Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6687 |
|---|---|
| ensemblid | ENSG00000197912.16 |
| hgncid | 11237 |
| symbol | SPG7 |
| name | SPG7 matrix AAA peptidase subunit, paraplegin |
| refseq_nuc | NM_003119.4 |
| refseq_prot | NP_003110.1 |
| ensembl_nuc | ENST00000645818.2 |
| ensembl_prot | ENSP00000495795.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 89508403 |
| end | 89557766 |
| strand | + |
| ver | v1.2 |
| region | chr16:89508403-89557766 |
| region5000 | chr16:89503403-89562766 |
| regionname0 | SPG7_chr16_89508403_89557766 |
| regionname5000 | SPG7_chr16_89503403_89562766 |
| 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 | 795 | 307 | 80 | 69 | 113 | 12 | 32 | 77 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0002 | 0/1 | 795 | 34 | 1 | 4 | 15 | 3 | 10 | 12 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0003 | 0/0 | 795 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0004 | 0/0 | 795 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0005 | 0/0 | 795 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0006 | 0/0 | 795 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0007 | 0/0 | 795 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0008 | 0/0 | 795 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0009 | 0/0 | 795 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0010 | 0/0 | 795 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2388 | 292 | 73 | 67 | 109 | 10 | 32 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0002 | 0/1 | 2388 | 33 | 1 | 4 | 15 | 3 | 9 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0003 | 0/0 | 2388 | 8 | 8 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0004 | 0/0 | 2388 | 4 | 1 | 0 | 2 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0005 | 0/0 | 2388 | 4 | 4 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0006 | 0/0 | 2388 | 2 | 0 | 1 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0007 | 0/0 | 2388 | 2 | 2 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0008 | 0/0 | 2388 | 2 | 1 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0009 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0010 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0011 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0012 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0013 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0014 | 0/0 | 2388 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0015 | 0/0 | 2388 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0016 | 0/0 | 2388 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0017 | 0/0 | 2388 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0018 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| c0019 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| 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 | 1/0 | 689 | 287 | 60 | 69 | 115 | 13 | 29 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| t0002 | 0/1 | 693 | 54 | 17 | 5 | 16 | 3 | 12 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| t0003 | 0/0 | 693 | 6 | 6 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| t0004 | 0/0 | 689 | 4 | 4 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| t0005 | 0/0 | 693 | 2 | 2 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| t0006 | 0/0 | 693 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| t0007 | 0/0 | 693 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| t0008 | 0/0 | 689 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| t0009 | 0/0 | 693 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| t0010 | 0/0 | 693 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0002 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0335 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2388 | 292 | 73 | 67 | 109 | 10 | 32 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0004 | 0/0 | 2388 | 4 | 1 | 0 | 2 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0005 | 0/0 | 2388 | 4 | 4 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0006 | 0/0 | 2388 | 2 | 0 | 1 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0011 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0012 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0013 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0016 | 0/0 | 2388 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0019 | 0/0 | 2388 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0002c0002 | 0/1 | 2388 | 33 | 1 | 4 | 15 | 3 | 9 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0002c0015 | 0/0 | 2388 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0003c0003 | 0/0 | 2388 | 8 | 8 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0004c0007 | 0/0 | 2388 | 2 | 2 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0005c0008 | 0/0 | 2388 | 2 | 1 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0006c0018 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0007c0017 | 0/0 | 2388 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0008c0010 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0009c0014 | 0/0 | 2388 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0010c0009 | 0/0 | 2388 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3076 | 271 | 57 | 66 | 108 | 10 | 29 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0001t0002 | 0/0 | 3080 | 11 | 7 | 1 | 1 | 0 | 2 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0001t0003 | 0/0 | 3080 | 4 | 4 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0001t0004 | 0/0 | 3076 | 4 | 4 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0001t0007 | 0/0 | 3080 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0001t0008 | 0/0 | 3076 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0004t0001 | 0/0 | 3076 | 4 | 1 | 0 | 2 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0005t0005 | 0/0 | 3080 | 2 | 2 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0005t0009 | 0/0 | 3080 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0005t0010 | 0/0 | 3080 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0006t0001 | 0/0 | 3076 | 2 | 0 | 1 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0011t0001 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0012t0001 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0013t0003 | 0/0 | 3080 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0016t0001 | 0/0 | 3076 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0001c0019t0003 | 0/0 | 3080 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0002c0002t0002 | 0/1 | 3080 | 32 | 1 | 4 | 14 | 3 | 9 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0002c0002t0006 | 0/0 | 3080 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0002c0015t0002 | 0/0 | 3080 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0003c0003t0002 | 0/0 | 3080 | 8 | 8 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0004c0007t0001 | 0/0 | 3076 | 2 | 2 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0005c0008t0002 | 0/0 | 3080 | 2 | 1 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0006c0018t0001 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0007c0017t0001 | 0/0 | 3076 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0008c0010t0001 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0009c0014t0001 | 0/0 | 3076 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| a0010c0009t0001 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | copy fasta | chr16 | 89503403 | 89562766 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0335 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0007g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0001t0008g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0004t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0004t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0004t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0005t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0005t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0005t0009g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0005t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0006t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0006t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0011t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0012t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0013t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0016t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0001c0019t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0002 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0002t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0002c0015t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0003c0003t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0004c0007t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0004c0007t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0005c0008t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0005c0008t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0006c0018t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0007c0017t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0008c0010t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0009c0014t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| a0010c0009t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0009 | c0014 | t0001 | g0259 | EUR | GBR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0260 | EUR | GBR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00280 | hp1 | a0001 | c0004 | t0001 | g0299 | EUR | FIN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0018 | EUR | FIN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | FIN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | CHS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01074 | hp1 | a0001 | c0006 | t0001 | g0057 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01106 | hp1 | a0007 | c0017 | t0001 | g0149 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0015 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0026 | EUR | IBS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01516 | hp2 | a0001 | c0006 | t0001 | g0104 | EUR | IBS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | IBS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0035 | EUR | IBS | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01884 | hp1 | a0005 | c0008 | t0002 | g0105 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01884 | hp2 | a0004 | c0007 | t0001 | g0296 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01891 | hp1 | a0003 | c0003 | t0002 | g0208 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01891 | hp2 | a0001 | c0013 | t0003 | g0340 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01928 | hp2 | a0001 | c0016 | t0001 | g0287 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0037 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0347 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02080 | hp1 | a0001 | c0012 | t0001 | g0062 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02145 | hp1 | a0004 | c0007 | t0001 | g0297 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CDX | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CDX | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CDX | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02258 | hp2 | a0001 | c0005 | t0010 | g0235 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0025 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02451 | hp2 | a0003 | c0003 | t0002 | g0233 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02615 | hp2 | a0003 | c0003 | t0002 | g0056 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02717 | hp1 | a0003 | c0003 | t0002 | g0231 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0017 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02965 | hp2 | a0001 | c0019 | t0003 | g0217 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02970 | hp1 | a0003 | c0003 | t0002 | g0234 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02970 | hp2 | a0003 | c0003 | t0002 | g0055 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0011 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03041 | hp2 | a0003 | c0003 | t0002 | g0232 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0306 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0344 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0295 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0012 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0033 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03579 | hp1 | a0001 | c0005 | t0009 | g0339 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0337 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0029 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0022 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03834 | hp1 | a0002 | c0015 | t0002 | g0040 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0036 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0032 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0168 | SAS | BEB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0021 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | YRI | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18747 | hp1 | a0010 | c0009 | t0001 | g0118 | EAS | CHB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18953 | hp1 | a0001 | c0004 | t0001 | g0308 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18960 | hp1 | a0002 | c0002 | t0006 | g0001 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0350 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0009 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18989 | hp1 | a0001 | c0011 | t0001 | g0178 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18991 | hp1 | a0005 | c0008 | t0002 | g0318 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18994 | hp2 | a0006 | c0018 | t0001 | g0243 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19010 | hp2 | a0008 | c0010 | t0001 | g0237 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | LWK | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19030 | hp2 | a0001 | c0005 | t0005 | g0304 | AFR | LWK | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | LWK | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0346 | AFR | LWK | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0176 | AFR | ASW | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ASW | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | TSI | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02559 | hp1 | a0001 | c0005 | t0005 | g0301 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | USA | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| HG06807 | hp2 | a0003 | c0003 | t0002 | g0054 | AFR | USA | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | USA | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | USA | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | LWK | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0002 | REF | REF | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0335 | REF | REF | SPG7_chr16_89503403_89562766 | SPG7 | chr16 | 89503403 | 89562766 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89513008
|
C | T | 1 | a0006 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.347C>T | p.Ser116Leu | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/17 | 362/3076 | 347/2388 | 116/795 | chr16 | 89513008 | ||
| chr16:89526366
|
T | C | 1 | a0010 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.656T>C | p.Ile219Thr | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/17 | 671/3076 | 656/2388 | 219/795 | chr16 | 89526366 | ||
| chr16:89530702
|
G | A | 1 | a0004 | 2 | HG01884.hp2 HG02145.hp1 |
missense_variant | MODERATE | c.881G>A | p.Arg294His | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/17 | 896/3076 | 881/2388 | 294/795 | chr16 | 89530702 | ||
| chr16:89530785
|
C | T | 1 | a0007 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.964C>T | p.Arg322Cys | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/17 | 979/3076 | 964/2388 | 322/795 | chr16 | 89530785 | ||
| chr16:89532480
|
G | C | 1 | a0008 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.1168G>C | p.Val390Leu | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/17 | 1183/3076 | 1168/2388 | 390/795 | chr16 | 89532480 | ||
| chr16:89546715
|
A | G | 1 | a0002 | 34 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(31): Show |
missense_variant | MODERATE | c.1507A>G | p.Thr503Ala | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/17 | 1522/3076 | 1507/2388 | 503/795 | chr16 | 89546715 | ||
| chr16:89546737
|
C | T | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1529C>T | p.Ala510Val | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/17 | 1544/3076 | 1529/2388 | 510/795 | chr16 | 89546737 | ||
| chr16:89553920
|
G | A | 2 | a0002a0005 | 36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
missense_variant | MODERATE | c.2063G>A | p.Arg688Gln | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/17 | 2078/3076 | 2063/2388 | 688/795 | chr16 | 89553920 | ||
| chr16:89556893
|
A | G | 1 | a0003 | 8 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
missense_variant | MODERATE | c.2188A>G | p.Asn730Asp | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 2203/3076 | 2188/2388 | 730/795 | chr16 | 89556893 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89508426
|
G | T | 1 | a0001c0019 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.9G>T | p.Val3Val | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/17 | 24/3076 | 9/2388 | 3/795 | chr16 | 89508426 | ||
| chr16:89508537
|
G | A | 1 | a0001c0006 | 2 | HG01074.hp1 HG01516.hp2 |
synonymous_variant | LOW | c.120G>A | p.Gly40Gly | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/17 | 135/3076 | 120/2388 | 40/795 | chr16 | 89508537 | ||
| chr16:89531909
|
A | G | 1 | a0001c0016 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.993A>G | p.Pro331Pro | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 8/17 | 1008/3076 | 993/2388 | 331/795 | chr16 | 89531909 | ||
| chr16:89550570
|
G | A | 1 | a0001c0011 | 1 | NA18989.hp1 | synonymous_variant | LOW | c.1740G>A | p.Leu580Leu | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/17 | 1755/3076 | 1740/2388 | 580/795 | chr16 | 89550570 | ||
| chr16:89550600
|
C | T | 2 | a0001c0013a0001c0019 | 2 | HG01891.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.1770C>T | p.Ala590Ala | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/17 | 1785/3076 | 1770/2388 | 590/795 | chr16 | 89550600 | ||
| chr16:89553011
|
G | A | 1 | a0001c0012 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.1812G>A | p.Leu604Leu | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/17 | 1827/3076 | 1812/2388 | 604/795 | chr16 | 89553011 | ||
| chr16:89553894
|
G | A | 2 | a0001c0013a0001c0019 | 2 | HG01891.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.2037G>A | p.Ala679Ala | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/17 | 2052/3076 | 2037/2388 | 679/795 | chr16 | 89553894 | ||
| chr16:89556985
|
G | A | 1 | a0001c0004 | 4 | HG00280.hp1 NA18953.hp1 NA18975.hp1 others(1): Show |
synonymous_variant | LOW | c.2280G>A | p.Pro760Pro | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 2295/3076 | 2280/2388 | 760/795 | chr16 | 89556985 | ||
| chr16:89556997
|
C | T | 1 | a0002c0015 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.2292C>T | p.Ile764Ile | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 2307/3076 | 2292/2388 | 764/795 | chr16 | 89556997 | ||
| chr16:89557000
|
C | T | 1 | a0001c0005 | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.2295C>T | p.Asp765Asp | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 2310/3076 | 2295/2388 | 765/795 | chr16 | 89557000 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89557104
|
T | A | 1 | a0002c0002t0006 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 11 | chr16 | 89557104 | |||||
| chr16:89557126
|
C | T | 6 | a0001c0001t0003a0001c0005t0005a0001c0005t0009others(3): Show | 10 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*33C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 33 | chr16 | 89557126 | |||||
| chr16:89557199
|
A | G | 3 | a0001c0005t0005a0001c0005t0009a0001c0005t0010 | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*106A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 106 | chr16 | 89557199 | |||||
| chr16:89557211
|
A | G | 3 | a0001c0005t0005a0001c0005t0009a0001c0005t0010 | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*118A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 118 | chr16 | 89557211 | |||||
| chr16:89557215
|
T | C | 3 | a0001c0005t0005a0001c0005t0009a0001c0005t0010 | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*122T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 122 | chr16 | 89557215 | |||||
| chr16:89557233
|
G | T | 3 | a0001c0005t0005a0001c0005t0009a0001c0005t0010 | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*140G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 140 | chr16 | 89557233 | |||||
| chr16:89557288
|
C | T | 3 | a0001c0005t0005a0001c0005t0009a0001c0005t0010 | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*195C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 195 | chr16 | 89557288 | |||||
| chr16:89557290
|
T | C | 1 | a0002c0002t0006 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*197T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 197 | chr16 | 89557290 | |||||
| chr16:89557455
|
C | T | 2 | a0001c0005t0009a0001c0005t0010 | 2 | HG02258.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*362C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 362 | chr16 | 89557455 | |||||
| chr16:89557491
|
G | A | 1 | a0001c0005t0009 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 398 | chr16 | 89557491 | |||||
| chr16:89557525
|
G | A | 1 | a0001c0001t0007 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*432G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 432 | chr16 | 89557525 | |||||
| chr16:89557528
|
A | G | 1 | a0001c0001t0008 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*435A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 435 | chr16 | 89557528 | |||||
| chr16:89557534
|
T | C | 1 | a0001c0001t0004 | 4 | HG02723.hp2 HG02896.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*441T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 441 | chr16 | 89557534 | |||||
| chr16:89557582
|
C | CCACA | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(10): Show | 66 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*491_*492insCACA | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 492 | INFO_REALIGN_3_PRIME | chr16 | 89557582 | ||||
| chr16:89557642
|
A | C | 2 | a0001c0005t0009a0001c0005t0010 | 2 | HG02258.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*549A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 549 | chr16 | 89557642 | |||||
| chr16:89557680
|
G | A | 3 | a0001c0005t0005a0001c0005t0009a0001c0005t0010 | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*587G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 587 | chr16 | 89557680 | |||||
| chr16:89557685
|
C | T | 3 | a0001c0005t0005a0001c0005t0009a0001c0005t0010 | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*592C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 592 | chr16 | 89557685 | |||||
| chr16:89557749
|
G | C | 3 | a0001c0005t0005a0001c0005t0009a0001c0005t0010 | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*656G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 17/17 | 656 | chr16 | 89557749 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89508712
|
C | T | 1 | a0001c0001t0001g0351 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.183+112C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89508712 | ||||||
| chr16:89508726
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.183+126G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89508726 | ||||||
| chr16:89509081
|
C | T | 1 | a0002c0002t0002g0350 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.183+481C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509081 | ||||||
| chr16:89509117
|
C | G | 1 | a0001c0001t0001g0349 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.183+517C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509117 | ||||||
| chr16:89509137
|
C | A | 1 | a0001c0004t0001g0009 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.183+537C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509137 | ||||||
| chr16:89509200
|
T | A | 36 | a0001c0001t0001g0014a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.183+600T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509200 | ||||||
| chr16:89509220
|
C | T | 5 | a0001c0001t0001g0345a0001c0001t0001g0348a0001c0001t0003g0344others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+620C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509220 | ||||||
| chr16:89509331
|
A | G | 1 | a0001c0001t0001g0343 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.183+731A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509331 | ||||||
| chr16:89509363
|
G | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.183+763G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509363 | ||||||
| chr16:89509426
|
T | A | 1 | a0001c0001t0001g0216 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.183+826T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509426 | ||||||
| chr16:89509483
|
