Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 80208 |
|---|---|
| ensemblid | ENSG00000104133.16 |
| hgncid | 11226 |
| symbol | SPG11 |
| name | SPG11 vesicle trafficking associated, spatacsin |
| refseq_nuc | NM_025137.4 |
| refseq_prot | NP_079413.3 |
| ensembl_nuc | ENST00000261866.12 |
| ensembl_prot | ENSP00000261866.7 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 44562696 |
| end | 44663662 |
| strand | - |
| ver | v1.2 |
| region | chr15:44562696-44663662 |
| region5000 | chr15:44557696-44668662 |
| regionname0 | SPG11_chr15_44562696_44663662 |
| regionname5000 | SPG11_chr15_44557696_44668662 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 2443 | 73 | 25 | 8 | 29 | 1 | 10 | 21 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0002 | 1/1 | 2443 | 52 | 19 | 8 | 15 | 3 | 5 | 10 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0003 | 0/0 | 2443 | 16 | 1 | 0 | 13 | 0 | 2 | 9 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0004 | 0/0 | 2443 | 12 | 0 | 0 | 12 | 0 | 0 | 9 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0005 | 0/0 | 2443 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0006 | 0/0 | 2443 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0007 | 0/0 | 2443 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0008 | 0/0 | 2443 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0009 | 0/0 | 2443 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0010 | 0/0 | 2443 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0011 | 0/0 | 2443 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0012 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0013 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0014 | 0/0 | 2443 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0015 | 0/0 | 2443 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0016 | 0/0 | 2443 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0017 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0018 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0019 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0020 | 0/0 | 2443 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0021 | 0/0 | 2443 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0022 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0023 | 0/0 | 2443 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0024 | 0/0 | 2443 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0025 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 7332 | 72 | 24 | 8 | 29 | 1 | 10 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0002 | 1/1 | 7332 | 51 | 19 | 8 | 15 | 2 | 5 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0003 | 0/0 | 7332 | 16 | 1 | 0 | 13 | 0 | 2 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0004 | 0/0 | 7332 | 12 | 0 | 0 | 12 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0005 | 0/0 | 7332 | 7 | 6 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0006 | 0/0 | 7332 | 4 | 4 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0007 | 0/0 | 7332 | 3 | 3 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0008 | 0/0 | 7332 | 3 | 3 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0009 | 0/0 | 7332 | 2 | 0 | 1 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0010 | 0/0 | 7332 | 2 | 2 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0011 | 0/0 | 7332 | 2 | 2 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0012 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0013 | 0/0 | 7332 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0014 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0015 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0016 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0017 | 0/0 | 7332 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0018 | 0/0 | 7332 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0019 | 0/0 | 7332 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0020 | 0/0 | 7332 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0021 | 0/0 | 7332 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0022 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0023 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0024 | 0/0 | 7332 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0025 | 0/0 | 7332 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0026 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| c0027 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 441 | 183 | 65 | 20 | 72 | 6 | 18 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| t0002 | 0/0 | 441 | 6 | 6 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| t0003 | 0/0 | 441 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 7332 | 72 | 24 | 8 | 29 | 1 | 10 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0001c0016 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0002c0002 | 1/1 | 7332 | 51 | 19 | 8 | 15 | 2 | 5 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0002c0021 | 0/0 | 7332 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0003c0003 | 0/0 | 7332 | 16 | 1 | 0 | 13 | 0 | 2 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0004c0004 | 0/0 | 7332 | 12 | 0 | 0 | 12 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0005c0005 | 0/0 | 7332 | 7 | 6 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0006c0006 | 0/0 | 7332 | 4 | 4 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0007c0008 | 0/0 | 7332 | 3 | 3 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0008c0007 | 0/0 | 7332 | 3 | 3 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0009c0011 | 0/0 | 7332 | 2 | 2 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0010c0010 | 0/0 | 7332 | 2 | 2 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0011c0009 | 0/0 | 7332 | 2 | 0 | 1 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0012c0012 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0013c0026 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0014c0024 | 0/0 | 7332 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0015c0020 | 0/0 | 7332 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0016c0019 | 0/0 | 7332 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0017c0022 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0018c0023 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0019c0015 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0020c0017 | 0/0 | 7332 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0021c0018 | 0/0 | 7332 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0022c0014 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0023c0013 | 0/0 | 7332 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0024c0025 | 0/0 | 7332 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0025c0027 | 0/0 | 7332 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7772 | 72 | 24 | 8 | 29 | 1 | 10 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0001c0016t0001 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0002c0002t0001 | 1/1 | 7772 | 45 | 13 | 8 | 15 | 2 | 5 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0002c0002t0002 | 0/0 | 7772 | 6 | 6 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0002c0021t0001 | 0/0 | 7772 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0003c0003t0001 | 0/0 | 7772 | 16 | 1 | 0 | 13 | 0 | 2 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0004c0004t0001 | 0/0 | 7772 | 12 | 0 | 0 | 12 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0005c0005t0001 | 0/0 | 7772 | 7 | 6 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0006c0006t0001 | 0/0 | 7772 | 4 | 4 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0007c0008t0001 | 0/0 | 7772 | 3 | 3 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0008c0007t0001 | 0/0 | 7772 | 3 | 3 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0009c0011t0001 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0009c0011t0003 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0010c0010t0001 | 0/0 | 7772 | 2 | 2 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0011c0009t0001 | 0/0 | 7772 | 2 | 0 | 1 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0012c0012t0001 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0013c0026t0001 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0014c0024t0001 | 0/0 | 7772 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0015c0020t0001 | 0/0 | 7772 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0016c0019t0001 | 0/0 | 7772 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0017c0022t0001 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0018c0023t0001 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0019c0015t0001 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0020c0017t0001 | 0/0 | 7772 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0021c0018t0001 | 0/0 | 7772 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0022c0014t0001 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0023c0013t0001 | 0/0 | 7772 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0024c0025t0001 | 0/0 | 7772 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| a0025c0027t0001 | 0/0 | 7772 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | copy fasta | chr15 | 44557696 | 44668662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0001c0016t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0002c0021t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0003c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0004c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0004c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0004c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0004c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0004c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0004c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0004c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0004c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0004c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0004c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0004c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0004c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0005c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0005c0005t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0005c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0005c0005t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0005c0005t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0005c0005t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0005c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0006c0006t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0006c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0006c0006t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0006c0006t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0007c0008t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0007c0008t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0007c0008t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0008c0007t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0008c0007t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0008c0007t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0009c0011t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0009c0011t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0010c0010t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0010c0010t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0011c0009t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0011c0009t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0012c0012t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0013c0026t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0014c0024t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0015c0020t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0016c0019t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0017c0022t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0018c0023t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0019c0015t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0020c0017t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0021c0018t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0022c0014t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0023c0013t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0024c0025t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| a0025c0027t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0011 | c0009 | t0001 | g0087 | EUR | GBR | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00140 | hp2 | a0002 | c0021 | t0001 | g0139 | EUR | GBR | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00408 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00423 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00597 | hp1 | a0003 | c0003 | t0001 | g0007 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG00673 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | CHS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01069 | hp2 | a0015 | c0020 | t0001 | g0123 | AMR | PUR | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01071 | hp2 | a0020 | c0017 | t0001 | g0065 | AMR | PUR | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | PUR | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0129 | AMR | CLM | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01258 | hp2 | a0011 | c0009 | t0001 | g0086 | AMR | CLM | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01496 | hp1 | a0005 | c0005 | t0001 | g0034 | AMR | CLM | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0042 | EUR | IBS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01891 | hp1 | a0009 | c0011 | t0001 | g0174 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01891 | hp2 | a0010 | c0010 | t0001 | g0181 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | PEL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02040 | hp1 | a0004 | c0004 | t0001 | g0166 | EAS | KHV | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02055 | hp1 | a0007 | c0008 | t0001 | g0188 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0131 | AMR | PEL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02155 | hp1 | a0004 | c0004 | t0001 | g0149 | EAS | CDX | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | CDX | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02257 | hp2 | a0005 | c0005 | t0001 | g0148 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02451 | hp2 | a0005 | c0005 | t0001 | g0146 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02523 | hp1 | a0004 | c0004 | t0001 | g0169 | EAS | KHV | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02572 | hp1 | a0007 | c0008 | t0001 | g0187 | AFR | GWD | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0004 | SAS | PJL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0024 | AFR | GWD | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02630 | hp1 | a0025 | c0027 | t0001 | g0140 | AFR | GWD | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0021 | AFR | GWD | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0019 | AFR | GWD | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02895 | hp1 | a0022 | c0014 | t0001 | g0185 | AFR | GWD | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02922 | hp1 | a0005 | c0005 | t0001 | g0032 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02970 | hp1 | a0006 | c0006 | t0001 | g0179 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0017 | SAS | PJL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03098 | hp1 | a0006 | c0006 | t0001 | g0178 | AFR | MSL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03130 | hp1 | a0010 | c0010 | t0001 | g0184 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03130 | hp2 | a0006 | c0006 | t0001 | g0044 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03139 | hp2 | a0006 | c0006 | t0001 | g0043 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | MSL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | MSL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03225 | hp2 | a0012 | c0012 | t0001 | g0046 | AFR | MSL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03453 | hp2 | a0005 | c0005 | t0001 | g0031 | AFR | MSL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03486 | hp1 | a0007 | c0008 | t0001 | g0186 | AFR | MSL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0124 | SAS | PJL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0153 | SAS | PJL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03516 | hp1 | a0005 | c0005 | t0001 | g0033 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03516 | hp2 | a0008 | c0007 | t0001 | g0151 | AFR | ESN | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03704 | hp1 | a0016 | c0019 | t0001 | g0115 | SAS | PJL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0133 | SAS | BEB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03927 | hp1 | a0003 | c0003 | t0001 | g0002 | SAS | BEB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | STU | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0118 | SAS | STU | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0155 | AFR | YRI | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18522 | hp2 | a0017 | c0022 | t0001 | g0114 | AFR | YRI | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18906 | hp1 | a0008 | c0007 | t0001 | g0152 | AFR | YRI | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | YRI | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18949 | hp2 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18951 | hp2 | a0024 | c0025 | t0001 | g0172 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0013 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18953 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18954 | hp1 | a0021 | c0018 | t0001 | g0097 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18960 | hp1 | a0004 | c0004 | t0001 | g0164 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18965 | hp2 | a0004 | c0004 | t0001 | g0168 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18966 | hp2 | a0004 | c0004 | t0001 | g0182 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18967 | hp2 | a0004 | c0004 | t0001 | g0170 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18971 | hp2 | a0004 | c0004 | t0001 | g0158 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18978 | hp2 | a0014 | c0024 | t0001 | g0159 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18985 | hp2 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18986 | hp1 | a0004 | c0004 | t0001 | g0171 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18990 | hp1 | a0004 | c0004 | t0001 | g0183 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19004 | hp2 | a0004 | c0004 | t0001 | g0167 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19007 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19030 | hp1 | a0019 | c0015 | t0001 | g0061 | AFR | LWK | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19030 | hp2 | a0013 | c0026 | t0001 | g0157 | AFR | LWK | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19043 | hp1 | a0008 | c0007 | t0001 | g0150 | AFR | LWK | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19063 | hp2 | a0004 | c0004 | t0001 | g0165 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19064 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19085 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | ASW | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ASW | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA20805 | hp1 | a0023 | c0013 | t0001 | g0064 | EUR | TSI | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0137 | EUR | TSI | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | CLM | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02109 | hp1 | a0018 | c0023 | t0001 | g0175 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02109 | hp2 | a0009 | c0011 | t0003 | g0173 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG02559 | hp2 | a0005 | c0005 | t0001 | g0147 | AFR | ACB | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0132 | AFR | MSL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | MSL | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0177 | AFR | USA | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | USA | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0163 | AFR | USA | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | USA | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA21309 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | LWK | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| NA21309 | hp2 | a0001 | c0016 | t0001 | g0108 | AFR | LWK | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0116 | REF | REF | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0156 | REF | REF | SPG11_chr15_44557696_44668662 | SPG11 | chr15 | 44557696 | 44668662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44563197
|
T | C | 3 | a0006a0007a0022 | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(5): Show |
missense_variant | MODERATE | c.7256A>G | p.Lys2419Arg | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 40/40 | 7271/7772 | 7256/7332 | 2419/2443 | chr15 | 44563197 | ||
| chr15:44564629
|
G | A | 2 | a0015a0020 | 2 | HG01069.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.7069C>T | p.Leu2357Phe | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/40 | 7084/7772 | 7069/7332 | 2357/2443 | chr15 | 44564629 | ||
| chr15:44565961
|
T | C | 1 | a0021 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.6892A>G | p.Ile2298Val | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 38/40 | 6907/7772 | 6892/7332 | 2298/2443 | chr15 | 44565961 | ||
| chr15:44572707
|
C | T | 2 | a0009a0010 | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
missense_variant | MODERATE | c.6319G>A | p.Val2107Ile | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/40 | 6334/7772 | 6319/7332 | 2107/2443 | chr15 | 44572707 | ||
| chr15:44585834
|
C | G | 1 | a0010 | 2 | HG01891.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.4923G>C | p.Lys1641Asn | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/40 | 4938/7772 | 4923/7332 | 1641/2443 | chr15 | 44585834 | ||
| chr15:44589348
|
A | G | 2 | a0008a0018 | 4 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
missense_variant | MODERATE | c.4810T>C | p.Phe1604Leu | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/40 | 4825/7772 | 4810/7332 | 1604/2443 | chr15 | 44589348 | ||
| chr15:44592387
|
T | C | 1 | a0006 | 4 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
missense_variant | MODERATE | c.4687A>G | p.Arg1563Gly | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/40 | 4702/7772 | 4687/7332 | 1563/2443 | chr15 | 44592387 | ||
| chr15:44592401
|
A | G | 1 | a0024 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.4673T>C | p.Leu1558Pro | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/40 | 4688/7772 | 4673/7332 | 1558/2443 | chr15 | 44592401 | ||
| chr15:44596199
|
C | T | 1 | a0016 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.4318G>A | p.Asp1440Asn | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 25/40 | 4333/7772 | 4318/7332 | 1440/2443 | chr15 | 44596199 | ||
| chr15:44598705
|
T | C | 1 | a0005 | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
missense_variant | MODERATE | c.3818A>G | p.Lys1273Arg | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 22/40 | 3833/7772 | 3818/7332 | 1273/2443 | chr15 | 44598705 | ||
| chr15:44608461
|
T | C | 1 | a0017 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.3436A>G | p.Ile1146Val | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/40 | 3451/7772 | 3436/7332 | 1146/2443 | chr15 | 44608461 | ||
| chr15:44613507
|
T | C | 1 | a0018 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.3068A>G | p.Glu1023Gly | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/40 | 3083/7772 | 3068/7332 | 1023/2443 | chr15 | 44613507 | ||
| chr15:44615364
|
T | C | 1 | a0011 | 2 | HG00140.hp1 HG01258.hp2 |
missense_variant&splice_region_variant | MODERATE | c.3037A>G | p.Lys1013Glu | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/40 | 3052/7772 | 3037/7332 | 1013/2443 | chr15 | 44615364 | ||
| chr15:44620368
|
A | G | 1 | a0019 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2656T>C | p.Tyr886His | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/40 | 2671/7772 | 2656/7332 | 886/2443 | chr15 | 44620368 | ||
| chr15:44626492
|
C | T | 1 | a0023 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.2083G>A | p.Ala695Thr | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/40 | 2098/7772 | 2083/7332 | 695/2443 | chr15 | 44626492 | ||
| chr15:44651559
|
A | G | 9 | a0001a0011a0012others(6): Show | 82 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
missense_variant | MODERATE | c.1388T>C | p.Phe463Ser | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/40 | 1403/7772 | 1388/7332 | 463/2443 | chr15 | 44651559 | ||
| chr15:44651599
|
T | C | 1 | a0003 | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
missense_variant | MODERATE | c.1348A>G | p.Ile450Val | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/40 | 1363/7772 | 1348/7332 | 450/2443 | chr15 | 44651599 | ||
| chr15:44651677
|
G | T | 1 | a0022 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.1270C>A | p.Pro424Thr | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/40 | 1285/7772 | 1270/7332 | 424/2443 | chr15 | 44651677 | ||
| chr15:44651760
|
T | C | 1 | a0014 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.1187A>G | p.Tyr396Cys | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/40 | 1202/7772 | 1187/7332 | 396/2443 | chr15 | 44651760 | ||
| chr15:44651839
|
C | T | 1 | a0023 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.1108G>A | p.Glu370Lys | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/40 | 1123/7772 | 1108/7332 | 370/2443 | chr15 | 44651839 | ||
| chr15:44657131
|
T | C | 2 | a0004a0024 | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
missense_variant | MODERATE | c.833A>G | p.Asn278Ser | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/40 | 848/7772 | 833/7332 | 278/2443 | chr15 | 44657131 | ||
| chr15:44657201
|
T | C | 1 | a0013 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.763A>G | p.Lys255Glu | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/40 | 778/7772 | 763/7332 | 255/2443 | chr15 | 44657201 | ||
| chr15:44659303
|
C | T | 1 | a0012 | 1 | HG03225.hp2 | missense_variant&splice_region_variant | MODERATE | c.443G>A | p.Ser148Asn | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/40 | 458/7772 | 443/7332 | 148/2443 | chr15 | 44659303 | ||
| chr15:44660497
|
T | C | 1 | a0025 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.377A>G | p.Asp126Gly | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 2/40 | 392/7772 | 377/7332 | 126/2443 | chr15 | 44660497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44564552
|
G | A | 1 | a0001c0016 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.7146C>T | p.Ser2382Ser | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/40 | 7161/7772 | 7146/7332 | 2382/2443 | chr15 | 44564552 | ||
| chr15:44564675
|
G | A | 1 | a0002c0021 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.7023C>T | p.Tyr2341Tyr | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/40 | 7038/7772 | 7023/7332 | 2341/2443 | chr15 | 44564675 | ||
| chr15:44572696
|
C | T | 1 | a0003c0003 | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
synonymous_variant | LOW | c.6330G>A | p.Gly2110Gly | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/40 | 6345/7772 | 6330/7332 | 2110/2443 | chr15 | 44572696 | ||
| chr15:44651600
|
G | A | 1 | a0003c0003 | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
synonymous_variant | LOW | c.1347C>T | p.Thr449Thr | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/40 | 1362/7772 | 1347/7332 | 449/2443 | chr15 | 44651600 | ||
| chr15:44651783
|
T | C | 1 | a0023c0013 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.1164A>G | p.Pro388Pro | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/40 | 1179/7772 | 1164/7332 | 388/2443 | chr15 | 44651783 | ||
| chr15:44652143
|
G | A | 2 | a0004c0004a0024c0025 | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
synonymous_variant | LOW | c.993C>T | p.Ser331Ser | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 5/40 | 1008/7772 | 993/7332 | 331/2443 | chr15 | 44652143 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44562732
|
T | A | 1 | a0009c0011t0003 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*389A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 40/40 | 389 | chr15 | 44562732 | |||||
| chr15:44562878
|
T | C | 1 | a0002c0002t0002 | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*243A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 40/40 | 243 | chr15 | 44562878 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44563338
|
G | A | 1 | a0006c0006t0001g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7152-37C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/39 | chr15 | 44563338 | ||||||
| chr15:44563391
|
T | A | 1 | a0004c0004t0001g0169 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.7152-90A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/39 | chr15 | 44563391 | ||||||
| chr15:44563399
|
A | C | 1 | a0003c0003t0001g0013 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.7152-98T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/39 | chr15 | 44563399 | ||||||
| chr15:44563402
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.7152-101T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/39 | chr15 | 44563402 | ||||||
| chr15:44563817
|
C | A | 2 | a0015c0020t0001g0123a0020c0017t0001g0065 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.7152-516G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/39 | chr15 | 44563817 | ||||||
| chr15:44563978
|
C | A | 1 | a0007c0008t0001g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7151+569G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/39 | chr15 | 44563978 | ||||||
