| geneid | 6585 |
|---|---|
| ensemblid | ENSG00000187122.17 |
| hgncid | 11085 |
| symbol | SLIT1 |
| name | slit guidance ligand 1 |
| refseq_nuc | NM_003061.3 |
| refseq_prot | NP_003052.2 |
| ensembl_nuc | ENST00000266058.9 |
| ensembl_prot | ENSP00000266058.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 96998038 |
| end | 97185959 |
| strand | - |
| ver | v1.2 |
| region | chr10:96998038-97185959 |
| region5000 | chr10:96993038-97190959 |
| regionname0 | SLIT1_chr10_96998038_97185959 |
| regionname5000 | SLIT1_chr10_96993038_97190959 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1534 | 247 | 87 | 38 | 80 | 8 | 32 | 54 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0002 | 0/0 | 1534 | 4 | 0 | 2 | 0 | 2 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0003 | 0/0 | 1534 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0004 | 0/0 | 1534 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0005 | 0/0 | 1534 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0006 | 0/0 | 1534 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0007 | 0/0 | 1534 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| 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 | 4605 | 132 | 42 | 17 | 54 | 5 | 14 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0002 | 0/0 | 4605 | 23 | 1 | 3 | 13 | 0 | 6 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0003 | 0/1 | 4605 | 22 | 9 | 5 | 1 | 3 | 3 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0004 | 0/0 | 4605 | 18 | 1 | 7 | 8 | 0 | 2 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0005 | 1/0 | 4605 | 9 | 6 | 2 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0006 | 0/0 | 4605 | 7 | 6 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0007 | 0/0 | 4605 | 6 | 6 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0008 | 0/0 | 4605 | 5 | 5 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0009 | 0/0 | 4605 | 5 | 1 | 2 | 0 | 0 | 2 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0010 | 0/0 | 4605 | 3 | 0 | 0 | 0 | 0 | 3 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0011 | 0/0 | 4605 | 2 | 2 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0012 | 0/0 | 4605 | 2 | 0 | 0 | 2 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0013 | 0/0 | 4605 | 2 | 0 | 0 | 0 | 2 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0014 | 0/0 | 4605 | 2 | 0 | 2 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0015 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0016 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0017 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0018 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0019 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0020 | 0/0 | 4605 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0021 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0022 | 0/0 | 4605 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0023 | 0/0 | 4605 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0024 | 0/0 | 4605 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0025 | 0/0 | 4605 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0026 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0027 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0028 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0029 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0030 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0031 | 0/0 | 4605 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| c0032 | 0/0 | 4605 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| 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 | 3360 | 162 | 48 | 30 | 56 | 4 | 22 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0002 | 0/0 | 3367 | 35 | 6 | 3 | 20 | 0 | 6 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0003 | 0/0 | 3364 | 10 | 9 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0004 | 0/0 | 3360 | 7 | 7 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0005 | 0/0 | 3360 | 6 | 0 | 2 | 0 | 2 | 2 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0006 | 0/0 | 3363 | 5 | 0 | 1 | 0 | 4 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0007 | 0/0 | 3360 | 3 | 2 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0008 | 0/0 | 3363 | 3 | 3 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0009 | 0/0 | 3364 | 3 | 3 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0010 | 0/0 | 3367 | 2 | 0 | 0 | 2 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0011 | 0/0 | 3364 | 2 | 2 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0012 | 0/0 | 3360 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0013 | 0/0 | 3360 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0014 | 0/0 | 3360 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0015 | 0/0 | 3360 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0016 | 0/0 | 3367 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0017 | 0/0 | 3367 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0018 | 0/0 | 3367 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0019 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0020 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0021 | 0/0 | 3360 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0022 | 0/0 | 3360 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0023 | 0/0 | 3360 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0024 | 0/0 | 3360 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0025 | 0/0 | 3364 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0026 | 0/0 | 3360 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0027 | 0/0 | 3360 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0028 | 0/0 | 3360 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| t0029 | 0/0 | 3360 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0191 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| 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 | 4605 | 132 | 42 | 17 | 54 | 5 | 14 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0002 | 0/0 | 4605 | 23 | 1 | 3 | 13 | 0 | 6 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0003 | 0/1 | 4605 | 22 | 9 | 5 | 1 | 3 | 3 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0004 | 0/0 | 4605 | 18 | 1 | 7 | 8 | 0 | 2 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0005 | 1/0 | 4605 | 9 | 6 | 2 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0006 | 0/0 | 4605 | 7 | 6 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0007 | 0/0 | 4605 | 6 | 6 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0008 | 0/0 | 4605 | 5 | 5 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0009 | 0/0 | 4605 | 5 | 1 | 2 | 0 | 0 | 2 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0010 | 0/0 | 4605 | 3 | 0 | 0 | 0 | 0 | 3 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0011 | 0/0 | 4605 | 2 | 2 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0012 | 