T | G | 1 | a0001c0001t0001g0042 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.183+883T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509483 | ||||||
| chr16:89509608
|
A | T | 36 | a0001c0001t0001g0014a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.184-882A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509608 | ||||||
| chr16:89509678
|
T | G | 185 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.184-812T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509678 | ||||||
| chr16:89509786
|
C | CT | 7 | a0001c0001t0001g0215a0001c0001t0001g0341a0001c0001t0001g0342others(4): Show | 7 | HG00673.hp2 HG01891.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-682dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 89509786 | |||||
| chr16:89509786
|
CT | C | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(165): Show | 170 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.184-682delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 89509786 | |||||
| chr16:89509786
|
CTT | C | 11 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(8): Show | 11 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-683_184-682del others(2): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 89509786 | |||||
| chr16:89509815
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.184-675A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509815 | ||||||
| chr16:89509827
|
C | T | 1 | a0001c0001t0002g0337 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.184-663C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509827 | ||||||
| chr16:89509978
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.184-512A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89509978 | ||||||
| chr16:89510001
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.184-489G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510001 | ||||||
| chr16:89510039
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.184-451A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510039 | ||||||
| chr16:89510057
|
C | G | 6 | a0001c0001t0001g0042a0001c0001t0002g0201a0001c0001t0004g0198others(3): Show | 6 | HG01167.hp2 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-433C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510057 | ||||||
| chr16:89510099
|
T | C | 236 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(233): Show | 239 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.184-391T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510099 | ||||||
| chr16:89510132
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.184-358G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510132 | ||||||
| chr16:89510255
|
G | A | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(179): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.184-235G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510255 | ||||||
| chr16:89510358
|
T | C | 185 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.184-132T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | chr16 | 89510358 | ||||||
| chr16:89510471
|
GT | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(174): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(176): Show |
splice_region_variant&intron_variant | LOW | c.184-4delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 89510471 | |||||
| chr16:89510638
|
C | T | 185 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.286+46C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89510638 | ||||||
| chr16:89510740
|
C | A | 4 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0338others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+148C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89510740 | ||||||
| chr16:89510810
|
G | A | 3 | a0003c0003t0002g0054a0003c0003t0002g0055a0003c0003t0002g0056 | 3 | HG02615.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.286+218G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89510810 | ||||||
| chr16:89510903
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.286+311C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89510903 | ||||||
| chr16:89510949
|
C | A | 1 | a0001c0006t0001g0057 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.286+357C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89510949 | ||||||
| chr16:89510958
|
A | G | 185 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.286+366A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89510958 | ||||||
| chr16:89511242
|
T | G | 1 | a0001c0001t0001g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.286+650T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511242 | ||||||
| chr16:89511282
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.286+690C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511282 | ||||||
| chr16:89511342
|
T | G | 1 | a0001c0001t0002g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.286+750T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511342 | ||||||
| chr16:89511363
|
T | G | 1 | a0001c0019t0003g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.286+771T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511363 | ||||||
| chr16:89511395
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.286+803C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511395 | ||||||
| chr16:89511411
|
T | A | 10 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(7): Show | 10 | HG01934.hp2 HG02080.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.286+819T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511411 | ||||||
| chr16:89511649
|
C | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(158): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.286+1057C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511649 | ||||||
| chr16:89511700
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.286+1108G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511700 | ||||||
| chr16:89511733
|
T | C | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.286+1141T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511733 | ||||||
| chr16:89511912
|
G | GTTTAA | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.287-1032_287-1031i others(7): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 89511912 | |||||
| chr16:89511915
|
T | G | 3 | a0002c0002t0002g0001a0002c0002t0002g0350a0002c0002t0006g0001 | 3 | NA18960.hp1 NA18972.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.287-1033T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511915 | ||||||
| chr16:89511916
|
A | T | 3 | a0002c0002t0002g0001a0002c0002t0002g0350a0002c0002t0006g0001 | 3 | NA18960.hp1 NA18972.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.287-1032A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511916 | ||||||
| chr16:89511946
|
C | G | 13 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0002g0219others(10): Show | 13 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.287-1002C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511946 | ||||||
| chr16:89511981
|
C | T | 2 | a0002c0002t0002g0038a0002c0002t0002g0039 | 2 | NA18942.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.287-967C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89511981 | ||||||
| chr16:89512090
|
T | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02074.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.287-858T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512090 | ||||||
| chr16:89512160
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.287-788C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512160 | ||||||
| chr16:89512348
|
C | G | 181 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(178): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.287-600C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512348 | ||||||
| chr16:89512554
|
A | T | 2 | a0001c0005t0009g0339a0001c0005t0010g0235 | 2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.287-394A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512554 | ||||||
| chr16:89512562
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.287-386C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512562 | ||||||
| chr16:89512668
|
A | G | 42 | a0001c0001t0001g0014a0001c0001t0001g0226a0001c0001t0001g0228others(39): Show | 43 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.287-280A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512668 | ||||||
| chr16:89512715
|
G | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.287-233G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512715 | ||||||
| chr16:89512807
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.287-141A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512807 | ||||||
| chr16:89512874
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.287-74G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 2/16 | chr16 | 89512874 | ||||||
| chr16:89513142
|
G | T | 2 | a0001c0001t0001g0218a0001c0019t0003g0217 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.376+105G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513142 | ||||||
| chr16:89513177
|
C | T | 2 | a0001c0001t0001g0218a0001c0019t0003g0217 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.376+140C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513177 | ||||||
| chr16:89513285
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.376+248A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513285 | ||||||
| chr16:89513388
|
C | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+351C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513388 | ||||||
| chr16:89513398
|
C | A | 3 | a0003c0003t0002g0054a0003c0003t0002g0055a0003c0003t0002g0056 | 3 | HG02615.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.376+361C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513398 | ||||||
| chr16:89513463
|
T | C | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+426T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513463 | ||||||
| chr16:89513500
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.376+463G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513500 | ||||||
| chr16:89513529
|
A | T | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.376+492A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513529 | ||||||
| chr16:89513539
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.376+502A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513539 | ||||||
| chr16:89513719
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.376+682T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89513719 | ||||||
| chr16:89513761
|
GT | G | 349 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(346): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.376+726delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89513761 | |||||
| chr16:89514071
|
G | T | 16 | a0001c0001t0001g0223a0001c0001t0001g0240a0001c0001t0001g0322others(13): Show | 16 | HG01192.hp1 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.376+1034G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514071 | ||||||
| chr16:89514276
|
A | T | 36 | a0001c0001t0001g0014a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.376+1239A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514276 | ||||||
| chr16:89514308
|
CT | C | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(97): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.376+1303delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514308 | |||||
| chr16:89514308
|
CTT | C | 30 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(27): Show | 30 | HG00621.hp2 HG01081.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.376+1302_376+1303d others(4): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514308 | |||||
| chr16:89514308
|
CTTT | C | 57 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(54): Show | 57 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.376+1301_376+1303d others(5): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514308 | |||||
| chr16:89514308
|
CTTTT | C | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(112): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.376+1300_376+1303d others(6): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514308 | |||||
| chr16:89514308
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0065 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.376+1287_376+1303d others(19): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514308 | |||||
| chr16:89514347
|
A | G | 1 | a0001c0001t0001g0321 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.376+1310A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514347 | ||||||
| chr16:89514361
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.376+1324C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514361 | ||||||
| chr16:89514445
|
G | C | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.376+1408G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514445 | ||||||
| chr16:89514448
|
G | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+1411G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514448 | ||||||
| chr16:89514532
|
G | A | 2 | a0001c0001t0001g0218a0001c0019t0003g0217 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.376+1495G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514532 | ||||||
| chr16:89514625
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.376+1588C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514625 | ||||||
| chr16:89514628
|
G | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+1591G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514628 | ||||||
| chr16:89514787
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.376+1750C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514787 | ||||||
| chr16:89514808
|
A | G | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+1771A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514808 | ||||||
| chr16:89514828
|
T | C | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.376+1791T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514828 | ||||||
| chr16:89514891
|
A | G | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0184 | 3 | NA18941.hp1 NA18964.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.376+1854A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514891 | ||||||
| chr16:89514922
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.376+1885G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514922 | ||||||
| chr16:89514935
|
C | CT | 10 | a0001c0001t0001g0247a0001c0001t0001g0300a0001c0001t0001g0333others(7): Show | 10 | HG00280.hp1 HG01978.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.376+1917dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514935 | |||||
| chr16:89514935
|
CT | C | 13 | a0001c0001t0001g0084a0001c0001t0001g0162a0001c0001t0001g0183others(10): Show | 13 | HG01081.hp1 HG01433.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.376+1917delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514935 | |||||
| chr16:89514935
|
CTT | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(179): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.376+1916_376+1917d others(4): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89514935 | |||||
| chr16:89514968
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.376+1931G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89514968 | ||||||
| chr16:89515017
|
A | G | 2 | a0001c0005t0009g0339a0001c0005t0010g0235 | 2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.376+1980A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515017 | ||||||
| chr16:89515048
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.376+2011T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515048 | ||||||
| chr16:89515181
|
G | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(196): Show | 201 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.376+2144G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515181 | ||||||
| chr16:89515242
|
C | CT | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+2217dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89515242 | |||||
| chr16:89515291
|
C | T | 6 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0002g0219others(3): Show | 6 | HG01081.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.376+2254C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515291 | ||||||
| chr16:89515304
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.376+2267T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515304 | ||||||
| chr16:89515378
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.376+2341C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515378 | ||||||
| chr16:89515503
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.376+2466G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515503 | ||||||
| chr16:89515516
|
T | C | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.376+2479T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515516 | ||||||
| chr16:89515610
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.376+2573C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515610 | ||||||
| chr16:89515660
|
A | C | 1 | a0001c0001t0001g0298 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.376+2623A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515660 | ||||||
| chr16:89515709
|
A | T | 1 | a0001c0019t0003g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.376+2672A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515709 | ||||||
| chr16:89515712
|
A | T | 19 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(16): Show | 19 | HG01081.hp1 HG02109.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.376+2675A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515712 | ||||||
| chr16:89515715
|
A | G | 1 | a0001c0005t0005g0301 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376+2678A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515715 | ||||||
| chr16:89515715
|
A | T | 241 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(238): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.376+2678A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515715 | ||||||
| chr16:89515721
|
T | G | 1 | a0001c0001t0001g0097 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.376+2684T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515721 | ||||||
| chr16:89515724
|
T | G | 181 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(178): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.376+2687T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515724 | ||||||
| chr16:89515724
|
T | TG | 5 | a0001c0001t0001g0345a0001c0001t0001g0348a0001c0001t0003g0344others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+2687_376+2688i others(3): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515724 | ||||||
| chr16:89515748
|
G | T | 2 | a0001c0001t0001g0294a0001c0001t0003g0295 | 2 | HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.376+2711G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89515748 | ||||||
| chr16:89516060
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.376+3023T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516060 | ||||||
| chr16:89516276
|
C | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+3239C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516276 | ||||||
| chr16:89516398
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.376+3361A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516398 | ||||||
| chr16:89516421
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.376+3384C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516421 | ||||||
| chr16:89516445
|
G | A | 13 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0002g0219others(10): Show | 13 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.376+3408G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516445 | ||||||
| chr16:89516504
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.376+3467T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516504 | ||||||
| chr16:89516520
|
C | T | 33 | a0001c0001t0001g0096a0001c0001t0001g0136a0001c0001t0001g0137others(30): Show | 33 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.376+3483C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516520 | ||||||
| chr16:89516523
|
C | G | 1 | a0001c0001t0001g0293 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.376+3486C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516523 | ||||||
| chr16:89516534
|
G | C | 36 | a0001c0001t0001g0014a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.376+3497G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516534 | ||||||
| chr16:89516659
|
G | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+3622G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516659 | ||||||
| chr16:89516679
|
T | C | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG02717.hp2 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.376+3642T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516679 | ||||||
| chr16:89516781
|
C | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+3744C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516781 | ||||||
| chr16:89516782
|
G | A | 1 | a0001c0001t0002g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.376+3745G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516782 | ||||||
| chr16:89516796
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.376+3759C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89516796 | ||||||
| chr16:89517038
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.376+4001G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517038 | ||||||
| chr16:89517170
|
G | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+4133G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517170 | ||||||
| chr16:89517202
|
C | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.376+4165C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517202 | ||||||
| chr16:89517220
|
T | TG | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.376+4184dupG | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89517220 | |||||
| chr16:89517239
|
A | ATTCCTGG others(32): Show |
1 | a0001c0001t0001g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.376+4211_376+4249d others(41): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89517239 | |||||
| chr16:89517248
|
AGGAATGG others(32): Show |
A | 11 | a0001c0001t0001g0136a0001c0001t0001g0155a0001c0001t0001g0156others(8): Show | 11 | HG00597.hp2 HG04204.hp1 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.376+4250_376+4288d others(41): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89517248 | |||||
| chr16:89517287
|
G | A | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(172): Show | 177 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.376+4250G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517287 | ||||||
| chr16:89517333
|
G | C | 1 | a0002c0002t0002g0013 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.376+4296G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517333 | ||||||
| chr16:89517401
|
C | T | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.376+4364C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517401 | ||||||
| chr16:89517614
|
G | T | 185 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.376+4577G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517614 | ||||||
| chr16:89517616
|
C | CT | 10 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0165others(7): Show | 10 | HG00438.hp2 HG01192.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.376+4599dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89517616 | |||||
| chr16:89517616
|
CT | C | 47 | a0001c0001t0001g0014a0001c0001t0001g0042a0001c0001t0001g0067others(44): Show | 48 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.376+4599delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89517616 | |||||
| chr16:89517616
|
CTT | C | 10 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0002g0027others(7): Show | 10 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.376+4598_376+4599d others(4): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89517616 | |||||
| chr16:89517777
|
G | T | 36 | a0001c0001t0001g0014a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.376+4740G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517777 | ||||||
| chr16:89517956
|
C | A | 5 | a0001c0001t0001g0226a0001c0001t0001g0248a0001c0001t0001g0249others(2): Show | 5 | HG02451.hp1 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+4919C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517956 | ||||||
| chr16:89517994
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.376+4957G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89517994 | ||||||
| chr16:89518249
|
A | C | 2 | a0001c0001t0001g0218a0001c0019t0003g0217 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.376+5212A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89518249 | ||||||
| chr16:89518748
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.377-5258C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89518748 | ||||||
| chr16:89518769
|
G | A | 2 | a0001c0001t0001g0014a0002c0015t0002g0040 | 2 | HG03834.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.377-5237G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89518769 | ||||||
| chr16:89518886
|
C | T | 4 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | HG02523.hp2 NA18945.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-5120C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89518886 | ||||||