| chr15:44563983
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.7151+564T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/39 | chr15 | 44563983 | ||||||
| chr15:44564056
|
C | T | 1 | a0009c0011t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7151+491G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/39 | chr15 | 44564056 | ||||||
| chr15:44564127
|
G | A | 11 | a0001c0001t0001g0083a0002c0002t0001g0017a0002c0002t0001g0025others(8): Show | 11 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.7151+420C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/39 | chr15 | 44564127 | ||||||
| chr15:44564240
|
G | A | 2 | a0008c0007t0001g0151a0008c0007t0001g0152 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7151+307C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/39 | chr15 | 44564240 | ||||||
| chr15:44564245
|
G | A | 12 | a0004c0004t0001g0158a0004c0004t0001g0164a0004c0004t0001g0165others(9): Show | 12 | HG02040.hp1 HG02523.hp1 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.7151+302C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 39/39 | chr15 | 44564245 | ||||||
| chr15:44564718
|
A | G | 2 | a0015c0020t0001g0123a0020c0017t0001g0065 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.7000-20T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 38/39 | chr15 | 44564718 | ||||||
| chr15:44564973
|
A | G | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7000-275T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 38/39 | chr15 | 44564973 | ||||||
| chr15:44565097
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.7000-399G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 38/39 | chr15 | 44565097 | ||||||
| chr15:44565295
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6999+559G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 38/39 | chr15 | 44565295 | ||||||
| chr15:44565339
|
C | T | 1 | a0014c0024t0001g0159 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.6999+515G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 38/39 | chr15 | 44565339 | ||||||
| chr15:44565385
|
T | C | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.6999+469A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 38/39 | chr15 | 44565385 | ||||||
| chr15:44565420
|
A | G | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.6999+434T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 38/39 | chr15 | 44565420 | ||||||
| chr15:44565572
|
T | G | 1 | a0002c0002t0001g0138 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.6999+282A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 38/39 | chr15 | 44565572 | ||||||
| chr15:44565706
|
C | G | 4 | a0001c0001t0001g0056a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG02559.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.6999+148G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 38/39 | chr15 | 44565706 | ||||||
| chr15:44566080
|
C | T | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.6844-71G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 37/39 | chr15 | 44566080 | ||||||
| chr15:44566319
|
AAAG | A | 17 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.6755-17_6755-15del others(3): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44566319 | ||||||
| chr15:44566599
|
A | G | 4 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(1): Show | 4 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.6755-294T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44566599 | ||||||
| chr15:44566632
|
C | T | 1 | a0002c0002t0001g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.6755-327G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44566632 | ||||||
| chr15:44566706
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.6755-401T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44566706 | ||||||
| chr15:44566743
|
C | T | 1 | a0002c0002t0001g0190 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.6755-438G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44566743 | ||||||
| chr15:44566770
|
G | C | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6755-465C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44566770 | ||||||
| chr15:44566792
|
C | T | 1 | a0002c0002t0001g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6755-487G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44566792 | ||||||
| chr15:44566793
|
G | A | 1 | a0021c0018t0001g0097 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.6755-488C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44566793 | ||||||
| chr15:44566970
|
T | C | 1 | a0008c0007t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6754+454A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44566970 | ||||||
| chr15:44566998
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6754+426C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44566998 | ||||||
| chr15:44567156
|
C | G | 1 | a0002c0002t0001g0136 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6754+268G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44567156 | ||||||
| chr15:44567184
|
TATTAAAA | T | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.6754+233_6754+239d others(9): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44567184 | ||||||
| chr15:44567349
|
C | CA | 31 | a0001c0001t0001g0058a0001c0001t0001g0092a0001c0001t0001g0110others(28): Show | 31 | HG00673.hp1 HG01496.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.6754+74dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44567349 | ||||||
| chr15:44567349
|
C | CAA | 31 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0089others(28): Show | 31 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.6754+73_6754+74dup others(2): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44567349 | ||||||
| chr15:44567349
|
CA | C | 14 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(11): Show | 14 | HG00140.hp2 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.6754+74delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44567349 | ||||||
| chr15:44567374
|
T | C | 7 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.6754+50A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44567374 | ||||||
| chr15:44567405
|
T | C | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.6754+19A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 36/39 | chr15 | 44567405 | ||||||
| chr15:44567646
|
A | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0111 | 2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.6586-54T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44567646 | ||||||
| chr15:44567703
|
G | A | 11 | a0001c0001t0001g0083a0002c0002t0001g0017a0002c0002t0001g0025others(8): Show | 11 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.6586-111C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44567703 | ||||||
| chr15:44568043
|
T | C | 2 | a0002c0002t0001g0176a0002c0002t0001g0177 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6586-451A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44568043 | ||||||
| chr15:44568146
|
C | T | 1 | a0002c0002t0002g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6586-554G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44568146 | ||||||
| chr15:44568196
|
T | G | 1 | a0002c0002t0001g0120 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.6586-604A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44568196 | ||||||
| chr15:44568281
|
G | A | 3 | a0002c0002t0001g0121a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG00609.hp1 HG00621.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.6586-689C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44568281 | ||||||
| chr15:44568364
|
T | C | 1 | a0002c0002t0001g0134 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.6586-772A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44568364 | ||||||
| chr15:44568427
|
C | G | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.6586-835G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44568427 | ||||||
| chr15:44568513
|
A | C | 13 | a0001c0001t0001g0101a0006c0006t0001g0043a0006c0006t0001g0044others(10): Show | 13 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.6585+885T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44568513 | ||||||
| chr15:44568556
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.6585+842A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44568556 | ||||||
| chr15:44568567
|
G | A | 7 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.6585+831C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44568567 | ||||||
| chr15:44568602
|
C | T | 2 | a0001c0001t0001g0057a0019c0015t0001g0061 | 2 | HG02895.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.6585+796G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44568602 | ||||||
| chr15:44568709
|
TCA | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0160others(1): Show | 4 | HG03704.hp1 HG04204.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.6585+687_6585+688d others(4): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44568709 | ||||||
| chr15:44568915
|
T | A | 14 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(11): Show | 14 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.6585+483A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44568915 | ||||||
| chr15:44568921
|
C | T | 4 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(1): Show | 4 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.6585+477G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44568921 | ||||||
| chr15:44569164
|
C | CA | 6 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.6585+233dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44569164 | ||||||
| chr15:44569188
|
A | G | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.6585+210T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44569188 | ||||||
| chr15:44569247
|
CT | C | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.6585+150delA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 35/39 | chr15 | 44569247 | ||||||
| chr15:44569718
|
C | CT | 5 | a0001c0001t0001g0093a0001c0001t0001g0101a0002c0002t0001g0042others(2): Show | 5 | HG01496.hp1 HG01515.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.6478-214dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 34/39 | chr15 | 44569718 | ||||||
| chr15:44569998
|
A | G | 1 | a0002c0002t0001g0119 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.6478-493T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 34/39 | chr15 | 44569998 | ||||||
| chr15:44570030
|
T | A | 2 | a0002c0002t0001g0029a0002c0002t0001g0030 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.6477+495A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 34/39 | chr15 | 44570030 | ||||||
| chr15:44570091
|
A | G | 1 | a0002c0002t0001g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.6477+434T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 34/39 | chr15 | 44570091 | ||||||
| chr15:44570174
|
G | A | 7 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.6477+351C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 34/39 | chr15 | 44570174 | ||||||
| chr15:44570359
|
A | G | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6477+166T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 34/39 | chr15 | 44570359 | ||||||
| chr15:44570428
|
C | T | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.6477+97G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 34/39 | chr15 | 44570428 | ||||||
| chr15:44570686
|
G | A | 1 | a0002c0002t0001g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.6344-28C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44570686 | ||||||
| chr15:44570732
|
G | A | 15 | a0003c0003t0001g0002a0003c0003t0001g0003a0003c0003t0001g0004others(12): Show | 15 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.6344-74C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44570732 | ||||||
| chr15:44570958
|
T | C | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.6344-300A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44570958 | ||||||
| chr15:44571042
|
C | G | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.6344-384G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44571042 | ||||||
| chr15:44571057
|
T | C | 1 | a0002c0002t0001g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.6344-399A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44571057 | ||||||
| chr15:44571146
|
CTG | C | 17 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.6344-490_6344-489d others(4): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44571146 | ||||||
| chr15:44571194
|
T | C | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.6344-536A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44571194 | ||||||
| chr15:44571205
|
G | A | 14 | a0001c0001t0001g0106a0004c0004t0001g0149a0004c0004t0001g0158others(11): Show | 14 | HG02040.hp1 HG02040.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.6344-547C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44571205 | ||||||
| chr15:44571279
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.6344-621G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44571279 | ||||||
| chr15:44571471
|
G | T | 1 | a0011c0009t0001g0086 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.6344-813C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44571471 | ||||||
| chr15:44571472
|
G | T | 1 | a0004c0004t0001g0171 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6344-814C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44571472 | ||||||
| chr15:44571496
|
C | CT | 37 | a0001c0001t0001g0060a0001c0001t0001g0106a0002c0002t0001g0018others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.6344-839dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44571496 | ||||||
| chr15:44571501
|
T | C | 15 | a0001c0001t0001g0110a0002c0002t0001g0017a0002c0002t0001g0025others(12): Show | 15 | HG00621.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.6344-843A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44571501 | ||||||
| chr15:44571778
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.6343+905A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44571778 | ||||||
| chr15:44572046
|
G | A | 12 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.6343+637C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44572046 | ||||||
| chr15:44572381
|
G | A | 1 | a0003c0003t0001g0015 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.6343+302C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44572381 | ||||||
| chr15:44572384
|
A | G | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6343+299T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 33/39 | chr15 | 44572384 | ||||||
| chr15:44572908
|
T | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.6206-88A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 32/39 | chr15 | 44572908 | ||||||
| chr15:44572939
|
T | C | 68 | a0001c0001t0001g0106a0002c0002t0001g0017a0002c0002t0001g0018others(65): Show | 68 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.6206-119A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 32/39 | chr15 | 44572939 | ||||||
| chr15:44572980
|
C | CG | 3 | a0002c0002t0002g0021a0002c0002t0002g0023a0002c0002t0002g0024 | 3 | HG02258.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.6206-161_6206-160i others(3): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 32/39 | chr15 | 44572980 | ||||||
| chr15:44572980
|
C | CGT | 2 | a0002c0002t0002g0019a0002c0002t0002g0020 | 2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.6206-161_6206-160i others(4): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 32/39 | chr15 | 44572980 | ||||||
| chr15:44572980
|
C | CT | 27 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0058others(24): Show | 27 | HG00621.hp2 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.6206-161dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 32/39 | chr15 | 44572980 | ||||||
| chr15:44572980
|
CT | C | 17 | a0001c0001t0001g0091a0002c0002t0001g0017a0002c0002t0001g0025others(14): Show | 17 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.6206-161delA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 32/39 | chr15 | 44572980 | ||||||
| chr15:44572981
|
T | G | 1 | a0002c0002t0002g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6206-161A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 32/39 | chr15 | 44572981 | ||||||
| chr15:44573120
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6206-300C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 32/39 | chr15 | 44573120 | ||||||
| chr15:44573133
|
CCCG | C | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.6206-316_6206-314d others(5): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 32/39 | chr15 | 44573133 | ||||||
| chr15:44573135
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.6206-315G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 32/39 | chr15 | 44573135 | ||||||
| chr15:44573156
|
T | C | 2 | a0001c0001t0001g0106a0004c0004t0001g0149 | 2 | HG02040.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.6206-336A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 32/39 | chr15 | 44573156 | ||||||
| chr15:44573353
|
GCATGTAT others(6): Show |
G | 3 | a0007c0008t0001g0186a0007c0008t0001g0187a0022c0014t0001g0185 | 3 | HG02572.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.6205+181_6205+193d others(15): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 32/39 | chr15 | 44573353 | ||||||
| chr15:44573892
|
G | A | 3 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152 | 3 | HG03516.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.6007-147C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 31/39 | chr15 | 44573892 | ||||||
| chr15:44573976
|
T | C | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6007-231A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 31/39 | chr15 | 44573976 | ||||||
| chr15:44574025
|
CAG | C | 38 | a0001c0001t0001g0106a0002c0002t0001g0018a0002c0002t0002g0019others(35): Show | 38 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.6007-282_6007-281d others(4): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 31/39 | chr15 | 44574025 | ||||||
| chr15:44574087
|
G | A | 2 | a0001c0001t0001g0095a0002c0002t0001g0153 | 2 | HG03490.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.6007-342C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 31/39 | chr15 | 44574087 | ||||||
| chr15:44574220
|
T | A | 1 | a0001c0001t0001g0036 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.6007-475A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 31/39 | chr15 | 44574220 | ||||||
| chr15:44574264
|
G | A | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6007-519C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 31/39 | chr15 | 44574264 | ||||||
| chr15:44574272
|
G | A | 4 | a0007c0008t0001g0186a0007c0008t0001g0187a0007c0008t0001g0188others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.6007-527C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 31/39 | chr15 | 44574272 | ||||||
| chr15:44574322
|
T | C | 1 | a0003c0003t0001g0003 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.6007-577A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 31/39 | chr15 | 44574322 | ||||||
| chr15:44574328
|
G | T | 17 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.6006+574C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 31/39 | chr15 | 44574328 | ||||||
| chr15:44574473
|
T | C | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.6006+429A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 31/39 | chr15 | 44574473 | ||||||
| chr15:44574649
|
A | C | 3 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152 | 3 | HG03516.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.6006+253T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 31/39 | chr15 | 44574649 | ||||||
| chr15:44574777
|
A | G | 1 | a0002c0002t0001g0026 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.6006+125T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 31/39 | chr15 | 44574777 | ||||||
| chr15:44575122
|
G | C | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.5867-81C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44575122 | ||||||
| chr15:44575419
|
A | G | 4 | a0009c0011t0001g0174a0009c0011t0003g0173a0010c0010t0001g0181others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.5867-378T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44575419 | ||||||
| chr15:44575493
|
C | CT | 8 | a0001c0001t0001g0142a0002c0002t0001g0017a0002c0002t0001g0025others(5): Show | 8 | HG00621.hp1 HG02602.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.5867-453dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44575493 | ||||||
| chr15:44575697
|
G | C | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5867-656C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44575697 | ||||||
| chr15:44575814
|
T | C | 1 | a0021c0018t0001g0097 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.5867-773A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44575814 | ||||||
| chr15:44575861
|
G | A | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.5867-820C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44575861 | ||||||
| chr15:44575870
|
C | T | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.5867-829G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44575870 | ||||||
| chr15:44575899
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.5867-858A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44575899 | ||||||
| chr15:44575905
|
G | A | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.5867-864C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44575905 | ||||||
| chr15:44575917
|
C | A | 4 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(1): Show | 4 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5867-876G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44575917 | ||||||
| chr15:44576073
|
C | T | 14 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(11): Show | 14 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.5867-1032G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576073 | ||||||
| chr15:44576082
|
C | T | 1 | a0008c0007t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5867-1041G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576082 | ||||||
| chr15:44576133
|
A | T | 38 | a0001c0001t0001g0106a0002c0002t0001g0018a0002c0002t0002g0019others(35): Show | 38 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.5867-1092T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576133 | ||||||
| chr15:44576142
|
CA | C | 103 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0041others(100): Show | 103 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.5867-1102delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576142 | ||||||
| chr15:44576142
|
CAA | C | 14 | a0001c0001t0001g0057a0001c0001t0001g0066a0002c0002t0001g0035others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.5867-1103_5867-110 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576142 | ||||||
| chr15:44576142
|
CAAA | C | 49 | a0001c0001t0001g0106a0002c0002t0001g0018a0002c0002t0001g0027others(46): Show | 49 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.5867-1104_5867-110 others(7): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576142 | ||||||
| chr15:44576142
|
CAAAA | C | 9 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(6): Show | 9 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.5867-1105_5867-110 others(8): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576142 | ||||||
| chr15:44576142
|
CAAAAAAA others(9): Show |
C | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.5867-1117_5867-110 others(20): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576142 | ||||||
| chr15:44576171
|
C | G | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.5867-1130G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576171 | ||||||
| chr15:44576305
|
T | C | 1 | a0002c0002t0001g0125 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5867-1264A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576305 | ||||||
| chr15:44576603
|
T | C | 53 | a0001c0001t0001g0106a0002c0002t0002g0019a0002c0002t0002g0020others(50): Show | 53 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.5867-1562A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576603 | ||||||
| chr15:44576609
|
A | C | 1 | a0003c0003t0001g0014 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.5867-1568T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576609 | ||||||
| chr15:44576635
|
C | T | 3 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152 | 3 | HG03516.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.5867-1594G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576635 | ||||||
| chr15:44576792
|
T | C | 38 | a0001c0001t0001g0106a0002c0002t0001g0018a0002c0002t0002g0019others(35): Show | 38 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.5867-1751A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576792 | ||||||
| chr15:44576857
|
C | T | 2 | a0009c0011t0001g0174a0009c0011t0003g0173 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.5867-1816G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576857 | ||||||
| chr15:44576874
|
T | C | 2 | a0015c0020t0001g0123a0020c0017t0001g0065 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5867-1833A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576874 | ||||||
| chr15:44576877
|
AGTGCAGT others(12): Show |
A | 2 | a0015c0020t0001g0123a0020c0017t0001g0065 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.5867-1855_5867-183 others(23): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44576877 | ||||||
| chr15:44577059
|
C | T | 4 | a0007c0008t0001g0186a0007c0008t0001g0187a0007c0008t0001g0188others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.5867-2018G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44577059 | ||||||
| chr15:44577167
|
A | G | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5867-2126T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44577167 | ||||||
| chr15:44577502
|
C | CA | 82 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0049others(79): Show | 82 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.5867-2462dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44577502 | ||||||
| chr15:44577502
|
C | CAA | 11 | a0001c0001t0001g0096a0001c0001t0001g0107a0001c0001t0001g0162others(8): Show | 11 | HG00609.hp2 HG00673.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.5867-2463_5867-246 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44577502 | ||||||
| chr15:44577514
|
A | C | 4 | a0009c0011t0001g0174a0009c0011t0003g0173a0010c0010t0001g0181others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.5867-2473T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44577514 | ||||||
| chr15:44577515
|
A | C | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.5867-2474T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44577515 | ||||||
| chr15:44577578
|
T | C | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.5867-2537A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44577578 | ||||||
| chr15:44577580
|
C | CTA | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.5867-2541_5867-254 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44577580 | ||||||
| chr15:44578014
|
C | CT | 9 | a0001c0001t0001g0106a0004c0004t0001g0149a0004c0004t0001g0164others(6): Show | 9 | HG02040.hp1 HG02040.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.5867-2974dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578014 | ||||||
| chr15:44578017
|
TCC | T | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5867-2978_5867-297 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578017 | ||||||
| chr15:44578018
|
C | T | 53 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0025others(50): Show | 53 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.5867-2977G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578018 | ||||||
| chr15:44578019
|
C | CT | 16 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0062others(13): Show | 16 | HG00423.hp1 HG01106.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.5867-2979dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578019 | ||||||
| chr15:44578019
|
C | T | 9 | a0001c0001t0001g0106a0004c0004t0001g0149a0004c0004t0001g0164others(6): Show | 9 | HG02040.hp1 HG02040.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.5867-2978G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578019 | ||||||
| chr15:44578019
|
CT | C | 40 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0025others(37): Show | 40 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.5867-2979delA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578019 | ||||||
| chr15:44578021
|
T | C | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5867-2980A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578021 | ||||||
| chr15:44578026
|
T | C | 1 | a0009c0011t0001g0174 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5867-2985A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578026 | ||||||
| chr15:44578041
|
T | C | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.5867-3000A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578041 | ||||||
| chr15:44578117
|
C | T | 4 | a0002c0002t0001g0112a0002c0002t0001g0113a0002c0002t0001g0130others(1): Show | 4 | HG02148.hp2 NA18986.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.5867-3076G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578117 | ||||||
| chr15:44578174
|
G | A | 1 | a0002c0002t0001g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5867-3133C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578174 | ||||||
| chr15:44578190
|
A | AT | 5 | a0001c0001t0001g0039a0001c0001t0001g0055a0002c0002t0001g0028others(2): Show | 5 | HG02257.hp1 HG02572.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.5867-3150dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578190 | ||||||
| chr15:44578190
|
