840 | ||||||
| chr1:118103840
|
A | AGTGTGTG others(3): Show |
12 | a0001c0001t0001g0195a0001c0004t0001g0226a0001c0004t0001g0235others(9): Show | 12 | HG00735.hp2 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.448-1924_448-1915d others(12): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103840 | ||||||
| chr1:118103840
|
A | AGTGTGTG others(5): Show |
70 | a0001c0001t0001g0171a0001c0001t0001g0198a0001c0004t0001g0220others(67): Show | 70 | HG00323.hp1 HG00438.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.448-1926_448-1915d others(14): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103840 | ||||||
| chr1:118103840
|
A | AGTGTGTG others(7): Show |
119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(116): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.448-1928_448-1915d others(16): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103840 | ||||||
| chr1:118103840
|
A | AGTGTGTG others(9): Show |
30 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(27): Show | 30 | HG00597.hp2 HG01099.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.448-1930_448-1915d others(18): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103840 | ||||||
| chr1:118103840
|
A | AGTGTGTG others(11): Show |
3 | a0001c0001t0001g0216a0001c0001t0001g0217a0004c0005t0001g0242 | 3 | HG02148.hp2 NA18967.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.448-1932_448-1915d others(20): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103840 | ||||||
| chr1:118103840
|
A | AGTGTGTG others(15): Show |
1 | a0004c0005t0001g0133 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.448-1936_448-1915d others(24): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103840 | ||||||
| chr1:118103840
|
A | AGTGTGTG others(17): Show |
1 | a0027c0041t0001g0093 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.448-1938_448-1915d others(26): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118103840 | ||||||
| chr1:118104051
|
C | T | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.448-2125G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118104051 | ||||||
| chr1:118104176
|
A | T | 3 | a0003c0003t0001g0108a0003c0003t0001g0114a0003c0003t0001g0115 | 3 | HG00642.hp1 HG01070.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.448-2250T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118104176 | ||||||
| chr1:118104479
|
T | G | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.448-2553A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118104479 | ||||||
| chr1:118104582
|
A | T | 1 | a0002c0002t0001g0069 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.448-2656T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118104582 | ||||||
| chr1:118104648
|
C | T | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.448-2722G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118104648 | ||||||
| chr1:118104771
|
G | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0171 | 2 | HG02602.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.448-2845C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118104771 | ||||||
| chr1:118104866
|
T | C | 5 | a0001c0001t0001g0003a0006c0007t0001g0187a0006c0007t0001g0188others(2): Show | 6 | HG01358.hp2 HG01433.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-2940A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118104866 | ||||||
| chr1:118104901
|
G | T | 54 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.448-2975C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118104901 | ||||||
| chr1:118105009
|
C | T | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | NA18990.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.448-3083G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118105009 | ||||||
| chr1:118105011
|
G | A | 58 | a0001c0032t0001g0067a0002c0002t0001g0001a0002c0002t0001g0010others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.448-3085C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118105011 | ||||||
| chr1:118105256
|
G | A | 4 | a0001c0006t0001g0252a0001c0006t0001g0253a0001c0006t0001g0255others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.448-3330C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118105256 | ||||||
| chr1:118105438
|
A | T | 1 | a0002c0002t0001g0011 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.448-3512T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118105438 | ||||||
| chr1:118105457
|
C | T | 3 | a0010c0013t0001g0121a0010c0013t0001g0132a0010c0013t0001g0135 | 3 | HG01496.hp2 HG01928.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.448-3531G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118105457 | ||||||
| chr1:118105647
|
G | A | 100 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(97): Show | 100 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.448-3721C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118105647 | ||||||
| chr1:118105682
|
G | A | 1 | a0001c0025t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.448-3756C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118105682 | ||||||
| chr1:118105716
|
A | C | 2 | a0002c0002t0001g0010a0002c0002t0001g0011 | 2 | HG02523.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.448-3790T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118105716 | ||||||
| chr1:118105729
|
G | A | 1 | a0002c0002t0001g0020 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.448-3803C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118105729 | ||||||
| chr1:118105856
|
G | GA | 161 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(158): Show | 162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.448-3931dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118105856 | ||||||
| chr1:118106273
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.448-4347C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118106273 | ||||||
| chr1:118106522
|
A | G | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.448-4596T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118106522 | ||||||
| chr1:118107206
|
A | C | 1 | a0003c0029t0001g0141 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.448-5280T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118107206 | ||||||
| chr1:118107217
|
G | T | 72 | a0001c0004t0003g0082a0003c0003t0001g0064a0003c0003t0001g0076others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.448-5291C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118107217 | ||||||
| chr1:118107418
|
C | T | 1 | a0003c0003t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.448-5492G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118107418 | ||||||
| chr1:118107619
|
C | T | 1 | a0004c0005t0001g0004 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.448-5693G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118107619 | ||||||
| chr1:118108101
|
C | T | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.448-6175G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118108101 | ||||||
| chr1:118108658
|
C | T | 1 | a0004c0005t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.447+6652G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118108658 | ||||||
| chr1:118108704
|
CT | C | 6 | a0001c0006t0001g0151a0001c0006t0001g0152a0002c0002t0001g0032others(3): Show | 6 | HG01346.hp2 NA18973.hp2 NA19079.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+6605delA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118108704 | ||||||
| chr1:118108925
|
T | G | 72 | a0001c0004t0003g0082a0003c0003t0001g0064a0003c0003t0001g0076others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.447+6385A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118108925 | ||||||
| chr1:118109126
|
T | C | 1 | a0008c0009t0002g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.447+6184A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118109126 | ||||||
| chr1:118109227
|
C | T | 1 | a0003c0003t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.447+6083G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118109227 | ||||||
| chr1:118109257
|
T | A | 1 | a0022c0037t0001g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.447+6053A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118109257 | ||||||
| chr1:118109367
|
G | A | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.447+5943C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118109367 | ||||||
| chr1:118109383
|
T | TA | 63 | a0001c0004t0001g0260a0001c0004t0003g0082a0002c0002t0001g0057others(60): Show | 63 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.447+5926dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118109383 | ||||||
| chr1:118109411
|
G | T | 1 | a0001c0001t0001g0177 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.447+5899C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118109411 | ||||||
| chr1:118109423
|
C | T | 1 | a0001c0004t0001g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.447+5887G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118109423 | ||||||
| chr1:118109509
|
C | T | 50 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(47): Show | 51 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.447+5801G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118109509 | ||||||
| chr1:118109556
|
A | AAAT | 57 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.447+5751_447+5753d others(5): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118109556 | ||||||
| chr1:118109556
|
A | AAATAAT | 5 | a0001c0032t0001g0067a0002c0002t0001g0017a0002c0002t0001g0018others(2): Show | 5 | HG02027.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.447+5748_447+5753d others(8): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118109556 | ||||||
| chr1:118109556
|
A | AAATAATA others(2): Show |
4 | a0002c0002t0001g0045a0011c0014t0001g0008a0011c0014t0001g0009others(1): Show | 4 | HG02572.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.447+5745_447+5753d others(11): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118109556 | ||||||
| chr1:118109556
|
AAAT | A | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(165): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.447+5751_447+5753d others(5): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118109556 | ||||||
| chr1:118109827
|
T | C | 1 | a0002c0002t0001g0030 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.447+5483A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118109827 | ||||||
| chr1:118110131
|
A | G | 50 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(47): Show | 51 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.447+5179T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118110131 | ||||||
| chr1:118110164
|
T | C | 1 | a0011c0014t0001g0009 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.447+5146A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118110164 | ||||||
| chr1:118110477
|
C | T | 2 | a0001c0025t0001g0063a0021c0024t0001g0006 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.447+4833G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118110477 | ||||||
| chr1:118110575
|
C | G | 58 | a0001c0032t0001g0067a0002c0002t0001g0001a0002c0002t0001g0010others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.447+4735G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118110575 | ||||||
| chr1:118110700
|
G | A | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.447+4610C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118110700 | ||||||
| chr1:118110734
|
T | A | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.447+4576A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118110734 | ||||||
| chr1:118111143
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(60): Show | 65 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.447+4167C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111143 | ||||||
| chr1:118111553
|
A | AAC | 48 | a0001c0019t0001g0205a0001c0019t0001g0208a0002c0002t0001g0001others(45): Show | 49 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.447+3755_447+3756d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111553 | ||||||
| chr1:118111553
|
A | AACAC | 6 | a0001c0001t0001g0144a0001c0004t0001g0060a0002c0002t0001g0012others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.447+3753_447+3756d others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111553 | ||||||
| chr1:118111553
|
A | AACACAC | 34 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0162others(31): Show | 34 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.447+3751_447+3756d others(8): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111553 | ||||||
| chr1:118111553
|
A | AACACACA others(1): Show |
60 | a0001c0001t0001g0145a0001c0001t0001g0159a0001c0001t0001g0160others(57): Show | 60 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.447+3749_447+3756d others(10): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111553 | ||||||
| chr1:118111553
|
A | AACACACA others(3): Show |
50 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0066others(47): Show | 51 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.447+3747_447+3756d others(12): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111553 | ||||||
| chr1:118111553
|
A | AACACACA others(5): Show |
35 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0170others(32): Show | 36 | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.447+3745_447+3756d others(14): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111553 | ||||||
| chr1:118111553
|
A | AACACACA others(7): Show |
11 | a0001c0001t0001g0215a0001c0004t0001g0224a0001c0004t0001g0232others(8): Show | 11 | HG02273.hp1 HG02615.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.447+3743_447+3756d others(16): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111553 | ||||||
| chr1:118111553
|
A | AACACACA others(9): Show |
2 | a0001c0004t0001g0220a0004c0005t0001g0125 | 2 | HG03239.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.447+3741_447+3756d others(18): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111553 | ||||||
| chr1:118111553
|
A | AACACACA others(11): Show |
4 | a0001c0004t0001g0223a0001c0004t0001g0238a0001c0006t0001g0252others(1): Show | 4 | HG01433.hp2 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.447+3739_447+3756d others(20): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111553 | ||||||