| chr16:89518992
|
A | T | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.377-5014A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89518992 | ||||||
| chr16:89519053
|
T | G | 2 | a0001c0001t0001g0322a0001c0001t0001g0333 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.377-4953T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519053 | ||||||
| chr16:89519076
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.377-4930C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519076 | ||||||
| chr16:89519087
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.377-4919G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519087 | ||||||
| chr16:89519219
|
A | G | 185 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.377-4787A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519219 | ||||||
| chr16:89519290
|
G | T | 5 | a0001c0001t0002g0221a0003c0003t0002g0231a0003c0003t0002g0232others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-4716G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519290 | ||||||
| chr16:89519380
|
T | A | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.377-4626T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519380 | ||||||
| chr16:89519381
|
T | G | 1 | a0001c0001t0001g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.377-4625T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519381 | ||||||
| chr16:89519406
|
A | G | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.377-4600A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519406 | ||||||
| chr16:89519467
|
G | A | 1 | a0001c0001t0007g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.377-4539G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519467 | ||||||
| chr16:89519594
|
CT | C | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.377-4410delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89519594 | |||||
| chr16:89519602
|
A | G | 185 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.377-4404A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519602 | ||||||
| chr16:89519609
|
C | T | 1 | a0001c0005t0005g0301 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.377-4397C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519609 | ||||||
| chr16:89519629
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.377-4377G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519629 | ||||||
| chr16:89519711
|
T | G | 1 | a0001c0001t0001g0253 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.377-4295T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89519711 | ||||||
| chr16:89520052
|
G | A | 1 | a0001c0019t0003g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.377-3954G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520052 | ||||||
| chr16:89520072
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.377-3934G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520072 | ||||||
| chr16:89520080
|
G | A | 36 | a0001c0001t0001g0014a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.377-3926G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520080 | ||||||
| chr16:89520148
|
G | A | 1 | a0001c0005t0005g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377-3858G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520148 | ||||||
| chr16:89520180
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.377-3826A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520180 | ||||||
| chr16:89520184
|
A | T | 36 | a0001c0001t0001g0014a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.377-3822A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520184 | ||||||
| chr16:89520251
|
A | C | 223 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(220): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.377-3755A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520251 | ||||||
| chr16:89520483
|
G | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0220 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.377-3523G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520483 | ||||||
| chr16:89520542
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.377-3464G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520542 | ||||||
| chr16:89520587
|
G | A | 36 | a0001c0001t0001g0014a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.377-3419G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520587 | ||||||
| chr16:89520622
|
C | T | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.377-3384C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520622 | ||||||
| chr16:89520672
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.377-3334C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520672 | ||||||
| chr16:89520710
|
GT | G | 185 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.377-3286delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89520710 | |||||
| chr16:89520720
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0322a0001c0001t0001g0333 | 3 | HG02647.hp2 HG02886.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.377-3286T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520720 | ||||||
| chr16:89520723
|
C | A | 1 | a0001c0001t0001g0254 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.377-3283C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520723 | ||||||
| chr16:89520879
|
T | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.377-3127T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89520879 | ||||||
| chr16:89521030
|
C | G | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.377-2976C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521030 | ||||||
| chr16:89521147
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.377-2859T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521147 | ||||||
| chr16:89521151
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.377-2855T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521151 | ||||||
| chr16:89521171
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.377-2835C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521171 | ||||||
| chr16:89521368
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.377-2638C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521368 | ||||||
| chr16:89521463
|
A | C | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.377-2543A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521463 | ||||||
| chr16:89521586
|
T | G | 1 | a0001c0006t0001g0104 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.377-2420T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521586 | ||||||
| chr16:89521600
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.377-2406G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521600 | ||||||
| chr16:89521612
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.377-2394G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521612 | ||||||
| chr16:89521767
|
C | A | 1 | a0001c0001t0001g0241 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.377-2239C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521767 | ||||||
| chr16:89521920
|
A | G | 2 | a0002c0002t0002g0026a0002c0002t0002g0035 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.377-2086A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521920 | ||||||
| chr16:89521972
|
G | A | 6 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(3): Show | 6 | HG01192.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.377-2034G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89521972 | ||||||
| chr16:89522080
|
A | G | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.377-1926A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522080 | ||||||
| chr16:89522158
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.377-1848G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522158 | ||||||
| chr16:89522164
|
G | T | 8 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(5): Show | 8 | HG01192.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.377-1842G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522164 | ||||||
| chr16:89522327
|
C | T | 5 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(2): Show | 5 | HG00639.hp1 HG02145.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.377-1679C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522327 | ||||||
| chr16:89522337
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.377-1669C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522337 | ||||||
| chr16:89522349
|
C | G | 1 | a0001c0019t0003g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.377-1657C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522349 | ||||||
| chr16:89522365
|
C | T | 1 | a0001c0001t0001g0348 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.377-1641C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522365 | ||||||
| chr16:89522367
|
C | T | 1 | a0001c0001t0001g0321 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.377-1639C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522367 | ||||||
| chr16:89522410
|
G | T | 16 | a0001c0001t0001g0223a0001c0001t0001g0240a0001c0001t0001g0322others(13): Show | 16 | HG01192.hp1 HG02280.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.377-1596G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522410 | ||||||
| chr16:89522439
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.377-1567G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522439 | ||||||
| chr16:89522443
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0207 | 2 | NA18989.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.377-1563C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522443 | ||||||
| chr16:89522444
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.377-1562G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522444 | ||||||
| chr16:89522488
|
A | G | 222 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(219): Show | 225 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.377-1518A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522488 | ||||||
| chr16:89522495
|
G | C | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.377-1511G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522495 | ||||||
| chr16:89522499
|
T | C | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-1507T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522499 | ||||||
| chr16:89522574
|
C | T | 13 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0002g0219others(10): Show | 13 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.377-1432C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522574 | ||||||
| chr16:89522612
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.377-1394G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522612 | ||||||
| chr16:89522699
|
C | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.377-1307C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522699 | ||||||
| chr16:89522717
|
G | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.377-1289G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522717 | ||||||
| chr16:89522869
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.377-1137C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522869 | ||||||
| chr16:89522902
|
C | T | 5 | a0001c0001t0002g0221a0003c0003t0002g0231a0003c0003t0002g0232others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-1104C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89522902 | ||||||
| chr16:89523000
|
G | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(217): Show | 223 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.377-1006G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523000 | ||||||
| chr16:89523033
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.377-973C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523033 | ||||||
| chr16:89523037
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.377-969C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523037 | ||||||
| chr16:89523287
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.377-719G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523287 | ||||||
| chr16:89523345
|
A | C | 5 | a0001c0001t0002g0221a0003c0003t0002g0231a0003c0003t0002g0232others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.377-661A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523345 | ||||||
| chr16:89523355
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02155.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.377-651G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523355 | ||||||
| chr16:89523571
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.377-435G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523571 | ||||||
| chr16:89523625
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.377-381A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523625 | ||||||
| chr16:89523652
|
G | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.377-354G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523652 | ||||||
| chr16:89523708
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.377-298G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523708 | ||||||
| chr16:89523730
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.377-276A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523730 | ||||||
| chr16:89523760
|
T | TATCTC | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(188): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.377-245_377-244ins others(5): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 89523760 | |||||
| chr16:89523804
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.377-202A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523804 | ||||||
| chr16:89523835
|
G | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.377-171G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523835 | ||||||
| chr16:89523857
|
G | A | 1 | a0005c0008t0002g0105 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.377-149G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523857 | ||||||
| chr16:89523949
|
C | T | 1 | a0002c0002t0002g0350 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.377-57C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 3/16 | chr16 | 89523949 | ||||||
| chr16:89524249
|
TGAGTGAG others(51): Show |
T | 1 | a0001c0001t0001g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.618+11_618+68delGT others(56): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 89524249 | |||||
| chr16:89524259
|
T | C | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(189): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.618+12T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524259 | ||||||
| chr16:89524338
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.618+91G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524338 | ||||||
| chr16:89524350
|
G | A | 1 | a0002c0002t0002g0350 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.618+103G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524350 | ||||||
| chr16:89524417
|
C | T | 36 | a0001c0001t0001g0014a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.618+170C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524417 | ||||||
| chr16:89524686
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.618+439C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524686 | ||||||
| chr16:89524724
|
C | T | 1 | a0001c0004t0001g0299 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.618+477C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524724 | ||||||
| chr16:89524768
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.618+521A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524768 | ||||||
| chr16:89524841
|
C | T | 5 | a0001c0001t0001g0328a0001c0001t0001g0331a0001c0001t0001g0332others(2): Show | 5 | HG02280.hp1 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+594C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524841 | ||||||
| chr16:89524865
|
G | A | 1 | a0001c0001t0002g0257 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.618+618G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524865 | ||||||
| chr16:89524881
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.618+634G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89524881 | ||||||
| chr16:89524953
|
C | CT | 94 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0043others(91): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.618+723dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 89524953 | |||||
| chr16:89524953
|
C | CTT | 10 | a0001c0001t0001g0094a0001c0001t0001g0131a0001c0001t0001g0159others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.618+722_618+723dup others(2): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr16 | 89524953 | |||||
| chr16:89525037
|
G | A | 2 | a0002c0002t0002g0038a0002c0002t0002g0039 | 2 | NA18942.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.618+790G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525037 | ||||||
| chr16:89525106
|
C | A | 2 | a0001c0001t0001g0218a0001c0019t0003g0217 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.618+859C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525106 | ||||||
| chr16:89525107
|
G | A | 5 | a0001c0001t0002g0221a0003c0003t0002g0231a0003c0003t0002g0232others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.618+860G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525107 | ||||||
| chr16:89525127
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.618+880T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525127 | ||||||
| chr16:89525624
|
T | A | 1 | a0001c0001t0001g0300 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.619-705T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525624 | ||||||
| chr16:89525645
|
G | A | 36 | a0001c0001t0001g0014a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.619-684G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525645 | ||||||
| chr16:89525669
|
G | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.619-660G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525669 | ||||||
| chr16:89525701
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.619-628T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525701 | ||||||
| chr16:89525840
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.619-489G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525840 | ||||||
| chr16:89525930
|
A | C | 36 | a0001c0001t0001g0014a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.619-399A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89525930 | ||||||
| chr16:89526003
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.619-326G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526003 | ||||||
| chr16:89526014
|
AACAAATT others(9): Show |
A | 1 | a0001c0001t0001g0083 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.619-314_619-299del others(16): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526014 | ||||||
| chr16:89526096
|
C | T | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.619-233C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526096 | ||||||
| chr16:89526101
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.619-228C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526101 | ||||||
| chr16:89526118
|
A | G | 1 | a0001c0016t0001g0287 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.619-211A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526118 | ||||||
| chr16:89526214
|
C | T | 51 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(48): Show | 52 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.619-115C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526214 | ||||||
| chr16:89526279
|
C | T | 8 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0002g0219others(5): Show | 8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.619-50C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526279 | ||||||
| chr16:89526282
|
G | A | 36 | a0001c0001t0001g0014a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.619-47G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 4/16 | chr16 | 89526282 | ||||||
| chr16:89526636
|
T | G | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | NA18950.hp2 NA18961.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.758+168T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526636 | ||||||
| chr16:89526679
|
C | T | 1 | a0001c0019t0003g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.758+211C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526679 | ||||||
| chr16:89526762
|
C | T | 4 | a0002c0002t0002g0012a0002c0002t0002g0033a0002c0002t0002g0034others(1): Show | 4 | HG00741.hp2 HG01978.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+294C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526762 | ||||||
| chr16:89526784
|
A | G | 1 | a0001c0019t0003g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.758+316A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526784 | ||||||
| chr16:89526790
|
C | T | 44 | a0001c0001t0001g0014a0001c0001t0001g0226a0001c0001t0001g0228others(41): Show | 45 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.758+322C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526790 | ||||||
| chr16:89526809
|
G | A | 8 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0002g0219others(5): Show | 8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.758+341G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526809 | ||||||
| chr16:89526817
|
G | GCGAAGTC others(21): Show |
176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(173): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.758+433_758+460dup others(28): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89526817 | |||||
| chr16:89526817
|
G | GCGAAGTC others(49): Show |
3 | a0001c0001t0001g0059a0001c0001t0001g0218a0001c0019t0003g0217 | 3 | HG02109.hp2 HG02300.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.758+405_758+460dup others(56): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89526817 | |||||
| chr16:89526901
|
CCGAAGTC others(21): Show |
C | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG03041.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.758+505_758+532del others(28): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89526901 | |||||
| chr16:89526929
|
G | C | 234 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(231): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.758+461G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526929 | ||||||
| chr16:89526945
|
C | T | 1 | a0001c0001t0001g0305 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.758+477C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526945 | ||||||
| chr16:89526957
|
G | C | 1 | a0001c0001t0001g0106 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.758+489G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526957 | ||||||
| chr16:89526974
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.758+506G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89526974 | ||||||
| chr16:89527084
|
C | G | 1 | a0001c0001t0001g0319 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.758+616C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527084 | ||||||
| chr16:89527183
|
C | T | 7 | a0001c0001t0001g0220a0001c0001t0001g0305a0001c0001t0002g0221others(4): Show | 7 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.758+715C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527183 | ||||||
| chr16:89527293
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.758+825T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527293 | ||||||
| chr16:89527294
|
G | C | 348 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(345): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.758+826G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527294 | ||||||
| chr16:89527388
|
G | A | 1 | a0001c0001t0001g0305 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.758+920G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527388 | ||||||
| chr16:89527433
|
C | T | 2 | a0001c0001t0001g0218a0001c0019t0003g0217 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.758+965C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527433 | ||||||
| chr16:89527568
|
C | T | 18 | a0001c0001t0001g0216a0001c0001t0001g0253a0001c0001t0001g0254others(15): Show | 18 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.758+1100C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527568 | ||||||
| chr16:89527663
|
C | A | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0184 | 3 | NA18941.hp1 NA18964.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.758+1195C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527663 | ||||||
| chr16:89527666
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.758+1198G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527666 | ||||||
| chr16:89527688
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0122a0001c0001t0001g0123 | 3 | HG01106.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.758+1220G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527688 | ||||||
| chr16:89527718
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.758+1250C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89527718 | ||||||
| chr16:89528068
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.759-1409G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528068 | ||||||
| chr16:89528161
|
C | A | 2 | a0001c0001t0001g0343a0001c0001t0001g0349 | 2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.759-1316C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528161 | ||||||