A | ATT | 13 | a0001c0001t0001g0106a0004c0004t0001g0149a0004c0004t0001g0158others(10): Show | 13 | HG02040.hp1 HG02040.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.5867-3151_5867-315 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578190 | ||||||
| chr15:44578190
|
AT | A | 27 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(24): Show | 27 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.5867-3150delA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578190 | ||||||
| chr15:44578190
|
ATT | A | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.5867-3151_5867-315 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578190 | ||||||
| chr15:44578250
|
G | C | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.5867-3209C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578250 | ||||||
| chr15:44578375
|
G | A | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5867-3334C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578375 | ||||||
| chr15:44578412
|
T | C | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.5867-3371A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578412 | ||||||
| chr15:44578418
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5867-3377G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578418 | ||||||
| chr15:44578464
|
G | T | 1 | a0002c0002t0001g0117 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.5867-3423C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578464 | ||||||
| chr15:44578514
|
AG | A | 68 | a0001c0001t0001g0106a0002c0002t0001g0017a0002c0002t0001g0018others(65): Show | 68 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.5867-3474delC | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578514 | ||||||
| chr15:44578793
|
A | C | 1 | a0001c0001t0001g0162 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.5867-3752T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578793 | ||||||
| chr15:44578887
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5867-3846C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578887 | ||||||
| chr15:44578910
|
C | A | 31 | a0001c0001t0001g0106a0003c0003t0001g0001a0003c0003t0001g0002others(28): Show | 31 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.5867-3869G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578910 | ||||||
| chr15:44578927
|
G | A | 10 | a0003c0003t0001g0007a0003c0003t0001g0008a0003c0003t0001g0009others(7): Show | 10 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(7): Show |
intron_variant | MODIFIER | c.5867-3886C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578927 | ||||||
| chr15:44578953
|
C | T | 1 | a0002c0002t0001g0136 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5867-3912G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578953 | ||||||
| chr15:44578973
|
T | C | 1 | a0003c0003t0001g0004 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5867-3932A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44578973 | ||||||
| chr15:44579155
|
C | T | 17 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.5867-4114G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579155 | ||||||
| chr15:44579223
|
T | A | 17 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.5867-4182A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579223 | ||||||
| chr15:44579290
|
C | G | 1 | a0001c0001t0001g0060 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5867-4249G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579290 | ||||||
| chr15:44579319
|
G | GT | 38 | a0001c0001t0001g0106a0002c0002t0001g0018a0002c0002t0002g0019others(35): Show | 38 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.5867-4279dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579319 | ||||||
| chr15:44579372
|
C | T | 9 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0072others(6): Show | 9 | HG00408.hp2 HG00423.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.5867-4331G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579372 | ||||||
| chr15:44579429
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.5866+4385T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579429 | ||||||
| chr15:44579473
|
G | A | 17 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.5866+4341C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579473 | ||||||
| chr15:44579496
|
T | A | 2 | a0004c0004t0001g0170a0024c0025t0001g0172 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.5866+4318A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579496 | ||||||
| chr15:44579526
|
C | CA | 24 | a0001c0001t0001g0038a0001c0001t0001g0063a0001c0001t0001g0072others(21): Show | 24 | HG01175.hp2 HG01496.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.5866+4287dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579526 | ||||||
| chr15:44579526
|
CA | C | 13 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(10): Show | 13 | HG00621.hp1 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.5866+4287delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579526 | ||||||
| chr15:44579542
|
A | G | 1 | a0002c0002t0001g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5866+4272T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579542 | ||||||
| chr15:44579619
|
T | C | 3 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152 | 3 | HG03516.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.5866+4195A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579619 | ||||||
| chr15:44579665
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5866+4149C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579665 | ||||||
| chr15:44579778
|
C | T | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5866+4036G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579778 | ||||||
| chr15:44579779
|
G | A | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.5866+4035C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579779 | ||||||
| chr15:44579881
|
T | C | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5866+3933A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579881 | ||||||
| chr15:44579998
|
CACTT | C | 11 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0068others(8): Show | 11 | HG00438.hp1 HG00673.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.5866+3812_5866+381 others(8): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44579998 | ||||||
| chr15:44580040
|
A | G | 17 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.5866+3774T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44580040 | ||||||
| chr15:44580155
|
C | T | 1 | a0019c0015t0001g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5866+3659G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44580155 | ||||||
| chr15:44580257
|
G | C | 1 | a0002c0002t0001g0026 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.5866+3557C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44580257 | ||||||
| chr15:44580292
|
A | C | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5866+3522T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44580292 | ||||||
| chr15:44580324
|
T | C | 38 | a0001c0001t0001g0106a0002c0002t0001g0018a0002c0002t0002g0019others(35): Show | 38 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.5866+3490A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44580324 | ||||||
| chr15:44580447
|
T | G | 1 | a0003c0003t0001g0002 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.5866+3367A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44580447 | ||||||
| chr15:44580517
|
G | A | 1 | a0014c0024t0001g0159 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.5866+3297C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44580517 | ||||||
| chr15:44580664
|
G | A | 4 | a0009c0011t0001g0174a0009c0011t0003g0173a0010c0010t0001g0181others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.5866+3150C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44580664 | ||||||
| chr15:44580740
|
G | A | 4 | a0009c0011t0001g0174a0009c0011t0003g0173a0010c0010t0001g0181others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.5866+3074C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44580740 | ||||||
| chr15:44580976
|
A | C | 14 | a0001c0001t0001g0106a0004c0004t0001g0149a0004c0004t0001g0158others(11): Show | 14 | HG02040.hp1 HG02040.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.5866+2838T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44580976 | ||||||
| chr15:44581073
|
C | T | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5866+2741G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44581073 | ||||||
| chr15:44581118
|
G | C | 1 | a0002c0002t0001g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5866+2696C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44581118 | ||||||
| chr15:44581189
|
C | G | 1 | a0001c0001t0001g0084 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.5866+2625G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44581189 | ||||||
| chr15:44581266
|
G | T | 14 | a0001c0001t0001g0106a0004c0004t0001g0149a0004c0004t0001g0158others(11): Show | 14 | HG02040.hp1 HG02040.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.5866+2548C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44581266 | ||||||
| chr15:44581286
|
AG | A | 2 | a0009c0011t0001g0174a0009c0011t0003g0173 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.5866+2527delC | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44581286 | ||||||
| chr15:44581310
|
G | A | 2 | a0004c0004t0001g0170a0024c0025t0001g0172 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.5866+2504C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44581310 | ||||||
| chr15:44581360
|
A | C | 184 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.5866+2454T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44581360 | ||||||
| chr15:44581597
|
TA | T | 38 | a0001c0001t0001g0106a0002c0002t0001g0018a0002c0002t0002g0019others(35): Show | 38 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.5866+2216delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44581597 | ||||||
| chr15:44581660
|
A | G | 54 | a0001c0001t0001g0106a0002c0002t0001g0018a0002c0002t0002g0019others(51): Show | 54 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.5866+2154T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44581660 | ||||||
| chr15:44581702
|
A | G | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.5866+2112T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44581702 | ||||||
| chr15:44581944
|
A | C | 1 | a0001c0016t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5866+1870T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44581944 | ||||||
| chr15:44582051
|
T | C | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.5866+1763A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44582051 | ||||||
| chr15:44582197
|
A | G | 4 | a0009c0011t0001g0174a0009c0011t0003g0173a0010c0010t0001g0181others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.5866+1617T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44582197 | ||||||
| chr15:44582289
|
G | A | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.5866+1525C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44582289 | ||||||
| chr15:44582495
|
C | G | 1 | a0002c0002t0001g0189 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.5866+1319G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44582495 | ||||||
| chr15:44582631
|
A | C | 14 | a0001c0001t0001g0106a0004c0004t0001g0149a0004c0004t0001g0158others(11): Show | 14 | HG02040.hp1 HG02040.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.5866+1183T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44582631 | ||||||
| chr15:44582653
|
A | G | 4 | a0007c0008t0001g0186a0007c0008t0001g0187a0007c0008t0001g0188others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.5866+1161T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44582653 | ||||||
| chr15:44582761
|
GA | G | 8 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.5866+1052delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44582761 | ||||||
| chr15:44582771
|
A | C | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5866+1043T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44582771 | ||||||
| chr15:44582855
|
C | T | 38 | a0001c0001t0001g0106a0002c0002t0001g0018a0002c0002t0002g0019others(35): Show | 38 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.5866+959G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44582855 | ||||||
| chr15:44582963
|
G | A | 5 | a0004c0004t0001g0158a0004c0004t0001g0170a0004c0004t0001g0171others(2): Show | 5 | NA18951.hp2 NA18967.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.5866+851C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44582963 | ||||||
| chr15:44582981
|
C | T | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.5866+833G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44582981 | ||||||
| chr15:44583078
|
A | ACTCT | 54 | a0001c0001t0001g0106a0002c0002t0001g0018a0002c0002t0002g0019others(51): Show | 54 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.5866+732_5866+735d others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44583078 | ||||||
| chr15:44583139
|
T | A | 1 | a0001c0001t0001g0090 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.5866+675A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44583139 | ||||||
| chr15:44583346
|
T | C | 1 | a0009c0011t0001g0174 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5866+468A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44583346 | ||||||
| chr15:44583427
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5866+387G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44583427 | ||||||
| chr15:44583436
|
C | T | 2 | a0008c0007t0001g0151a0008c0007t0001g0152 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5866+378G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44583436 | ||||||
| chr15:44583682
|
C | T | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.5866+132G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 30/39 | chr15 | 44583682 | ||||||
| chr15:44584647
|
TG | T | 4 | a0007c0008t0001g0186a0007c0008t0001g0187a0007c0008t0001g0188others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.5122-90delC | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/39 | chr15 | 44584647 | ||||||
| chr15:44584785
|
A | G | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.5122-227T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/39 | chr15 | 44584785 | ||||||
| chr15:44584829
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5122-271T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/39 | chr15 | 44584829 | ||||||
| chr15:44585014
|
G | T | 1 | a0011c0009t0001g0087 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5122-456C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/39 | chr15 | 44585014 | ||||||
| chr15:44585316
|
G | A | 2 | a0002c0002t0001g0176a0002c0002t0001g0177 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5121+320C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/39 | chr15 | 44585316 | ||||||
| chr15:44585430
|
C | CA | 118 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.5121+205dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/39 | chr15 | 44585430 | ||||||
| chr15:44585430
|
C | CAA | 56 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0100others(53): Show | 56 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.5121+204_5121+205d others(4): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/39 | chr15 | 44585430 | ||||||
| chr15:44585459
|
G | A | 1 | a0016c0019t0001g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5121+177C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/39 | chr15 | 44585459 | ||||||
| chr15:44585554
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.5121+82T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/39 | chr15 | 44585554 | ||||||
| chr15:44585556
|
C | T | 1 | a0003c0003t0001g0001 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5121+80G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/39 | chr15 | 44585556 | ||||||
| chr15:44585602
|
T | TA | 27 | a0001c0001t0001g0092a0001c0001t0001g0098a0003c0003t0001g0001others(24): Show | 27 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.5121+33dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/39 | chr15 | 44585602 | ||||||
| chr15:44585602
|
T | TAA | 14 | a0001c0001t0001g0106a0004c0004t0001g0149a0004c0004t0001g0158others(11): Show | 14 | HG02040.hp1 HG02040.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.5121+32_5121+33dup others(2): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/39 | chr15 | 44585602 | ||||||
| chr15:44585602
|
TA | T | 5 | a0001c0001t0001g0057a0002c0002t0001g0030a0002c0002t0002g0024others(2): Show | 5 | HG01069.hp2 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.5121+33delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 29/39 | chr15 | 44585602 | ||||||
| chr15:44585983
|
G | GT | 33 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0062others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.4907-134dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44585983 | ||||||
| chr15:44585983
|
G | GTT | 26 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0103others(23): Show | 26 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.4907-135_4907-134d others(4): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44585983 | ||||||
| chr15:44586043
|
G | A | 17 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.4907-193C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44586043 | ||||||
| chr15:44586136
|
C | T | 1 | a0002c0021t0001g0139 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4907-286G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44586136 | ||||||
| chr15:44586215
|
G | A | 67 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0047others(64): Show | 67 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.4907-365C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44586215 | ||||||
| chr15:44586373
|
T | C | 54 | a0001c0001t0001g0106a0002c0002t0001g0018a0002c0002t0002g0019others(51): Show | 54 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.4907-523A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44586373 | ||||||
| chr15:44586570
|
G | A | 3 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152 | 3 | HG03516.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4907-720C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44586570 | ||||||
| chr15:44586830
|
G | C | 1 | a0016c0019t0001g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4907-980C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44586830 | ||||||
| chr15:44587153
|
G | A | 14 | a0001c0001t0001g0106a0004c0004t0001g0149a0004c0004t0001g0158others(11): Show | 14 | HG02040.hp1 HG02040.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.4907-1303C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587153 | ||||||
| chr15:44587232
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4907-1382T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587232 | ||||||
| chr15:44587693
|
C | CA | 43 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0048others(40): Show | 43 | HG00408.hp2 HG00609.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.4906+1558dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587693 | ||||||
| chr15:44587693
|
C | CAA | 19 | a0001c0001t0001g0059a0001c0001t0001g0092a0001c0001t0001g0098others(16): Show | 19 | HG00423.hp1 HG00673.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.4906+1557_4906+155 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587693 | ||||||
| chr15:44587693
|
C | CAAAAAAA others(12): Show |
2 | a0002c0002t0002g0020a0002c0002t0002g0024 | 2 | HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4906+1540_4906+155 others(23): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587693 | ||||||
| chr15:44587693
|
C | CAAAAAAA others(13): Show |
2 | a0002c0002t0002g0021a0002c0002t0002g0022 | 2 | HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4906+1539_4906+155 others(24): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587693 | ||||||
| chr15:44587693
|
CA | C | 28 | a0001c0001t0001g0058a0001c0001t0001g0095a0001c0001t0001g0104others(25): Show | 28 | HG00438.hp2 HG00609.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.4906+1558delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587693 | ||||||
| chr15:44587693
|
CAAAA | C | 12 | a0003c0003t0001g0001a0003c0003t0001g0003a0003c0003t0001g0004others(9): Show | 12 | HG00423.hp2 HG00597.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.4906+1555_4906+155 others(8): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587693 | ||||||
| chr15:44587694
|
A | C | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4906+1558T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587694 | ||||||
| chr15:44587697
|
A | AAAAAAAA others(7): Show |
1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4906+1554_4906+155 others(18): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587697 | ||||||
| chr15:44587707
|
A | AAAAAAAC others(11): Show |
2 | a0002c0002t0002g0019a0002c0002t0002g0023 | 2 | HG02258.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.4906+1544_4906+154 others(22): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587707 | ||||||
| chr15:44587709
|
A | AAAAAAAA others(9): Show |
1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4906+1542_4906+154 others(20): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587709 | ||||||
| chr15:44587718
|
A | AAAAAAAA others(8): Show |
1 | a0006c0006t0001g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4906+1533_4906+153 others(19): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587718 | ||||||
| chr15:44587718
|
A | AAAAAAAA others(7): Show |
5 | a0006c0006t0001g0044a0006c0006t0001g0179a0007c0008t0001g0187others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4906+1533_4906+153 others(18): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587718 | ||||||
| chr15:44587718
|
A | AAAAAAAA others(6): Show |
2 | a0006c0006t0001g0043a0007c0008t0001g0186 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4906+1533_4906+153 others(17): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587718 | ||||||
| chr15:44587740
|
CAAAT | C | 8 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.4906+1508_4906+151 others(8): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587740 | ||||||
| chr15:44587772
|
A | G | 14 | a0001c0001t0001g0106a0004c0004t0001g0149a0004c0004t0001g0158others(11): Show | 14 | HG02040.hp1 HG02040.hp2 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.4906+1480T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587772 | ||||||
| chr15:44587788
|
T | TA | 3 | a0008c0007t0001g0151a0008c0007t0001g0152a0018c0023t0001g0175 | 3 | HG02109.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4906+1463dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44587788 | ||||||
| chr15:44588072
|
C | G | 1 | a0011c0009t0001g0086 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.4906+1180G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44588072 | ||||||
| chr15:44588294
|
C | CA | 13 | a0001c0001t0001g0106a0004c0004t0001g0149a0004c0004t0001g0158others(10): Show | 13 | HG02040.hp1 HG02040.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.4906+957dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44588294 | ||||||
| chr15:44588585
|
C | T | 2 | a0002c0002t0001g0137a0002c0002t0001g0138 | 2 | HG01106.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.4906+667G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44588585 | ||||||
| chr15:44588664
|
T | C | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4906+588A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44588664 | ||||||
| chr15:44589056
|
T | C | 1 | a0002c0002t0001g0137 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4906+196A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 28/39 | chr15 | 44589056 | ||||||
| chr15:44589520
|
C | T | 1 | a0008c0007t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4744-106G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44589520 | ||||||
| chr15:44589560
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4744-146A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44589560 | ||||||
| chr15:44589757
|
C | T | 32 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.4744-343G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44589757 | ||||||
| chr15:44589766
|
A | G | 69 | a0001c0001t0001g0106a0002c0002t0001g0017a0002c0002t0001g0018others(66): Show | 69 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.4744-352T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44589766 | ||||||
| chr15:44589829
|
G | A | 17 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.4744-415C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44589829 | ||||||
| chr15:44589837
|
A | G | 68 | a0001c0001t0001g0106a0002c0002t0001g0017a0002c0002t0001g0018others(65): Show | 68 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.4744-423T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44589837 | ||||||
| chr15:44589898
|
C | T | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.4744-484G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44589898 | ||||||
| chr15:44589954
|
A | G | 36 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(33): Show | 36 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.4744-540T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44589954 | ||||||
| chr15:44589971
|
T | C | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4744-557A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44589971 | ||||||
| chr15:44590191
|
C | T | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.4744-777G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44590191 | ||||||
| chr15:44590195
|
C | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4744-781G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44590195 | ||||||
| chr15:44590432
|
G | GT | 8 | a0004c0004t0001g0165a0005c0005t0001g0031a0005c0005t0001g0032others(5): Show | 8 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4744-1019dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44590432 | ||||||
| chr15:44590730
|
G | C | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4744-1316C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44590730 | ||||||
| chr15:44590762
|
C | T | 68 | a0001c0001t0001g0106a0002c0002t0001g0017a0002c0002t0001g0018others(65): Show | 68 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.4744-1348G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44590762 | ||||||
| chr15:44590802
|
C | T | 4 | a0009c0011t0001g0174a0009c0011t0003g0173a0010c0010t0001g0181others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.4744-1388G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44590802 | ||||||
| chr15:44590814
|
T | C | 1 | a0003c0003t0001g0010 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4744-1400A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44590814 | ||||||
| chr15:44591090
|
C | T | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4743+1241G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44591090 | ||||||
| chr15:44591170
|
C | T | 1 | a0002c0002t0001g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4743+1161G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44591170 | ||||||
| chr15:44591284
|
A | C | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.4743+1047T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44591284 | ||||||
| chr15:44591348
|
T | A | 1 | a0002c0002t0001g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4743+983A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44591348 | ||||||
| chr15:44591349
|
A | T | 10 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(7): Show | 10 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.4743+982T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44591349 | ||||||
| chr15:44591366
|
T | G | 10 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(7): Show | 10 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.4743+965A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44591366 | ||||||
| chr15:44591541
|
G | C | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.4743+790C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44591541 | ||||||
| chr15:44591744
|
A | G | 68 | a0001c0001t0001g0106a0002c0002t0001g0017a0002c0002t0001g0018others(65): Show | 68 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.4743+587T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44591744 | ||||||
| chr15:44591748
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4743+583C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44591748 | ||||||
| chr15:44591831
|
C | T | 1 | a0011c0009t0001g0086 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.4743+500G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44591831 | ||||||
| chr15:44591925
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.4743+406G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44591925 | ||||||
| chr15:44592040
|
G | A | 46 | a0001c0001t0001g0106a0002c0002t0001g0018a0002c0002t0002g0019others(43): Show | 46 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.4743+291C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44592040 | ||||||
| chr15:44592097
|
C | T | 49 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0049others(46): Show | 49 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.4743+234G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44592097 | ||||||
| chr15:44592110
|
C | CA | 10 | a0002c0002t0001g0133a0002c0002t0001g0137a0006c0006t0001g0043others(7): Show | 10 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.4743+220dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44592110 | ||||||
| chr15:44592110
|
CA | C | 6 | a0001c0001t0001g0085a0001c0001t0001g0088a0009c0011t0001g0174others(3): Show | 6 | HG01515.hp2 HG01891.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.4743+220delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44592110 | ||||||