| chr1:118111553
|
A | AACACACA others(13): Show |
1 | a0001c0004t0001g0222 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.447+3737_447+3756d others(22): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111553 | ||||||
| chr1:118111553
|
AACACAC | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0201 | 2 | NA18941.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.447+3751_447+3756d others(8): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111553 | ||||||
| chr1:118111592
|
A | ACACACAC others(6): Show |
1 | a0003c0003t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.447+3717_447+3718i others(15): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111592 | ||||||
| chr1:118111625
|
C | T | 1 | a0001c0001t0001g0003 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.447+3685G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111625 | ||||||
| chr1:118111628
|
A | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(78): Show | 83 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.447+3682T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118111628 | ||||||
| chr1:118112671
|
C | T | 54 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.447+2639G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118112671 | ||||||
| chr1:118112841
|
T | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.447+2469A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118112841 | ||||||
| chr1:118113244
|
C | T | 2 | a0001c0004t0001g0220a0001c0004t0001g0222 | 2 | HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.447+2066G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118113244 | ||||||
| chr1:118113259
|
G | T | 54 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.447+2051C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118113259 | ||||||
| chr1:118113718
|
C | T | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.447+1592G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118113718 | ||||||
| chr1:118114535
|
T | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.447+775A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118114535 | ||||||
| chr1:118114540
|
T | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.447+770A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118114540 | ||||||
| chr1:118114617
|
A | G | 1 | a0001c0006t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.447+693T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118114617 | ||||||
| chr1:118114773
|
T | C | 26 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(23): Show | 26 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.447+537A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118114773 | ||||||
| chr1:118114911
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.447+399T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118114911 | ||||||
| chr1:118114920
|
C | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.447+390G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118114920 | ||||||
| chr1:118114967
|
C | G | 2 | a0001c0004t0001g0060a0001c0004t0001g0061 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.447+343G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118114967 | ||||||
| chr1:118114996
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.447+314G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118114996 | ||||||
| chr1:118115208
|
T | C | 1 | a0001c0006t0001g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.447+102A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 4/48 | chr1 | 118115208 | ||||||
| chr1:118115462
|
T | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-21A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118115462 | ||||||
| chr1:118115815
|
C | T | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.316-374G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118115815 | ||||||
| chr1:118116053
|
G | A | 1 | a0003c0003t0001g0099 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.316-612C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118116053 | ||||||
| chr1:118116229
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.316-788C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118116229 | ||||||
| chr1:118116339
|
T | G | 54 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.316-898A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118116339 | ||||||
| chr1:118116370
|
T | C | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-929A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118116370 | ||||||
| chr1:118116405
|
C | A | 2 | a0001c0025t0001g0063a0021c0024t0001g0006 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.316-964G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118116405 | ||||||
| chr1:118116443
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.316-1002T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118116443 | ||||||
| chr1:118116584
|
T | G | 1 | a0028c0040t0001g0122 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.316-1143A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118116584 | ||||||
| chr1:118116666
|
T | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-1225A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118116666 | ||||||
| chr1:118116983
|
C | T | 1 | a0001c0006t0001g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.316-1542G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118116983 | ||||||
| chr1:118117242
|
T | G | 61 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(58): Show | 62 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.316-1801A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118117242 | ||||||
| chr1:118117549
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.316-2108C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118117549 | ||||||
| chr1:118117984
|
G | A | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-2543C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118117984 | ||||||
| chr1:118118304
|
C | A | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-2863G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118118304 | ||||||
| chr1:118118382
|
G | T | 4 | a0003c0003t0001g0101a0003c0003t0001g0111a0003c0003t0001g0127others(1): Show | 4 | HG02056.hp1 HG02074.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-2941C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118118382 | ||||||
| chr1:118118394
|
A | G | 1 | a0008c0009t0002g0107 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.316-2953T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118118394 | ||||||
| chr1:118118558
|
C | T | 1 | a0004c0005t0001g0243 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.316-3117G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118118558 | ||||||
| chr1:118118581
|
T | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-3140A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118118581 | ||||||
| chr1:118118590
|
A | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-3149T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118118590 | ||||||
| chr1:118118662
|
C | T | 53 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.316-3221G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118118662 | ||||||
| chr1:118118677
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.316-3236G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118118677 | ||||||
| chr1:118118779
|
T | C | 2 | a0005c0011t0001g0106a0005c0011t0002g0104 | 2 | HG02273.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.316-3338A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118118779 | ||||||
| chr1:118118931
|
A | G | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.316-3490T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118118931 | ||||||
| chr1:118119019
|
T | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-3578A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118119019 | ||||||
| chr1:118119079
|
C | T | 1 | a0003c0003t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.316-3638G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118119079 | ||||||
| chr1:118119099
|
A | G | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-3658T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118119099 | ||||||
| chr1:118119129
|
A | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.316-3688T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118119129 | ||||||
| chr1:118119210
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0199a0001c0001t0001g0209 | 3 | NA18971.hp1 NA19081.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.316-3769A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118119210 | ||||||
| chr1:118119567
|
C | A | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.316-4126G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118119567 | ||||||
| chr1:118119679
|
A | C | 35 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0022others(32): Show | 35 | HG00438.hp2 HG00621.hp2 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.316-4238T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118119679 | ||||||
| chr1:118119868
|
C | T | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-4427G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118119868 | ||||||
| chr1:118120010
|
T | C | 3 | a0002c0002t0001g0033a0002c0002t0001g0034a0002c0002t0001g0052 | 3 | NA18946.hp2 NA18948.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.316-4569A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118120010 | ||||||
| chr1:118120108
|
A | C | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-4667T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118120108 | ||||||
| chr1:118120271
|
T | A | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-4830A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118120271 | ||||||
| chr1:118120283
|
T | TA | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(258): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.316-4843dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118120283 | ||||||
| chr1:118120318
|
GATTAAA | G | 6 | a0002c0002t0001g0001a0002c0002t0001g0019a0002c0002t0001g0020others(3): Show | 7 | HG00735.hp2 HG01346.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.316-4883_316-4878d others(8): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118120318 | ||||||
| chr1:118120583
|
T | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-5142A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118120583 | ||||||
| chr1:118120834
|
A | G | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.316-5393T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118120834 | ||||||
| chr1:118120948
|
T | C | 12 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0022others(9): Show | 12 | HG00621.hp2 HG02074.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.316-5507A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118120948 | ||||||
| chr1:118121096
|
C | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.316-5655G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118121096 | ||||||
| chr1:118121134
|
C | G | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-5693G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118121134 | ||||||
| chr1:118121144
|
G | T | 1 | a0002c0002t0001g0057 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.316-5703C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118121144 | ||||||
| chr1:118121321
|
C | G | 4 | a0003c0003t0001g0076a0003c0003t0001g0078a0012c0015t0002g0079others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.316-5880G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118121321 | ||||||
| chr1:118121338
|
G | A | 1 | a0004c0005t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.316-5897C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118121338 | ||||||
| chr1:118121415
|
T | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-5974A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118121415 | ||||||
| chr1:118121416
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.316-5975G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118121416 | ||||||
| chr1:118121706
|
G | T | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-6265C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118121706 | ||||||
| chr1:118121748
|
T | G | 100 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(97): Show | 100 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.316-6307A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118121748 | ||||||
| chr1:118122153
|
C | CTG | 5 | a0001c0001t0001g0169a0001c0001t0001g0204a0002c0002t0001g0033others(2): Show | 5 | HG01934.hp2 HG02071.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.316-6714_316-6713d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118122153 | ||||||
| chr1:118122153
|
C | CTGTG | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-6716_316-6713d others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118122153 | ||||||
| chr1:118122153
|
CTG | C | 98 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(95): Show | 98 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.316-6714_316-6713d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118122153 | ||||||
| chr1:118122279
|
G | GA | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-6839dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118122279 | ||||||
| chr1:118122413
|
C | T | 3 | a0001c0006t0001g0164a0001c0006t0001g0165a0001c0006t0001g0193 | 3 | HG02055.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.316-6972G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118122413 | ||||||
| chr1:118122438
|
C | A | 1 | a0001c0001t0001g0184 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.316-6997G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118122438 | ||||||
| chr1:118122533
|
G | A | 2 | a0001c0010t0001g0150a0001c0010t0001g0156 | 2 | NA18949.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.316-7092C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118122533 | ||||||
| chr1:118122871
|
G | A | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-7430C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118122871 | ||||||
| chr1:118122928
|
T | A | 5 | a0003c0003t0001g0136a0003c0003t0001g0137a0003c0003t0001g0139others(2): Show | 5 | HG01167.hp1 HG01358.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.316-7487A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118122928 | ||||||