| chr16:89528162
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.759-1315G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528162 | ||||||
| chr16:89528218
|
G | A | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(179): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.759-1259G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528218 | ||||||
| chr16:89528293
|
G | T | 8 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0002g0219others(5): Show | 8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.759-1184G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528293 | ||||||
| chr16:89528316
|
C | T | 8 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0002g0219others(5): Show | 8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.759-1161C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528316 | ||||||
| chr16:89528317
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.759-1160G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528317 | ||||||
| chr16:89528323
|
C | T | 181 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(178): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.759-1154C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528323 | ||||||
| chr16:89528331
|
A | G | 7 | a0001c0001t0001g0220a0001c0001t0001g0305a0001c0001t0002g0221others(4): Show | 7 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.759-1146A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528331 | ||||||
| chr16:89528395
|
C | CA | 6 | a0001c0001t0001g0107a0001c0001t0001g0135a0001c0001t0001g0205others(3): Show | 6 | HG02602.hp2 HG03471.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.759-1066dupA | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89528395 | |||||
| chr16:89528409
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.759-1068A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528409 | ||||||
| chr16:89528411
|
A | AT | 32 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(29): Show | 32 | HG00621.hp2 HG00642.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.759-1066_759-1065i others(3): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528411 | ||||||
| chr16:89528483
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.759-994G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528483 | ||||||
| chr16:89528531
|
A | G | 7 | a0001c0001t0001g0220a0001c0001t0001g0305a0001c0001t0002g0221others(4): Show | 7 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.759-946A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528531 | ||||||
| chr16:89528603
|
C | CA | 47 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0053others(44): Show | 47 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.759-874_759-873ins others(1): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528603 | ||||||
| chr16:89528603
|
C | CT | 68 | a0001c0001t0001g0014a0001c0001t0001g0222a0001c0001t0001g0226others(65): Show | 69 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.759-854dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89528603 | |||||
| chr16:89528603
|
C | CTT | 13 | a0001c0001t0001g0228a0001c0001t0002g0024a0001c0001t0002g0229others(10): Show | 13 | HG00741.hp2 HG01978.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.759-855_759-854dup others(2): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89528603 | |||||
| chr16:89528603
|
CTT | C | 7 | a0001c0001t0001g0220a0001c0001t0002g0221a0001c0019t0003g0217others(4): Show | 7 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.759-855_759-854del others(2): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 89528603 | |||||
| chr16:89528604
|
T | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(130): Show | 135 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.759-873T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528604 | ||||||
| chr16:89528606
|
T | A | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-871T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528606 | ||||||
| chr16:89528628
|
T | A | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(187): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.759-849T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528628 | ||||||
| chr16:89528651
|
G | T | 1 | a0001c0019t0003g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.759-826G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528651 | ||||||
| chr16:89528673
|
C | G | 1 | a0001c0001t0002g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.759-804C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528673 | ||||||
| chr16:89528678
|
C | T | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-799C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528678 | ||||||
| chr16:89528808
|
C | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0122a0001c0001t0001g0123 | 3 | HG01106.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.759-669C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528808 | ||||||
| chr16:89528853
|
T | C | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(188): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.759-624T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528853 | ||||||
| chr16:89528932
|
C | G | 1 | a0001c0001t0001g0271 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.759-545C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528932 | ||||||
| chr16:89528967
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.759-510A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89528967 | ||||||
| chr16:89529101
|
C | G | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-376C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529101 | ||||||
| chr16:89529101
|
C | T | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.759-376C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529101 | ||||||
| chr16:89529108
|
G | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.759-369G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529108 | ||||||
| chr16:89529144
|
G | A | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.759-333G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529144 | ||||||
| chr16:89529296
|
G | A | 1 | a0009c0014t0001g0259 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.759-181G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529296 | ||||||
| chr16:89529312
|
C | T | 1 | a0001c0004t0001g0009 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.759-165C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529312 | ||||||
| chr16:89529315
|
G | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.759-162G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529315 | ||||||
| chr16:89529322
|
C | A | 1 | a0002c0015t0002g0040 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.759-155C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529322 | ||||||
| chr16:89529351
|
C | T | 8 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0002g0219others(5): Show | 8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.759-126C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529351 | ||||||
| chr16:89529375
|
G | A | 1 | a0002c0002t0002g0013 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.759-102G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 5/16 | chr16 | 89529375 | ||||||
| chr16:89529698
|
C | T | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.861+119C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529698 | ||||||
| chr16:89529748
|
C | A | 2 | a0001c0001t0001g0252a0001c0001t0008g0306 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.861+169C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529748 | ||||||
| chr16:89529775
|
C | T | 1 | a0001c0001t0001g0316 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.861+196C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529775 | ||||||
| chr16:89529784
|
C | A | 1 | a0003c0003t0002g0231 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.861+205C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529784 | ||||||
| chr16:89529892
|
T | C | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.861+313T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529892 | ||||||
| chr16:89529894
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.861+315C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529894 | ||||||
| chr16:89529900
|
T | C | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.861+321T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529900 | ||||||
| chr16:89529951
|
T | A | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.861+372T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529951 | ||||||
| chr16:89529958
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.861+379G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529958 | ||||||
| chr16:89529964
|
C | A | 8 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0002g0219others(5): Show | 8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.861+385C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529964 | ||||||
| chr16:89529965
|
G | A | 1 | a0001c0001t0002g0257 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.861+386G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89529965 | ||||||
| chr16:89530072
|
C | T | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.861+493C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530072 | ||||||
| chr16:89530147
|
T | G | 1 | a0001c0001t0001g0260 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.862-536T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530147 | ||||||
| chr16:89530147
|
TTG | T | 46 | a0001c0001t0001g0014a0001c0001t0001g0218a0001c0001t0001g0226others(43): Show | 47 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.862-519_862-518del others(2): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 89530147 | |||||
| chr16:89530149
|
G | T | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0042others(185): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.862-534G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530149 | ||||||
| chr16:89530151
|
G | T | 38 | a0001c0001t0001g0014a0001c0001t0001g0218a0001c0001t0002g0024others(35): Show | 39 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.862-532G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530151 | ||||||
| chr16:89530245
|
A | G | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.862-438A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530245 | ||||||
| chr16:89530306
|
A | G | 235 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(232): Show | 238 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.862-377A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530306 | ||||||
| chr16:89530342
|
C | T | 1 | a0001c0001t0007g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.862-341C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530342 | ||||||
| chr16:89530360
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0012t0001g0062 | 3 | HG02080.hp1 HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.862-323G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530360 | ||||||
| chr16:89530382
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.862-301G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530382 | ||||||
| chr16:89530600
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.862-83C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530600 | ||||||
| chr16:89530606
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.862-77C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530606 | ||||||
| chr16:89530649
|
G | T | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.862-34G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 6/16 | chr16 | 89530649 | ||||||
| chr16:89530813
|
A | G | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(189): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
splice_region_variant&intron_variant | LOW | c.987+5A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89530813 | ||||||
| chr16:89530827
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.987+19G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89530827 | ||||||
| chr16:89530865
|
C | T | 1 | a0001c0019t0003g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.987+57C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89530865 | ||||||
| chr16:89530938
|
C | T | 1 | a0002c0002t0002g0031 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.987+130C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89530938 | ||||||
| chr16:89530959
|
T | C | 5 | a0001c0001t0002g0201a0001c0001t0004g0198a0001c0001t0004g0199others(2): Show | 5 | HG02723.hp2 HG02896.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.987+151T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89530959 | ||||||
| chr16:89531024
|
A | G | 2 | a0001c0001t0001g0218a0001c0019t0003g0217 | 2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.987+216A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531024 | ||||||
| chr16:89531098
|
C | A | 8 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0002g0219others(5): Show | 8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.987+290C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531098 | ||||||
| chr16:89531120
|
T | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0261a0001c0001t0001g0272others(2): Show | 6 | HG01074.hp2 HG01255.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.987+312T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531120 | ||||||
| chr16:89531151
|
C | T | 1 | a0001c0005t0005g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.987+343C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531151 | ||||||
| chr16:89531156
|
C | CT | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+350dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 89531156 | |||||
| chr16:89531184
|
C | T | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+376C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531184 | ||||||
| chr16:89531185
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.987+377G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531185 | ||||||
| chr16:89531225
|
CAT | C | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+418_987+419del others(2): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531225 | ||||||
| chr16:89531332
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0187 | 2 | NA18954.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.987+524G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531332 | ||||||
| chr16:89531436
|
C | A | 36 | a0001c0001t0001g0014a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.988-468C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531436 | ||||||
| chr16:89531456
|
C | T | 5 | a0001c0001t0001g0052a0001c0001t0001g0102a0001c0001t0001g0129others(2): Show | 5 | HG00735.hp2 HG01070.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-448C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531456 | ||||||
| chr16:89531460
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.988-444A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531460 | ||||||
| chr16:89531468
|
A | G | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.988-436A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531468 | ||||||
| chr16:89531663
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.988-241C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531663 | ||||||
| chr16:89531669
|
T | G | 1 | a0001c0005t0005g0301 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.988-235T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531669 | ||||||
| chr16:89531700
|
G | GCGTGGTG others(6): Show |
1 | a0001c0001t0001g0211 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.988-203_988-191dup others(13): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 89531700 | |||||
| chr16:89531772
|
GTTTGAGG others(11): Show |
G | 4 | a0002c0002t0002g0017a0002c0002t0002g0018a0002c0002t0002g0022others(1): Show | 4 | HG00323.hp1 HG02300.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-130_988-113del others(18): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr16 | 89531772 | |||||
| chr16:89531779
|
G | A | 1 | a0001c0001t0001g0351 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.988-125G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531779 | ||||||
| chr16:89531789
|
G | A | 1 | a0001c0005t0010g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.988-115G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531789 | ||||||
| chr16:89531794
|
C | T | 1 | a0001c0005t0009g0339 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.988-110C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 7/16 | chr16 | 89531794 | ||||||
| chr16:89532283
|
C | G | 1 | a0001c0001t0001g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1151-180C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 8/16 | chr16 | 89532283 | ||||||
| chr16:89532329
|
G | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG02080.hp1 HG02129.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-134G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 8/16 | chr16 | 89532329 | ||||||
| chr16:89532352
|
A | G | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(189): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1151-111A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 8/16 | chr16 | 89532352 | ||||||
| chr16:89532724
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1324+88C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532724 | ||||||
| chr16:89532772
|
G | GA | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1324+148dupA | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89532772 | |||||
| chr16:89532801
|
A | T | 1 | a0010c0009t0001g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1324+165A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532801 | ||||||
| chr16:89532821
|
C | T | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+185C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532821 | ||||||
| chr16:89532833
|
C | T | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(187): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1324+197C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532833 | ||||||
| chr16:89532858
|
C | T | 3 | a0003c0003t0002g0054a0003c0003t0002g0055a0003c0003t0002g0056 | 3 | HG02615.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1324+222C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532858 | ||||||
| chr16:89532908
|
A | G | 3 | a0001c0001t0001g0228a0001c0001t0002g0227a0001c0001t0002g0230 | 3 | HG02109.hp1 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1324+272A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532908 | ||||||
| chr16:89532938
|
C | T | 2 | a0004c0007t0001g0296a0004c0007t0001g0297 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1324+302C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532938 | ||||||
| chr16:89532944
|
G | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1324+308G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532944 | ||||||
| chr16:89532947
|
G | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(181): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1324+311G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532947 | ||||||
| chr16:89532957
|
C | A | 2 | a0004c0007t0001g0296a0004c0007t0001g0297 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1324+321C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532957 | ||||||
| chr16:89532994
|
C | T | 2 | a0001c0001t0002g0024a0001c0001t0002g0030 | 2 | HG02071.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1324+358C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89532994 | ||||||
| chr16:89533004
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1324+368A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533004 | ||||||
| chr16:89533073
|
C | CA | 164 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(161): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1324+457dupA | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89533073 | |||||
| chr16:89533073
|
C | CAA | 19 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0069others(16): Show | 19 | HG00438.hp2 HG01109.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1324+456_1324+457d others(4): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89533073 | |||||
| chr16:89533073
|
CA | C | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(80): Show | 86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1324+457delA | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89533073 | |||||
| chr16:89533091
|
A | AC | 3 | a0003c0003t0002g0054a0003c0003t0002g0055a0003c0003t0002g0056 | 3 | HG02615.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1324+455_1324+456i others(3): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533091 | ||||||
| chr16:89533094
|
C | A | 4 | a0001c0001t0001g0093a0001c0001t0001g0101a0001c0001t0001g0108others(1): Show | 4 | HG02015.hp1 HG02074.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+458C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533094 | ||||||
| chr16:89533122
|
A | G | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(189): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1324+486A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533122 | ||||||
| chr16:89533172
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1324+536C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533172 | ||||||
| chr16:89533182
|
CTT | C | 7 | a0001c0001t0001g0220a0001c0001t0001g0328a0001c0001t0002g0221others(4): Show | 7 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324+551_1324+552d others(4): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89533182 | |||||
| chr16:89533192
|
T | C | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(190): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1324+556T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533192 | ||||||
| chr16:89533208
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+572C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533208 | ||||||
| chr16:89533220
|
C | T | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1324+584C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533220 | ||||||
| chr16:89533221
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0183 | 3 | HG02717.hp2 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1324+585G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533221 | ||||||
| chr16:89533261
|
G | A | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+625G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533261 | ||||||
| chr16:89533267
|
T | A | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1324+631T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533267 | ||||||
| chr16:89533302
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1324+666A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533302 | ||||||
| chr16:89533436
|
A | G | 4 | a0001c0001t0001g0228a0001c0001t0002g0227a0001c0001t0002g0230others(1): Show | 4 | HG02109.hp1 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+800A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533436 | ||||||
| chr16:89533578
|
G | C | 1 | a0001c0001t0004g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1324+942G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533578 | ||||||
| chr16:89533629
|
G | A | 9 | a0001c0001t0001g0218a0001c0001t0001g0239a0001c0001t0001g0248others(6): Show | 9 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1324+993G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533629 | ||||||
| chr16:89533666
|
A | T | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(1): Show | 4 | HG02451.hp1 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+1030A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533666 | ||||||
| chr16:89533753
|
T | C | 1 | a0001c0005t0009g0339 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1324+1117T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533753 | ||||||
| chr16:89533769
|
A | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1324+1133A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533769 | ||||||
| chr16:89533808
|
T | G | 9 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00597.hp2 NA18946.hp2 NA18974.hp1 others(6): Show |
intron_variant | MODIFIER | c.1324+1172T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533808 | ||||||
| chr16:89533823
|
T | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(188): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1324+1187T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533823 | ||||||
| chr16:89533837
|
T | C | 333 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(330): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1324+1201T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533837 | ||||||
| chr16:89533926
|
G | T | 1 | a0003c0003t0002g0208 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1324+1290G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533926 | ||||||
| chr16:89533946
|
A | T | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1324+1310A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533946 | ||||||
| chr16:89533953
|
C | T | 1 | a0001c0005t0005g0301 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1324+1317C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533953 | ||||||
| chr16:89533994
|