0/0 | 4605 | 2 | 0 | 0 | 2 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0015 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0016 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0017 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0018 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0019 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0020 | 0/0 | 4605 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0021 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0022 | 0/0 | 4605 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0023 | 0/0 | 4605 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0024 | 0/0 | 4605 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0026 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0030 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0032 | 0/0 | 4605 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0002c0013 | 0/0 | 4605 | 2 | 0 | 0 | 0 | 2 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0002c0014 | 0/0 | 4605 | 2 | 0 | 2 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0003c0029 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0004c0028 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0005c0025 | 0/0 | 4605 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0006c0027 | 0/0 | 4605 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0007c0031 | 0/0 | 4605 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7964 | 87 | 26 | 13 | 35 | 3 | 10 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0002 | 0/0 | 7971 | 19 | 3 | 1 | 13 | 0 | 2 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0003 | 0/0 | 7968 | 3 | 2 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0004 | 0/0 | 7964 | 4 | 4 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0005 | 0/0 | 7964 | 3 | 0 | 1 | 0 | 1 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0006 | 0/0 | 7967 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0010 | 0/0 | 7971 | 2 | 0 | 0 | 2 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0011 | 0/0 | 7968 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0013 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0016 | 0/0 | 7971 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0017 | 0/0 | 7971 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0018 | 0/0 | 7971 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0019 | 0/0 | 7964 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0020 | 0/0 | 7964 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0021 | 0/0 | 7964 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0022 | 0/0 | 7964 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0023 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0024 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0028 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0001t0029 | 0/0 | 7964 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0002t0001 | 0/0 | 7964 | 17 | 1 | 2 | 9 | 0 | 5 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0002t0002 | 0/0 | 7971 | 5 | 0 | 1 | 4 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0002t0012 | 0/0 | 7964 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0003t0001 | 0/1 | 7964 | 14 | 5 | 4 | 1 | 1 | 2 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0003t0002 | 0/0 | 7971 | 2 | 1 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0003t0005 | 0/0 | 7964 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0003t0006 | 0/0 | 7967 | 2 | 0 | 1 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0003t0011 | 0/0 | 7968 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0003t0015 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0003t0026 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0004t0001 | 0/0 | 7964 | 17 | 0 | 7 | 8 | 0 | 2 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0004t0003 | 0/0 | 7968 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0005t0001 | 1/0 | 7964 | 6 | 3 | 2 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0005t0002 | 0/0 | 7971 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0005t0004 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0005t0009 | 0/0 | 7968 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0006t0001 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0006t0004 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0006t0007 | 0/0 | 7964 | 3 | 2 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0006t0009 | 0/0 | 7968 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0006t0014 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0007t0001 | 0/0 | 7964 | 5 | 5 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0007t0003 | 0/0 | 7968 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0008t0003 | 0/0 | 7968 | 5 | 5 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0009t0001 | 0/0 | 7964 | 2 | 1 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0009t0005 | 0/0 | 7964 | 2 | 0 | 1 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0009t0027 | 0/0 | 7964 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0010t0002 | 0/0 | 7971 | 3 | 0 | 0 | 0 | 0 | 3 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0011t0001 | 0/0 | 7964 | 2 | 2 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0012t0001 | 0/0 | 7964 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0012t0002 | 0/0 | 7971 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0015t0001 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0016t0001 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0017t0008 | 0/0 | 7967 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0018t0009 | 0/0 | 7968 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0019t0008 | 0/0 | 7967 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0020t0001 | 0/0 | 7964 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0021t0008 | 0/0 | 7967 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0022t0002 | 0/0 | 7971 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0023t0002 | 0/0 | 7971 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0024t0001 | 0/0 | 7964 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0026t0004 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0030t0001 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0001c0032t0001 | 0/0 | 7964 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0002c0013t0006 | 0/0 | 7967 | 2 | 0 | 0 | 0 | 2 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0002c0014t0001 | 0/0 | 7964 | 2 | 0 | 2 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0003c0029t0002 | 0/0 | 7971 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0004c0028t0001 | 0/0 | 7964 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0005c0025t0002 | 0/0 | 7971 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0006c0027t0025 | 0/0 | 7968 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| a0007c0031t0001 | 0/0 | 7964 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | copy