| chr1:118123088
|
G | A | 1 | a0004c0005t0001g0133 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.316-7647C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118123088 | ||||||
| chr1:118123227
|
C | T | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-7786G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118123227 | ||||||
| chr1:118123660
|
C | T | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.316-8219G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118123660 | ||||||
| chr1:118123706
|
C | T | 2 | a0001c0018t0001g0229a0014c0016t0002g0228 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.316-8265G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118123706 | ||||||
| chr1:118123951
|
T | C | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.316-8510A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118123951 | ||||||
| chr1:118124783
|
C | T | 1 | a0002c0002t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.316-9342G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118124783 | ||||||
| chr1:118124800
|
G | A | 2 | a0001c0004t0001g0225a0001c0004t0001g0237 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.316-9359C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118124800 | ||||||
| chr1:118124933
|
T | C | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.316-9492A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118124933 | ||||||
| chr1:118125003
|
G | A | 3 | a0003c0003t0001g0108a0003c0003t0001g0114a0003c0003t0001g0115 | 3 | HG00642.hp1 HG01070.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.316-9562C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125003 | ||||||
| chr1:118125094
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.316-9653G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125094 | ||||||
| chr1:118125195
|
T | G | 2 | a0004c0005t0001g0119a0004c0005t0001g0120 | 2 | HG00323.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.316-9754A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125195 | ||||||
| chr1:118125230
|
C | CATATATA others(3): Show |
2 | a0001c0004t0001g0222a0001c0004t0001g0223 | 2 | HG01433.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.316-9799_316-9790d others(12): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125230 | ||||||
| chr1:118125245
|
A | ATATATAT others(7): Show |
1 | a0001c0004t0001g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.316-9805_316-9804i others(16): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125245 | ||||||
| chr1:118125245
|
A | ATATATAT others(5): Show |
1 | a0001c0004t0001g0224 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.316-9805_316-9804i others(14): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125245 | ||||||
| chr1:118125245
|
A | ATATATAT others(3): Show |
4 | a0001c0004t0001g0220a0001c0018t0001g0229a0001c0027t0001g0221others(1): Show | 4 | HG02280.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-9805_316-9804i others(12): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125245 | ||||||
| chr1:118125245
|
A | ATATATAT others(5): Show |
1 | a0001c0004t0001g0235 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.316-9805_316-9804i others(14): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125245 | ||||||
| chr1:118125245
|
A | ATATATAT others(3): Show |
10 | a0001c0004t0001g0219a0001c0004t0001g0227a0001c0004t0001g0231others(7): Show | 10 | HG02145.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.316-9805_316-9804i others(12): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125245 | ||||||
| chr1:118125245
|
A | ATATATTT others(3): Show |
3 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0026t0001g0261 | 3 | HG02965.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.316-9805_316-9804i others(12): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125245 | ||||||
| chr1:118125245
|
A | ATATTTTT others(3): Show |
1 | a0001c0004t0001g0237 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.316-9805_316-9804i others(12): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125245 | ||||||
| chr1:118125245
|
A | T | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.316-9804T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125245 | ||||||
| chr1:118125319
|
T | G | 1 | a0001c0001t0001g0192 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.316-9878A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125319 | ||||||
| chr1:118125328
|
C | T | 2 | a0001c0004t0001g0225a0001c0004t0001g0237 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.316-9887G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125328 | ||||||
| chr1:118125346
|
T | C | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.316-9905A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125346 | ||||||
| chr1:118125445
|
C | T | 1 | a0001c0004t0001g0061 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316-10004G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125445 | ||||||
| chr1:118125453
|
C | T | 1 | a0003c0003t0001g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.316-10012G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125453 | ||||||
| chr1:118125563
|
G | A | 5 | a0001c0004t0001g0257a0001c0004t0001g0258a0001c0004t0001g0259others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.316-10122C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125563 | ||||||
| chr1:118125643
|
G | A | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.316-10202C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125643 | ||||||
| chr1:118125808
|
A | G | 1 | a0003c0003t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.316-10367T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118125808 | ||||||
| chr1:118126043
|
G | GT | 122 | a0001c0001t0001g0065a0001c0004t0003g0082a0001c0006t0001g0251others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.316-10603dupA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118126043 | ||||||
| chr1:118126043
|
G | GTT | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(99): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.316-10604_316-1060 others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118126043 | ||||||
| chr1:118126043
|
G | GTTT | 5 | a0001c0001t0001g0181a0001c0006t0001g0124a0001c0018t0001g0148others(2): Show | 5 | HG00621.hp1 HG01952.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.316-10605_316-1060 others(7): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118126043 | ||||||
| chr1:118126080
|
T | A | 2 | a0010c0013t0001g0132a0010c0013t0001g0135 | 2 | HG01928.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.316-10639A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118126080 | ||||||
| chr1:118126203
|
C | CT | 120 | a0001c0001t0001g0161a0001c0001t0001g0200a0001c0001t0001g0210others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.316-10763dupA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118126203 | ||||||
| chr1:118126203
|
C | CTT | 8 | a0002c0002t0001g0025a0002c0002t0001g0043a0002c0002t0001g0044others(5): Show | 8 | HG00738.hp2 HG04184.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.316-10764_316-1076 others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118126203 | ||||||
| chr1:118126203
|
CTTTTTTT others(3): Show |
C | 1 | a0018c0031t0002g0007 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.316-10772_316-1076 others(14): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118126203 | ||||||
| chr1:118126287
|
G | A | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.316-10846C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118126287 | ||||||
| chr1:118126403
|
C | T | 1 | a0001c0025t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.316-10962G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118126403 | ||||||
| chr1:118126509
|
G | A | 1 | a0001c0004t0001g0234 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.316-11068C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118126509 | ||||||
| chr1:118126878
|
AGAGGTCT others(12): Show |
A | 54 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.316-11456_316-1143 others(23): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118126878 | ||||||
| chr1:118127277
|
G | T | 1 | a0001c0004t0001g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.316-11836C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118127277 | ||||||
| chr1:118127339
|
G | A | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-11898C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118127339 | ||||||
| chr1:118127339
|
G | T | 73 | a0001c0004t0003g0082a0003c0003t0001g0064a0003c0003t0001g0076others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.316-11898C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118127339 | ||||||
| chr1:118127477
|
C | G | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.316-12036G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118127477 | ||||||
| chr1:118127547
|
C | G | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.316-12106G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118127547 | ||||||
| chr1:118127880
|
T | C | 6 | a0001c0001t0001g0168a0001c0001t0001g0177a0001c0001t0001g0178others(3): Show | 6 | HG00733.hp1 HG01099.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-12439A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118127880 | ||||||
| chr1:118127890
|
A | C | 2 | a0007c0017t0001g0015a0007c0017t0001g0016 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.316-12449T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118127890 | ||||||
| chr1:118128037
|
G | A | 3 | a0004c0005t0001g0096a0004c0005t0001g0097a0004c0005t0001g0098 | 3 | NA18990.hp2 NA19084.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.316-12596C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118128037 | ||||||
| chr1:118128281
|
A | G | 2 | a0001c0018t0001g0229a0014c0016t0002g0228 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.316-12840T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118128281 | ||||||
| chr1:118128330
|
C | T | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.316-12889G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118128330 | ||||||
| chr1:118128614
|
A | G | 1 | a0001c0004t0001g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.316-13173T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118128614 | ||||||
| chr1:118128827
|
T | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-13386A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118128827 | ||||||
| chr1:118129190
|
G | A | 2 | a0001c0001t0001g0211a0001c0010t0001g0154 | 2 | NA19006.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.316-13749C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118129190 | ||||||
| chr1:118129489
|
C | T | 1 | a0001c0001t0001g0003 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.316-14048G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118129489 | ||||||
| chr1:118129495
|
A | T | 1 | a0017c0034t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.316-14054T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118129495 | ||||||
| chr1:118129753
|
T | C | 2 | a0003c0003t0001g0101a0003c0003t0001g0134 | 2 | HG02056.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.316-14312A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118129753 | ||||||
| chr1:118129906
|
C | T | 3 | a0010c0013t0001g0121a0010c0013t0001g0132a0010c0013t0001g0135 | 3 | HG01496.hp2 HG01928.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.316-14465G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118129906 | ||||||
| chr1:118129910
|
T | A | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-14469A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118129910 | ||||||
| chr1:118129976
|
T | G | 54 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.316-14535A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118129976 | ||||||
| chr1:118130442
|
C | A | 1 | a0001c0001t0001g0161 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.316-15001G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118130442 | ||||||
| chr1:118130651
|
G | A | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.316-15210C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118130651 | ||||||
| chr1:118130653
|
G | A | 1 | a0001c0006t0001g0251 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.316-15212C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118130653 | ||||||
| chr1:118130810
|
G | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.316-15369C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118130810 | ||||||
| chr1:118130830
|
C | T | 2 | a0001c0001t0001g0211a0001c0010t0001g0154 | 2 | NA19006.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.316-15389G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118130830 | ||||||
| chr1:118131251
|
C | T | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.316-15810G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118131251 | ||||||
| chr1:118131395
|
T | C | 56 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.316-15954A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118131395 | ||||||
| chr1:118131684
|
C | T | 6 | a0003c0003t0001g0256a0003c0003t0003g0100a0008c0009t0002g0077others(3): Show | 6 | HG02258.hp1 HG02818.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-16243G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118131684 | ||||||
| chr1:118132113
|
G | A | 3 | a0003c0003t0001g0087a0003c0003t0001g0088a0003c0003t0001g0089 | 3 | HG01069.hp2 HG01071.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.316-16672C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118132113 | ||||||
| chr1:118132267
|
A | G | 56 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.316-16826T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118132267 | ||||||
| chr1:118132273
|
G | A | 3 | a0001c0006t0001g0151a0001c0006t0001g0152a0001c0006t0001g0153 | 3 | HG00280.hp2 HG01346.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.316-16832C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118132273 | ||||||
| chr1:118132278
|
A | T | 1 | a0001c0006t0001g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.316-16837T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118132278 | ||||||