C | T | 1 | a0002c0002t0002g0022 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1324+1358C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89533994 | ||||||
| chr16:89534035
|
A | G | 1 | a0001c0004t0001g0176 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1324+1399A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534035 | ||||||
| chr16:89534136
|
G | A | 6 | a0001c0001t0001g0220a0001c0001t0002g0221a0003c0003t0002g0231others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+1500G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534136 | ||||||
| chr16:89534199
|
G | C | 8 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0002g0219others(5): Show | 8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1324+1563G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534199 | ||||||
| chr16:89534231
|
A | G | 1 | a0002c0002t0002g0350 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1324+1595A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534231 | ||||||
| chr16:89534310
|
C | T | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(188): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1324+1674C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534310 | ||||||
| chr16:89534370
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+1734G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534370 | ||||||
| chr16:89534394
|
T | C | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(189): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1324+1758T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534394 | ||||||
| chr16:89534569
|
G | T | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1324+1933G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534569 | ||||||
| chr16:89534821
|
C | A | 1 | a0001c0001t0001g0278 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1324+2185C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534821 | ||||||
| chr16:89534826
|
C | T | 35 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0030others(32): Show | 36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1324+2190C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89534826 | ||||||
| chr16:89535064
|
C | G | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(188): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1324+2428C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535064 | ||||||
| chr16:89535076
|
A | G | 35 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0030others(32): Show | 36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1324+2440A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535076 | ||||||
| chr16:89535084
|
A | G | 35 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0030others(32): Show | 36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1324+2448A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535084 | ||||||
| chr16:89535146
|
T | C | 37 | a0001c0001t0001g0103a0001c0001t0001g0278a0001c0001t0002g0024others(34): Show | 38 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1324+2510T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535146 | ||||||
| chr16:89535176
|
G | T | 1 | a0001c0001t0002g0227 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1324+2540G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535176 | ||||||
| chr16:89535280
|
C | T | 1 | a0004c0007t0001g0297 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1324+2644C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535280 | ||||||
| chr16:89535305
|
G | A | 2 | a0001c0001t0001g0218a0001c0013t0003g0340 | 2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1324+2669G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535305 | ||||||
| chr16:89535357
|
A | T | 43 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0216others(40): Show | 45 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1324+2721A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535357 | ||||||
| chr16:89535427
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1324+2791G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535427 | ||||||
| chr16:89535485
|
C | T | 133 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0068others(130): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1324+2849C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535485 | ||||||
| chr16:89535501
|
C | T | 1 | a0001c0001t0001g0331 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1324+2865C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535501 | ||||||
| chr16:89535548
|
C | T | 1 | a0001c0001t0001g0051 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1324+2912C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535548 | ||||||
| chr16:89535582
|
G | A | 36 | a0001c0001t0001g0218a0001c0001t0002g0024a0001c0001t0002g0027others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1324+2946G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535582 | ||||||
| chr16:89535598
|
C | G | 135 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1324+2962C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535598 | ||||||
| chr16:89535620
|
T | G | 35 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0030others(32): Show | 36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1324+2984T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535620 | ||||||
| chr16:89535659
|
G | A | 1 | a0001c0001t0001g0305 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1324+3023G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535659 | ||||||
| chr16:89535741
|
C | T | 192 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(189): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1324+3105C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535741 | ||||||
| chr16:89535745
|
G | C | 157 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(154): Show | 161 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1324+3109G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535745 | ||||||
| chr16:89535746
|
A | G | 1 | a0001c0001t0001g0315 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1324+3110A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535746 | ||||||
| chr16:89535755
|
C | T | 5 | a0001c0001t0002g0221a0003c0003t0002g0231a0003c0003t0002g0232others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324+3119C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535755 | ||||||
| chr16:89535815
|
A | ATGTGGCC others(365): Show |
1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+3209_1324+321 others(376): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535815 | |||||
| chr16:89535815
|
A | ATGTGGCC others(272): Show |
2 | a0001c0013t0003g0340a0001c0019t0003g0217 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1324+3292_1324+329 others(283): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535815 | |||||
| chr16:89535854
|
TCTCTGGT others(394): Show |
T | 1 | a0001c0001t0003g0295 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1324+3241_1324+364 others(4): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535854 | |||||
| chr16:89535877
|
C | G | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1324+3241C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535877 | ||||||
| chr16:89535908
|
C | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG00639.hp1 HG01069.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+3272C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535908 | ||||||
| chr16:89535916
|
T | TCTCTGGT others(24): Show |
1 | a0001c0001t0001g0047 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1324+3292_1324+329 others(35): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535916 | |||||
| chr16:89535916
|
T | TCTCTGGT others(272): Show |
4 | a0001c0001t0001g0074a0001c0001t0001g0075a0003c0003t0002g0054others(1): Show | 4 | HG01346.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+3292_1324+329 others(283): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535916 | |||||
| chr16:89535929
|
A | G | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(187): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1324+3293A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535929 | ||||||
| chr16:89535939
|
G | GTGTGGCC others(86): Show |
1 | a0001c0001t0001g0008 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1324+3310_1324+331 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | |||||
| chr16:89535939
|
G | GTGTGGCC others(55): Show |
5 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 5 | HG00639.hp1 HG01069.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324+3310_1324+331 others(66): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | |||||
| chr16:89535939
|
G | GTGTGGCC others(55): Show |
1 | a0001c0001t0001g0189 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1324+3333_1324+333 others(66): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | |||||
| chr16:89535939
|
G | GTGTGGCC others(86): Show |
158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(155): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1324+3333_1324+333 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | |||||
| chr16:89535939
|
G | GTGTGGCC others(117): Show |
2 | a0001c0001t0001g0106a0010c0009t0001g0118 | 2 | NA18747.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1324+3333_1324+333 others(128): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | |||||
| chr16:89535939
|
G | GTGTGGCC others(673): Show |
3 | a0001c0001t0001g0107a0001c0001t0001g0194a0001c0001t0001g0211 | 3 | HG00408.hp2 HG02129.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1324+3333_1324+333 others(684): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | |||||
| chr16:89535939
|
G | GTGTGGCC others(86): Show |
6 | a0001c0001t0001g0225a0001c0001t0001g0345a0001c0001t0001g0348others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+3316_1324+331 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | |||||
| chr16:89535939
|
GTGTGGCC others(24): Show |
G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+3396_1324+342 others(35): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535939 | |||||
| chr16:89535947
|
T | TCTCTGGT others(24): Show |
2 | a0001c0001t0001g0185a0001c0001t0001g0196 | 2 | HG03491.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1324+3333_1324+333 others(35): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535947 | |||||
| chr16:89535947
|
T | TCTCTGGT others(86): Show |
1 | a0001c0001t0001g0134 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1324+3333_1324+333 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89535947 | |||||
| chr16:89535970
|
C | G | 12 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0077others(9): Show | 12 | HG01243.hp1 HG01346.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.1324+3334C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535970 | ||||||
| chr16:89535978
|
T | G | 4 | a0001c0001t0001g0045a0001c0001t0001g0077a0001c0001t0001g0084others(1): Show | 4 | HG02647.hp1 HG03654.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+3342T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89535978 | ||||||
| chr16:89536001
|
C | G | 7 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0077others(4): Show | 7 | HG01243.hp1 HG01346.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324+3365C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536001 | ||||||
| chr16:89536032
|
C | CTGTGGCC others(415): Show |
1 | a0001c0001t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1324+3426_1324+342 others(426): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536032 | |||||
| chr16:89536032
|
C | CTGTGGCC others(365): Show |
1 | a0001c0001t0001g0084 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1324+3426_1324+342 others(376): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536032 | |||||
| chr16:89536032
|
C | CTGTGGCC others(209): Show |
1 | a0001c0001t0001g0142 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1324+3426_1324+342 others(220): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536032 | |||||
| chr16:89536032
|
C | G | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3396C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536032 | ||||||
| chr16:89536040
|
T | G | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3404T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536040 | ||||||
| chr16:89536063
|
G | C | 8 | a0001c0001t0001g0185a0001c0001t0001g0228a0001c0001t0002g0219others(5): Show | 8 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1324+3427G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536063 | ||||||
| chr16:89536071
|
G | T | 6 | a0001c0001t0001g0142a0001c0001t0001g0185a0001c0001t0001g0189others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+3435G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536071 | ||||||
| chr16:89536094
|
G | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0185 | 2 | NA18961.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1324+3458G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536094 | ||||||
| chr16:89536102
|
G | GCTCTGGT others(148): Show |
1 | a0001c0001t0001g0189 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1324+3496_1324+349 others(159): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536102 | |||||
| chr16:89536102
|
G | GCTCTGGT others(117): Show |
1 | a0001c0001t0001g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1324+3527_1324+352 others(128): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536102 | |||||
| chr16:89536102
|
G | GCTCTGGT others(551): Show |
4 | a0001c0001t0002g0219a0001c0001t0002g0229a0001c0005t0009g0339others(1): Show | 4 | HG01081.hp1 HG02258.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+3527_1324+352 others(562): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536102 | |||||
| chr16:89536102
|
G | GCTCTGGT others(551): Show |
3 | a0001c0001t0001g0228a0001c0001t0002g0227a0001c0001t0002g0230 | 3 | HG02109.hp1 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1324+3527_1324+352 others(562): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536102 | |||||
| chr16:89536102
|
G | T | 8 | a0001c0001t0001g0106a0001c0001t0001g0142a0001c0001t0001g0185others(5): Show | 8 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324+3466G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536102 | ||||||
| chr16:89536102
|
GCTCTGGT others(24): Show |
G | 35 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0030others(32): Show | 36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1324+3497_1324+352 others(35): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536102 | |||||
| chr16:89536123
|
C | A | 3 | a0001c0001t0001g0218a0001c0013t0003g0340a0001c0019t0003g0217 | 3 | HG01891.hp2 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1324+3487C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536123 | ||||||
| chr16:89536125
|
G | C | 1 | a0001c0001t0001g0185 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1324+3489G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536125 | ||||||
| chr16:89536133
|
T | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0189 | 2 | HG03516.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1324+3497T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536133 | ||||||
| chr16:89536133
|
T | TCTCTGGT others(117): Show |
1 | a0003c0003t0002g0056 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1324+3527_1324+352 others(128): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536133 | |||||
| chr16:89536133
|
T | TCTCTGGT others(86): Show |
2 | a0001c0001t0001g0106a0010c0009t0001g0118 | 2 | NA18747.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1324+3527_1324+352 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536133 | |||||
| chr16:89536133
|
T | TCTCTGGT others(117): Show |
83 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0042others(80): Show | 83 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1324+3527_1324+352 others(128): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536133 | |||||
| chr16:89536136
|
C | CTGGTGCT others(148): Show |
1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+3524_1324+352 others(159): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536136 | |||||
| chr16:89536136
|
C | CTGGTGCT others(148): Show |
2 | a0001c0013t0003g0340a0001c0019t0003g0217 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1324+3527_1324+352 others(159): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536136 | |||||
| chr16:89536164
|
G | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(98): Show | 102 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1324+3528G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536164 | ||||||
| chr16:89536195
|
T | G | 1 | a0001c0001t0001g0185 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1324+3559T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536195 | ||||||
| chr16:89536195
|
T | TCTCTGGT others(22): Show |
9 | a0001c0001t0001g0014a0001c0001t0001g0046a0001c0001t0001g0047others(6): Show | 9 | HG00639.hp1 HG01069.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1324+3564_1324+359 others(33): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536195 | |||||
| chr16:89536206
|
G | C | 1 | a0001c0001t0003g0346 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1324+3570G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536206 | ||||||
| chr16:89536211
|
G | T | 35 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0030others(32): Show | 36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1324+3575G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536211 | ||||||
| chr16:89536218
|
G | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0043others(117): Show | 122 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1324+3582G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536218 | ||||||
| chr16:89536249
|
G | C | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+3613G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536249 | ||||||
| chr16:89536255
|
C | CCG | 13 | a0001c0001t0001g0014a0001c0001t0001g0046a0001c0001t0001g0047others(10): Show | 13 | HG00639.hp1 HG01069.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1324+3620_1324+362 others(6): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | |||||
| chr16:89536255
|
C | CCGCTCTG others(150): Show |
9 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0076others(6): Show | 9 | HG00621.hp2 HG01243.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.1324+3620_1324+362 others(161): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | |||||
| chr16:89536255
|
C | CCGCTCTG others(148): Show |
1 | a0001c0001t0001g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1324+3620_1324+362 others(159): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | |||||
| chr16:89536255
|
C | CCGCTCTG others(179): Show |
73 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0043others(70): Show | 74 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1324+3620_1324+362 others(190): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | |||||
| chr16:89536255
|
C | CCGCTCTG others(86): Show |
4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3620_1324+362 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | |||||
| chr16:89536255
|
C | CCTCTCTG others(117): Show |
1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+3623_1324+362 others(128): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | |||||
| chr16:89536255
|
C | CCTCTCTG others(88): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG01346.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1324+3623_1324+362 others(99): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | |||||
| chr16:89536255
|
C | CCTCTCTG others(86): Show |
1 | a0001c0001t0001g0185 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1324+3623_1324+362 others(97): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536255 | |||||
| chr16:89536286
|
T | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(101): Show | 105 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1324+3650T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536286 | ||||||
| chr16:89536286
|
T | TCTCTGGT others(55): Show |
1 | a0001c0001t0001g0187 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1324+3710_1324+371 others(66): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536286 | |||||
| chr16:89536317
|
G | GCTCTGGT others(55): Show |
86 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0045others(83): Show | 86 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1324+3710_1324+371 others(66): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536317 | |||||
| chr16:89536317
|
G | GCTCTGGT others(55): Show |
1 | a0001c0001t0001g0042 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1324+3710_1324+371 others(66): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536317 | |||||
| chr16:89536317
|
G | GCTCTGGT others(24): Show |
11 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0076others(8): Show | 11 | HG00621.hp2 HG01243.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.1324+3710_1324+371 others(35): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536317 | |||||
| chr16:89536317
|
G | T | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(89): Show | 93 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1324+3681G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536317 | ||||||
| chr16:89536372
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0001g0171a0001c0001t0001g0195 | 3 | HG01099.hp2 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1324+3736T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536372 | ||||||
| chr16:89536381
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1324+3745G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536381 | ||||||
| chr16:89536451
|
CGGTGAGG others(2): Show |
C | 37 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0030others(34): Show | 38 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1324+3841_1324+384 others(13): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536451 | |||||
| chr16:89536451
|
CGGTGAGG others(11): Show |
C | 1 | a0001c0001t0001g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1324+3832_1324+384 others(22): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536451 | |||||
| chr16:89536468
|
C | CCGGGTGA others(69): Show |
1 | a0001c0001t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1324+3832_1324+383 others(80): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536468 | ||||||
| chr16:89536469
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1324+3833G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536469 | ||||||
| chr16:89536469
|
G | GGGTGAGG others(45): Show |
4 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0087others(1): Show | 4 | HG01074.hp1 HG01243.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3841_1324+384 others(56): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536469 | |||||
| chr16:89536469
|
G | GGGTGAGG others(78): Show |
179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(176): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1324+3841_1324+384 others(89): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536469 | |||||
| chr16:89536469
|
G | GGGTGAGG others(40): Show |
3 | a0001c0001t0001g0218a0001c0013t0003g0340a0001c0019t0003g0217 | 3 | HG01891.hp2 HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1324+3849_1324+385 others(51): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536469 | |||||
| chr16:89536469
|
G | GGGTGAGG others(12): Show |
1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1324+3842_1324+386 others(23): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536469 | |||||
| chr16:89536469
|
G | GGGTGAGG others(45): Show |
1 | a0001c0001t0002g0257 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1324+3903_1324+395 others(56): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536469 | |||||
| chr16:89536469
|
GGGTGAGG others(26): Show |
G | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3861_1324+389 others(37): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536469 | |||||
| chr16:89536472
|
T | TGAGGCCG others(12): Show |
3 | a0001c0001t0001g0096a0001c0001t0001g0226a0007c0017t0001g0149 | 3 | HG00741.hp1 HG01106.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1324+3841_1324+384 others(23): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536472 | |||||
| chr16:89536481
|
T | C | 4 | a0001c0001t0001g0096a0001c0001t0001g0226a0001c0001t0002g0221others(1): Show | 4 | HG00741.hp1 HG01106.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+3845T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536481 | ||||||
| chr16:89536486
|
T | C | 4 | a0001c0001t0001g0096a0001c0001t0001g0226a0001c0001t0002g0221others(1): Show | 4 | HG00741.hp1 HG01106.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+3850T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536486 | ||||||
| chr16:89536488
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1324+3852A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536488 | ||||||
| chr16:89536491
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1324+3855T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536491 | ||||||
| chr16:89536497
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0002g0221 | 2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3861A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536497 | ||||||
| chr16:89536500