fasta | chr10 | 96993038 | 97190959 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0010g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0010g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0013g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0016g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0017g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0018g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0019g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0020g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0021g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0022g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0023g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0024g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0028g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0001t0029g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0002t0012g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0006g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0006g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0015g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0003t0026g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0004t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0005t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0005t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0005t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0005t0001g0191 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0005t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0005t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0005t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0005t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0006t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0006t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0006t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0006t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0006t0007g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0006t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0006t0014g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0007t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0007t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0007t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0007t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0007t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0007t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0008t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0008t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0008t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0008t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0008t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0009t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0009t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0009t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0009t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0009t0027g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0010t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0010t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0010t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0011t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0011t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0012t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0012t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0015t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0016t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0017t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0018t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0019t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0020t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0021t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0022t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0023t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0024t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0026t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0030t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0001c0032t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0002c0013t0006g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0002c0013t0006g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0002c0014t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0002c0014t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0003c0029t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0004c0028t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0005c0025t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0006c0027t0025g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| a0007c0031t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0006 | g0036 | EUR | GBR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00140 | hp2 | a0001 | c0003 | t0005 | g0183 | EUR | GBR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | FIN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0139 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00544 | hp2 | a0001 | c0001 | t0019 | g0155 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00558 | hp1 | a0001 | c0004 | t0001 | g0044 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00597 | hp1 | a0001 | c0032 | t0001 | g0061 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00642 | hp1 | a0001 | c0023 | t0002 | g0146 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0255 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00735 | hp2 | a0001 | c0001 | t0022 | g0254 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00738 | hp2 | a0001 | c0003 | t0006 | g0190 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00741 | hp1 | a0001 | c0004 | t0001 | g0166 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01070 | hp1 | a0001 | c0009 | t0005 | g0032 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01070 | hp2 | a0001 | c0004 | t0001 | g0075 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0076 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01081 | hp1 | a0001 | c0005 | t0001 | g0192 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01081 | hp2 | a0001 | c0004 | t0001 | g0165 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01106 | hp1 | a0001 | c0009 | t0027 | g0223 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01106 | hp2 | a0001 | c0004 | t0001 | g0065 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01109 | hp2 | a0001 | c0006 | t0007 | g0209 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0212 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01243 | hp1 | a0001 | c0005 | t0001 | g0005 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0126 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01257 | hp2 | a0001 | c0004 | t0001 | g0127 