| chr15:44592260
|
A | C | 8 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.4743+71T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44592260 | ||||||
| chr15:44592269
|
A | G | 1 | a0007c0008t0001g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4743+62T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 27/39 | chr15 | 44592269 | ||||||
| chr15:44592501
|
T | C | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4636-63A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44592501 | ||||||
| chr15:44592560
|
T | C | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.4636-122A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44592560 | ||||||
| chr15:44592819
|
C | CAATA | 9 | a0001c0001t0001g0075a0001c0001t0001g0076a0002c0002t0001g0018others(6): Show | 9 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.4636-385_4636-382d others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44592819 | ||||||
| chr15:44592970
|
G | A | 1 | a0002c0002t0001g0045 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4636-532C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44592970 | ||||||
| chr15:44593078
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4636-640A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44593078 | ||||||
| chr15:44593098
|
C | A | 2 | a0009c0011t0001g0174a0009c0011t0003g0173 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.4636-660G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44593098 | ||||||
| chr15:44593123
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4636-685A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44593123 | ||||||
| chr15:44593607
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | NA18965.hp1 NA18985.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.4636-1169A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44593607 | ||||||
| chr15:44593712
|
T | G | 1 | a0002c0002t0001g0121 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4636-1274A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44593712 | ||||||
| chr15:44593754
|
C | CT | 15 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(12): Show | 15 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.4636-1317dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44593754 | ||||||
| chr15:44593899
|
G | A | 1 | a0005c0005t0001g0033 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4635+1360C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44593899 | ||||||
| chr15:44594179
|
C | T | 5 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(2): Show | 5 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.4635+1080G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44594179 | ||||||
| chr15:44594350
|
C | T | 7 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4635+909G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44594350 | ||||||
| chr15:44594358
|
G | A | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4635+901C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44594358 | ||||||
| chr15:44594596
|
G | GA | 8 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0142others(5): Show | 8 | HG00621.hp2 HG01106.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.4635+662dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44594596 | ||||||
| chr15:44594596
|
GA | G | 59 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0063others(56): Show | 59 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.4635+662delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44594596 | ||||||
| chr15:44594704
|
A | G | 1 | a0009c0011t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4635+555T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44594704 | ||||||
| chr15:44594816
|
TTTG | T | 4 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(1): Show | 4 | HG02559.hp1 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.4635+440_4635+442d others(5): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44594816 | ||||||
| chr15:44594966
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4635+293C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44594966 | ||||||
| chr15:44595083
|
C | T | 2 | a0008c0007t0001g0151a0008c0007t0001g0152 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4635+176G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44595083 | ||||||
| chr15:44595108
|
C | T | 1 | a0003c0003t0001g0001 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4635+151G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 26/39 | chr15 | 44595108 | ||||||
| chr15:44595626
|
T | C | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4435-167A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 25/39 | chr15 | 44595626 | ||||||
| chr15:44595923
|
C | T | 3 | a0007c0008t0001g0186a0007c0008t0001g0187a0022c0014t0001g0185 | 3 | HG02572.hp1 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4434+160G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 25/39 | chr15 | 44595923 | ||||||
| chr15:44596072
|
A | G | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4434+11T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 25/39 | chr15 | 44596072 | ||||||
| chr15:44596428
|
A | C | 3 | a0008c0007t0001g0151a0008c0007t0001g0152a0018c0023t0001g0175 | 3 | HG02109.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4162-73T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 24/39 | chr15 | 44596428 | ||||||
| chr15:44596599
|
C | T | 4 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(1): Show | 4 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4161+185G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 24/39 | chr15 | 44596599 | ||||||
| chr15:44596660
|
CA | C | 111 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(108): Show | 111 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.4161+123delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 24/39 | chr15 | 44596660 | ||||||
| chr15:44596660
|
CAA | C | 10 | a0002c0002t0001g0018a0002c0002t0001g0029a0002c0002t0001g0030others(7): Show | 10 | HG01069.hp1 HG01069.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.4161+122_4161+123d others(4): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 24/39 | chr15 | 44596660 | ||||||
| chr15:44596660
|
CAAA | C | 14 | a0002c0002t0001g0027a0002c0002t0001g0028a0003c0003t0001g0003others(11): Show | 14 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.4161+121_4161+123d others(5): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 24/39 | chr15 | 44596660 | ||||||
| chr15:44596660
|
CAAAA | C | 19 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(16): Show | 19 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.4161+120_4161+123d others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 24/39 | chr15 | 44596660 | ||||||
| chr15:44596660
|
CAAAAAA | C | 11 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(8): Show | 11 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.4161+118_4161+123d others(8): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 24/39 | chr15 | 44596660 | ||||||
| chr15:44596660
|
CAAAAAAA others(8): Show |
C | 1 | a0009c0011t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4161+109_4161+123d others(17): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 24/39 | chr15 | 44596660 | ||||||
| chr15:44596661
|
A | C | 3 | a0006c0006t0001g0043a0007c0008t0001g0186a0007c0008t0001g0188 | 3 | HG02055.hp1 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4161+123T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 24/39 | chr15 | 44596661 | ||||||
| chr15:44596662
|
A | C | 4 | a0006c0006t0001g0044a0006c0006t0001g0178a0006c0006t0001g0179others(1): Show | 4 | HG02895.hp1 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.4161+122T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 24/39 | chr15 | 44596662 | ||||||
| chr15:44596750
|
C | G | 1 | a0008c0007t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4161+34G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 24/39 | chr15 | 44596750 | ||||||
| chr15:44597110
|
CT | C | 39 | a0002c0002t0001g0113a0002c0002t0002g0019a0002c0002t0002g0020others(36): Show | 39 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.4002-168delA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44597110 | ||||||
| chr15:44597110
|
CTT | C | 11 | a0004c0004t0001g0166a0006c0006t0001g0043a0006c0006t0001g0044others(8): Show | 11 | HG02040.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.4002-169_4002-168d others(4): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44597110 | ||||||
| chr15:44597358
|
C | T | 4 | a0007c0008t0001g0186a0007c0008t0001g0187a0007c0008t0001g0188others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4002-415G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44597358 | ||||||
| chr15:44597381
|
G | C | 2 | a0011c0009t0001g0086a0011c0009t0001g0087 | 2 | HG00140.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.4002-438C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44597381 | ||||||
| chr15:44597417
|
C | A | 49 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(46): Show | 49 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.4002-474G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44597417 | ||||||
| chr15:44597465
|
G | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0111 | 2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4002-522C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44597465 | ||||||
| chr15:44597568
|
G | A | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4002-625C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44597568 | ||||||
| chr15:44597570
|
G | A | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.4002-627C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44597570 | ||||||
| chr15:44597658
|
C | A | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.4001+607G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44597658 | ||||||
| chr15:44597730
|
G | A | 2 | a0004c0004t0001g0167a0004c0004t0001g0168 | 2 | NA18965.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.4001+535C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44597730 | ||||||
| chr15:44597800
|
C | T | 1 | a0002c0002t0002g0020 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4001+465G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44597800 | ||||||
| chr15:44597904
|
T | C | 5 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(2): Show | 5 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.4001+361A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44597904 | ||||||
| chr15:44597906
|
C | T | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4001+359G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44597906 | ||||||
| chr15:44598060
|
T | C | 1 | a0002c0002t0001g0026 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4001+205A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44598060 | ||||||
| chr15:44598061
|
A | T | 2 | a0005c0005t0001g0031a0005c0005t0001g0034 | 2 | HG01496.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.4001+204T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44598061 | ||||||
| chr15:44598256
|
C | A | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.4001+9G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 23/39 | chr15 | 44598256 | ||||||
| chr15:44599118
|
A | G | 3 | a0008c0007t0001g0151a0008c0007t0001g0152a0018c0023t0001g0175 | 3 | HG02109.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3687-282T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 21/39 | chr15 | 44599118 | ||||||
| chr15:44599393
|
G | A | 1 | a0008c0007t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3687-557C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 21/39 | chr15 | 44599393 | ||||||
| chr15:44599440
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0160 | 2 | NA18978.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.3687-604G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 21/39 | chr15 | 44599440 | ||||||
| chr15:44599960
|
T | A | 1 | a0002c0002t0001g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3686+507A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 21/39 | chr15 | 44599960 | ||||||
| chr15:44599995
|
C | T | 2 | a0001c0001t0001g0076a0002c0002t0001g0117 | 2 | NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.3686+472G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 21/39 | chr15 | 44599995 | ||||||
| chr15:44600027
|
T | C | 73 | a0001c0001t0001g0050a0001c0001t0001g0081a0001c0001t0001g0102others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.3686+440A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 21/39 | chr15 | 44600027 | ||||||
| chr15:44600201
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0141 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3686+266A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 21/39 | chr15 | 44600201 | ||||||
| chr15:44600216
|
G | GAATGT | 8 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0110others(5): Show | 8 | HG03704.hp1 HG04204.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.3686+250_3686+251i others(7): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 21/39 | chr15 | 44600216 | ||||||
| chr15:44600235
|
T | C | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.3686+232A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 21/39 | chr15 | 44600235 | ||||||
| chr15:44600762
|
T | C | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3521-130A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44600762 | ||||||
| chr15:44600928
|
C | T | 3 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152 | 3 | HG03516.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3521-296G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44600928 | ||||||
| chr15:44600981
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3521-349G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44600981 | ||||||
| chr15:44601107
|
G | A | 1 | a0008c0007t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3521-475C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601107 | ||||||
| chr15:44601131
|
A | G | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.3521-499T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601131 | ||||||
| chr15:44601220
|
A | ATTTAACT | 53 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(50): Show | 53 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.3521-589_3521-588i others(9): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601220 | ||||||
| chr15:44601267
|
A | T | 46 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(43): Show | 46 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.3521-635T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601267 | ||||||
| chr15:44601402
|
A | C | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3521-770T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601402 | ||||||
| chr15:44601447
|
G | C | 1 | a0002c0002t0001g0138 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3521-815C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601447 | ||||||
| chr15:44601552
|
CTCT | C | 44 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(41): Show | 44 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.3521-923_3521-921d others(5): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601552 | ||||||
| chr15:44601557
|
C | CT | 18 | a0001c0001t0001g0071a0001c0001t0001g0072a0002c0002t0001g0017others(15): Show | 18 | HG00621.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.3521-926dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601557 | ||||||
| chr15:44601557
|
CT | C | 5 | a0001c0001t0001g0063a0001c0001t0001g0085a0001c0001t0001g0104others(2): Show | 5 | HG01496.hp2 HG01515.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3521-926delA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601557 | ||||||
| chr15:44601644
|
G | A | 1 | a0007c0008t0001g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3521-1012C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601644 | ||||||
| chr15:44601735
|
TTACAG | T | 2 | a0008c0007t0001g0151a0008c0007t0001g0152 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3521-1108_3521-110 others(9): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601735 | ||||||
| chr15:44601792
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3521-1160G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601792 | ||||||
| chr15:44601793
|
G | A | 15 | a0003c0003t0001g0002a0003c0003t0001g0003a0003c0003t0001g0004others(12): Show | 15 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.3521-1161C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601793 | ||||||
| chr15:44601794
|
G | C | 3 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152 | 3 | HG03516.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3521-1162C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601794 | ||||||
| chr15:44601841
|
G | A | 1 | a0003c0003t0001g0002 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3521-1209C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601841 | ||||||
| chr15:44601844
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3521-1212G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601844 | ||||||
| chr15:44601853
|
C | G | 1 | a0009c0011t0001g0174 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3521-1221G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601853 | ||||||
| chr15:44601871
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3521-1239G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601871 | ||||||
| chr15:44601896
|
C | T | 1 | a0002c0002t0001g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3521-1264G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44601896 | ||||||
| chr15:44602201
|
CCTTT | C | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3521-1573_3521-157 others(8): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602201 | ||||||
| chr15:44602237
|
C | T | 1 | a0002c0002t0001g0154 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3521-1605G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602237 | ||||||
| chr15:44602240
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3521-1608G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602240 | ||||||
| chr15:44602349
|
G | C | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.3521-1717C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602349 | ||||||
| chr15:44602414
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3521-1782A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602414 | ||||||
| chr15:44602483
|
C | CT | 16 | a0001c0001t0001g0099a0002c0002t0001g0028a0005c0005t0001g0031others(13): Show | 16 | HG00408.hp2 HG01496.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3521-1852dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602483 | ||||||
| chr15:44602572
|
G | A | 1 | a0002c0002t0001g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3521-1940C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602572 | ||||||
| chr15:44602583
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3521-1951T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602583 | ||||||
| chr15:44602591
|
G | A | 2 | a0002c0002t0001g0029a0002c0002t0001g0030 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3521-1959C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602591 | ||||||
| chr15:44602683
|
C | T | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.3521-2051G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602683 | ||||||
| chr15:44602684
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3521-2052C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602684 | ||||||
| chr15:44602693
|
A | G | 53 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(50): Show | 53 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.3521-2061T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602693 | ||||||
| chr15:44602717
|
C | T | 1 | a0002c0002t0001g0190 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3521-2085G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602717 | ||||||
| chr15:44602819
|
T | C | 4 | a0001c0001t0001g0110a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | NA18949.hp1 NA18977.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.3521-2187A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602819 | ||||||
| chr15:44602825
|
A | G | 1 | a0002c0002t0001g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3521-2193T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44602825 | ||||||
| chr15:44603053
|
A | AT | 74 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(71): Show | 74 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.3521-2422dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44603053 | ||||||
| chr15:44603053
|
A | ATT | 5 | a0006c0006t0001g0178a0009c0011t0001g0174a0009c0011t0003g0173others(2): Show | 5 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.3521-2423_3521-242 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44603053 | ||||||
| chr15:44603128
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3521-2496G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44603128 | ||||||
| chr15:44603322
|
G | A | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3521-2690C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44603322 | ||||||
| chr15:44603498
|
T | A | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3520+2527A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44603498 | ||||||
| chr15:44603657
|
C | A | 2 | a0003c0003t0001g0005a0003c0003t0001g0006 | 2 | NA19007.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3520+2368G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44603657 | ||||||
| chr15:44603934
|
T | C | 1 | a0002c0002t0001g0035 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3520+2091A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44603934 | ||||||
| chr15:44604007
|
C | T | 53 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(50): Show | 53 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.3520+2018G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604007 | ||||||
| chr15:44604103
|
A | G | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3520+1922T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604103 | ||||||
| chr15:44604129
|
G | A | 7 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3520+1896C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604129 | ||||||
| chr15:44604199
|
T | TA | 5 | a0001c0001t0001g0143a0002c0002t0001g0028a0002c0002t0001g0029others(2): Show | 5 | HG01891.hp1 HG03209.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.3520+1825dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604199 | ||||||
| chr15:44604200
|
A | T | 4 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(1): Show | 4 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3520+1825T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604200 | ||||||
| chr15:44604218
|
T | C | 1 | a0021c0018t0001g0097 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3520+1807A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604218 | ||||||
| chr15:44604385
|
C | T | 1 | a0002c0021t0001g0139 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3520+1640G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604385 | ||||||
| chr15:44604460
|
G | T | 1 | a0002c0002t0001g0133 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3520+1565C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604460 | ||||||
| chr15:44604498
|
T | G | 10 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.3520+1527A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604498 | ||||||
| chr15:44604695
|
G | A | 8 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3520+1330C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604695 | ||||||
| chr15:44604931
|
C | CA | 54 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0050others(51): Show | 54 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.3520+1093dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604931 | ||||||
| chr15:44604931
|
C | CAA | 9 | a0001c0001t0001g0040a0001c0001t0001g0063a0002c0002t0001g0025others(6): Show | 9 | HG01106.hp1 HG01496.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.3520+1092_3520+109 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604931 | ||||||
| chr15:44604931
|
C | CAAAAAAA others(3): Show |
1 | a0010c0010t0001g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3520+1084_3520+109 others(14): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604931 | ||||||
| chr15:44604931
|
C | CAAAAAAA others(4): Show |
2 | a0008c0007t0001g0151a0009c0011t0003g0173 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3520+1083_3520+109 others(15): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604931 | ||||||
| chr15:44604931
|
C | CAAAAAAA others(5): Show |
1 | a0008c0007t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3520+1082_3520+109 others(16): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604931 | ||||||
| chr15:44604931
|
C | CAAAAAAA others(6): Show |
1 | a0008c0007t0001g0152 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3520+1081_3520+109 others(17): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604931 | ||||||
| chr15:44604931
|
CA | C | 19 | a0001c0001t0001g0058a0001c0001t0001g0088a0001c0001t0001g0093others(16): Show | 19 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.3520+1093delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604931 | ||||||
| chr15:44604931
|
CAAA | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0099others(2): Show | 5 | HG00408.hp2 HG00423.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3520+1091_3520+109 others(7): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44604931 | ||||||
| chr15:44605044
|
A | T | 1 | a0001c0001t0001g0082 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3520+981T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44605044 | ||||||
| chr15:44605137
|
G | C | 1 | a0015c0020t0001g0123 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3520+888C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44605137 | ||||||
| chr15:44605194
|
G | A | 4 | a0009c0011t0001g0174a0009c0011t0003g0173a0010c0010t0001g0181others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.3520+831C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44605194 | ||||||
| chr15:44605261
|
T | C | 8 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3520+764A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44605261 | ||||||
| chr15:44605348
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3520+677G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44605348 | ||||||
| chr15:44605508
|
A | C | 1 | a0002c0002t0002g0020 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3520+517T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44605508 | ||||||
| chr15:44605541
|
G | C | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.3520+484C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44605541 | ||||||
| chr15:44605547
|
A | G | 73 | a0001c0001t0001g0050a0001c0001t0001g0081a0001c0001t0001g0102others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.3520+478T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44605547 | ||||||
| chr15:44605695
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3520+330C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44605695 | ||||||
| chr15:44605696
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3520+329A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44605696 | ||||||
| chr15:44605923
|
T | A | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3520+102A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 20/39 | chr15 | 44605923 | ||||||
| chr15:44606120
|
T | C | 1 | a0002c0002t0001g0137 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3454-29A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44606120 | ||||||
| chr15:44606176
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0160 | 2 | NA18978.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.3454-85C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44606176 | ||||||
| chr15:44606366
|
G | T | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.3454-275C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44606366 | ||||||
| chr15:44606444
|
C | T | 1 | a0002c0002t0001g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3454-353G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44606444 | ||||||
| chr15:44606458
|
CATG | C | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.3454-370_3454-368d others(5): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44606458 | ||||||
| chr15:44606608
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3454-517T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44606608 | ||||||
| chr15:44606629
|
G | A | 32 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.3454-538C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44606629 | ||||||
| chr15:44607013
|
T | A | 7 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3454-922A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44607013 | ||||||
| chr15:44607058
|
A | T | 4 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(1): Show | 4 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3454-967T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44607058 | ||||||
| chr15:44607256
|
A | G | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.3454-1165T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44607256 | ||||||
| chr15:44607313
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3453+1131C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44607313 | ||||||
| chr15:44607345
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3453+1099C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44607345 | ||||||
| chr15:44607366
|