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1324+3864T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536500 | ||||||
| chr16:89536505
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1324+3869T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536505 | ||||||
| chr16:89536506
|
G | C | 2 | a0001c0001t0001g0180a0001c0001t0002g0221 | 2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3870G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536506 | ||||||
| chr16:89536510
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0002g0221 | 2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3874C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536510 | ||||||
| chr16:89536512
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0002g0221 | 2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3876G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536512 | ||||||
| chr16:89536514
|
T | C | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3878T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536514 | ||||||
| chr16:89536514
|
T | G | 2 | a0001c0001t0001g0180a0001c0001t0002g0221 | 2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3878T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536514 | ||||||
| chr16:89536515
|
G | C | 2 | a0001c0001t0001g0180a0001c0001t0002g0221 | 2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3879G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536515 | ||||||
| chr16:89536519
|
T | C | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3883T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536519 | ||||||
| chr16:89536520
|
C | CAGGTGAA others(7): Show |
2 | a0001c0001t0001g0051a0001c0001t0001g0185 | 2 | NA18957.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1324+3890_1324+389 others(18): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536520 | |||||
| chr16:89536520
|
C | CAGGTGAG others(7): Show |
183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1324+3893_1324+389 others(18): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536520 | |||||
| chr16:89536520
|
C | CAGGTGAG others(40): Show |
2 | a0001c0001t0001g0141a0001c0006t0001g0057 | 2 | HG01074.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1324+3893_1324+389 others(51): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536520 | |||||
| chr16:89536520
|
C | G | 2 | a0001c0001t0001g0180a0001c0001t0002g0221 | 2 | HG01175.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1324+3884C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536520 | ||||||
| chr16:89536530
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+3894G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536530 | ||||||
| chr16:89536549
|
A | G | 2 | a0001c0001t0001g0141a0001c0001t0002g0221 | 2 | HG02809.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1324+3913A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536549 | ||||||
| chr16:89536550
|
G | T | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+3914G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536550 | ||||||
| chr16:89536561
|
GCGGGTGA others(3): Show |
G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+3927_1324+393 others(14): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536561 | |||||
| chr16:89536563
|
G | A | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3927G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536563 | ||||||
| chr16:89536577
|
G | C | 13 | a0001c0001t0001g0240a0001c0001t0001g0323a0001c0001t0001g0324others(10): Show | 13 | HG01192.hp1 HG02280.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1324+3941G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536577 | ||||||
| chr16:89536582
|
G | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0180a0001c0001t0002g0221others(2): Show | 5 | HG00741.hp1 HG01074.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324+3946G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536582 | ||||||
| chr16:89536583
|
G | T | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3947G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536583 | ||||||
| chr16:89536586
|
G | GAGGTGAG others(2): Show |
4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3959_1324+396 others(13): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536586 | |||||
| chr16:89536586
|
G | GAGGTGAG others(12): Show |
1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1324+3959_1324+396 others(23): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536586 | |||||
| chr16:89536596
|
A | AGGTGAGG others(7): Show |
1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1324+3972_1324+397 others(18): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536596 | |||||
| chr16:89536596
|
A | G | 3 | a0001c0001t0001g0096a0001c0006t0001g0057a0007c0017t0001g0149 | 3 | HG00741.hp1 HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1324+3960A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536596 | ||||||
| chr16:89536605
|
G | C | 1 | a0001c0006t0001g0057 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1324+3969G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536605 | ||||||
| chr16:89536618
|
C | T | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3982C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536618 | ||||||
| chr16:89536624
|
AG | A | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+3991delG | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536624 | |||||
| chr16:89536634
|
A | AG | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+4000dupG | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89536634 | |||||
| chr16:89536641
|
C | T | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+4005C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536641 | ||||||
| chr16:89536646
|
T | C | 4 | a0003c0003t0002g0231a0003c0003t0002g0232a0003c0003t0002g0233others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+4010T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536646 | ||||||
| chr16:89536647
|
G | GAGGCAGG others(3): Show |
1 | a0001c0001t0001g0305 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1324+4011_1324+401 others(14): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536647 | ||||||
| chr16:89536650
|
C | T | 1 | a0001c0001t0001g0305 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1324+4014C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536650 | ||||||
| chr16:89536656
|
A | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(193): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1324+4020A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536656 | ||||||
| chr16:89536659
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0226 | 2 | HG01361.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1324+4023C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536659 | ||||||
| chr16:89536722
|
A | G | 5 | a0001c0001t0002g0221a0003c0003t0002g0231a0003c0003t0002g0232others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324+4086A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536722 | ||||||
| chr16:89536809
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1324+4173C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536809 | ||||||
| chr16:89536860
|
C | T | 4 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | HG02523.hp2 NA18945.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1324+4224C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536860 | ||||||
| chr16:89536948
|
G | T | 5 | a0001c0001t0002g0221a0003c0003t0002g0231a0003c0003t0002g0232others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324+4312G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536948 | ||||||
| chr16:89536978
|
A | G | 1 | a0002c0002t0002g0021 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1324+4342A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536978 | ||||||
| chr16:89536982
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+4346C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89536982 | ||||||
| chr16:89537007
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1324+4371C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537007 | ||||||
| chr16:89537050
|
CTGAAGGC others(7): Show |
C | 4 | a0001c0001t0001g0110a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG01928.hp1 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+4418_1324+443 others(18): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89537050 | |||||
| chr16:89537178
|
A | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(194): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1324+4542A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537178 | ||||||
| chr16:89537290
|
C | CT | 146 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(143): Show | 150 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1324+4654_1324+465 others(5): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537290 | ||||||
| chr16:89537318
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1324+4682G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537318 | ||||||
| chr16:89537344
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0182 | 2 | NA18984.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1324+4708G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537344 | ||||||
| chr16:89537358
|
T | G | 1 | a0001c0001t0001g0143 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1324+4722T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537358 | ||||||
| chr16:89537375
|
GGGGAGCG others(18): Show |
G | 5 | a0001c0001t0001g0254a0001c0001t0001g0284a0001c0001t0001g0285others(2): Show | 5 | HG00408.hp1 HG00438.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324+4746_1324+477 others(29): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89537375 | |||||
| chr16:89537454
|
C | T | 5 | a0001c0001t0002g0221a0003c0003t0002g0231a0003c0003t0002g0232others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324+4818C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537454 | ||||||
| chr16:89537532
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+4896C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537532 | ||||||
| chr16:89537733
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1324+5097C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537733 | ||||||
| chr16:89537972
|
T | A | 1 | a0001c0001t0001g0351 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1324+5336T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89537972 | ||||||
| chr16:89538202
|
A | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(193): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1324+5566A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538202 | ||||||
| chr16:89538235
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+5599C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538235 | ||||||
| chr16:89538339
|
C | G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+5703C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538339 | ||||||
| chr16:89538429
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1324+5793C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538429 | ||||||
| chr16:89538617
|
C | G | 1 | a0001c0001t0001g0144 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1324+5981C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538617 | ||||||
| chr16:89538663
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-5985C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538663 | ||||||
| chr16:89538700
|
T | G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-5948T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538700 | ||||||
| chr16:89538747
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-5901C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538747 | ||||||
| chr16:89538846
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-5802G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538846 | ||||||
| chr16:89538955
|
T | TGAACACT others(14): Show |
7 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0227others(4): Show | 7 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325-5692_1325-567 others(25): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89538955 | |||||
| chr16:89538961
|
C | T | 1 | a0002c0002t0002g0037 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1325-5687C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538961 | ||||||
| chr16:89538996
|
G | T | 7 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0227others(4): Show | 7 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325-5652G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89538996 | ||||||
| chr16:89539087
|
C | T | 141 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(138): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1325-5561C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539087 | ||||||
| chr16:89539157
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-5491C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539157 | ||||||
| chr16:89539300
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1325-5348G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539300 | ||||||
| chr16:89539325
|
C | A | 2 | a0002c0002t0002g0012a0002c0002t0002g0033 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1325-5323C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539325 | ||||||
| chr16:89539488
|
G | A | 6 | a0001c0001t0001g0044a0001c0001t0001g0124a0001c0001t0001g0126others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325-5160G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539488 | ||||||
| chr16:89539556
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0088 | 2 | HG00621.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1325-5092C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539556 | ||||||
| chr16:89539630
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1325-5018G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539630 | ||||||
| chr16:89539688
|
T | G | 3 | a0001c0001t0002g0221a0001c0013t0003g0340a0001c0019t0003g0217 | 3 | HG01891.hp2 HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1325-4960T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539688 | ||||||
| chr16:89539706
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1325-4942A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539706 | ||||||
| chr16:89539950
|
G | A | 4 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0030others(1): Show | 4 | HG02071.hp1 HG02602.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325-4698G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89539950 | ||||||
| chr16:89540118
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1325-4530C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540118 | ||||||
| chr16:89540376
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1325-4272C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540376 | ||||||
| chr16:89540420
|
C | G | 3 | a0001c0001t0002g0221a0001c0013t0003g0340a0001c0019t0003g0217 | 3 | HG01891.hp2 HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1325-4228C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540420 | ||||||
| chr16:89540547
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1325-4101C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540547 | ||||||
| chr16:89540734
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(50): Show | 54 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1325-3914G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540734 | ||||||
| chr16:89540755
|
G | A | 1 | a0001c0012t0001g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1325-3893G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540755 | ||||||
| chr16:89540836
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0053 | 2 | HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1325-3812C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540836 | ||||||
| chr16:89540849
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1325-3799C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540849 | ||||||
| chr16:89540950
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-3698A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89540950 | ||||||
| chr16:89541006
|
G | A | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(187): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1325-3642G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541006 | ||||||
| chr16:89541006
|
G | GACTAGAA others(191): Show |
1 | a0001c0001t0001g0214 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1325-3557_1325-355 others(202): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541006 | |||||
| chr16:89541006
|
G | GACTAGAA others(288): Show |
1 | a0003c0003t0002g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1325-3412_1325-341 others(299): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541006 | |||||
| chr16:89541008
|
C | CTAGAAGA others(42): Show |
3 | a0001c0001t0001g0223a0001c0001t0001g0240a0001c0001t0001g0327 | 3 | HG02886.hp1 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1325-3552_1325-350 others(53): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541008 | |||||
| chr16:89541008
|
CTAGAAGA others(42): Show |
C | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-3552_1325-350 others(53): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541008 | |||||
| chr16:89541047
|
GTACGCAG others(91): Show |
G | 1 | a0001c0001t0001g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1325-3552_1325-345 others(102): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541047 | |||||
| chr16:89541096
|
GTACGCAG others(42): Show |
G | 140 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1325-3446_1325-339 others(53): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541096 | |||||
| chr16:89541100
|
G | A | 13 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0074others(10): Show | 13 | HG00621.hp2 HG01243.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1325-3548G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541100 | ||||||
| chr16:89541145
|
C | CTACGCAG others(42): Show |
1 | a0001c0001t0001g0236 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1325-3455_1325-345 others(53): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89541145 | |||||
| chr16:89541145
|
C | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0117 | 2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1325-3503C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541145 | ||||||
| chr16:89541147
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-3501A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541147 | ||||||
| chr16:89541197
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1325-3451C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541197 | ||||||
| chr16:89541202
|
A | C | 2 | a0001c0013t0003g0340a0001c0019t0003g0217 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1325-3446A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541202 | ||||||
| chr16:89541258
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-3390A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541258 | ||||||
| chr16:89541271
|
G | A | 142 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(139): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1325-3377G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541271 | ||||||
| chr16:89541295
|
T | C | 2 | a0001c0013t0003g0340a0001c0019t0003g0217 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1325-3353T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541295 | ||||||
| chr16:89541427
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1325-3221G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541427 | ||||||
| chr16:89541521
|
T | C | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-3127T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541521 | ||||||
| chr16:89541532
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1325-3116G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541532 | ||||||
| chr16:89541560
|
A | G | 1 | a0001c0005t0010g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1325-3088A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541560 | ||||||
| chr16:89541561
|
C | G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-3087C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541561 | ||||||
| chr16:89541758
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1325-2890G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541758 | ||||||
| chr16:89541827
|
A | G | 235 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(232): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1325-2821A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541827 | ||||||
| chr16:89541887
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1325-2761A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541887 | ||||||
| chr16:89541897
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1325-2751G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541897 | ||||||
| chr16:89541934
|
T | C | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(141): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1325-2714T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89541934 | ||||||
| chr16:89542035
|
CAT | C | 9 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00597.hp2 NA18946.hp2 NA18974.hp1 others(6): Show |
intron_variant | MODIFIER | c.1325-2611_1325-261 others(6): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89542035 | |||||
| chr16:89542052
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1325-2596C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542052 | ||||||
| chr16:89542062
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-2586G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542062 | ||||||
| chr16:89542125
|
A | T | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-2523A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542125 | ||||||
| chr16:89542150
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1325-2498G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542150 | ||||||
| chr16:89542170
|
A | C | 1 | a0001c0001t0001g0334 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1325-2478A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542170 | ||||||
| chr16:89542289
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0203 | 2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1325-2359G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542289 | ||||||
| chr16:89542294
|
G | A | 99 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1325-2354G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542294 | ||||||
| chr16:89542359
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1325-2289C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542359 | ||||||
| chr16:89542435
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-2213G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542435 | ||||||
| chr16:89542589
|
C | G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-2059C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542589 | ||||||
| chr16:89542622
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1325-2026T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542622 | ||||||
| chr16:89542705
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0240a0001c0001t0001g0327 | 3 | HG02886.hp1 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1325-1943C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542705 | ||||||
| chr16:89542833
|
C | G | 155 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(152): Show | 159 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1325-1815C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542833 | ||||||
| chr16:89542900
|
C | T | 4 | a0001c0001t0001g0322a0001c0001t0001g0333a0004c0007t0001g0296others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325-1748C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542900 | ||||||
| chr16:89542941
|
C | CT | 12 | a0001c0001t0001g0050a0001c0001t0001g0072a0001c0001t0001g0086others(9): Show | 12 | HG01106.hp2 HG01192.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1325-1683dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89542941 | |||||
| chr16:89542941
|
CT | C | 10 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0085others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.1325-1683delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89542941 | |||||
| chr16:89542941
|
CTT | C | 105 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 108 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1325-1684_1325-168 others(6): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89542941 | |||||
| chr16:89542941
|
CTTT | C | 57 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0075others(54): Show | 58 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1325-1685_1325-168 others(7): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89542941 | |||||
| chr16:89542978
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1325-1670T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89542978 | ||||||
| chr16:89543010
|
T | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1325-1638T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543010 | ||||||
| chr16:89543017
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-1631G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543017 | ||||||
| chr16:89543022
|