| chr1:118132761
|
G | A | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.316-17320C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118132761 | ||||||
| chr1:118132803
|
T | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(256): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.316-17362A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118132803 | ||||||
| chr1:118132928
|
T | C | 163 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(160): Show | 164 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.316-17487A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118132928 | ||||||
| chr1:118132962
|
A | C | 2 | a0003c0003t0001g0129a0003c0003t0001g0130 | 2 | HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.316-17521T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118132962 | ||||||
| chr1:118133230
|
T | C | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.315+17313A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118133230 | ||||||
| chr1:118133358
|
G | A | 2 | a0002c0002t0001g0024a0002c0002t0001g0037 | 2 | NA18972.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.315+17185C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118133358 | ||||||
| chr1:118133732
|
T | C | 1 | a0001c0025t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.315+16811A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118133732 | ||||||
| chr1:118133966
|
G | C | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.315+16577C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118133966 | ||||||
| chr1:118134033
|
A | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.315+16510T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118134033 | ||||||
| chr1:118134044
|
C | A | 1 | a0001c0006t0001g0255 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.315+16499G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118134044 | ||||||
| chr1:118134802
|
C | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.315+15741G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118134802 | ||||||
| chr1:118134882
|
C | T | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.315+15661G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118134882 | ||||||
| chr1:118135184
|
G | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.315+15359C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135184 | ||||||
| chr1:118135325
|
G | T | 2 | a0001c0018t0001g0229a0014c0016t0002g0228 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.315+15218C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135325 | ||||||
| chr1:118135371
|
A | ATG | 16 | a0001c0001t0001g0168a0001c0001t0001g0194a0001c0001t0001g0195others(13): Show | 16 | HG00323.hp2 HG02129.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.315+15170_315+1517 others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135371 | ||||||
| chr1:118135371
|
A | ATGTG | 7 | a0001c0001t0001g0166a0001c0006t0001g0151a0001c0006t0001g0152others(4): Show | 7 | HG01346.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.315+15168_315+1517 others(8): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135371 | ||||||
| chr1:118135371
|
ATG | A | 109 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0181others(106): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.315+15170_315+1517 others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135371 | ||||||
| chr1:118135371
|
ATGTG | A | 49 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(46): Show | 49 | HG00423.hp1 HG00597.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.315+15168_315+1517 others(8): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135371 | ||||||
| chr1:118135371
|
ATGTGTG | A | 6 | a0002c0002t0001g0031a0004c0005t0001g0249a0007c0033t0001g0014others(3): Show | 6 | HG02040.hp1 HG02258.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.315+15166_315+1517 others(10): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135371 | ||||||
| chr1:118135371
|
ATGTGTGT others(1): Show |
A | 5 | a0001c0004t0001g0226a0001c0004t0001g0227a0001c0004t0001g0231others(2): Show | 5 | HG02055.hp2 HG02976.hp1 NA19079.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+15164_315+1517 others(12): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135371 | ||||||
| chr1:118135371
|
ATGTGTGT others(3): Show |
A | 2 | a0001c0032t0001g0067a0026c0039t0002g0262 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.315+15162_315+1517 others(14): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135371 | ||||||
| chr1:118135407
|
G | A | 1 | a0009c0012t0001g0247 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.315+15136C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135407 | ||||||
| chr1:118135409
|
G | A | 2 | a0001c0001t0001g0159a0003c0003t0001g0076 | 2 | HG01928.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.315+15134C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135409 | ||||||
| chr1:118135411
|
A | G | 3 | a0001c0001t0001g0159a0002c0002t0001g0010a0003c0003t0001g0076 | 3 | HG01928.hp1 HG02109.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.315+15132T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135411 | ||||||
| chr1:118135432
|
G | T | 164 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(161): Show | 165 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.315+15111C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135432 | ||||||
| chr1:118135955
|
G | A | 1 | a0001c0006t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.315+14588C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118135955 | ||||||
| chr1:118136020
|
G | T | 1 | a0003c0003t0001g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.315+14523C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136020 | ||||||
| chr1:118136168
|
C | G | 78 | a0001c0004t0003g0082a0001c0006t0001g0103a0001c0006t0001g0124others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.315+14375G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136168 | ||||||
| chr1:118136196
|
G | A | 1 | a0003c0003t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.315+14347C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136196 | ||||||
| chr1:118136330
|
C | T | 77 | a0001c0004t0003g0082a0001c0006t0001g0103a0001c0006t0001g0124others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.315+14213G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136330 | ||||||
| chr1:118136595
|
G | A | 53 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.315+13948C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136595 | ||||||
| chr1:118136791
|
G | T | 1 | a0004c0005t0001g0119 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.315+13752C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136791 | ||||||
| chr1:118136801
|
A | ATGTGTG | 3 | a0001c0004t0001g0062a0002c0002t0001g0047a0021c0024t0001g0006 | 3 | HG02451.hp2 HG03486.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.315+13736_315+1374 others(10): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136801 | ||||||
| chr1:118136801
|
A | ATGTGTGT others(1): Show |
6 | a0002c0002t0001g0011a0002c0002t0001g0030a0002c0002t0001g0058others(3): Show | 6 | HG01109.hp1 HG02135.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+13734_315+1374 others(12): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136801 | ||||||
| chr1:118136801
|
A | ATGTGTGT others(3): Show |
24 | a0002c0002t0001g0010a0002c0002t0001g0012a0002c0002t0001g0013others(21): Show | 24 | HG00597.hp1 HG00621.hp2 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.315+13732_315+1374 others(14): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136801 | ||||||
| chr1:118136801
|
A | ATGTGTGT others(5): Show |
16 | a0002c0002t0001g0001a0002c0002t0001g0019a0002c0002t0001g0020others(13): Show | 17 | HG00438.hp2 HG00735.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.315+13730_315+1374 others(16): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136801 | ||||||
| chr1:118136801
|
A | ATGTGTGT others(7): Show |
6 | a0002c0002t0001g0043a0002c0002t0001g0044a0002c0002t0001g0045others(3): Show | 6 | HG02735.hp1 NA18971.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.315+13728_315+1374 others(18): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136801 | ||||||
| chr1:118136801
|
ATG | A | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.315+13740_315+1374 others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136801 | ||||||
| chr1:118136832
|
T | TGTGTGTG others(4): Show |
1 | a0002c0002t0001g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.315+13710_315+1371 others(15): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136832 | ||||||
| chr1:118136833
|
T | G | 4 | a0002c0002t0001g0021a0007c0017t0001g0015a0007c0017t0001g0016others(1): Show | 4 | HG00597.hp1 HG02109.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+13710A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118136833 | ||||||
| chr1:118137088
|
T | A | 1 | a0001c0004t0001g0234 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.315+13455A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118137088 | ||||||
| chr1:118137311
|
G | C | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.315+13232C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118137311 | ||||||
| chr1:118137689
|
C | T | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.315+12854G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118137689 | ||||||
| chr1:118137714
|
G | C | 1 | a0003c0003t0001g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.315+12829C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118137714 | ||||||
| chr1:118137824
|
T | C | 1 | a0001c0004t0001g0230 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.315+12719A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118137824 | ||||||
| chr1:118138100
|
C | A | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.315+12443G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118138100 | ||||||
| chr1:118138177
|
C | T | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG00140.hp1 HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.315+12366G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118138177 | ||||||
| chr1:118138229
|
A | T | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.315+12314T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118138229 | ||||||
| chr1:118138523
|
CCACACAT others(3): Show |
C | 53 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.315+12010_315+1201 others(14): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118138523 | ||||||
| chr1:118138700
|
T | G | 1 | a0004c0005t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.315+11843A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118138700 | ||||||
| chr1:118138746
|
T | G | 2 | a0002c0002t0001g0058a0002c0002t0001g0059 | 2 | NA18973.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.315+11797A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118138746 | ||||||
| chr1:118138853
|
G | T | 1 | a0001c0001t0001g0196 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.315+11690C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118138853 | ||||||
| chr1:118138907
|
T | G | 1 | a0001c0025t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.315+11636A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118138907 | ||||||
| chr1:118139131
|
A | T | 29 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(26): Show | 29 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.315+11412T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118139131 | ||||||
| chr1:118139515
|
A | T | 1 | a0005c0038t0002g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.315+11028T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118139515 | ||||||
| chr1:118139813
|
G | T | 1 | a0004c0005t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.315+10730C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118139813 | ||||||
| chr1:118140001
|
G | T | 1 | a0003c0003t0001g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.315+10542C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118140001 | ||||||
| chr1:118140110
|
G | T | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.315+10433C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118140110 | ||||||
| chr1:118140130
|
C | G | 1 | a0001c0001t0001g0166 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.315+10413G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118140130 | ||||||
| chr1:118140246
|
G | A | 2 | a0002c0002t0001g0036a0002c0002t0001g0039 | 2 | NA18981.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.315+10297C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118140246 | ||||||
| chr1:118140398
|
C | G | 53 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.315+10145G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118140398 | ||||||
| chr1:118140443
|
C | A | 1 | a0004c0005t0001g0125 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.315+10100G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118140443 | ||||||
| chr1:118140549
|
C | T | 58 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.315+9994G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118140549 | ||||||
| chr1:118141038
|
C | T | 2 | a0001c0004t0001g0060a0001c0004t0001g0061 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.315+9505G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118141038 | ||||||
| chr1:118141129
|
GT | G | 58 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.315+9413delA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118141129 | ||||||
| chr1:118141152
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.315+9391C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118141152 | ||||||
| chr1:118141432
|
G | A | 6 | a0001c0001t0001g0186a0001c0001t0001g0191a0001c0001t0001g0213others(3): Show | 6 | HG01255.hp2 HG01981.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+9111C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118141432 | ||||||
| chr1:118141655
|
T | C | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.315+8888A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118141655 | ||||||
| chr1:118141888
|