T | C | 73 | a0001c0001t0001g0050a0001c0001t0001g0081a0001c0001t0001g0102others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.3453+1078A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44607366 | ||||||
| chr15:44607422
|
T | C | 1 | a0002c0002t0001g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3453+1022A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44607422 | ||||||
| chr15:44607539
|
G | A | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3453+905C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44607539 | ||||||
| chr15:44607562
|
C | T | 1 | a0008c0007t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3453+882G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44607562 | ||||||
| chr15:44608016
|
C | T | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3453+428G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44608016 | ||||||
| chr15:44608019
|
C | T | 2 | a0005c0005t0001g0147a0005c0005t0001g0148 | 2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.3453+425G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44608019 | ||||||
| chr15:44608151
|
T | C | 1 | a0008c0007t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3453+293A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44608151 | ||||||
| chr15:44608364
|
C | T | 1 | a0008c0007t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3453+80G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 19/39 | chr15 | 44608364 | ||||||
| chr15:44608706
|
G | T | 1 | a0009c0011t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3292-101C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44608706 | ||||||
| chr15:44608892
|
T | G | 4 | a0007c0008t0001g0186a0007c0008t0001g0187a0007c0008t0001g0188others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3292-287A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44608892 | ||||||
| chr15:44608899
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3292-294T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44608899 | ||||||
| chr15:44608953
|
GAT | G | 7 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3292-350_3292-349d others(4): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44608953 | ||||||
| chr15:44609194
|
C | T | 4 | a0007c0008t0001g0186a0007c0008t0001g0187a0007c0008t0001g0188others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3292-589G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44609194 | ||||||
| chr15:44609254
|
C | T | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3292-649G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44609254 | ||||||
| chr15:44609309
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3292-704A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44609309 | ||||||
| chr15:44609599
|
C | A | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3292-994G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44609599 | ||||||
| chr15:44609729
|
G | A | 32 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.3291+1111C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44609729 | ||||||
| chr15:44609895
|
A | AT | 16 | a0001c0001t0001g0052a0001c0001t0001g0074a0001c0001t0001g0079others(13): Show | 16 | HG01123.hp2 HG02040.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.3291+944dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44609895 | ||||||
| chr15:44609895
|
A | ATT | 5 | a0001c0001t0001g0145a0002c0002t0002g0020a0002c0002t0002g0021others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.3291+943_3291+944d others(4): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44609895 | ||||||
| chr15:44609895
|
AT | A | 41 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0073others(38): Show | 41 | HG00621.hp1 HG01496.hp1 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.3291+944delA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44609895 | ||||||
| chr15:44609895
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0081a0025c0027t0001g0140 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3291+935_3291+944d others(12): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44609895 | ||||||
| chr15:44609959
|
C | G | 4 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(1): Show | 4 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3291+881G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44609959 | ||||||
| chr15:44610149
|
C | T | 3 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152 | 3 | HG03516.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3291+691G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44610149 | ||||||
| chr15:44610166
|
G | C | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3291+674C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44610166 | ||||||
| chr15:44610360
|
A | C | 188 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(185): Show | 188 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.3291+480T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44610360 | ||||||
| chr15:44610390
|
T | C | 14 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(11): Show | 14 | HG02040.hp1 HG02109.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.3291+450A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44610390 | ||||||
| chr15:44610410
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3291+430A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44610410 | ||||||
| chr15:44610413
|
C | T | 3 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152 | 3 | HG03516.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3291+427G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44610413 | ||||||
| chr15:44610546
|
T | C | 72 | a0001c0001t0001g0081a0001c0001t0001g0102a0001c0001t0001g0103others(69): Show | 72 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.3291+294A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44610546 | ||||||
| chr15:44610579
|
C | T | 72 | a0001c0001t0001g0081a0001c0001t0001g0102a0001c0001t0001g0103others(69): Show | 72 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.3291+261G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 18/39 | chr15 | 44610579 | ||||||
| chr15:44611052
|
T | G | 1 | a0017c0022t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3146-67A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611052 | ||||||
| chr15:44611087
|
C | A | 189 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(186): Show | 189 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.3146-102G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611087 | ||||||
| chr15:44611091
|
T | TA | 11 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0049others(8): Show | 11 | HG00597.hp2 HG01123.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3146-107dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
T | TAAAAAAA others(3): Show |
3 | a0006c0006t0001g0044a0006c0006t0001g0178a0006c0006t0001g0179 | 3 | HG02970.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3146-116_3146-107d others(12): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
T | TAAAAAAA others(4): Show |
5 | a0002c0002t0002g0020a0002c0002t0002g0021a0002c0002t0002g0022others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3146-117_3146-107d others(13): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
T | TAAAAAAA others(5): Show |
5 | a0003c0003t0001g0003a0003c0003t0001g0005a0003c0003t0001g0006others(2): Show | 5 | HG00423.hp2 NA18949.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.3146-118_3146-107d others(14): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
T | TAAAAAAA others(6): Show |
6 | a0002c0002t0002g0023a0003c0003t0001g0001a0003c0003t0001g0009others(3): Show | 6 | HG00408.hp1 HG00673.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3146-119_3146-107d others(15): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
T | TAAAAAAA others(7): Show |
4 | a0003c0003t0001g0002a0003c0003t0001g0004a0003c0003t0001g0008others(1): Show | 4 | HG02602.hp2 HG03927.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.3146-120_3146-107d others(16): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
T | TAAAAAAA others(8): Show |
6 | a0004c0004t0001g0149a0004c0004t0001g0164a0004c0004t0001g0166others(3): Show | 6 | HG02040.hp1 HG02155.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.3146-121_3146-107d others(17): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
T | TAAAAAAA others(9): Show |
7 | a0004c0004t0001g0158a0004c0004t0001g0165a0004c0004t0001g0167others(4): Show | 7 | HG02523.hp1 NA18965.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.3146-122_3146-107d others(18): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
T | TAAAAAAA others(10): Show |
1 | a0003c0003t0001g0012 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3146-123_3146-107d others(19): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
T | TAAAAAAA others(12): Show |
2 | a0008c0007t0001g0150a0010c0010t0001g0184 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3146-125_3146-107d others(21): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
T | TAAAAAAA others(13): Show |
1 | a0009c0011t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3146-126_3146-107d others(22): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
T | TAAAAAAA others(14): Show |
1 | a0010c0010t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3146-127_3146-107d others(23): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
TA | T | 37 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0001t0001g0076others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.3146-107delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
TAAAAAAA others(2): Show |
T | 10 | a0001c0001t0001g0081a0001c0001t0001g0102a0001c0001t0001g0103others(7): Show | 10 | HG01496.hp1 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.3146-115_3146-107d others(11): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611091
|
TAAAAAAA others(3): Show |
T | 9 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(6): Show | 9 | HG00621.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3146-116_3146-107d others(12): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611091 | ||||||
| chr15:44611126
|
A | T | 1 | a0002c0002t0001g0128 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3146-141T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611126 | ||||||
| chr15:44611397
|
T | C | 9 | a0001c0001t0001g0081a0001c0001t0001g0102a0001c0001t0001g0103others(6): Show | 9 | HG02559.hp1 HG02630.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.3146-412A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611397 | ||||||
| chr15:44611398
|
A | G | 1 | a0006c0006t0001g0044 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3146-413T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611398 | ||||||
| chr15:44611501
|
T | C | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3146-516A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611501 | ||||||
| chr15:44611539
|
A | G | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.3146-554T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611539 | ||||||
| chr15:44611718
|
C | T | 1 | a0003c0003t0001g0003 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3146-733G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611718 | ||||||
| chr15:44611727
|
T | A | 2 | a0008c0007t0001g0151a0008c0007t0001g0152 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3146-742A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611727 | ||||||
| chr15:44611809
|
C | CT | 174 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.3146-825dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611809 | ||||||
| chr15:44611809
|
C | CTTT | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3146-827_3146-825d others(5): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611809 | ||||||
| chr15:44611865
|
G | C | 1 | a0002c0002t0001g0128 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3146-880C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611865 | ||||||
| chr15:44611954
|
C | T | 15 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(12): Show | 15 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.3146-969G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611954 | ||||||
| chr15:44611955
|
G | A | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3146-970C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611955 | ||||||
| chr15:44611999
|
C | T | 11 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(8): Show | 11 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3146-1014G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44611999 | ||||||
| chr15:44612011
|
G | A | 1 | a0004c0004t0001g0182 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3146-1026C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44612011 | ||||||
| chr15:44612028
|
C | T | 20 | a0001c0001t0001g0081a0001c0001t0001g0102a0001c0001t0001g0103others(17): Show | 20 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.3146-1043G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44612028 | ||||||
| chr15:44612088
|
C | G | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3146-1103G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44612088 | ||||||
| chr15:44612119
|
A | G | 4 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(1): Show | 4 | HG00621.hp1 HG03017.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.3146-1134T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44612119 | ||||||
| chr15:44612301
|
A | C | 4 | a0007c0008t0001g0186a0007c0008t0001g0187a0007c0008t0001g0188others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3145+1129T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44612301 | ||||||
| chr15:44612309
|
T | C | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3145+1121A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44612309 | ||||||
| chr15:44612327
|
T | C | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3145+1103A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44612327 | ||||||
| chr15:44612547
|
T | C | 20 | a0001c0001t0001g0081a0001c0001t0001g0102a0001c0001t0001g0103others(17): Show | 20 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.3145+883A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44612547 | ||||||
| chr15:44612718
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3145+712A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44612718 | ||||||
| chr15:44612731
|
A | AT | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.3145+698dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44612731 | ||||||
| chr15:44613297
|
G | A | 1 | a0010c0010t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3145+133C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 17/39 | chr15 | 44613297 | ||||||
| chr15:44614139
|
C | T | 40 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(37): Show | 40 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.3039-603G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/39 | chr15 | 44614139 | ||||||
| chr15:44614250
|
G | A | 19 | a0001c0001t0001g0081a0001c0001t0001g0102a0001c0001t0001g0103others(16): Show | 19 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.3039-714C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/39 | chr15 | 44614250 | ||||||
| chr15:44614514
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3038+849C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/39 | chr15 | 44614514 | ||||||
| chr15:44614520
|
G | A | 1 | a0009c0011t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3038+843C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/39 | chr15 | 44614520 | ||||||
| chr15:44614609
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0106a0014c0024t0001g0159 | 3 | HG02040.hp2 NA18966.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.3038+754C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/39 | chr15 | 44614609 | ||||||
| chr15:44614646
|
G | A | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.3038+717C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/39 | chr15 | 44614646 | ||||||
| chr15:44614661
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3038+702G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/39 | chr15 | 44614661 | ||||||
| chr15:44614787
|
A | G | 1 | a0002c0002t0001g0154 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3038+576T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/39 | chr15 | 44614787 | ||||||
| chr15:44614898
|
C | T | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3038+465G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/39 | chr15 | 44614898 | ||||||
| chr15:44614900
|
A | G | 72 | a0001c0001t0001g0081a0001c0001t0001g0102a0001c0001t0001g0103others(69): Show | 72 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.3038+463T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/39 | chr15 | 44614900 | ||||||
| chr15:44615093
|
C | T | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3038+270G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/39 | chr15 | 44615093 | ||||||
| chr15:44615143
|
A | C | 4 | a0009c0011t0001g0174a0009c0011t0003g0173a0010c0010t0001g0181others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.3038+220T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/39 | chr15 | 44615143 | ||||||
| chr15:44615289
|
G | A | 1 | a0019c0015t0001g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3038+74C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 16/39 | chr15 | 44615289 | ||||||
| chr15:44615630
|
G | T | 3 | a0002c0002t0001g0028a0002c0002t0001g0029a0002c0002t0001g0030 | 3 | HG02965.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2835-64C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44615630 | ||||||
| chr15:44615695
|
T | C | 1 | a0002c0002t0001g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2835-129A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44615695 | ||||||
| chr15:44615843
|
G | T | 1 | a0009c0011t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2835-277C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44615843 | ||||||
| chr15:44615868
|
G | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0077 | 2 | HG01175.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2835-302C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44615868 | ||||||
| chr15:44615892
|
C | T | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2835-326G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44615892 | ||||||
| chr15:44616136
|
T | C | 40 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(37): Show | 40 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.2835-570A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44616136 | ||||||
| chr15:44616453
|
C | T | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2835-887G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44616453 | ||||||
| chr15:44616534
|
G | A | 1 | a0002c0002t0002g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2835-968C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44616534 | ||||||
| chr15:44617002
|
C | T | 2 | a0008c0007t0001g0151a0008c0007t0001g0152 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2835-1436G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44617002 | ||||||
| chr15:44617031
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2835-1465C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44617031 | ||||||
| chr15:44617050
|
G | T | 2 | a0009c0011t0001g0174a0009c0011t0003g0173 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2835-1484C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44617050 | ||||||
| chr15:44617064
|
A | G | 1 | a0002c0002t0001g0130 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2835-1498T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44617064 | ||||||
| chr15:44617412
|
G | T | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2835-1846C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44617412 | ||||||
| chr15:44617424
|
G | C | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2835-1858C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44617424 | ||||||
| chr15:44617582
|
C | T | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2835-2016G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44617582 | ||||||
| chr15:44617605
|
C | T | 4 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(1): Show | 4 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2835-2039G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44617605 | ||||||
| chr15:44617947
|
A | T | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.2834+2243T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44617947 | ||||||
| chr15:44618017
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2834+2173T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44618017 | ||||||
| chr15:44618160
|
T | A | 2 | a0002c0002t0001g0112a0002c0002t0001g0113 | 2 | NA18986.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2834+2030A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44618160 | ||||||
| chr15:44618301
|
G | C | 1 | a0009c0011t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2834+1889C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44618301 | ||||||
| chr15:44618311
|
A | C | 1 | a0015c0020t0001g0123 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2834+1879T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44618311 | ||||||
| chr15:44618336
|
G | A | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2834+1854C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44618336 | ||||||
| chr15:44618516
|
C | CA | 29 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0067others(26): Show | 29 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.2834+1673dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44618516 | ||||||
| chr15:44618599
|
C | T | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2834+1591G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44618599 | ||||||
| chr15:44618600
|
G | A | 4 | a0007c0008t0001g0186a0007c0008t0001g0187a0007c0008t0001g0188others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2834+1590C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44618600 | ||||||
| chr15:44618672
|
C | T | 40 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(37): Show | 40 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.2834+1518G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44618672 | ||||||
| chr15:44618680
|
C | T | 1 | a0007c0008t0001g0186 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2834+1510G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44618680 | ||||||
| chr15:44618735
|
G | T | 1 | a0002c0002t0001g0124 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2834+1455C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44618735 | ||||||
| chr15:44618817
|
C | CA | 8 | a0002c0002t0001g0018a0002c0002t0001g0027a0002c0002t0002g0019others(5): Show | 8 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2834+1372dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44618817 | ||||||
| chr15:44618841
|
C | T | 4 | a0006c0006t0001g0043a0006c0006t0001g0044a0006c0006t0001g0178others(1): Show | 4 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2834+1349G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44618841 | ||||||
| chr15:44619250
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2834+940A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44619250 | ||||||
| chr15:44619390
|
C | G | 2 | a0002c0002t0001g0176a0002c0002t0001g0177 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2834+800G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44619390 | ||||||
| chr15:44619473
|
A | G | 3 | a0005c0005t0001g0146a0005c0005t0001g0147a0005c0005t0001g0148 | 3 | HG02257.hp2 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2834+717T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44619473 | ||||||
| chr15:44619721
|
A | AT | 7 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0143others(4): Show | 7 | HG01175.hp1 HG02602.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2834+468dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44619721 | ||||||
| chr15:44619721
|
AT | A | 60 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0025others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.2834+468delA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44619721 | ||||||
| chr15:44619865
|
C | T | 15 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(12): Show | 15 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2834+325G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44619865 | ||||||
| chr15:44619936
|
G | A | 1 | a0003c0003t0001g0003 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2834+254C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 15/39 | chr15 | 44619936 | ||||||
| chr15:44620418
|
A | C | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2621-15T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44620418 | ||||||
| chr15:44620429
|
A | G | 4 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(1): Show | 4 | HG01496.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2621-26T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44620429 | ||||||
| chr15:44620431
|
T | C | 4 | a0007c0008t0001g0186a0007c0008t0001g0187a0007c0008t0001g0188others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2621-28A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44620431 | ||||||
| chr15:44620487
|
A | C | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2621-84T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44620487 | ||||||
| chr15:44620552
|
CTTTT | C | 31 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(28): Show | 31 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2621-153_2621-150d others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44620552 | ||||||
| chr15:44620702
|
A | AT | 65 | a0001c0001t0001g0106a0002c0002t0001g0017a0002c0002t0001g0018others(62): Show | 65 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.2621-300dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44620702 | ||||||
| chr15:44620900
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2621-497A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44620900 | ||||||
| chr15:44620934
|
G | A | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.2621-531C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44620934 | ||||||
| chr15:44620990
|
C | T | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2621-587G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44620990 | ||||||
| chr15:44621222
|
G | A | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2620+537C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44621222 | ||||||
| chr15:44621321
|
A | G | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.2620+438T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44621321 | ||||||
| chr15:44621489
|
A | C | 32 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.2620+270T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44621489 | ||||||
| chr15:44621575
|
T | G | 1 | a0002c0002t0001g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2620+184A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44621575 | ||||||
| chr15:44621594
|
C | G | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2620+165G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44621594 | ||||||
| chr15:44621622
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2620+137G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 14/39 | chr15 | 44621622 | ||||||
| chr15:44621953
|
AT | A | 17 | a0001c0001t0001g0053a0002c0002t0001g0018a0002c0002t0002g0019others(14): Show | 17 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.2445-20delA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 13/39 | chr15 | 44621953 | ||||||
| chr15:44622026
|
G | A | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2445-92C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 13/39 | chr15 | 44622026 | ||||||
| chr15:44622518
|
G | A | 32 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.2317-171C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 12/39 | chr15 | 44622518 | ||||||
| chr15:44622536
|
T | C | 1 | a0002c0002t0002g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2317-189A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 12/39 | chr15 | 44622536 | ||||||
| chr15:44622556
|
T | C | 4 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(1): Show | 4 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2316+172A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 12/39 | chr15 | 44622556 | ||||||
| chr15:44622646
|
G | T | 1 | a0003c0003t0001g0004 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2316+82C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 12/39 | chr15 | 44622646 | ||||||
| chr15:44622665
|
C | A | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.2316+63G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 12/39 | chr15 | 44622665 | ||||||
| chr15:44623304
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2245-505C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44623304 | ||||||
| chr15:44623474
|
G | A | 2 | a0002c0002t0001g0029a0002c0002t0001g0030 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2245-675C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44623474 | ||||||
| chr15:44623503
|
C | T | 10 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(7): Show | 10 | HG02559.hp1 HG02572.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.2245-704G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44623503 | ||||||
| chr15:44623563
|
CA | C | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.2245-765delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44623563 | ||||||
| chr15:44623682
|
A | G | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2245-883T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44623682 | ||||||
| chr15:44623719
|
C | T | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2245-920G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44623719 | ||||||
| chr15:44623734
|