C | A | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1325-1626C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543022 | ||||||
| chr16:89543032
|
C | G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-1616C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543032 | ||||||
| chr16:89543034
|
A | G | 173 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(170): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1325-1614A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543034 | ||||||
| chr16:89543048
|
C | T | 36 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0060others(33): Show | 38 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1325-1600C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543048 | ||||||
| chr16:89543080
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1325-1568T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543080 | ||||||
| chr16:89543096
|
C | T | 13 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0074others(10): Show | 13 | HG00621.hp2 HG01243.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1325-1552C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543096 | ||||||
| chr16:89543097
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1325-1551G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543097 | ||||||
| chr16:89543100
|
A | G | 1 | a0002c0002t0002g0016 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1325-1548A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543100 | ||||||
| chr16:89543105
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1325-1543G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543105 | ||||||
| chr16:89543109
|
A | G | 2 | a0001c0001t0001g0298a0001c0013t0003g0340 | 2 | HG01891.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1325-1539A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543109 | ||||||
| chr16:89543136
|
A | G | 2 | a0001c0001t0001g0106a0010c0009t0001g0118 | 2 | NA18747.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1325-1512A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543136 | ||||||
| chr16:89543148
|
T | C | 10 | a0001c0001t0001g0050a0001c0001t0001g0106a0001c0001t0001g0189others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1325-1500T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543148 | ||||||
| chr16:89543149
|
G | A | 2 | a0001c0001t0001g0106a0010c0009t0001g0118 | 2 | NA18747.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1325-1499G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543149 | ||||||
| chr16:89543154
|
A | G | 4 | a0001c0001t0001g0331a0001c0001t0001g0343a0001c0001t0001g0349others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325-1494A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543154 | ||||||
| chr16:89543161
|
A | C | 3 | a0001c0001t0001g0223a0001c0001t0002g0219a0001c0005t0010g0235 | 3 | HG01081.hp1 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1325-1487A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543161 | ||||||
| chr16:89543164
|
C | G | 104 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(101): Show | 106 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1325-1484C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543164 | ||||||
| chr16:89543169
|
C | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0109 | 2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1325-1479C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543169 | ||||||
| chr16:89543182
|
T | A | 2 | a0001c0001t0002g0027a0002c0002t0002g0032 | 2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1325-1466T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543182 | ||||||
| chr16:89543182
|
T | C | 4 | a0001c0001t0001g0106a0001c0001t0001g0214a0001c0001t0002g0221others(1): Show | 4 | HG01256.hp1 HG02809.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325-1466T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543182 | ||||||
| chr16:89543190
|
G | A | 2 | a0001c0001t0001g0180a0001c0005t0010g0235 | 2 | HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1325-1458G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543190 | ||||||
| chr16:89543193
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1325-1455C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543193 | ||||||
| chr16:89543194
|
T | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0246 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1325-1454T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543194 | ||||||
| chr16:89543225
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1325-1423G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543225 | ||||||
| chr16:89543232
|
C | A | 1 | a0001c0001t0001g0298 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1325-1416C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543232 | ||||||
| chr16:89543237
|
G | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0173a0001c0001t0001g0345 | 3 | HG00642.hp1 HG00735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1325-1411G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543237 | ||||||
| chr16:89543238
|
C | T | 10 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0075others(7): Show | 10 | HG00621.hp2 HG01243.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.1325-1410C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543238 | ||||||
| chr16:89543239
|
G | A | 34 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0001g0218others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1325-1409G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543239 | ||||||
| chr16:89543242
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1325-1406T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543242 | ||||||
| chr16:89543270
|
C | CGGT | 57 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0075others(54): Show | 58 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1325-1376_1325-137 others(7): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543270 | |||||
| chr16:89543286
|
A | G | 37 | a0001c0001t0001g0211a0001c0001t0002g0024a0001c0001t0002g0027others(34): Show | 38 | HG00323.hp1 HG00408.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1325-1362A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543286 | ||||||
| chr16:89543347
|
C | CTTTTTTT others(3): Show |
4 | a0002c0002t0002g0026a0002c0002t0002g0035a0002c0002t0002g0039others(1): Show | 4 | HG01515.hp2 HG01517.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325-1293_1325-128 others(14): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543347 | |||||
| chr16:89543347
|
C | CTTTTTTT others(4): Show |
52 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0074others(49): Show | 53 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1325-1294_1325-128 others(15): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543347 | |||||
| chr16:89543347
|
C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0213others(5): Show | 8 | HG01243.hp2 HG02148.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.1325-1295_1325-128 others(16): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543347 | |||||
| chr16:89543347
|
C | CTTTTTTT others(6): Show |
3 | a0001c0005t0005g0301a0001c0005t0005g0304a0002c0002t0002g0028 | 3 | HG02559.hp1 NA18940.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1325-1296_1325-128 others(17): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543347 | |||||
| chr16:89543347
|
C | CTTTTTTT others(7): Show |
3 | a0003c0003t0002g0054a0003c0003t0002g0055a0003c0003t0002g0056 | 3 | HG02615.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1325-1297_1325-128 others(18): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543347 | |||||
| chr16:89543347
|
CT | C | 8 | a0001c0001t0001g0046a0001c0001t0001g0089a0001c0001t0001g0136others(5): Show | 8 | HG01109.hp2 HG01169.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1325-1284delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543347 | |||||
| chr16:89543365
|
G | T | 1 | a0001c0001t0001g0255 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1325-1283G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543365 | ||||||
| chr16:89543367
|
G | C | 13 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0074others(10): Show | 13 | HG00621.hp2 HG01243.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1325-1281G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543367 | ||||||
| chr16:89543445
|
G | A | 35 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0030others(32): Show | 36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1325-1203G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543445 | ||||||
| chr16:89543613
|
C | T | 67 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0074others(64): Show | 68 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1325-1035C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543613 | ||||||
| chr16:89543646
|
ATTCTTTT others(2): Show |
A | 30 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0074others(27): Show | 30 | HG00621.hp2 HG01081.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1325-999_1325-991d others(11): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543646 | |||||
| chr16:89543646
|
ATTCTTTT others(3): Show |
A | 36 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0030others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1325-999_1325-990d others(12): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543646 | |||||
| chr16:89543649
|
C | CT | 18 | a0001c0001t0001g0096a0001c0001t0001g0103a0001c0001t0001g0116others(15): Show | 18 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1325-978dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543649 | |||||
| chr16:89543649
|
CT | C | 6 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0119others(3): Show | 6 | HG01943.hp1 HG02895.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325-978delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 89543649 | |||||
| chr16:89543699
|
G | C | 4 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0030others(1): Show | 4 | HG02071.hp1 HG02602.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325-949G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543699 | ||||||
| chr16:89543776
|
C | G | 2 | a0001c0001t0001g0223a0001c0001t0001g0240 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1325-872C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543776 | ||||||
| chr16:89543784
|
A | G | 1 | a0001c0001t0001g0334 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1325-864A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543784 | ||||||
| chr16:89543796
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-852G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543796 | ||||||
| chr16:89543836
|
G | C | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-812G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543836 | ||||||
| chr16:89543938
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0210 | 2 | HG00140.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.1325-710C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543938 | ||||||
| chr16:89543974
|
A | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0171a0001c0001t0001g0195 | 3 | HG01099.hp2 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1325-674A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89543974 | ||||||
| chr16:89544100
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1325-548C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89544100 | ||||||
| chr16:89544162
|
G | T | 1 | a0001c0001t0001g0315 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1325-486G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89544162 | ||||||
| chr16:89544256
|
C | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0088 | 2 | HG00621.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1325-392C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89544256 | ||||||
| chr16:89544346
|
G | A | 1 | a0001c0005t0005g0301 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1325-302G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89544346 | ||||||
| chr16:89544355
|
A | G | 1 | a0002c0002t0002g0038 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1325-293A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89544355 | ||||||
| chr16:89544438
|
C | T | 1 | a0001c0005t0010g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1325-210C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 9/16 | chr16 | 89544438 | ||||||
| chr16:89544791
|
G | A | 47 | a0001c0001t0001g0008a0001c0001t0001g0045a0001c0001t0001g0058others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1449+19G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89544791 | ||||||
| chr16:89544827
|
C | G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1449+55C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89544827 | ||||||
| chr16:89544856
|
C | T | 1 | a0001c0005t0009g0339 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1449+84C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89544856 | ||||||
| chr16:89544946
|
C | T | 2 | a0001c0013t0003g0340a0001c0019t0003g0217 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1449+174C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89544946 | ||||||
| chr16:89544950
|
CGGCTGCA others(54): Show |
C | 1 | a0001c0001t0001g0189 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1449+195_1449+255d others(63): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 89544950 | |||||
| chr16:89544956
|
C | T | 1 | a0001c0016t0001g0287 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1449+184C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89544956 | ||||||
| chr16:89545039
|
A | G | 1 | a0001c0001t0001g0345 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1449+267A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545039 | ||||||
| chr16:89545153
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1449+381T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545153 | ||||||
| chr16:89545378
|
C | T | 5 | a0001c0001t0002g0201a0001c0001t0004g0198a0001c0001t0004g0199others(2): Show | 5 | HG02723.hp2 HG02896.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1449+606C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545378 | ||||||
| chr16:89545540
|
C | T | 1 | a0001c0012t0001g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1449+768C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545540 | ||||||
| chr16:89545549
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1449+777T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545549 | ||||||
| chr16:89545588
|
CTTCTCCA others(11): Show |
C | 1 | a0001c0001t0008g0306 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1449+847_1449+864d others(20): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 89545588 | |||||
| chr16:89545649
|
C | G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1449+877C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545649 | ||||||
| chr16:89545697
|
G | A | 5 | a0001c0001t0001g0254a0001c0001t0001g0284a0001c0001t0001g0285others(2): Show | 5 | HG00408.hp1 HG00438.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+925G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545697 | ||||||
| chr16:89545795
|
C | T | 1 | a0003c0003t0002g0208 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1450-863C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545795 | ||||||
| chr16:89545850
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1450-808T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545850 | ||||||
| chr16:89545852
|
A | AT | 65 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0074others(62): Show | 66 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1450-801dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 89545852 | |||||
| chr16:89545866
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1450-792T>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545866 | ||||||
| chr16:89545910
|
T | C | 17 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(14): Show | 17 | HG00408.hp2 HG01934.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1450-748T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545910 | ||||||
| chr16:89545990
|
G | A | 13 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0074others(10): Show | 13 | HG00621.hp2 HG01243.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1450-668G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89545990 | ||||||
| chr16:89546103
|
T | G | 27 | a0001c0001t0001g0008a0001c0001t0001g0045a0001c0001t0001g0070others(24): Show | 27 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.1450-555T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546103 | ||||||
| chr16:89546144
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1450-514C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546144 | ||||||
| chr16:89546227
|
C | T | 2 | a0001c0005t0005g0301a0001c0005t0005g0304 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1450-431C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546227 | ||||||
| chr16:89546230
|
G | A | 62 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0074others(59): Show | 63 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1450-428G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546230 | ||||||
| chr16:89546236
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1450-422G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546236 | ||||||
| chr16:89546571
|
A | AC | 91 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0051others(88): Show | 91 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1450-75dupC | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 89546571 | |||||
| chr16:89546571
|
AC | A | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(76): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1450-75delC | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 89546571 | |||||
| chr16:89546574
|
C | T | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0184 | 3 | NA18941.hp1 NA18964.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1450-84C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546574 | ||||||
| chr16:89546578
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1450-80C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546578 | ||||||
| chr16:89546580
|
C | T | 2 | a0001c0013t0003g0340a0001c0019t0003g0217 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1450-78C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546580 | ||||||
| chr16:89546583
|
C | A | 2 | a0001c0005t0005g0301a0001c0005t0005g0304 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1450-75C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546583 | ||||||
| chr16:89546584
|
A | C | 1 | a0001c0005t0010g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1450-74A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546584 | ||||||
| chr16:89546629
|
G | A | 65 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0074others(62): Show | 66 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1450-29G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 10/16 | chr16 | 89546629 | ||||||
| chr16:89546810
|
G | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0133 | 3 | HG00639.hp1 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1552+50G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89546810 | ||||||
| chr16:89546825
|
A | C | 63 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0074others(60): Show | 64 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.1552+65A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89546825 | ||||||
| chr16:89546863
|
C | T | 2 | a0001c0005t0005g0301a0001c0005t0005g0304 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1552+103C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89546863 | ||||||
| chr16:89546939
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1552+179G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89546939 | ||||||
| chr16:89546965
|
G | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(42): Show | 46 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1552+205G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89546965 | ||||||
| chr16:89546991
|
C | T | 2 | a0001c0013t0003g0340a0001c0019t0003g0217 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1552+231C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89546991 | ||||||
| chr16:89547004
|
T | C | 336 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(333): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1552+244T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547004 | ||||||
| chr16:89547057
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1552+297G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547057 | ||||||
| chr16:89547113
|
G | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0274 | 2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1552+353G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547113 | ||||||
| chr16:89547122
|
G | A | 64 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0074others(61): Show | 65 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1552+362G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547122 | ||||||
| chr16:89547312
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0203 | 2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1552+552A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547312 | ||||||
| chr16:89547315
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1552+555C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547315 | ||||||
| chr16:89547362
|
A | G | 2 | a0001c0005t0005g0301a0001c0005t0005g0304 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1552+602A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547362 | ||||||
| chr16:89547416
|
G | T | 2 | a0001c0005t0005g0301a0001c0005t0005g0304 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1553-587G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547416 | ||||||
| chr16:89547490
|
G | T | 1 | a0001c0001t0001g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1553-513G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547490 | ||||||
| chr16:89547538
|
G | T | 1 | a0001c0001t0001g0236 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1553-465G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547538 | ||||||
| chr16:89547552
|
G | C | 335 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(332): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1553-451G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547552 | ||||||
| chr16:89547711
|
C | T | 1 | a0001c0001t0007g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1553-292C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547711 | ||||||
| chr16:89547753
|
C | G | 1 | a0003c0003t0002g0208 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1553-250C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547753 | ||||||
| chr16:89547788
|
T | G | 1 | a0001c0001t0002g0337 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1553-215T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547788 | ||||||
| chr16:89547872
|
C | G | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1553-131C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547872 | ||||||
| chr16:89547975
|
C | G | 1 | a0001c0001t0001g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1553-28C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 11/16 | chr16 | 89547975 | ||||||
| chr16:89548126
|
C | T | 2 | a0001c0001t0001g0289a0009c0014t0001g0259 | 2 | HG00099.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1663+13C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548126 | ||||||
| chr16:89548170
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1663+57A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548170 | ||||||
| chr16:89548225
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1663+112C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548225 | ||||||
| chr16:89548274
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1663+161T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548274 | ||||||
| chr16:89548296
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1663+183T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548296 | ||||||
| chr16:89548481
|
C | T | 1 | a0001c0001t0004g0202 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1663+368C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548481 | ||||||
| chr16:89548509
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1663+396C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548509 | ||||||
| chr16:89548583
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1663+470C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548583 | ||||||
| chr16:89548653
|
G | A | 7 | a0001c0001t0001g0222a0001c0001t0001g0242a0001c0001t0001g0290others(4): Show | 7 | HG00280.hp1 NA18612.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.1663+540G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548653 | ||||||
| chr16:89548800
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1663+687C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548800 | ||||||
| chr16:89548844
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1663+731G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548844 | ||||||
| chr16:89548905
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1663+792C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548905 | ||||||