T | G | 24 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0222others(21): Show | 24 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.315+8655A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118141888 | ||||||
| chr1:118142316
|
A | G | 58 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.315+8227T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118142316 | ||||||
| chr1:118142387
|
T | A | 2 | a0001c0004t0001g0060a0001c0004t0001g0061 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.315+8156A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118142387 | ||||||
| chr1:118142558
|
G | A | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.315+7985C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118142558 | ||||||
| chr1:118142641
|
T | C | 1 | a0001c0025t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.315+7902A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118142641 | ||||||
| chr1:118142737
|
G | T | 1 | a0005c0038t0002g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.315+7806C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118142737 | ||||||
| chr1:118142798
|
G | A | 2 | a0002c0002t0001g0024a0002c0002t0001g0037 | 2 | NA18972.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.315+7745C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118142798 | ||||||
| chr1:118143031
|
C | T | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.315+7512G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118143031 | ||||||
| chr1:118143217
|
A | G | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.315+7326T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118143217 | ||||||
| chr1:118143228
|
C | G | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.315+7315G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118143228 | ||||||
| chr1:118143432
|
T | C | 2 | a0001c0004t0001g0060a0001c0004t0001g0061 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.315+7111A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118143432 | ||||||
| chr1:118143497
|
A | G | 58 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.315+7046T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118143497 | ||||||
| chr1:118143822
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.315+6721A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118143822 | ||||||
| chr1:118143941
|
T | C | 4 | a0001c0004t0001g0234a0001c0018t0001g0229a0004c0005t0001g0084others(1): Show | 4 | HG02280.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+6602A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118143941 | ||||||
| chr1:118144267
|
C | T | 1 | a0004c0005t0001g0125 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.315+6276G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118144267 | ||||||
| chr1:118144344
|
A | T | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.315+6199T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118144344 | ||||||
| chr1:118144762
|
T | C | 1 | a0005c0011t0002g0202 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.315+5781A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118144762 | ||||||
| chr1:118144804
|
A | G | 1 | a0002c0002t0001g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.315+5739T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118144804 | ||||||
| chr1:118144851
|
TAATC | T | 4 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(1): Show | 4 | HG01433.hp2 HG03098.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+5688_315+5691d others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118144851 | ||||||
| chr1:118144909
|
T | C | 1 | a0002c0002t0001g0011 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.315+5634A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118144909 | ||||||
| chr1:118144972
|
T | C | 1 | a0001c0004t0001g0230 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.315+5571A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118144972 | ||||||
| chr1:118145253
|
T | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(76): Show | 81 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.315+5290A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118145253 | ||||||
| chr1:118145371
|
A | T | 1 | a0001c0001t0001g0166 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.315+5172T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118145371 | ||||||
| chr1:118145496
|
T | C | 2 | a0001c0018t0001g0229a0014c0016t0002g0228 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.315+5047A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118145496 | ||||||
| chr1:118145716
|
TA | T | 7 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0250others(4): Show | 7 | HG02055.hp2 HG02451.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.315+4826delT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118145716 | ||||||
| chr1:118145973
|
AT | A | 15 | a0001c0004t0001g0225a0001c0004t0001g0226a0001c0004t0001g0227others(12): Show | 15 | HG00741.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.315+4569delA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118145973 | ||||||
| chr1:118146077
|
G | A | 26 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(23): Show | 26 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.315+4466C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118146077 | ||||||
| chr1:118146108
|
C | T | 2 | a0003c0003t0001g0129a0003c0003t0001g0130 | 2 | HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.315+4435G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118146108 | ||||||
| chr1:118146646
|
T | C | 1 | a0005c0020t0002g0157 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.315+3897A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118146646 | ||||||
| chr1:118146777
|
C | G | 1 | a0002c0002t0001g0057 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.315+3766G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118146777 | ||||||
| chr1:118146778
|
T | G | 1 | a0002c0002t0001g0057 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.315+3765A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118146778 | ||||||
| chr1:118146851
|
T | C | 53 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.315+3692A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118146851 | ||||||
| chr1:118146883
|
T | C | 4 | a0004c0005t0001g0244a0009c0012t0001g0245a0009c0012t0001g0246others(1): Show | 4 | NA18949.hp1 NA18973.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+3660A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118146883 | ||||||
| chr1:118147269
|
T | C | 24 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0222others(21): Show | 24 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.315+3274A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118147269 | ||||||
| chr1:118147303
|
T | C | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.315+3240A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118147303 | ||||||
| chr1:118147461
|
T | C | 3 | a0001c0006t0001g0073a0001c0006t0001g0074a0001c0006t0001g0075 | 3 | HG00140.hp1 HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.315+3082A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118147461 | ||||||
| chr1:118147496
|
CAT | C | 56 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0230others(53): Show | 57 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.315+3045_315+3046d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118147496 | ||||||
| chr1:118147581
|
C | T | 1 | a0004c0005t0001g0242 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.315+2962G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118147581 | ||||||
| chr1:118147597
|
T | C | 4 | a0001c0006t0001g0252a0001c0006t0001g0253a0001c0006t0001g0255others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+2946A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118147597 | ||||||
| chr1:118147703
|
C | A | 1 | a0004c0005t0001g0081 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.315+2840G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118147703 | ||||||
| chr1:118147829
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.315+2714C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118147829 | ||||||
| chr1:118147941
|
T | C | 1 | a0001c0004t0001g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.315+2602A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118147941 | ||||||
| chr1:118147991
|
G | T | 1 | a0004c0005t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.315+2552C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118147991 | ||||||
| chr1:118148117
|
A | G | 1 | a0001c0004t0001g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.315+2426T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148117 | ||||||
| chr1:118148163
|
G | A | 5 | a0001c0001t0001g0003a0006c0007t0001g0187a0006c0007t0001g0188others(2): Show | 6 | HG01358.hp2 HG01433.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.315+2380C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148163 | ||||||
| chr1:118148180
|
C | T | 53 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.315+2363G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148180 | ||||||
| chr1:118148181
|
G | A | 1 | a0001c0018t0001g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.315+2362C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148181 | ||||||
| chr1:118148195
|
T | C | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.315+2348A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148195 | ||||||
| chr1:118148343
|
T | C | 1 | a0002c0002t0001g0050 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.315+2200A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148343 | ||||||
| chr1:118148344
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.315+2199A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148344 | ||||||
| chr1:118148362
|
A | C | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0162 | 3 | HG01167.hp2 HG01928.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.315+2181T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148362 | ||||||
| chr1:118148368
|
T | C | 2 | a0007c0017t0001g0015a0007c0017t0001g0016 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.315+2175A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148368 | ||||||
| chr1:118148371
|
T | G | 1 | a0001c0001t0001g0195 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.315+2172A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148371 | ||||||
| chr1:118148385
|
G | T | 1 | a0002c0002t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.315+2158C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148385 | ||||||
| chr1:118148414
|
C | T | 24 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0222others(21): Show | 24 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.315+2129G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148414 | ||||||
| chr1:118148484
|
CGCTGATT others(17): Show |
C | 53 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(50): Show | 54 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.315+2035_315+2058d others(26): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148484 | ||||||
| chr1:118148518
|
TCCATTTT others(17): Show |
T | 1 | a0001c0006t0001g0070 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.315+2001_315+2024d others(26): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148518 | ||||||
| chr1:118148658
|
G | A | 2 | a0002c0002t0001g0041a0002c0002t0001g0042 | 2 | NA19064.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.315+1885C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148658 | ||||||
| chr1:118148944
|
A | G | 1 | a0003c0003t0001g0092 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.315+1599T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118148944 | ||||||
| chr1:118149034
|
T | C | 1 | a0001c0004t0001g0231 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.315+1509A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118149034 | ||||||
| chr1:118149558
|
G | T | 2 | a0001c0004t0001g0060a0001c0004t0001g0061 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.315+985C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118149558 | ||||||
| chr1:118149586
|
C | T | 4 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014others(1): Show | 4 | HG02109.hp1 HG02735.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+957G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118149586 | ||||||
| chr1:118150325
|
A | G | 1 | a0002c0002t0001g0032 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.315+218T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118150325 | ||||||
| chr1:118150393
|
T | G | 32 | a0001c0004t0001g0143a0004c0005t0001g0004a0004c0005t0001g0080others(29): Show | 32 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.315+150A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 3/48 | chr1 | 118150393 | ||||||
| chr1:118150666
|
C | T | 7 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(4): Show | 7 | HG01433.hp2 HG02055.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.229-37G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 2/48 | chr1 | 118150666 | ||||||
| chr1:118150697
|
C | T | 2 | a0001c0004t0001g0060a0001c0004t0001g0061 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.229-68G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 2/48 | chr1 | 118150697 | ||||||
| chr1:118150747
|
G | A | 13 | a0002c0002t0001g0024a0002c0002t0001g0032a0002c0002t0001g0033others(10): Show | 13 | HG00438.hp2 HG02080.hp2 NA18946.hp2 others(10): Show |
intron_variant | MODIFIER | c.229-118C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 2/48 | chr1 | 118150747 | ||||||
| chr1:118151532
|
C | T | 48 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(45): Show | 49 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.88-163G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118151532 | ||||||
| chr1:118151910
|
G | A | 2 | a0005c0020t0002g0157a0005c0020t0002g0197 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.88-541C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118151910 | ||||||
| chr1:118152041
|
T | C | 1 | a0001c0004t0001g0224 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.88-672A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118152041 | ||||||
| chr1:118152316
|