A | G | 4 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0098others(1): Show | 4 | HG00423.hp1 HG01978.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-935T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44623734 | ||||||
| chr15:44623748
|
ACTTTT | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0056 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2245-954_2245-950d others(7): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44623748 | ||||||
| chr15:44623788
|
G | T | 31 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(28): Show | 31 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.2245-989C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44623788 | ||||||
| chr15:44624056
|
C | T | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2245-1257G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44624056 | ||||||
| chr15:44624266
|
T | C | 2 | a0002c0002t0001g0109a0002c0002t0001g0131 | 2 | HG02148.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2245-1467A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44624266 | ||||||
| chr15:44624285
|
C | T | 1 | a0002c0002t0001g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2245-1486G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44624285 | ||||||
| chr15:44624332
|
GA | G | 15 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0052others(12): Show | 15 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2245-1534delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44624332 | ||||||
| chr15:44624772
|
T | C | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2244+1559A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44624772 | ||||||
| chr15:44624863
|
G | A | 1 | a0009c0011t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2244+1468C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44624863 | ||||||
| chr15:44624903
|
G | C | 3 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152 | 3 | HG03516.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2244+1428C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44624903 | ||||||
| chr15:44625071
|
G | A | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2244+1260C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44625071 | ||||||
| chr15:44625088
|
C | A | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2244+1243G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44625088 | ||||||
| chr15:44625134
|
C | CA | 5 | a0001c0001t0001g0052a0001c0001t0001g0074a0003c0003t0001g0012others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2244+1196dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44625134 | ||||||
| chr15:44625415
|
G | A | 2 | a0011c0009t0001g0086a0011c0009t0001g0087 | 2 | HG00140.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2244+916C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44625415 | ||||||
| chr15:44625505
|
T | C | 10 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(7): Show | 10 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2244+826A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44625505 | ||||||
| chr15:44625589
|
C | T | 1 | a0002c0002t0001g0026 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2244+742G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44625589 | ||||||
| chr15:44625590
|
A | G | 1 | a0002c0002t0001g0026 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2244+741T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44625590 | ||||||
| chr15:44625817
|
T | C | 1 | a0005c0005t0001g0031 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2244+514A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44625817 | ||||||
| chr15:44625828
|
C | T | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.2244+503G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44625828 | ||||||
| chr15:44625976
|
G | A | 2 | a0009c0011t0001g0174a0009c0011t0003g0173 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2244+355C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44625976 | ||||||
| chr15:44626051
|
T | G | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.2244+280A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44626051 | ||||||
| chr15:44626052
|
A | AT | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.2244+278dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44626052 | ||||||
| chr15:44626116
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2244+215C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44626116 | ||||||
| chr15:44626162
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2244+169C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44626162 | ||||||
| chr15:44626289
|
A | T | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.2244+42T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44626289 | ||||||
| chr15:44626321
|
C | A | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2244+10G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 11/39 | chr15 | 44626321 | ||||||
| chr15:44626724
|
T | A | 1 | a0022c0014t0001g0185 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2068-217A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 10/39 | chr15 | 44626724 | ||||||
| chr15:44626835
|
T | A | 2 | a0002c0002t0001g0176a0002c0002t0001g0177 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2068-328A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 10/39 | chr15 | 44626835 | ||||||
| chr15:44627150
|
T | C | 42 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(39): Show | 42 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2068-643A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 10/39 | chr15 | 44627150 | ||||||
| chr15:44627285
|
A | C | 42 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(39): Show | 42 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2068-778T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 10/39 | chr15 | 44627285 | ||||||
| chr15:44627569
|
A | G | 4 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(1): Show | 4 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2068-1062T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 10/39 | chr15 | 44627569 | ||||||
| chr15:44627593
|
AT | A | 5 | a0002c0002t0001g0154a0009c0011t0001g0174a0009c0011t0003g0173others(2): Show | 5 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2067+1075delA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 10/39 | chr15 | 44627593 | ||||||
| chr15:44627621
|
G | A | 1 | a0002c0002t0001g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2067+1048C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 10/39 | chr15 | 44627621 | ||||||
| chr15:44627840
|
C | T | 1 | a0005c0005t0001g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2067+829G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 10/39 | chr15 | 44627840 | ||||||
| chr15:44628240
|
T | C | 1 | a0011c0009t0001g0087 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2067+429A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 10/39 | chr15 | 44628240 | ||||||
| chr15:44628447
|
T | G | 10 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(7): Show | 10 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2067+222A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 10/39 | chr15 | 44628447 | ||||||
| chr15:44628489
|
T | C | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.2067+180A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 10/39 | chr15 | 44628489 | ||||||
| chr15:44628509
|
T | G | 1 | a0002c0002t0002g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2067+160A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 10/39 | chr15 | 44628509 | ||||||
| chr15:44628538
|
G | A | 2 | a0003c0003t0001g0002a0003c0003t0001g0004 | 2 | HG02602.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2067+131C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 10/39 | chr15 | 44628538 | ||||||
| chr15:44629136
|
G | A | 2 | a0009c0011t0001g0174a0009c0011t0003g0173 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1891+97C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 9/39 | chr15 | 44629136 | ||||||
| chr15:44629531
|
C | T | 16 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(13): Show | 16 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1736-143G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44629531 | ||||||
| chr15:44629581
|
T | G | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1736-193A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44629581 | ||||||
| chr15:44629673
|
C | A | 1 | a0001c0001t0001g0059 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1736-285G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44629673 | ||||||
| chr15:44629710
|
C | T | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1736-322G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44629710 | ||||||
| chr15:44629978
|
G | A | 3 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152 | 3 | HG03516.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1736-590C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44629978 | ||||||
| chr15:44630057
|
G | A | 2 | a0004c0004t0001g0170a0024c0025t0001g0172 | 2 | NA18951.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1736-669C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630057 | ||||||
| chr15:44630084
|
G | A | 16 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(13): Show | 16 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1736-696C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630084 | ||||||
| chr15:44630181
|
G | T | 35 | a0002c0002t0001g0018a0002c0002t0001g0027a0002c0002t0001g0028others(32): Show | 35 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.1736-793C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630181 | ||||||
| chr15:44630284
|
G | A | 6 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1736-896C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630284 | ||||||
| chr15:44630346
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1736-958G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630346 | ||||||
| chr15:44630405
|
A | C | 1 | a0010c0010t0001g0184 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1736-1017T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630405 | ||||||
| chr15:44630569
|
T | C | 35 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(32): Show | 35 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.1736-1181A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630569 | ||||||
| chr15:44630575
|
G | A | 1 | a0002c0002t0001g0130 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1736-1187C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630575 | ||||||
| chr15:44630643
|
G | A | 2 | a0002c0002t0001g0176a0002c0002t0001g0177 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1736-1255C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630643 | ||||||
| chr15:44630648
|
C | T | 1 | a0002c0002t0001g0154 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1736-1260G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630648 | ||||||
| chr15:44630724
|
C | T | 1 | a0002c0002t0001g0120 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1736-1336G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630724 | ||||||
| chr15:44630740
|
T | C | 2 | a0001c0001t0001g0142a0003c0003t0001g0015 | 2 | HG00423.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1736-1352A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630740 | ||||||
| chr15:44630781
|
C | T | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1736-1393G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630781 | ||||||
| chr15:44630782
|
G | A | 8 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(5): Show | 8 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1736-1394C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630782 | ||||||
| chr15:44630829
|
CG | C | 10 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(7): Show | 10 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1736-1442delC | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630829 | ||||||
| chr15:44630853
|
T | G | 34 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1736-1465A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630853 | ||||||
| chr15:44630895
|
A | G | 20 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0051others(17): Show | 20 | HG01981.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1736-1507T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630895 | ||||||
| chr15:44630956
|
A | AT | 4 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(1): Show | 4 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1736-1569dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44630956 | ||||||
| chr15:44631289
|
T | G | 4 | a0009c0011t0001g0174a0009c0011t0003g0173a0010c0010t0001g0181others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1736-1901A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44631289 | ||||||
| chr15:44631310
|
T | C | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1736-1922A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44631310 | ||||||
| chr15:44631352
|
G | GA | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1736-1965dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44631352 | ||||||
| chr15:44631434
|
G | C | 2 | a0009c0011t0001g0174a0009c0011t0003g0173 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1736-2046C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44631434 | ||||||
| chr15:44631440
|
T | C | 1 | a0003c0003t0001g0001 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1736-2052A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44631440 | ||||||
| chr15:44631455
|
G | C | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1735+2050C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44631455 | ||||||
| chr15:44631534
|
G | A | 1 | a0002c0002t0001g0133 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1735+1971C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44631534 | ||||||
| chr15:44631622
|
A | C | 1 | a0002c0002t0001g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1735+1883T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44631622 | ||||||
| chr15:44631661
|
C | CT | 19 | a0001c0001t0001g0051a0001c0001t0001g0071a0001c0001t0001g0091others(16): Show | 19 | HG00423.hp2 HG02040.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.1735+1843dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44631661 | ||||||
| chr15:44631701
|
C | T | 2 | a0008c0007t0001g0151a0008c0007t0001g0152 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1735+1804G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44631701 | ||||||
| chr15:44631803
|
C | CT | 16 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0069others(13): Show | 16 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1735+1701dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44631803 | ||||||
| chr15:44631803
|
C | CTTTTTTT others(11): Show |
1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1735+1684_1735+170 others(22): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44631803 | ||||||
| chr15:44631984
|
T | G | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1735+1521A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44631984 | ||||||
| chr15:44632002
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1735+1503A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44632002 | ||||||
| chr15:44632036
|
T | C | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1735+1469A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44632036 | ||||||
| chr15:44632112
|
A | G | 42 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(39): Show | 42 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1735+1393T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44632112 | ||||||
| chr15:44632200
|
T | A | 17 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(14): Show | 17 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1735+1305A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44632200 | ||||||
| chr15:44632372
|
C | T | 1 | a0002c0002t0001g0125 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1735+1133G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44632372 | ||||||
| chr15:44632517
|
A | AT | 6 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(3): Show | 6 | HG00621.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1735+987dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44632517 | ||||||
| chr15:44632593
|
C | T | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1735+912G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44632593 | ||||||
| chr15:44632746
|
C | T | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1735+759G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44632746 | ||||||
| chr15:44632762
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1735+743C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44632762 | ||||||
| chr15:44633163
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1735+342G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633163 | ||||||
| chr15:44633205
|
G | A | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1735+300C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633205 | ||||||
| chr15:44633324
|
C | CA | 29 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0040others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1735+180dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
C | CAA | 26 | a0001c0001t0001g0052a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 26 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.1735+179_1735+180d others(4): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
C | CAAA | 15 | a0001c0001t0001g0048a0001c0001t0001g0060a0001c0001t0001g0077others(12): Show | 15 | HG00140.hp1 HG01175.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.1735+178_1735+180d others(5): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
C | CAAAA | 13 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0053others(10): Show | 13 | HG01106.hp1 HG01981.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1735+177_1735+180d others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
C | CAAAAA | 6 | a0001c0001t0001g0041a0001c0001t0001g0162a0004c0004t0001g0164others(3): Show | 6 | HG02257.hp2 HG03453.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.1735+176_1735+180d others(7): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
C | CAAAAAA | 8 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0055others(5): Show | 8 | HG01496.hp1 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1735+175_1735+180d others(8): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
C | CAAAAAAA | 5 | a0002c0002t0002g0023a0004c0004t0001g0149a0004c0004t0001g0166others(2): Show | 5 | HG02040.hp1 HG02155.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1735+174_1735+180d others(9): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
C | CAAAAAAA others(3): Show |
1 | a0005c0005t0001g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1735+171_1735+180d others(12): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0102 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1735+169_1735+180d others(14): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0050a0004c0004t0001g0167a0004c0004t0001g0168 | 3 | NA18965.hp2 NA19004.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1735+168_1735+180d others(15): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0105 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1735+166_1735+180d others(17): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
C | CAAAAAAA others(10): Show |
1 | a0005c0005t0001g0033 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1735+164_1735+180d others(19): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0101 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1735+160_1735+180d others(23): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
CAAAAAAA others(3): Show |
C | 1 | a0008c0007t0001g0151 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1735+171_1735+180d others(12): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
CAAAAAAA others(4): Show |
C | 2 | a0003c0003t0001g0007a0003c0003t0001g0012 | 2 | HG00597.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1735+170_1735+180d others(13): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
CAAAAAAA others(5): Show |
C | 17 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.1735+169_1735+180d others(14): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
CAAAAAAA others(6): Show |
C | 1 | a0002c0002t0001g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1735+168_1735+180d others(15): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0056 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1735+166_1735+180d others(17): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0072 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1735+165_1735+180d others(18): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
CAAAAAAA others(10): Show |
C | 1 | a0002c0002t0001g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1735+164_1735+180d others(19): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0001g0110a0008c0007t0001g0150 | 2 | NA18977.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1735+163_1735+180d others(20): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
CAAAAAAA others(13): Show |
C | 1 | a0002c0002t0001g0026 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1735+161_1735+180d others(22): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633324
|
CAAAAAAA others(14): Show |
C | 8 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1735+160_1735+180d others(23): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633324 | ||||||
| chr15:44633343
|
AAAAAAAA others(13): Show |
A | 2 | a0002c0002t0001g0029a0002c0002t0001g0030 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1735+142_1735+161d others(22): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633343 | ||||||
| chr15:44633458
|
G | A | 1 | a0001c0016t0001g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1735+47C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 8/39 | chr15 | 44633458 | ||||||
| chr15:44633682
|
G | GA | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1603-46dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44633682 | ||||||
| chr15:44633946
|
C | G | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1603-309G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44633946 | ||||||
| chr15:44634026
|
A | T | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603-389T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44634026 | ||||||
| chr15:44634130
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1603-493G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44634130 | ||||||
| chr15:44634415
|
C | T | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1603-778G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44634415 | ||||||
| chr15:44634441
|
A | AT | 20 | a0001c0001t0001g0073a0001c0001t0001g0075a0002c0002t0001g0029others(17): Show | 20 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.1603-805dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44634441 | ||||||
| chr15:44634441
|
A | C | 4 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(1): Show | 4 | HG00621.hp1 HG03017.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-804T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44634441 | ||||||
| chr15:44634638
|
G | A | 7 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1603-1001C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44634638 | ||||||
| chr15:44634813
|
GTGAGGAT others(16): Show |
G | 1 | a0002c0002t0001g0035 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1603-1199_1603-117 others(27): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44634813 | ||||||
| chr15:44634827
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1603-1190C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44634827 | ||||||
| chr15:44634917
|
A | T | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1603-1280T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44634917 | ||||||
| chr15:44635042
|
C | T | 1 | a0019c0015t0001g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1603-1405G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44635042 | ||||||
| chr15:44635141
|
G | A | 1 | a0003c0003t0001g0004 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1603-1504C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44635141 | ||||||
| chr15:44635286
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1603-1649G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44635286 | ||||||
| chr15:44635424
|
A | G | 1 | a0017c0022t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1603-1787T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44635424 | ||||||
| chr15:44635522
|
C | T | 2 | a0009c0011t0001g0174a0009c0011t0003g0173 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1603-1885G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44635522 | ||||||
| chr15:44635595
|
CA | C | 112 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0040others(109): Show | 112 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1603-1959delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44635595 | ||||||
| chr15:44635595
|
CAA | C | 30 | a0001c0001t0001g0060a0001c0001t0001g0091a0002c0002t0001g0017others(27): Show | 30 | HG00621.hp1 HG01496.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1603-1960_1603-195 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44635595 | ||||||
| chr15:44635595
|
CAAAAAAA others(4): Show |
C | 34 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1603-1969_1603-195 others(15): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44635595 | ||||||
| chr15:44635623
|
A | G | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-1986T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44635623 | ||||||
| chr15:44635917
|
T | TA | 15 | a0003c0003t0001g0002a0003c0003t0001g0003a0003c0003t0001g0004others(12): Show | 15 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.1603-2281dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44635917 | ||||||
| chr15:44635932
|
A | C | 1 | a0001c0001t0001g0056 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1603-2295T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44635932 | ||||||
| chr15:44636020
|
C | T | 1 | a0008c0007t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1603-2383G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636020 | ||||||
| chr15:44636084
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1603-2447A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636084 | ||||||
| chr15:44636186
|
T | C | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1603-2549A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636186 | ||||||
| chr15:44636239
|
G | A | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1603-2602C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636239 | ||||||
| chr15:44636268
|
T | C | 3 | a0002c0002t0001g0028a0002c0002t0001g0029a0002c0002t0001g0030 | 3 | HG02965.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1603-2631A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636268 | ||||||
| chr15:44636477
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1603-2840A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636477 | ||||||
| chr15:44636491
|
C | T | 4 | a0009c0011t0001g0174a0009c0011t0003g0173a0010c0010t0001g0181others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-2854G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636491 | ||||||
| chr15:44636518
|
C | T | 3 | a0005c0005t0001g0146a0005c0005t0001g0147a0005c0005t0001g0148 | 3 | HG02257.hp2 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1603-2881G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636518 | ||||||
| chr15:44636519
|
G | A | 4 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(1): Show | 4 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-2882C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636519 | ||||||
| chr15:44636591
|
G | A | 1 | a0002c0002t0001g0025 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1603-2954C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636591 | ||||||
| chr15:44636617
|
G | A | 17 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(14): Show | 17 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1603-2980C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636617 | ||||||
| chr15:44636669
|
A | G | 2 | a0008c0007t0001g0151a0008c0007t0001g0152 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1603-3032T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636669 | ||||||
| chr15:44636828
|
A | G | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1603-3191T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636828 | ||||||
| chr15:44636852
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1603-3215C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636852 | ||||||
| chr15:44636877
|
G | A | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603-3240C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636877 | ||||||
| chr15:44636925
|
C | CA | 22 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1603-3289dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636925 | ||||||
| chr15:44636925
|
C | CAA | 12 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0111others(9): Show | 12 | HG00621.hp2 HG02258.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603-3290_1603-328 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636925 | ||||||
| chr15:44636925
|
C | CAAA | 5 | a0001c0001t0001g0052a0001c0001t0001g0055a0002c0002t0001g0117others(2): Show | 5 | HG02055.hp2 HG02257.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603-3291_1603-328 others(7): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636925 | ||||||
| chr15:44636925
|
CAAAAAAA others(8): Show |