| chr16:89548924
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1663+811C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548924 | ||||||
| chr16:89548925
|
C | T | 52 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0221others(49): Show | 53 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.1663+812C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89548925 | ||||||
| chr16:89549045
|
A | C | 50 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0221others(47): Show | 51 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1663+932A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549045 | ||||||
| chr16:89549058
|
C | T | 2 | a0001c0005t0005g0301a0001c0005t0005g0304 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1663+945C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549058 | ||||||
| chr16:89549134
|
G | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG01928.hp1 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663+1021G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549134 | ||||||
| chr16:89549141
|
C | T | 2 | a0001c0001t0001g0106a0010c0009t0001g0118 | 2 | NA18747.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1663+1028C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549141 | ||||||
| chr16:89549271
|
C | G | 1 | a0003c0003t0002g0208 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1663+1158C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549271 | ||||||
| chr16:89549357
|
T | G | 35 | a0001c0005t0005g0301a0001c0005t0005g0304a0002c0002t0002g0001others(32): Show | 36 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1664-1137T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549357 | ||||||
| chr16:89549631
|
G | A | 148 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1664-863G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549631 | ||||||
| chr16:89549747
|
G | T | 33 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0010others(30): Show | 34 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.1664-747G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549747 | ||||||
| chr16:89549755
|
G | A | 1 | a0003c0003t0002g0208 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1664-739G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549755 | ||||||
| chr16:89549759
|
T | C | 49 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0221others(46): Show | 50 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1664-735T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549759 | ||||||
| chr16:89549770
|
G | A | 49 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0221others(46): Show | 50 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1664-724G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549770 | ||||||
| chr16:89549824
|
G | A | 48 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0227others(45): Show | 49 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1664-670G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549824 | ||||||
| chr16:89549894
|
C | G | 1 | a0002c0002t0002g0013 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1664-600C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89549894 | ||||||
| chr16:89550033
|
C | T | 8 | a0003c0003t0002g0054a0003c0003t0002g0055a0003c0003t0002g0056others(5): Show | 8 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1664-461C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550033 | ||||||
| chr16:89550150
|
T | C | 50 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0221others(47): Show | 51 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1664-344T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550150 | ||||||
| chr16:89550166
|
C | G | 1 | a0001c0005t0005g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1664-328C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550166 | ||||||
| chr16:89550317
|
C | T | 50 | a0001c0001t0001g0008a0001c0001t0001g0228a0001c0001t0002g0219others(47): Show | 51 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1664-177C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550317 | ||||||
| chr16:89550364
|
G | T | 50 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0221others(47): Show | 51 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1664-130G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550364 | ||||||
| chr16:89550382
|
G | A | 49 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0227others(46): Show | 50 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1664-112G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550382 | ||||||
| chr16:89550392
|
C | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0309a0001c0001t0001g0311others(2): Show | 6 | HG01168.hp1 HG01169.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1664-102C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550392 | ||||||
| chr16:89550440
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1664-54T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550440 | ||||||
| chr16:89550479
|
C | A | 2 | a0001c0013t0003g0340a0001c0019t0003g0217 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1664-15C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 12/16 | chr16 | 89550479 | ||||||
| chr16:89550656
|
G | C | 52 | a0001c0001t0001g0228a0001c0001t0002g0219a0001c0001t0002g0221others(49): Show | 53 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.1779+47G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89550656 | ||||||
| chr16:89550656
|
GTGGGGAG others(23): Show |
G | 1 | a0001c0001t0001g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1779+103_1779+132d others(32): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 89550656 | |||||
| chr16:89550847
|
A | G | 17 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(14): Show | 17 | HG00597.hp1 HG01934.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1779+238A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89550847 | ||||||
| chr16:89550901
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1779+292G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89550901 | ||||||
| chr16:89551065
|
TCAAA | T | 50 | a0001c0001t0001g0113a0001c0001t0001g0228a0001c0001t0002g0219others(47): Show | 51 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.1779+469_1779+472d others(6): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 89551065 | |||||
| chr16:89551110
|
C | T | 34 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0010others(31): Show | 35 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1779+501C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551110 | ||||||
| chr16:89551182
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1779+573G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551182 | ||||||
| chr16:89551194
|
G | C | 2 | a0001c0005t0009g0339a0001c0005t0010g0235 | 2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1779+585G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551194 | ||||||
| chr16:89551334
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1779+725C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551334 | ||||||
| chr16:89551363
|
T | G | 2 | a0001c0001t0002g0221a0001c0001t0007g0011 | 2 | HG02809.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1779+754T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551363 | ||||||
| chr16:89551757
|
G | A | 2 | a0001c0001t0002g0221a0001c0001t0007g0011 | 2 | HG02809.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1779+1148G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551757 | ||||||
| chr16:89551978
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1780-1001A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89551978 | ||||||
| chr16:89552063
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1780-916T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552063 | ||||||
| chr16:89552064
|
C | T | 7 | a0001c0001t0002g0221a0001c0001t0007g0011a0001c0005t0005g0301others(4): Show | 7 | HG01891.hp2 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1780-915C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552064 | ||||||
| chr16:89552086
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1780-893T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552086 | ||||||
| chr16:89552087
|
C | G | 1 | a0001c0001t0001g0265 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1780-892C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552087 | ||||||
| chr16:89552122
|
G | A | 46 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0044others(43): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.1780-857G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552122 | ||||||
| chr16:89552194
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1780-785G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552194 | ||||||
| chr16:89552214
|
G | T | 2 | a0001c0013t0003g0340a0001c0019t0003g0217 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1780-765G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552214 | ||||||
| chr16:89552267
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1780-712C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552267 | ||||||
| chr16:89552275
|
A | T | 2 | a0001c0001t0002g0221a0001c0001t0007g0011 | 2 | HG02809.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1780-704A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552275 | ||||||
| chr16:89552324
|
G | A | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0013t0003g0340others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1780-655G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552324 | ||||||
| chr16:89552341
|
G | A | 1 | a0001c0019t0003g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1780-638G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552341 | ||||||
| chr16:89552467
|
C | G | 2 | a0001c0005t0010g0235a0001c0019t0003g0217 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1780-512C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552467 | ||||||
| chr16:89552468
|
G | A | 2 | a0001c0001t0001g0289a0009c0014t0001g0259 | 2 | HG00099.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1780-511G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552468 | ||||||
| chr16:89552523
|
C | T | 5 | a0001c0001t0002g0230a0001c0005t0005g0301a0001c0005t0005g0304others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1780-456C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552523 | ||||||
| chr16:89552720
|
T | G | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0183 | 3 | HG02717.hp2 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1780-259T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552720 | ||||||
| chr16:89552791
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1780-188G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552791 | ||||||
| chr16:89552885
|
C | T | 1 | a0001c0005t0010g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1780-94C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 13/16 | chr16 | 89552885 | ||||||
| chr16:89553162
|
A | C | 2 | a0001c0001t0001g0281a0008c0010t0001g0237 | 2 | HG00673.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1936+27A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553162 | ||||||
| chr16:89553289
|
G | T | 7 | a0001c0001t0002g0221a0001c0001t0007g0011a0001c0005t0005g0301others(4): Show | 7 | HG01891.hp2 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1936+154G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553289 | ||||||
| chr16:89553390
|
A | T | 1 | a0001c0001t0001g0205 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1936+255A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553390 | ||||||
| chr16:89553667
|
G | A | 8 | a0001c0001t0001g0070a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG00597.hp1 HG02040.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1937-127G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553667 | ||||||
| chr16:89553740
|
A | G | 58 | a0001c0001t0001g0100a0001c0001t0002g0024a0001c0001t0002g0027others(55): Show | 59 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.1937-54A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553740 | ||||||
| chr16:89553750
|
G | A | 6 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325others(3): Show | 6 | HG01192.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1937-44G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553750 | ||||||
| chr16:89553778
|
C | G | 2 | a0001c0001t0002g0221a0001c0001t0007g0011 | 2 | HG02809.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1937-16C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553778 | ||||||
| chr16:89553792
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG02647.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1937-2A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 14/16 | chr16 | 89553792 | ||||||
| chr16:89554043
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2103+83G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/16 | chr16 | 89554043 | ||||||
| chr16:89554055
|
G | T | 2 | a0001c0005t0005g0301a0001c0005t0005g0304 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2103+95G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/16 | chr16 | 89554055 | ||||||
| chr16:89554255
|
C | T | 1 | a0001c0019t0003g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2104-231C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/16 | chr16 | 89554255 | ||||||
| chr16:89554447
|
G | A | 3 | a0001c0001t0001g0328a0001c0001t0001g0332a0001c0005t0009g0339 | 3 | HG03098.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2104-39G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/16 | chr16 | 89554447 | ||||||
| chr16:89554474
|
C | G | 1 | a0001c0001t0001g0334 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2104-12C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 15/16 | chr16 | 89554474 | ||||||
| chr16:89554681
|
A | G | 1 | a0001c0005t0010g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+118A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554681 | ||||||
| chr16:89554761
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2181+198C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554761 | ||||||
| chr16:89554798
|
C | G | 1 | a0001c0005t0010g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+235C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554798 | ||||||
| chr16:89554818
|
C | G | 2 | a0001c0001t0002g0221a0001c0001t0007g0011 | 2 | HG02809.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2181+255C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554818 | ||||||
| chr16:89554856
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2181+293C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554856 | ||||||
| chr16:89554893
|
C | T | 1 | a0001c0005t0010g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+330C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554893 | ||||||
| chr16:89554971
|
G | A | 1 | a0001c0005t0010g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+408G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554971 | ||||||
| chr16:89554982
|
C | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0109 | 2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.2181+419C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554982 | ||||||
| chr16:89554986
|
G | C | 1 | a0001c0001t0007g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2181+423G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89554986 | ||||||
| chr16:89555008
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2181+445C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555008 | ||||||
| chr16:89555075
|
T | C | 1 | a0001c0005t0010g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+512T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555075 | ||||||
| chr16:89555084
|
C | CT | 12 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0084others(9): Show | 12 | HG01346.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2181+537dupT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 89555084 | |||||
| chr16:89555084
|
C | T | 1 | a0001c0005t0010g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+521C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555084 | ||||||
| chr16:89555084
|
CT | C | 11 | a0001c0001t0001g0067a0001c0001t0001g0111a0001c0001t0001g0155others(8): Show | 11 | HG01515.hp2 HG02735.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.2181+537delT | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 89555084 | |||||
| chr16:89555185
|
A | G | 1 | a0001c0005t0010g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2181+622A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555185 | ||||||
| chr16:89555270
|
G | T | 1 | a0001c0013t0003g0340 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2181+707G>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555270 | ||||||
| chr16:89555283
|
A | G | 3 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0010g0235 | 3 | HG02258.hp2 HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2181+720A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555283 | ||||||
| chr16:89555305
|
T | C | 3 | a0001c0001t0001g0323a0001c0001t0001g0329a0001c0001t0001g0330 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2181+742T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555305 | ||||||
| chr16:89555333
|
G | A | 4 | a0001c0001t0002g0221a0001c0001t0007g0011a0001c0013t0003g0340others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2181+770G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555333 | ||||||
| chr16:89555339
|
C | A | 9 | a0001c0001t0001g0100a0001c0001t0002g0221a0001c0001t0003g0295others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2181+776C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555339 | ||||||
| chr16:89555462
|
C | G | 3 | a0001c0001t0001g0336a0001c0005t0009g0339a0001c0005t0010g0235 | 3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2181+899C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555462 | ||||||
| chr16:89555500
|
C | A | 1 | a0001c0001t0007g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2181+937C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555500 | ||||||
| chr16:89555520
|
C | T | 1 | a0001c0005t0005g0304 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2181+957C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555520 | ||||||
| chr16:89555528
|
A | G | 7 | a0001c0001t0001g0100a0001c0001t0003g0295a0001c0001t0003g0344others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2181+965A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555528 | ||||||
| chr16:89555537
|
G | C | 7 | a0001c0001t0001g0100a0001c0001t0003g0295a0001c0001t0003g0344others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2181+974G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555537 | ||||||
| chr16:89555565
|
G | C | 2 | a0001c0005t0005g0301a0001c0005t0005g0304 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2181+1002G>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555565 | ||||||
| chr16:89555574
|
C | T | 1 | a0001c0001t0004g0202 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2181+1011C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555574 | ||||||
| chr16:89555575
|
A | G | 350 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(347): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.2181+1012A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555575 | ||||||
| chr16:89555589
|
C | T | 2 | a0001c0001t0002g0227a0001c0001t0002g0230 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2181+1026C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555589 | ||||||
| chr16:89555649
|
C | T | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+1086C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555649 | ||||||
| chr16:89555699
|
C | G | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+1136C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555699 | ||||||
| chr16:89555709
|
A | G | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2181+1146A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555709 | ||||||
| chr16:89555748
|
T | G | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-1139T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555748 | ||||||
| chr16:89555795
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2182-1092C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555795 | ||||||
| chr16:89555800
|
CTTTGTCC others(2): Show |
C | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-1085_2182-107 others(13): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 89555800 | |||||
| chr16:89555860
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2182-1027C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555860 | ||||||
| chr16:89555917
|
T | C | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-970T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555917 | ||||||
| chr16:89555934
|
G | A | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-953G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555934 | ||||||
| chr16:89555946
|
C | T | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-941C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89555946 | ||||||
| chr16:89556044
|
G | A | 2 | a0001c0001t0002g0221a0001c0001t0007g0011 | 2 | HG02809.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2182-843G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556044 | ||||||
| chr16:89556088
|
A | G | 14 | a0001c0001t0002g0201a0001c0001t0002g0219a0001c0001t0002g0227others(11): Show | 14 | HG01081.hp1 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2182-799A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556088 | ||||||
| chr16:89556092
|
C | G | 1 | a0002c0002t0002g0037 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2182-795C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556092 | ||||||
| chr16:89556099
|
C | T | 2 | a0001c0005t0005g0301a0001c0005t0005g0304 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2182-788C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556099 | ||||||
| chr16:89556116
|
T | G | 38 | a0001c0001t0002g0024a0001c0001t0002g0027a0001c0001t0002g0030others(35): Show | 39 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.2182-771T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556116 | ||||||
| chr16:89556209
|
T | C | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-678T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556209 | ||||||
| chr16:89556219
|
A | C | 1 | a0001c0001t0002g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2182-668A>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556219 | ||||||
| chr16:89556305
|
TAAC | T | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-567_2182-565d others(5): Show |
SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 89556305 | |||||
| chr16:89556320
|
C | A | 4 | a0001c0001t0002g0219a0001c0001t0002g0227a0001c0001t0002g0229others(1): Show | 4 | HG01081.hp1 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-567C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556320 | ||||||
| chr16:89556354
|
C | A | 6 | a0001c0001t0001g0069a0001c0001t0001g0076a0001c0001t0001g0088others(3): Show | 6 | HG00621.hp2 NA18980.hp2 NA19054.hp2 others(3): Show |
intron_variant | MODIFIER | c.2182-533C>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556354 | ||||||
| chr16:89556366
|
G | A | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-521G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556366 | ||||||
| chr16:89556391
|
T | G | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-496T>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556391 | ||||||
| chr16:89556453
|
C | T | 9 | a0001c0001t0002g0201a0001c0001t0002g0221a0001c0001t0003g0295others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2182-434C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556453 | ||||||
| chr16:89556468
|
A | T | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-419A>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556468 | ||||||
| chr16:89556469
|
A | G | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-418A>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556469 | ||||||
| chr16:89556480
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2182-407T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556480 | ||||||
| chr16:89556603
|
C | T | 1 | a0001c0004t0001g0176 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2182-284C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556603 | ||||||
| chr16:89556604
|
G | A | 4 | a0001c0005t0005g0301a0001c0005t0005g0304a0001c0005t0009g0339others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182-283G>A | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556604 | ||||||
| chr16:89556729
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0309a0001c0001t0001g0311others(2): Show | 6 | HG01168.hp1 HG01169.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.2182-158T>C | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556729 | ||||||
| chr16:89556815
|
C | G | 1 | a0001c0001t0001g0334 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2182-72C>G | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556815 | ||||||
| chr16:89556839
|
C | T | 1 | a0001c0005t0010g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2182-48C>T | SPG7 | ENSG00000197912.16 | transcript | ENST00000645818.2 | protein_coding | 16/16 | chr16 | 89556839 |