A | G | 2 | a0002c0002t0001g0012a0002c0002t0001g0013 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.88-947T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118152316 | ||||||
| chr1:118152331
|
C | T | 2 | a0001c0006t0001g0103a0001c0006t0001g0124 | 2 | HG01109.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.88-962G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118152331 | ||||||
| chr1:118152761
|
T | G | 1 | a0002c0002t0001g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.88-1392A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118152761 | ||||||
| chr1:118152783
|
A | G | 19 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0022others(16): Show | 19 | HG00621.hp2 HG02071.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.88-1414T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118152783 | ||||||
| chr1:118153032
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.88-1663A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118153032 | ||||||
| chr1:118153092
|
G | A | 1 | a0001c0006t0001g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.88-1723C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118153092 | ||||||
| chr1:118153284
|
C | A | 1 | a0001c0001t0001g0192 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.88-1915G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118153284 | ||||||
| chr1:118153508
|
A | G | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.88-2139T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118153508 | ||||||
| chr1:118153709
|
T | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(256): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.88-2340A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118153709 | ||||||
| chr1:118154074
|
G | A | 1 | a0004c0005t0001g0125 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.88-2705C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118154074 | ||||||
| chr1:118154340
|
T | C | 26 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(23): Show | 26 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.88-2971A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118154340 | ||||||
| chr1:118154390
|
G | A | 1 | a0001c0006t0001g0193 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.88-3021C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118154390 | ||||||
| chr1:118154456
|
A | G | 15 | a0001c0004t0001g0224a0001c0004t0001g0225a0001c0004t0001g0226others(12): Show | 15 | HG00741.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.88-3087T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118154456 | ||||||
| chr1:118154461
|
T | A | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.88-3092A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118154461 | ||||||
| chr1:118154468
|
C | T | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.88-3099G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118154468 | ||||||
| chr1:118154519
|
C | A | 1 | a0003c0003t0001g0099 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.88-3150G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118154519 | ||||||
| chr1:118154764
|
T | C | 1 | a0003c0003t0001g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.88-3395A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118154764 | ||||||
| chr1:118154961
|
T | C | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.88-3592A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118154961 | ||||||
| chr1:118155057
|
G | A | 52 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(49): Show | 53 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.88-3688C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118155057 | ||||||
| chr1:118155134
|
G | A | 1 | a0003c0003t0001g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.88-3765C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118155134 | ||||||
| chr1:118155230
|
T | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.88-3861A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118155230 | ||||||
| chr1:118155965
|
C | T | 24 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0222others(21): Show | 24 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.88-4596G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118155965 | ||||||
| chr1:118156013
|
T | C | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.88-4644A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118156013 | ||||||
| chr1:118156094
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.88-4725A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118156094 | ||||||
| chr1:118156141
|
T | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.88-4772A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118156141 | ||||||
| chr1:118156391
|
C | T | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.88-5022G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118156391 | ||||||
| chr1:118156617
|
T | C | 1 | a0001c0004t0001g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88-5248A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118156617 | ||||||
| chr1:118156715
|
G | A | 57 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.88-5346C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118156715 | ||||||
| chr1:118156885
|
G | A | 1 | a0003c0003t0001g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.88-5516C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118156885 | ||||||
| chr1:118157010
|
C | G | 164 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(161): Show | 165 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.88-5641G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118157010 | ||||||
| chr1:118157011
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.88-5642C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118157011 | ||||||
| chr1:118157055
|
A | G | 1 | a0001c0004t0001g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88-5686T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118157055 | ||||||
| chr1:118157099
|
C | T | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(256): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.88-5730G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118157099 | ||||||
| chr1:118157153
|
G | T | 24 | a0001c0004t0001g0219a0001c0004t0001g0220a0001c0004t0001g0222others(21): Show | 24 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.88-5784C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118157153 | ||||||
| chr1:118157203
|
C | T | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.88-5834G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118157203 | ||||||
| chr1:118157235
|
T | C | 52 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(49): Show | 53 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.88-5866A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118157235 | ||||||
| chr1:118157482
|
G | A | 49 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(46): Show | 50 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.88-6113C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118157482 | ||||||
| chr1:118157854
|
A | G | 2 | a0001c0006t0001g0070a0001c0006t0001g0071 | 2 | HG02129.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.88-6485T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118157854 | ||||||
| chr1:118157878
|
A | G | 1 | a0002c0002t0001g0010 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.88-6509T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118157878 | ||||||
| chr1:118158251
|
T | G | 1 | a0013c0021t0002g0158 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.88-6882A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118158251 | ||||||
| chr1:118158885
|
G | A | 26 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(23): Show | 26 | HG00741.hp1 HG01433.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.88-7516C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118158885 | ||||||
| chr1:118159413
|
T | C | 2 | a0003c0003t0001g0129a0003c0003t0001g0130 | 2 | HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.88-8044A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118159413 | ||||||
| chr1:118159664
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(72): Show | 77 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.88-8295C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118159664 | ||||||
| chr1:118159667
|
T | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.88-8298A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118159667 | ||||||
| chr1:118159704
|
G | A | 2 | a0002c0002t0001g0041a0002c0002t0001g0042 | 2 | NA19064.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.88-8335C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118159704 | ||||||
| chr1:118160644
|
A | C | 1 | a0012c0015t0002g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.88-9275T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118160644 | ||||||
| chr1:118160658
|
A | G | 55 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(52): Show | 56 | HG00438.hp2 HG00621.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.88-9289T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118160658 | ||||||
| chr1:118160772
|
T | C | 1 | a0001c0004t0001g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88-9403A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118160772 | ||||||
| chr1:118160868
|
A | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.88-9499T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118160868 | ||||||
| chr1:118160988
|
A | T | 4 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014others(1): Show | 4 | HG02109.hp1 HG02735.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-9619T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118160988 | ||||||
| chr1:118161335
|
A | G | 50 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(47): Show | 51 | HG00438.hp2 HG00621.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.88-9966T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118161335 | ||||||
| chr1:118161544
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.88-10175A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118161544 | ||||||
| chr1:118161599
|
A | G | 1 | a0003c0003t0001g0101 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.88-10230T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118161599 | ||||||
| chr1:118161682
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.88-10313G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118161682 | ||||||
| chr1:118161778
|
G | A | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.88-10409C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118161778 | ||||||
| chr1:118162267
|
TG | T | 47 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(44): Show | 48 | HG00438.hp2 HG00621.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.88-10899delC | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118162267 | ||||||
| chr1:118162407
|
G | T | 4 | a0003c0003t0001g0076a0003c0003t0001g0078a0008c0009t0002g0077others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-11038C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118162407 | ||||||
| chr1:118162485
|
G | T | 47 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(44): Show | 48 | HG00438.hp2 HG00621.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.88-11116C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118162485 | ||||||
| chr1:118162889
|
T | C | 1 | a0002c0002t0001g0045 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.88-11520A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118162889 | ||||||
| chr1:118163359
|
C | A | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.88-11990G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118163359 | ||||||
| chr1:118163387
|
T | C | 1 | a0001c0004t0001g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88-12018A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118163387 | ||||||
| chr1:118163474
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.88-12105A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118163474 | ||||||
| chr1:118163876
|
A | G | 1 | a0001c0004t0001g0224 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.88-12507T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118163876 | ||||||
| chr1:118164013
|
G | A | 51 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(48): Show | 52 | HG00438.hp2 HG00621.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.88-12644C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118164013 | ||||||
| chr1:118164025
|
T | C | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.88-12656A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118164025 | ||||||
| chr1:118164109
|
C | T | 51 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(48): Show | 52 | HG00438.hp2 HG00621.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.88-12740G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118164109 | ||||||
| chr1:118164305
|
A | C | 1 | a0001c0001t0001g0149 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.88-12936T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118164305 | ||||||
| chr1:118164319
|
A | C | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.88-12950T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118164319 | ||||||
| chr1:118164407
|
TGTCA | T | 165 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(162): Show | 166 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.88-13042_88-13039d others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118164407 | ||||||
| chr1:118164733
|
T | C | 1 | a0001c0004t0001g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88-13364A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118164733 | ||||||
| chr1:118164764
|
A | G | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.88-13395T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118164764 | ||||||
| chr1:118164803
|
C | A | 2 | a0007c0017t0001g0015a0007c0017t0001g0016 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.88-13434G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118164803 | ||||||
| chr1:118165402
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.88-14033C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118165402 | ||||||
| chr1:118165573
|
A | G | 2 | a0002c0002t0001g0017a0002c0002t0001g0018 | 2 | HG02027.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.88-14204T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118165573 | ||||||