C | 1 | a0025c0027t0001g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1603-3303_1603-328 others(19): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636925 | ||||||
| chr15:44636925
|
CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0001g0091a0001c0001t0001g0094 | 2 | HG01106.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1603-3307_1603-328 others(23): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636925 | ||||||
| chr15:44636934
|
A | C | 2 | a0002c0002t0001g0035a0021c0018t0001g0097 | 2 | NA18954.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1603-3297T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636934 | ||||||
| chr15:44636934
|
AAAAAAAA others(17): Show |
A | 21 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(18): Show | 21 | HG00621.hp1 HG01496.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.1603-3321_1603-329 others(28): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636934 | ||||||
| chr15:44636935
|
A | C | 1 | a0023c0013t0001g0064 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1603-3298T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636935 | ||||||
| chr15:44636935
|
AAAAAAAA others(16): Show |
A | 7 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(4): Show | 7 | HG00609.hp1 HG02257.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1603-3321_1603-329 others(27): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636935 | ||||||
| chr15:44636936
|
A | C | 1 | a0001c0001t0001g0080 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1603-3299T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636936 | ||||||
| chr15:44636937
|
AAAAAAAA others(14): Show |
A | 15 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(12): Show | 15 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.1603-3321_1603-330 others(25): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636937 | ||||||
| chr15:44636938
|
A | AC | 9 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0068others(6): Show | 9 | HG00438.hp1 HG01515.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.1603-3302_1603-330 others(5): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636938 | ||||||
| chr15:44636938
|
AAAAAAAA others(13): Show |
A | 1 | a0003c0003t0001g0004 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1603-3321_1603-330 others(24): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636938 | ||||||
| chr15:44636939
|
A | C | 38 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0063others(35): Show | 38 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1603-3302T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636939 | ||||||
| chr15:44636941
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1603-3304T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636941 | ||||||
| chr15:44636941
|
AAAAAAAA others(10): Show |
A | 7 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(4): Show | 7 | HG02572.hp1 HG02895.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1603-3321_1603-330 others(21): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636941 | ||||||
| chr15:44636942
|
A | C | 1 | a0001c0001t0001g0080 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1603-3305T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636942 | ||||||
| chr15:44636942
|
AAAAAAAA others(9): Show |
A | 8 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(5): Show | 8 | HG02055.hp1 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1603-3321_1603-330 others(20): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636942 | ||||||
| chr15:44636943
|
A | C | 8 | a0001c0001t0001g0072a0001c0001t0001g0079a0001c0001t0001g0095others(5): Show | 8 | HG00140.hp1 HG01258.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.1603-3306T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636943 | ||||||
| chr15:44636943
|
AAAAAAAA others(8): Show |
A | 3 | a0002c0002t0001g0018a0002c0002t0002g0020a0002c0002t0002g0024 | 3 | HG02615.hp1 HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1603-3321_1603-330 others(19): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636943 | ||||||
| chr15:44636944
|
A | C | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0085others(3): Show | 6 | HG01515.hp2 HG02040.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603-3307T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636944 | ||||||
| chr15:44636945
|
AAAAAAAA others(6): Show |
A | 2 | a0002c0002t0001g0112a0002c0002t0001g0113 | 2 | NA18986.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1603-3321_1603-330 others(17): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636945 | ||||||
| chr15:44636946
|
A | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0160 | 2 | NA18978.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1603-3309T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636946 | ||||||
| chr15:44636946
|
AAAAAAAA others(5): Show |
A | 2 | a0002c0002t0001g0130a0002c0002t0001g0131 | 2 | HG02148.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1603-3321_1603-331 others(16): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636946 | ||||||
| chr15:44636947
|
AAAAAAAA others(4): Show |
A | 1 | a0002c0002t0001g0154 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1603-3321_1603-331 others(15): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636947 | ||||||
| chr15:44636950
|
A | C | 5 | a0001c0001t0001g0067a0009c0011t0001g0174a0009c0011t0003g0173others(2): Show | 5 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1603-3313T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636950 | ||||||
| chr15:44636957
|
AC | A | 2 | a0001c0001t0001g0073a0018c0023t0001g0175 | 2 | HG02109.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1603-3321delG | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636957 | ||||||
| chr15:44636958
|
C | A | 38 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0056others(35): Show | 38 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1603-3321G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636958 | ||||||
| chr15:44636959
|
A | C | 2 | a0002c0002t0001g0035a0021c0018t0001g0097 | 2 | NA18954.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1603-3322T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44636959 | ||||||
| chr15:44637286
|
C | G | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1603-3649G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44637286 | ||||||
| chr15:44637469
|
T | C | 49 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0049others(46): Show | 49 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.1603-3832A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44637469 | ||||||
| chr15:44637482
|
T | G | 10 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(7): Show | 10 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1603-3845A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44637482 | ||||||
| chr15:44637565
|
C | T | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603-3928G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44637565 | ||||||
| chr15:44637981
|
T | C | 4 | a0009c0011t0001g0174a0009c0011t0003g0173a0010c0010t0001g0181others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-4344A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44637981 | ||||||
| chr15:44638002
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1603-4365T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44638002 | ||||||
| chr15:44638341
|
T | C | 1 | a0002c0002t0001g0121 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1603-4704A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44638341 | ||||||
| chr15:44638401
|
G | A | 34 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1603-4764C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44638401 | ||||||
| chr15:44638492
|
A | C | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1603-4855T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44638492 | ||||||
| chr15:44638496
|
CA | C | 9 | a0001c0001t0001g0082a0002c0002t0001g0017a0002c0002t0001g0025others(6): Show | 9 | HG00621.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1603-4860delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44638496 | ||||||
| chr15:44638500
|
A | AC | 23 | a0001c0001t0001g0055a0001c0001t0001g0142a0001c0001t0001g0144others(20): Show | 23 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1603-4864dupG | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44638500 | ||||||
| chr15:44638500
|
A | C | 10 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0180others(7): Show | 10 | HG02109.hp1 HG02965.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1603-4863T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44638500 | ||||||
| chr15:44638500
|
AC | A | 57 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0049others(54): Show | 57 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1603-4864delG | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44638500 | ||||||
| chr15:44638585
|
C | G | 3 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152 | 3 | HG03516.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1603-4948G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44638585 | ||||||
| chr15:44638636
|
G | A | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1603-4999C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44638636 | ||||||
| chr15:44638762
|
G | A | 34 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1603-5125C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44638762 | ||||||
| chr15:44638994
|
C | CA | 18 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(15): Show | 18 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.1603-5358dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44638994 | ||||||
| chr15:44638994
|
C | CAA | 13 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.1603-5359_1603-535 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44638994 | ||||||
| chr15:44639005
|
T | A | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1603-5368A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639005 | ||||||
| chr15:44639062
|
C | G | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603-5425G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639062 | ||||||
| chr15:44639252
|
A | AAC | 3 | a0001c0001t0001g0081a0001c0001t0001g0111a0025c0027t0001g0140 | 3 | HG02630.hp1 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1603-5617_1603-561 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639252 | ||||||
| chr15:44639252
|
AAC | A | 6 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603-5617_1603-561 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639252 | ||||||
| chr15:44639276
|
T | TAC | 13 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0067others(10): Show | 13 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.1603-5641_1603-564 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639276 | ||||||
| chr15:44639276
|
T | TACAC | 3 | a0001c0001t0001g0072a0001c0001t0001g0096a0002c0002t0001g0109 | 3 | HG03139.hp1 NA18953.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1603-5643_1603-564 others(8): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639276 | ||||||
| chr15:44639276
|
TAC | T | 23 | a0001c0001t0001g0079a0001c0001t0001g0143a0001c0001t0001g0145others(20): Show | 23 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1603-5641_1603-564 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639276 | ||||||
| chr15:44639276
|
TACAC | T | 23 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(20): Show | 23 | HG00621.hp1 HG02040.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1603-5643_1603-564 others(8): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639276 | ||||||
| chr15:44639276
|
TACACAC | T | 19 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(16): Show | 19 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.1603-5645_1603-564 others(10): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639276 | ||||||
| chr15:44639276
|
TACACACA others(1): Show |
T | 8 | a0004c0004t0001g0149a0008c0007t0001g0150a0008c0007t0001g0151others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1603-5647_1603-564 others(12): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639276 | ||||||
| chr15:44639320
|
CAGAG | C | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603-5687_1603-568 others(8): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639320 | ||||||
| chr15:44639385
|
T | C | 32 | a0001c0001t0001g0093a0002c0002t0001g0042a0002c0002t0001g0112others(29): Show | 32 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.1603-5748A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639385 | ||||||
| chr15:44639580
|
G | A | 2 | a0009c0011t0001g0174a0009c0011t0003g0173 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1603-5943C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639580 | ||||||
| chr15:44639609
|
G | C | 1 | a0007c0008t0001g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1603-5972C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639609 | ||||||
| chr15:44639643
|
A | C | 1 | a0003c0003t0001g0003 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1603-6006T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639643 | ||||||
| chr15:44639773
|
A | T | 1 | a0002c0002t0001g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1603-6136T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639773 | ||||||
| chr15:44639824
|
GATTA | G | 2 | a0002c0002t0001g0133a0015c0020t0001g0123 | 2 | HG01069.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1603-6191_1603-618 others(8): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44639824 | ||||||
| chr15:44640015
|
C | T | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1603-6378G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44640015 | ||||||
| chr15:44640052
|
T | C | 1 | a0017c0022t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1603-6415A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44640052 | ||||||
| chr15:44640426
|
C | T | 1 | a0002c0002t0001g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1603-6789G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44640426 | ||||||
| chr15:44640599
|
A | C | 1 | a0002c0002t0001g0117 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1603-6962T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44640599 | ||||||
| chr15:44640677
|
A | C | 1 | a0002c0002t0001g0117 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1603-7040T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44640677 | ||||||
| chr15:44640771
|
G | A | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603-7134C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44640771 | ||||||
| chr15:44640966
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1603-7329C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44640966 | ||||||
| chr15:44641017
|
C | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0074others(2): Show | 5 | NA18965.hp1 NA18967.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603-7380G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641017 | ||||||
| chr15:44641123
|
C | T | 2 | a0002c0002t0001g0117a0002c0002t0001g0122 | 2 | NA18952.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1603-7486G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641123 | ||||||
| chr15:44641288
|
T | C | 1 | a0002c0002t0001g0128 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1602+7578A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641288 | ||||||
| chr15:44641436
|
T | C | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1602+7430A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641436 | ||||||
| chr15:44641586
|
T | TAC | 26 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0053others(23): Show | 26 | HG00140.hp2 HG00408.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1602+7278_1602+727 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641586 | ||||||
| chr15:44641586
|
T | TACAC | 39 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0055others(36): Show | 39 | HG00140.hp1 HG00597.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1602+7276_1602+727 others(8): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641586 | ||||||
| chr15:44641586
|
T | TACACAC | 29 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0041others(26): Show | 29 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1602+7274_1602+727 others(10): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641586 | ||||||
| chr15:44641586
|
T | TACACACA others(1): Show |
9 | a0001c0001t0001g0039a0001c0001t0001g0069a0001c0001t0001g0070others(6): Show | 9 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.1602+7272_1602+727 others(12): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641586 | ||||||
| chr15:44641586
|
T | TACACACA others(3): Show |
5 | a0001c0001t0001g0057a0001c0001t0001g0071a0001c0001t0001g0100others(2): Show | 5 | HG00597.hp1 HG02895.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602+7270_1602+727 others(14): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641586 | ||||||
| chr15:44641586
|
T | TACACACA others(5): Show |
1 | a0002c0002t0001g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1602+7268_1602+727 others(16): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641586 | ||||||
| chr15:44641586
|
TAC | T | 12 | a0001c0001t0001g0101a0002c0002t0001g0025a0002c0002t0001g0028others(9): Show | 12 | HG00609.hp1 HG01123.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1602+7278_1602+727 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641586 | ||||||
| chr15:44641586
|
TACAC | T | 3 | a0004c0004t0001g0158a0007c0008t0001g0186a0007c0008t0001g0187 | 3 | HG02572.hp1 HG03486.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1602+7276_1602+727 others(8): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641586 | ||||||
| chr15:44641586
|
TACACAC | T | 14 | a0001c0001t0001g0078a0004c0004t0001g0149a0004c0004t0001g0164others(11): Show | 14 | HG02040.hp1 HG02055.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.1602+7274_1602+727 others(10): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641586 | ||||||
| chr15:44641586
|
TACACACA others(1): Show |
T | 2 | a0002c0002t0001g0027a0002c0002t0002g0020 | 2 | HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1602+7272_1602+727 others(12): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641586 | ||||||
| chr15:44641586
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0077 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1602+7268_1602+727 others(16): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641586 | ||||||
| chr15:44641586
|
TACACACA others(11): Show |
T | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1602+7262_1602+727 others(22): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641586 | ||||||
| chr15:44641586
|
TACACACA others(23): Show |
T | 1 | a0009c0011t0001g0174 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1602+7250_1602+727 others(34): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641586 | ||||||
| chr15:44641863
|
G | A | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1602+7003C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641863 | ||||||
| chr15:44641922
|
G | GA | 36 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0144others(33): Show | 36 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.1602+6943dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641922 | ||||||
| chr15:44641922
|
G | GAA | 17 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(14): Show | 17 | HG02040.hp1 HG02109.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.1602+6942_1602+694 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641922 | ||||||
| chr15:44641922
|
GA | G | 8 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0072others(5): Show | 8 | HG02109.hp2 NA18955.hp1 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1602+6943delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641922 | ||||||
| chr15:44641972
|
A | G | 1 | a0009c0011t0003g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1602+6894T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641972 | ||||||
| chr15:44641983
|
T | C | 2 | a0003c0003t0001g0008a0003c0003t0001g0009 | 2 | NA18953.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1602+6883A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641983 | ||||||
| chr15:44641997
|
G | A | 1 | a0002c0002t0001g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1602+6869C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44641997 | ||||||
| chr15:44642020
|
G | A | 4 | a0007c0008t0001g0186a0007c0008t0001g0187a0007c0008t0001g0188others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602+6846C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642020 | ||||||
| chr15:44642057
|
T | G | 2 | a0002c0002t0001g0116a0002c0002t0001g0132 | 2 | HG03471.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1602+6809A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642057 | ||||||
| chr15:44642163
|
C | T | 34 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1602+6703G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642163 | ||||||
| chr15:44642189
|
A | T | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1602+6677T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642189 | ||||||
| chr15:44642280
|
A | G | 34 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1602+6586T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642280 | ||||||
| chr15:44642287
|
C | T | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1602+6579G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642287 | ||||||
| chr15:44642364
|
C | CA | 30 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(27): Show | 30 | HG00621.hp2 HG02040.hp1 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.1602+6501dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642364 | ||||||
| chr15:44642364
|
CA | C | 5 | a0002c0002t0001g0029a0007c0008t0001g0186a0007c0008t0001g0187others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602+6501delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642364 | ||||||
| chr15:44642425
|
A | C | 3 | a0005c0005t0001g0146a0005c0005t0001g0147a0005c0005t0001g0148 | 3 | HG02257.hp2 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1602+6441T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642425 | ||||||
| chr15:44642443
|
TAC | T | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602+6421_1602+642 others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642443 | ||||||
| chr15:44642445
|
C | T | 1 | a0002c0002t0001g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1602+6421G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642445 | ||||||
| chr15:44642697
|
C | CA | 12 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(9): Show | 12 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.1602+6168dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642697 | ||||||
| chr15:44642709
|
A | AT | 4 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(1): Show | 4 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602+6156_1602+615 others(5): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642709 | ||||||
| chr15:44642709
|
A | T | 8 | a0001c0001t0001g0057a0002c0002t0001g0018a0002c0002t0002g0019others(5): Show | 8 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1602+6157T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642709 | ||||||
| chr15:44642838
|
C | T | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1602+6028G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642838 | ||||||
| chr15:44642933
|
G | A | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1602+5933C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642933 | ||||||
| chr15:44642954
|
T | C | 4 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(1): Show | 4 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602+5912A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44642954 | ||||||
| chr15:44643017
|
G | C | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602+5849C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44643017 | ||||||
| chr15:44643092
|
T | C | 4 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(1): Show | 4 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602+5774A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44643092 | ||||||
| chr15:44643429
|
A | G | 1 | a0002c0002t0001g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1602+5437T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44643429 | ||||||
| chr15:44643471
|
G | C | 2 | a0003c0003t0001g0010a0003c0003t0001g0011 | 2 | HG00408.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1602+5395C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44643471 | ||||||
| chr15:44643597
|
C | G | 1 | a0002c0002t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1602+5269G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44643597 | ||||||
| chr15:44643659
|
C | T | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1602+5207G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44643659 | ||||||
| chr15:44643698
|
A | G | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1602+5168T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44643698 | ||||||
| chr15:44643746
|
A | G | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1602+5120T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44643746 | ||||||
| chr15:44643768
|
C | T | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602+5098G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44643768 | ||||||
| chr15:44643906
|
G | GT | 15 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(12): Show | 15 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1602+4959dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44643906 | ||||||
| chr15:44643980
|
G | A | 15 | a0003c0003t0001g0002a0003c0003t0001g0003a0003c0003t0001g0004others(12): Show | 15 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.1602+4886C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44643980 | ||||||
| chr15:44643987
|
C | T | 7 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602+4879G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44643987 | ||||||
| chr15:44644166
|
C | CA | 18 | a0001c0001t0001g0107a0001c0001t0001g0142a0003c0003t0001g0003others(15): Show | 18 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.1602+4699dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644166 | ||||||
| chr15:44644166
|
CA | C | 5 | a0001c0001t0001g0041a0002c0002t0001g0117a0002c0002t0001g0153others(2): Show | 5 | HG01071.hp2 HG02055.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602+4699delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644166 | ||||||
| chr15:44644202
|
T | A | 4 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(1): Show | 4 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602+4664A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644202 | ||||||
| chr15:44644342
|
G | C | 3 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152 | 3 | HG03516.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1602+4524C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644342 | ||||||
| chr15:44644381
|
T | C | 1 | a0002c0002t0001g0138 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1602+4485A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644381 | ||||||
| chr15:44644465
|
T | A | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1602+4401A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644465 | ||||||
| chr15:44644584
|
C | T | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1602+4282G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644584 | ||||||
| chr15:44644773
|
T | C | 1 | a0004c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1602+4093A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644773 | ||||||
| chr15:44644776
|
A | T | 1 | a0004c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1602+4090T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644776 | ||||||
| chr15:44644777
|
C | A | 1 | a0004c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1602+4089G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644777 | ||||||
| chr15:44644778
|
C | G | 1 | a0004c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1602+4088G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644778 | ||||||
| chr15:44644780
|
A | T | 1 | a0004c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1602+4086T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644780 | ||||||
| chr15:44644782
|
A | G | 1 | a0004c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1602+4084T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644782 | ||||||
| chr15:44644783
|
A | C | 1 | a0004c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1602+4083T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644783 | ||||||
| chr15:44644784
|
C | G | 1 | a0004c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1602+4082G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644784 | ||||||
| chr15:44644785
|
A | T | 1 | a0004c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1602+4081T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644785 | ||||||
| chr15:44644786
|
T | G | 1 | a0004c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1602+4080A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644786 | ||||||
| chr15:44644788
|
C | T | 1 | a0004c0004t0001g0170 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1602+4078G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644788 | ||||||
| chr15:44644877
|
G | T | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | HG00438.hp1 HG01981.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1602+3989C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44644877 | ||||||
| chr15:44645146
|
A | C | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1602+3720T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44645146 | ||||||
| chr15:44645219
|