| chr1:118165627
|
TA | T | 7 | a0001c0004t0001g0257a0001c0004t0001g0258a0001c0004t0001g0259others(4): Show | 7 | HG02145.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.88-14259delT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118165627 | ||||||
| chr1:118165645
|
C | CT | 160 | a0001c0001t0001g0144a0001c0001t0001g0159a0001c0001t0001g0160others(157): Show | 161 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.88-14277dupA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118165645 | ||||||
| chr1:118165645
|
C | CTT | 11 | a0001c0010t0001g0150a0002c0002t0001g0025a0002c0008t0001g0046others(8): Show | 11 | HG00423.hp1 HG02976.hp2 HG04184.hp1 others(8): Show |
intron_variant | MODIFIER | c.88-14278_88-14277d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118165645 | ||||||
| chr1:118165645
|
C | T | 1 | a0001c0004t0001g0235 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.88-14276G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118165645 | ||||||
| chr1:118165692
|
T | C | 1 | a0004c0005t0001g0091 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.88-14323A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118165692 | ||||||
| chr1:118165697
|
C | G | 1 | a0004c0005t0001g0091 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.88-14328G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118165697 | ||||||
| chr1:118165889
|
C | T | 1 | a0001c0018t0001g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.88-14520G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118165889 | ||||||
| chr1:118165967
|
C | T | 9 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0022others(6): Show | 9 | HG00621.hp2 HG02523.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.88-14598G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118165967 | ||||||
| chr1:118166089
|
C | A | 1 | a0003c0003t0001g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.88-14720G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118166089 | ||||||
| chr1:118166382
|
C | T | 51 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(48): Show | 52 | HG00438.hp2 HG00621.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.88-15013G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118166382 | ||||||
| chr1:118166483
|
A | G | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.88-15114T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118166483 | ||||||
| chr1:118166758
|
T | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0216 | 2 | HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.88-15389A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118166758 | ||||||
| chr1:118167007
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0201 | 2 | NA18941.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.88-15638A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118167007 | ||||||
| chr1:118167233
|
G | A | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.88-15864C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118167233 | ||||||
| chr1:118167397
|
T | C | 1 | a0001c0004t0001g0235 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.88-16028A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118167397 | ||||||
| chr1:118167624
|
A | T | 1 | a0004c0005t0001g0090 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.88-16255T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118167624 | ||||||
| chr1:118167674
|
A | G | 13 | a0003c0003t0001g0092a0003c0003t0001g0099a0004c0005t0001g0081others(10): Show | 13 | HG02155.hp2 NA18943.hp2 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.88-16305T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118167674 | ||||||
| chr1:118167784
|
C | T | 1 | a0002c0002t0001g0019 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.88-16415G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118167784 | ||||||
| chr1:118167824
|
T | C | 1 | a0001c0006t0001g0236 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.88-16455A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118167824 | ||||||
| chr1:118168152
|
T | C | 4 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014others(1): Show | 4 | HG02109.hp1 HG02735.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-16783A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118168152 | ||||||
| chr1:118168457
|
T | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(77): Show | 82 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.87+16614A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118168457 | ||||||
| chr1:118168762
|
A | AT | 4 | a0003c0003t0001g0086a0003c0003t0001g0087a0003c0003t0001g0088others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+16308dupA | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118168762 | ||||||
| chr1:118168820
|
G | A | 3 | a0003c0003t0001g0256a0018c0031t0002g0007a0021c0024t0001g0006 | 3 | HG02451.hp2 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.87+16251C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118168820 | ||||||
| chr1:118169109
|
C | T | 54 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(51): Show | 55 | HG00438.hp2 HG00621.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.87+15962G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118169109 | ||||||
| chr1:118169521
|
G | T | 1 | a0001c0001t0001g0213 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.87+15550C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118169521 | ||||||
| chr1:118169578
|
G | A | 1 | a0001c0018t0001g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.87+15493C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118169578 | ||||||
| chr1:118169612
|
T | C | 1 | a0005c0020t0002g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.87+15459A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118169612 | ||||||
| chr1:118169683
|
C | G | 4 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014others(1): Show | 4 | HG02109.hp1 HG02735.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+15388G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118169683 | ||||||
| chr1:118170144
|
C | A | 1 | a0001c0004t0001g0237 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.87+14927G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118170144 | ||||||
| chr1:118170455
|
G | T | 1 | a0021c0024t0001g0006 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.87+14616C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118170455 | ||||||
| chr1:118170483
|
G | C | 55 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(52): Show | 56 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.87+14588C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118170483 | ||||||
| chr1:118170634
|
G | A | 3 | a0002c0002t0001g0043a0002c0002t0001g0044a0002c0002t0001g0045 | 3 | NA18971.hp2 NA19056.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.87+14437C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118170634 | ||||||
| chr1:118170650
|
C | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0018 | 2 | HG02027.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.87+14421G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118170650 | ||||||
| chr1:118170779
|
C | A | 2 | a0003c0003t0001g0129a0003c0003t0001g0130 | 2 | HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.87+14292G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118170779 | ||||||
| chr1:118170904
|
C | A | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.87+14167G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118170904 | ||||||
| chr1:118170940
|
A | G | 4 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014others(1): Show | 4 | HG02109.hp1 HG02735.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+14131T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118170940 | ||||||
| chr1:118170990
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.87+14081C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118170990 | ||||||
| chr1:118171036
|
G | A | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.87+14035C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118171036 | ||||||
| chr1:118171133
|
G | T | 1 | a0014c0016t0002g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.87+13938C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118171133 | ||||||
| chr1:118171236
|
A | C | 2 | a0003c0003t0001g0136a0003c0003t0001g0137 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.87+13835T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118171236 | ||||||
| chr1:118171300
|
T | C | 1 | a0001c0004t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.87+13771A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118171300 | ||||||
| chr1:118171357
|
C | T | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.87+13714G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118171357 | ||||||
| chr1:118171546
|
G | T | 2 | a0001c0006t0001g0252a0001c0006t0001g0253 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.87+13525C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118171546 | ||||||
| chr1:118171598
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18988.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.87+13473C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118171598 | ||||||
| chr1:118172283
|
A | T | 5 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+12788T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118172283 | ||||||
| chr1:118172467
|
T | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.87+12604A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118172467 | ||||||
| chr1:118172851
|
T | A | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(256): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.87+12220A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118172851 | ||||||
| chr1:118172957
|
A | T | 1 | a0002c0002t0001g0024 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.87+12114T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118172957 | ||||||
| chr1:118173143
|
C | A | 2 | a0002c0002t0001g0017a0002c0002t0001g0018 | 2 | HG02027.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.87+11928G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118173143 | ||||||
| chr1:118173281
|
C | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0201 | 2 | NA18941.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.87+11790G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118173281 | ||||||
| chr1:118173843
|
G | A | 1 | a0001c0025t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.87+11228C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118173843 | ||||||
| chr1:118173858
|
T | TA | 155 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0004t0001g0060others(152): Show | 156 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.87+11212dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118173858 | ||||||
| chr1:118173858
|
T | TAA | 12 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0022others(9): Show | 12 | HG00621.hp2 HG00735.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.87+11211_87+11212d others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118173858 | ||||||
| chr1:118173859
|
A | T | 1 | a0001c0018t0001g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.87+11212T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118173859 | ||||||
| chr1:118174072
|
T | C | 1 | a0010c0013t0001g0132 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.87+10999A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118174072 | ||||||
| chr1:118174386
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.87+10685A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118174386 | ||||||
| chr1:118174406
|
C | T | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.87+10665G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118174406 | ||||||
| chr1:118174466
|
A | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.87+10605T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118174466 | ||||||
| chr1:118175021
|
CTTAT | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(256): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.87+10046_87+10049d others(6): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118175021 | ||||||
| chr1:118175322
|
G | A | 1 | a0001c0025t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.87+9749C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118175322 | ||||||
| chr1:118175378
|
A | G | 55 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(52): Show | 56 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.87+9693T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118175378 | ||||||
| chr1:118175422
|
A | G | 79 | a0001c0004t0003g0082a0001c0006t0001g0103a0001c0006t0001g0124others(76): Show | 79 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.87+9649T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118175422 | ||||||
| chr1:118175555
|
G | A | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.87+9516C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118175555 | ||||||
| chr1:118175572
|
T | C | 1 | a0003c0029t0001g0141 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.87+9499A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118175572 | ||||||
| chr1:118175574
|
C | CA | 16 | a0001c0001t0001g0201a0001c0001t0001g0203a0001c0001t0001g0204others(13): Show | 16 | HG00140.hp1 HG00621.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.87+9496dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118175574 | ||||||
| chr1:118175587
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.87+9484T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118175587 | ||||||
| chr1:118175861
|
T | A | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.87+9210A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118175861 | ||||||
| chr1:118175881
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.87+9190T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118175881 | ||||||
| chr1:118175959
|
G | A | 5 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(2): Show | 5 | HG01433.hp2 HG02055.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+9112C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118175959 | ||||||
| chr1:118176354
|
A | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(256): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.87+8717T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118176354 | ||||||
| chr1:118176378
|
T | A | 2 | a0011c0014t0001g0008a0011c0014t0001g0009 | 2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.87+8693A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118176378 | ||||||
| chr1:118176755
|
T | C | 1 | a0001c0004t0001g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.87+8316A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118176755 | ||||||
| chr1:118176875
|
A | C | 1 | a0026c0039t0002g0262 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.87+8196T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118176875 | ||||||
| chr1:118177007
|
T | C | 1 | a0001c0025t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.87+8064A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118177007 | ||||||
| chr1:118177116
|
A | T | 36 | a0002c0002t0001g0010a0002c0002t0001g0011a0002c0002t0001g0022others(33): Show | 36 | HG00438.hp2 HG00621.hp2 HG02071.hp1 others(33): Show |
intron_variant | MODIFIER | c.87+7955T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118177116 | ||||||
| chr1:118177161
|
A | G | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG00621.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.87+7910T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118177161 | ||||||
| chr1:118177172
|
G | C | 2 | a0002c0002t0001g0058a0002c0002t0001g0059 | 2 | NA18973.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.87+7899C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118177172 | ||||||
| chr1:118177232
|
A | C | 4 | a0001c0004t0001g0220a0001c0004t0001g0222a0001c0004t0001g0223others(1): Show | 4 | HG01433.hp2 HG03098.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+7839T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118177232 | ||||||
| chr1:118177333
|
T | C | 55 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(52): Show | 56 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.87+7738A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118177333 | ||||||
| chr1:118177417
|
C | A | 1 | a0001c0001t0001g0209 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.87+7654G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118177417 | ||||||
| chr1:118177614
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.87+7457G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118177614 | ||||||
| chr1:118177687
|
A | G | 1 | a0001c0004t0003g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.87+7384T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118177687 | ||||||
| chr1:118177878
|
T | A | 6 | a0003c0003t0001g0136a0003c0003t0001g0137a0003c0003t0001g0139others(3): Show | 6 | HG00733.hp2 HG01167.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.87+7193A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118177878 | ||||||
| chr1:118177985
|
C | T | 3 | a0002c0002t0001g0001a0002c0002t0001g0019a0002c0002t0001g0020 | 4 | HG01346.hp1 HG02698.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+7086G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118177985 | ||||||
| chr1:118178143
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18988.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.87+6928A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118178143 | ||||||
| chr1:118178345
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.87+6726T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118178345 | ||||||
| chr1:118178449
|
G | A | 5 | a0001c0004t0001g0257a0001c0004t0001g0258a0001c0004t0001g0259others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.87+6622C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118178449 | ||||||
| chr1:118178721
|
TATTCAGT others(24): Show |
T | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.87+6319_87+6349del others(31): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118178721 | ||||||
| chr1:118178858
|
G | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0018 | 2 | HG02027.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.87+6213C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118178858 | ||||||
| chr1:118178993
|
T | C | 2 | a0001c0006t0001g0241a0001c0006t0001g0251 | 2 | NA19058.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.87+6078A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118178993 | ||||||
| chr1:118179113
|
A | C | 1 | a0004c0005t0001g0081 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.87+5958T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118179113 | ||||||
| chr1:118179174
|
G | C | 1 | a0004c0005t0001g0142 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.87+5897C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118179174 | ||||||
| chr1:118179295
|
C | T | 1 | a0004c0005t0001g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.87+5776G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118179295 | ||||||
| chr1:118179546
|
T | G | 1 | a0005c0038t0002g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.87+5525A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118179546 | ||||||
| chr1:118179762
|
C | A | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.87+5309G>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118179762 | ||||||
| chr1:118179853
|
G | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(1): Show | 4 | HG01981.hp2 HG02148.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+5218C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118179853 | ||||||
| chr1:118180317
|
C | T | 3 | a0007c0017t0001g0015a0007c0017t0001g0016a0007c0033t0001g0014 | 3 | HG02109.hp1 HG02735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.87+4754G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118180317 | ||||||
| chr1:118180356
|
C | T | 1 | a0001c0004t0001g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.87+4715G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118180356 | ||||||
| chr1:118180374
|
T | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | NA19063.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.87+4697A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118180374 | ||||||
| chr1:118180740
|
T | A | 1 | a0001c0001t0001g0065 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.87+4331A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118180740 | ||||||
| chr1:118180741
|
A | T | 1 | a0001c0001t0001g0065 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.87+4330T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118180741 | ||||||
| chr1:118180769
|
T | C | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.87+4302A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118180769 | ||||||
| chr1:118181059
|
CAATTT | C | 3 | a0001c0001t0001g0144a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG00735.hp1 HG03490.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.87+4007_87+4011del others(5): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118181059 | ||||||
| chr1:118181062
|
T | C | 111 | a0001c0004t0001g0143a0001c0004t0001g0219a0001c0004t0001g0220others(108): Show | 111 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.87+4009A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118181062 | ||||||
| chr1:118181072
|
A | G | 52 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(49): Show | 53 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.87+3999T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118181072 | ||||||
| chr1:118181509
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.87+3562G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118181509 | ||||||
| chr1:118181605
|
T | C | 2 | a0001c0006t0001g0241a0001c0006t0001g0251 | 2 | NA19058.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.87+3466A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118181605 | ||||||
| chr1:118181931
|
C | T | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.87+3140G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118181931 | ||||||
| chr1:118181998
|
A | G | 1 | a0001c0004t0001g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.87+3073T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118181998 | ||||||
| chr1:118182085
|
C | CAATG | 79 | a0001c0004t0003g0082a0001c0006t0001g0103a0001c0006t0001g0124others(76): Show | 79 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.87+2982_87+2985dup others(4): Show |
SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118182085 | ||||||
| chr1:118182203
|
A | G | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.87+2868T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118182203 | ||||||
| chr1:118182504
|
A | T | 1 | a0001c0025t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.87+2567T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118182504 | ||||||
| chr1:118182698
|
A | T | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.87+2373T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118182698 | ||||||
| chr1:118182719
|
T | G | 8 | a0004c0005t0001g0242a0004c0005t0001g0243a0004c0005t0001g0244others(5): Show | 8 | HG00423.hp1 HG00597.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.87+2352A>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118182719 | ||||||
| chr1:118182728
|
T | C | 1 | a0001c0004t0001g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.87+2343A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118182728 | ||||||
| chr1:118182921
|
T | C | 1 | a0001c0006t0001g0251 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.87+2150A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118182921 | ||||||
| chr1:118183171
|
A | G | 1 | a0007c0033t0001g0014 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.87+1900T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118183171 | ||||||
| chr1:118183274
|
A | G | 4 | a0003c0003t0001g0076a0003c0003t0001g0078a0008c0009t0002g0077others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+1797T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118183274 | ||||||
| chr1:118183659
|
C | T | 7 | a0001c0006t0001g0070a0001c0006t0001g0071a0001c0006t0001g0072others(4): Show | 7 | HG00140.hp1 HG01109.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.87+1412G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118183659 | ||||||
| chr1:118183922
|
G | A | 4 | a0001c0006t0001g0252a0001c0006t0001g0253a0001c0006t0001g0255others(1): Show | 4 | HG02451.hp1 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+1149C>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118183922 | ||||||
| chr1:118184080
|
G | GA | 58 | a0001c0004t0001g0257a0001c0004t0001g0258a0001c0004t0001g0259others(55): Show | 59 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.87+990dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184080 | ||||||
| chr1:118184187
|
C | T | 1 | a0016c0023t0001g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.87+884G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184187 | ||||||
| chr1:118184189
|
A | C | 1 | a0001c0032t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.87+882T>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184189 | ||||||
| chr1:118184208
|
G | GA | 52 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(49): Show | 53 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.87+862dupT | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184208 | ||||||
| chr1:118184218
|
T | A | 54 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(51): Show | 55 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.87+853A>T | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184218 | ||||||
| chr1:118184330
|
G | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG02015.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.87+741C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184330 | ||||||
| chr1:118184515
|
C | T | 57 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062others(54): Show | 58 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.87+556G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184515 | ||||||
| chr1:118184590
|
T | C | 52 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(49): Show | 53 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.87+481A>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184590 | ||||||
| chr1:118184599
|
C | T | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.87+472G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184599 | ||||||
| chr1:118184602
|
G | C | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.87+469C>G | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184602 | ||||||
| chr1:118184712
|
C | G | 1 | a0003c0003t0001g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.87+359G>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184712 | ||||||
| chr1:118184737
|
A | G | 1 | a0001c0025t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.87+334T>C | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184737 | ||||||
| chr1:118184858
|
C | T | 2 | a0018c0031t0002g0007a0021c0024t0001g0006 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.87+213G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184858 | ||||||
| chr1:118184932
|
TG | T | 3 | a0001c0004t0001g0060a0001c0004t0001g0061a0001c0004t0001g0062 | 3 | HG02615.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.87+138delC | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184932 | ||||||
| chr1:118184944
|
TC | T | 51 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(48): Show | 52 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.87+126delG | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184944 | ||||||
| chr1:118184977
|
A | T | 4 | a0011c0014t0001g0008a0011c0014t0001g0009a0018c0031t0002g0007others(1): Show | 4 | HG02451.hp2 HG02572.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+94T>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118184977 | ||||||
| chr1:118185049
|
G | T | 1 | a0001c0001t0001g0005 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.87+22C>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118185049 | ||||||
| chr1:118185050
|
C | T | 1 | a0004c0005t0001g0004 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.87+21G>A | SPAG17 | ENSG00000155761.14 | transcript | ENST00000336338.10 | protein_coding | 1/48 | chr1 | 118185050 |