T | C | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1602+3647A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44645219 | ||||||
| chr15:44645239
|
CA | C | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1602+3626delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44645239 | ||||||
| chr15:44645282
|
T | C | 15 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(12): Show | 15 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1602+3584A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44645282 | ||||||
| chr15:44645348
|
G | C | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1602+3518C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44645348 | ||||||
| chr15:44645392
|
T | C | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1602+3474A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44645392 | ||||||
| chr15:44645452
|
C | T | 38 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(35): Show | 38 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1602+3414G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44645452 | ||||||
| chr15:44645528
|
T | C | 1 | a0002c0002t0001g0135 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1602+3338A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44645528 | ||||||
| chr15:44645606
|
A | G | 1 | a0003c0003t0001g0001 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1602+3260T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44645606 | ||||||
| chr15:44645725
|
G | A | 4 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(1): Show | 4 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602+3141C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44645725 | ||||||
| chr15:44645843
|
A | C | 6 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1602+3023T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44645843 | ||||||
| chr15:44645871
|
A | G | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1602+2995T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44645871 | ||||||
| chr15:44646334
|
C | T | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1602+2532G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44646334 | ||||||
| chr15:44646344
|
T | C | 69 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0025others(66): Show | 69 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1602+2522A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44646344 | ||||||
| chr15:44646568
|
G | C | 4 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602+2298C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44646568 | ||||||
| chr15:44646598
|
T | C | 34 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1602+2268A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44646598 | ||||||
| chr15:44646757
|
A | G | 1 | a0002c0021t0001g0139 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1602+2109T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44646757 | ||||||
| chr15:44646883
|
T | C | 1 | a0025c0027t0001g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1602+1983A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44646883 | ||||||
| chr15:44646949
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1602+1917G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44646949 | ||||||
| chr15:44647127
|
T | C | 7 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602+1739A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44647127 | ||||||
| chr15:44647365
|
T | C | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1602+1501A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44647365 | ||||||
| chr15:44647866
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1602+1000A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44647866 | ||||||
| chr15:44648130
|
C | T | 1 | a0002c0002t0001g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1602+736G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44648130 | ||||||
| chr15:44648293
|
T | C | 10 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(7): Show | 10 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1602+573A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44648293 | ||||||
| chr15:44648512
|
C | CA | 18 | a0001c0001t0001g0162a0001c0016t0001g0108a0002c0002t0001g0027others(15): Show | 18 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.1602+353dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44648512 | ||||||
| chr15:44648512
|
CA | C | 15 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0066others(12): Show | 15 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1602+353delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44648512 | ||||||
| chr15:44648745
|
T | C | 1 | a0004c0004t0001g0169 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1602+121A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 7/39 | chr15 | 44648745 | ||||||
| chr15:44649086
|
A | G | 2 | a0009c0011t0001g0174a0009c0011t0003g0173 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1457-75T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44649086 | ||||||
| chr15:44649331
|
T | C | 1 | a0002c0002t0001g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1457-320A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44649331 | ||||||
| chr15:44649398
|
A | T | 1 | a0002c0002t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1457-387T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44649398 | ||||||
| chr15:44649455
|
A | G | 7 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1457-444T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44649455 | ||||||
| chr15:44649665
|
G | GCAGACCA | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1457-661_1457-655d others(9): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44649665 | ||||||
| chr15:44649848
|
C | G | 1 | a0005c0005t0001g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1457-837G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44649848 | ||||||
| chr15:44649855
|
T | C | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1457-844A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44649855 | ||||||
| chr15:44649894
|
C | CA | 15 | a0001c0001t0001g0040a0004c0004t0001g0149a0004c0004t0001g0158others(12): Show | 15 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.1457-884dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44649894 | ||||||
| chr15:44650004
|
T | C | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1457-993A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44650004 | ||||||
| chr15:44650131
|
G | A | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1457-1120C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44650131 | ||||||
| chr15:44650256
|
C | T | 2 | a0008c0007t0001g0151a0008c0007t0001g0152 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1456+1235G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44650256 | ||||||
| chr15:44650329
|
G | A | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1456+1162C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44650329 | ||||||
| chr15:44650340
|
G | C | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1456+1151C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44650340 | ||||||
| chr15:44650405
|
A | G | 42 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(39): Show | 42 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1456+1086T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44650405 | ||||||
| chr15:44650475
|
G | A | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1456+1016C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44650475 | ||||||
| chr15:44650558
|
G | A | 5 | a0004c0004t0001g0166a0004c0004t0001g0167a0004c0004t0001g0168others(2): Show | 5 | HG02040.hp1 HG02523.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1456+933C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44650558 | ||||||
| chr15:44650624
|
TA | T | 18 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(15): Show | 18 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.1456+866delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44650624 | ||||||
| chr15:44650655
|
A | G | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1456+836T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44650655 | ||||||
| chr15:44650711
|
T | C | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1456+780A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44650711 | ||||||
| chr15:44650751
|
A | G | 17 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(14): Show | 17 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1456+740T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44650751 | ||||||
| chr15:44650896
|
G | A | 28 | a0002c0002t0001g0042a0002c0002t0001g0112a0002c0002t0001g0113others(25): Show | 28 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.1456+595C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44650896 | ||||||
| chr15:44651028
|
G | A | 14 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(11): Show | 14 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1456+463C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44651028 | ||||||
| chr15:44651216
|
G | T | 1 | a0020c0017t0001g0065 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1456+275C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44651216 | ||||||
| chr15:44651232
|
T | C | 3 | a0005c0005t0001g0146a0005c0005t0001g0147a0005c0005t0001g0148 | 3 | HG02257.hp2 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1456+259A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44651232 | ||||||
| chr15:44651377
|
T | A | 6 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1456+114A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 6/39 | chr15 | 44651377 | ||||||
| chr15:44651962
|
CTT | C | 6 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1008-25_1008-24del others(2): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 5/39 | chr15 | 44651962 | ||||||
| chr15:44652026
|
A | G | 70 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0025others(67): Show | 70 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1008-87T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 5/39 | chr15 | 44652026 | ||||||
| chr15:44652073
|
C | G | 7 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007+56G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 5/39 | chr15 | 44652073 | ||||||
| chr15:44652371
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.870-105A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44652371 | ||||||
| chr15:44652420
|
C | T | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.870-154G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44652420 | ||||||
| chr15:44652473
|
T | C | 4 | a0009c0011t0001g0174a0009c0011t0003g0173a0010c0010t0001g0181others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-207A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44652473 | ||||||
| chr15:44652519
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.870-253G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44652519 | ||||||
| chr15:44652637
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.870-371G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44652637 | ||||||
| chr15:44652658
|
C | CT | 28 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0051others(25): Show | 28 | HG01981.hp2 HG02055.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.870-393dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44652658 | ||||||
| chr15:44652715
|
C | T | 1 | a0002c0002t0001g0116 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.870-449G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44652715 | ||||||
| chr15:44652972
|
C | T | 3 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp1 HG03017.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.870-706G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44652972 | ||||||
| chr15:44653077
|
C | T | 6 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.870-811G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44653077 | ||||||
| chr15:44653592
|
TAGTTC | T | 14 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(11): Show | 14 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.870-1331_870-1327d others(7): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44653592 | ||||||
| chr15:44653680
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.870-1414A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44653680 | ||||||
| chr15:44653754
|
A | C | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.870-1488T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44653754 | ||||||
| chr15:44653882
|
T | C | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.870-1616A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44653882 | ||||||
| chr15:44654070
|
C | T | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.870-1804G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44654070 | ||||||
| chr15:44654149
|
T | C | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.870-1883A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44654149 | ||||||
| chr15:44654249
|
T | C | 161 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.870-1983A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44654249 | ||||||
| chr15:44654260
|
AG | A | 17 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(14): Show | 17 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.870-1995delC | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44654260 | ||||||
| chr15:44654327
|
T | C | 17 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(14): Show | 17 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.870-2061A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44654327 | ||||||
| chr15:44654440
|
G | A | 1 | a0002c0002t0001g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.870-2174C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44654440 | ||||||
| chr15:44654497
|
G | A | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.870-2231C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44654497 | ||||||
| chr15:44654531
|
C | T | 18 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(15): Show | 18 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.870-2265G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44654531 | ||||||
| chr15:44654535
|
CTTA | C | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.870-2272_870-2270d others(5): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44654535 | ||||||
| chr15:44654630
|
A | C | 1 | a0008c0007t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.870-2364T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44654630 | ||||||
| chr15:44654843
|
GA | G | 10 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0051others(7): Show | 10 | HG01981.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.869+2251delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44654843 | ||||||
| chr15:44654914
|
C | T | 8 | a0004c0004t0001g0149a0004c0004t0001g0164a0004c0004t0001g0165others(5): Show | 8 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.869+2181G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44654914 | ||||||
| chr15:44654915
|
G | A | 1 | a0003c0003t0001g0001 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.869+2180C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44654915 | ||||||
| chr15:44655236
|
T | C | 2 | a0002c0002t0001g0137a0002c0002t0001g0138 | 2 | HG01106.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.869+1859A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44655236 | ||||||
| chr15:44655404
|
G | C | 6 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.869+1691C>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44655404 | ||||||
| chr15:44655473
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.869+1622G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44655473 | ||||||
| chr15:44655624
|
T | TA | 18 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(15): Show | 18 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.869+1470dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44655624 | ||||||
| chr15:44655632
|
A | G | 1 | a0016c0019t0001g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.869+1463T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44655632 | ||||||
| chr15:44655659
|
C | T | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.869+1436G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44655659 | ||||||
| chr15:44655870
|
A | G | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.869+1225T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44655870 | ||||||
| chr15:44656082
|
G | A | 1 | a0002c0021t0001g0139 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.869+1013C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44656082 | ||||||
| chr15:44656104
|
G | A | 7 | a0005c0005t0001g0031a0005c0005t0001g0032a0005c0005t0001g0033others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.869+991C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44656104 | ||||||
| chr15:44656132
|
A | T | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.869+963T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44656132 | ||||||
| chr15:44656457
|
G | A | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02970.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.869+638C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44656457 | ||||||
| chr15:44656626
|
C | T | 1 | a0005c0005t0001g0146 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.869+469G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44656626 | ||||||
| chr15:44656721
|
C | T | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.869+374G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44656721 | ||||||
| chr15:44656858
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.869+237G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44656858 | ||||||
| chr15:44657040
|
C | A | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.869+55G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 4/39 | chr15 | 44657040 | ||||||
| chr15:44657459
|
A | C | 1 | a0018c0023t0001g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.668-163T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44657459 | ||||||
| chr15:44657509
|
C | T | 1 | a0017c0022t0001g0114 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.668-213G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44657509 | ||||||
| chr15:44657625
|
A | G | 2 | a0002c0002t0001g0112a0002c0002t0001g0113 | 2 | NA18986.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.668-329T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44657625 | ||||||
| chr15:44657899
|
T | C | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.668-603A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44657899 | ||||||
| chr15:44658115
|
C | T | 13 | a0004c0004t0001g0149a0004c0004t0001g0158a0004c0004t0001g0164others(10): Show | 13 | HG02040.hp1 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.668-819G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44658115 | ||||||
| chr15:44658248
|
T | C | 18 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(15): Show | 18 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.667+831A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44658248 | ||||||
| chr15:44658364
|
C | T | 20 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(17): Show | 20 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.667+715G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44658364 | ||||||
| chr15:44658461
|
C | CT | 21 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(18): Show | 21 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.667+617dupA | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44658461 | ||||||
| chr15:44658584
|
G | A | 2 | a0010c0010t0001g0181a0010c0010t0001g0184 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.667+495C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44658584 | ||||||
| chr15:44658616
|
G | T | 14 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(11): Show | 14 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.667+463C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44658616 | ||||||
| chr15:44658739
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.667+340C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44658739 | ||||||
| chr15:44658845
|
T | C | 3 | a0008c0007t0001g0151a0008c0007t0001g0152a0018c0023t0001g0175 | 3 | HG02109.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.667+234A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44658845 | ||||||
| chr15:44658975
|
C | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.667+104G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44658975 | ||||||
| chr15:44658976
|
A | G | 158 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(155): Show | 158 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.667+103T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 3/39 | chr15 | 44658976 | ||||||
| chr15:44659482
|
G | A | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.443-179C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 2/39 | chr15 | 44659482 | ||||||
| chr15:44659515
|
C | G | 14 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(11): Show | 14 | HG00621.hp1 HG01496.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.443-212G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 2/39 | chr15 | 44659515 | ||||||
| chr15:44659619
|
A | C | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.443-316T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 2/39 | chr15 | 44659619 | ||||||
| chr15:44659717
|
G | A | 10 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(7): Show | 10 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.443-414C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 2/39 | chr15 | 44659717 | ||||||
| chr15:44659741
|
T | C | 4 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(1): Show | 4 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-438A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 2/39 | chr15 | 44659741 | ||||||
| chr15:44659831
|
T | C | 4 | a0003c0003t0001g0012a0003c0003t0001g0013a0003c0003t0001g0014others(1): Show | 4 | HG00673.hp2 NA18949.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.443-528A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 2/39 | chr15 | 44659831 | ||||||
| chr15:44659881
|
C | A | 1 | a0009c0011t0001g0174 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.442+551G>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 2/39 | chr15 | 44659881 | ||||||
| chr15:44659927
|
G | A | 1 | a0007c0008t0001g0188 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.442+505C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 2/39 | chr15 | 44659927 | ||||||
| chr15:44660048
|
G | A | 4 | a0008c0007t0001g0150a0008c0007t0001g0151a0008c0007t0001g0152others(1): Show | 4 | HG02109.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+384C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 2/39 | chr15 | 44660048 | ||||||
| chr15:44660271
|
T | C | 1 | a0013c0026t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+161A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 2/39 | chr15 | 44660271 | ||||||
| chr15:44660333
|
G | A | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.442+99C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 2/39 | chr15 | 44660333 | ||||||
| chr15:44660383
|
G | T | 1 | a0002c0002t0001g0017 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.442+49C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 2/39 | chr15 | 44660383 | ||||||
| chr15:44660621
|
GA | G | 6 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.258-6delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44660621 | ||||||
| chr15:44660665
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.258-49A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44660665 | ||||||
| chr15:44660709
|
A | G | 1 | a0010c0010t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.258-93T>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44660709 | ||||||
| chr15:44660729
|
G | T | 69 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0025others(66): Show | 69 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.258-113C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44660729 | ||||||
| chr15:44660974
|
T | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02970.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-358A>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44660974 | ||||||
| chr15:44661007
|
T | TA | 6 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-392dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44661007 | ||||||
| chr15:44661244
|
G | A | 69 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0025others(66): Show | 69 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.258-628C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44661244 | ||||||
| chr15:44661832
|
T | A | 1 | a0002c0002t0001g0153 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.258-1216A>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44661832 | ||||||
| chr15:44661868
|
A | T | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.258-1252T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44661868 | ||||||
| chr15:44661896
|
T | C | 1 | a0002c0002t0001g0035 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.258-1280A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44661896 | ||||||
| chr15:44661944
|
T | C | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-1328A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44661944 | ||||||
| chr15:44661962
|
C | T | 1 | a0002c0002t0002g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.258-1346G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44661962 | ||||||
| chr15:44661989
|
C | G | 1 | a0002c0002t0001g0045 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.258-1373G>C | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44661989 | ||||||
| chr15:44662077
|
T | C | 1 | a0002c0002t0001g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.257+1314A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44662077 | ||||||
| chr15:44662145
|
T | C | 1 | a0002c0002t0001g0154 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.257+1246A>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44662145 | ||||||
| chr15:44662254
|
G | T | 188 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(185): Show | 188 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.257+1137C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44662254 | ||||||
| chr15:44662285
|
G | T | 34 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.257+1106C>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44662285 | ||||||
| chr15:44662288
|
AGAGGAGC others(2): Show |
A | 34 | a0002c0002t0001g0018a0002c0002t0001g0176a0002c0002t0001g0177others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.257+1094_257+1102d others(11): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44662288 | ||||||
| chr15:44662339
|
TAAAG | T | 6 | a0002c0002t0001g0176a0002c0002t0001g0177a0006c0006t0001g0043others(3): Show | 6 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+1048_257+1051d others(6): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44662339 | ||||||
| chr15:44662458
|
A | C | 1 | a0002c0002t0001g0042 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.257+933T>G | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44662458 | ||||||
| chr15:44662567
|
C | T | 1 | a0004c0004t0001g0158 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.257+824G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44662567 | ||||||
| chr15:44662650
|
T | TA | 31 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(28): Show | 31 | HG00408.hp1 HG00597.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.257+740dupT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44662650 | ||||||
| chr15:44662650
|
T | TAA | 16 | a0001c0001t0001g0180a0002c0002t0001g0018a0002c0002t0001g0176others(13): Show | 16 | HG00423.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.257+739_257+740dup others(2): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44662650 | ||||||
| chr15:44662650
|
T | TAAAA | 6 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0021others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+737_257+740dup others(4): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44662650 | ||||||
| chr15:44662650
|
TA | T | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG01069.hp1 HG02572.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+740delT | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44662650 | ||||||
| chr15:44662650
|
TAAAAAAA others(3): Show |
T | 12 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0026others(9): Show | 12 | HG00621.hp1 HG01496.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.257+731_257+740del others(10): Show |
SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44662650 | ||||||
| chr15:44663047
|
G | A | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+344C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44663047 | ||||||
| chr15:44663115
|
C | T | 7 | a0002c0002t0001g0018a0002c0002t0002g0019a0002c0002t0002g0020others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+276G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44663115 | ||||||
| chr15:44663180
|
G | A | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.257+211C>T | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44663180 | ||||||
| chr15:44663301
|
A | T | 1 | a0002c0002t0001g0017 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.257+90T>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44663301 | ||||||
| chr15:44663356
|
C | T | 16 | a0003c0003t0001g0001a0003c0003t0001g0002a0003c0003t0001g0003others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.257+35G>A | SPG11 | ENSG00000104133.16 | transcript | ENST00000261866.12 | protein_coding | 1/39 | chr15 | 44663356 |