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01258 | hp2 | a0001 | c0004 | t0001 | g0074 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01261 | hp1 | a0002 | c0014 | t0001 | g0202 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0171 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0230 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01361 | hp2 | a0002 | c0014 | t0001 | g0227 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01433 | hp2 | a0001 | c0001 | t0021 | g0031 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01515 | hp1 | a0002 | c0013 | t0006 | g0029 | EUR | IBS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | IBS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01517 | hp1 | a0002 | c0013 | t0006 | g0030 | EUR | IBS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0240 | EUR | IBS | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01884 | hp1 | a0001 | c0003 | t0011 | g0012 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01891 | hp1 | a0001 | c0016 | t0001 | g0159 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | PEL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02055 | hp1 | a0001 | c0007 | t0001 | g0248 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02055 | hp2 | a0001 | c0009 | t0001 | g0239 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02071 | hp1 | a0001 | c0012 | t0002 | g0047 | EAS | KHV | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0244 | EAS | KHV | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02145 | hp2 | a0001 | c0007 | t0001 | g0218 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | CDX | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02155 | hp2 | a0001 | c0004 | t0001 | g0117 | EAS | CDX | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | CDX | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02165 | hp2 | a0001 | c0004 | t0001 | g0173 | EAS | CDX | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02257 | hp2 | a0001 | c0006 | t0007 | g0013 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02258 | hp2 | a0001 | c0004 | t0003 | g0176 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0052 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02280 | hp2 | a0001 | c0005 | t0002 | g0020 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02451 | hp1 | a0001 | c0011 | t0001 | g0187 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02602 | hp1 | a0001 | c0024 | t0001 | g0252 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0096 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02615 | hp1 | a0001 | c0008 | t0003 | g0082 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02615 | hp2 | a0001 | c0007 | t0001 | g0180 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0250 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02630 | hp1 | a0001 | c0001 | t0028 | g0093 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02630 | hp2 | a0001 | c0001 | t0023 | g0046 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02717 | hp1 | a0001 | c0006 | t0004 | g0204 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02717 | hp2 | a0001 | c0030 | t0001 | g0010 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02723 | hp1 | a0001 | c0003 | t0002 | g0219 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02738 | hp1 | a0001 | c0002 | t0012 | g0001 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02738 | hp2 | a0001 | c0009 | t0001 | g0039 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02809 | hp1 | a0001 | c0008 | t0003 | g0086 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02809 | hp2 | a0001 | c0006 | t0009 | g0055 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02886 | hp2 | a0001 | c0018 | t0009 | g0217 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02895 | hp2 | a0001 | c0003 | t0026 | g0170 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02896 | hp1 | a0001 | c0003 | t0015 | g0087 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02965 | hp2 | a0001 | c0008 | t0003 | g0060 | AFR | ESN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02970 | hp1 | a0001 | c0019 | t0008 | g0059 | AFR | ESN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02976 | hp2 | a0004 | c0028 | t0001 | g0216 | AFR | ESN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03017 | hp1 | a0001 | c0010 | t0002 | g0003 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0168 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03041 | hp2 | a0001 | c0005 | t0009 | g0091 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03098 | hp1 | a0006 | c0027 | t0025 | g0220 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03098 | hp2 | a0001 | c0008 | t0003 | g0085 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0179 | AFR | ESN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03130 | hp2 | a0001 | c0007 | t0001 | g0058 | AFR | ESN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03139 | hp2 | a0001 | c0026 | t0004 | g0090 | AFR | ESN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03225 | hp1 | a0003 | c0029 | t0002 | g0014 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0045 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03453 | hp2 | a0001 | c0005 | t0004 | g0153 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0002 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0035 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03516 | hp2 | a0001 | c0006 | t0001 | g0056 | AFR | ESN | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03540 | hp1 | a0001 | c0001 | t0024 | g0027 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03579 | hp1 | a0001 | c0017 | t0008 | g0123 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03579 | hp2 | a0001 | c0006 | t0014 | g0213 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0243 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03654 | hp2 | a0001 | c0003 | t0002 | g0125 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03688 | hp2 | a0001 | c0004 | t0001 | g0228 | SAS | STU | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03704 | hp2 | a0001 | c0010 | t0002 | g0107 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0256 | SAS | BEB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0251 | SAS | BEB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03942 | hp2 | a0001 | c0020 | t0001 | g0079 | SAS | BEB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG04115 | hp2 | a0001 | c0004 | t0001 | g0069 | SAS | STU | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG04184 | hp2 | a0001 | c0001 | t0016 | g0229 | SAS | BEB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0193 | SAS | STU | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG04199 | hp2 | a0001 | c0010 | t0002 | g0253 | SAS | STU | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0130 | SAS | STU | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | STU | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0120 | SAS | STU | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18522 | hp1 | a0001 | c0007 | t0001 | g0057 | AFR | YRI | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18522 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | YRI | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18906 | hp1 | a0001 | c0007 | t0003 | g0114 | AFR | YRI | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18906 | hp2 | a0001 | c0015 | t0001 | g0177 | AFR | YRI | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18943 | hp2 | a0001 | c0004 | t0001 | g0024 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18954 | hp2 | a0001 | c0001 | t0010 | g0197 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18960 | hp1 | a0001 | c0004 | t0001 | g0147 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18993 | hp1 | a0001 | c0004 | t0001 | g0195 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18998 | hp2 | a0001 | c0022 | t0002 | g0226 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18999 | hp1 | a0001 | c0001 | t0020 | g0109 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19000 | hp1 | a0001 | c0012 | t0001 | g0053 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19007 | hp1 | a0005 | c0025 | t0002 | g0163 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | LWK | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | LWK | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19043 | hp2 | a0001 | c0011 | t0001 | g0157 | AFR | LWK | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19063 | hp1 | a0001 | c0001 | t0029 | g0206 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19063 | hp2 | a0007 | c0031 | t0001 | g0152 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19070 | hp1 | a0001 | c0001 | t0010 | g0137 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19082 | hp1 | a0001 | c0004 | t0001 | g0140 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19087 | hp2 | a0001 | c0004 | t0001 | g0210 | EAS | JPT | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0089 | AFR | YRI | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA19240 | hp2 | a0001 | c0008 | t0003 | g0084 | AFR | YRI | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0237 | AFR | ASW | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ASW | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0038 | EUR | TSI | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0184 | EUR | TSI | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA20905 | hp1 | a0001 | c0009 | t0005 | g0238 | SAS | GIH | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | GIH | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0136 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02109 | hp1 | a0001 | c0001 | t0017 | g0015 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG02559 | hp2 | a0001 | c0021 | t0008 | g0028 | AFR | ACB | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0064 | AFR | MSL | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG06807 | hp1 | a0001 | c0006 | t0007 | g0088 | AFR | USA | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | USA | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA20300 | hp1 | a0001 | c0001 | t0011 | g0150 | AFR | USA | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | USA | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0172 | REF | REF | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| homoSapiens_grch38 | hp1 | a0001 | c0005 | t0001 | g0191 | REF | REF | SLIT1_chr10_96993038_97190959 | SLIT1 | chr10 | 96993038 | 97190959 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:97002301
|
G | A | 1 | a0005 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.4223C>T | p.Ser1408Leu | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/37 | 4508/7964 | 4223/4605 | 1408/1534 | chr10 | 97002301 | ||
| chr10:97031645
|
G | A | 1 | a0004 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.2471C>T | p.Pro824Leu | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 24/37 | 2756/7964 | 2471/4605 | 824/1534 | chr10 | 97031645 | ||
| chr10:97049069
|
C | A | 1 | a0006 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1351G>T | p.Ala451Ser | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/37 | 1636/7964 | 1351/4605 | 451/1534 | chr10 | 97049069 | ||
| chr10:97056342
|
G | A | 1 | a0003 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.1280C>T | p.Ser427Phe | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/37 | 1565/7964 | 1280/4605 | 427/1534 | chr10 | 97056342 | ||
| chr10:97066067
|
T | C | 1 | a0007 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.433A>G | p.Ile145Val | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/37 | 718/7964 | 433/4605 | 145/1534 | chr10 | 97066067 | ||
| chr10:97164843
|
G | A | 1 | a0002 | 4 | HG01261.hp1 HG01361.hp2 HG01515.hp1 others(1): Show |
missense_variant | MODERATE | c.245C>T | p.Ala82Val | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/37 | 530/7964 | 245/4605 | 82/1534 | chr10 | 97164843 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:97002246
|
C | T | 3 | a0001c0017a0001c0019a0001c0021 | 3 | HG02559.hp2 HG02970.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.4278G>A | p.Gln1426Gln | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/37 | 4563/7964 | 4278/4605 | 1426/1534 | chr10 | 97002246 | ||
| chr10:97002294
|
T | G | 6 | a0001c0004a0001c0012a0001c0017others(3): Show | 24 | HG00558.hp1 HG00741.hp1 HG01070.hp2 others(21): Show |
synonymous_variant | LOW | c.4230A>C | p.Ala1410Ala | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/37 | 4515/7964 | 4230/4605 | 1410/1534 | chr10 | 97002294 | ||
| chr10:97006489
|
C | T | 1 | a0001c0012 | 2 | HG02071.hp1 NA19000.hp1 |
synonymous_variant | LOW | c.3573G>A | p.Thr1191Thr | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 32/37 | 3858/7964 | 3573/4605 | 1191/1534 | chr10 | 97006489 | ||
| chr10:97030810
|
G | A | 6 | a0001c0006a0001c0015a0001c0018others(3): Show | 12 | HG01109.hp2 HG02257.hp2 HG02559.hp2 others(9): Show |
synonymous_variant | LOW | c.2529C>T | p.Asp843Asp | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/37 | 2814/7964 | 2529/4605 | 843/1534 | chr10 | 97030810 | ||
| chr10:97031635
|
G | A | 1 | a0001c0022 | 1 | NA18998.hp2 | synonymous_variant | LOW | c.2481C>T | p.Ala827Ala | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 24/37 | 2766/7964 | 2481/4605 | 827/1534 | chr10 | 97031635 | ||
| chr10:97034506
|
A | G | 1 | a0001c0023 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.2403T>C | p.Asn801Asn | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/37 | 2688/7964 | 2403/4605 | 801/1534 | chr10 | 97034506 | ||
| chr10:97043495
|
G | A | 1 | a0001c0009 | 5 | HG01070.hp1 HG01106.hp1 HG02055.hp2 others(2): Show |
synonymous_variant | LOW | c.1872C>T | p.Arg624Arg | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 19/37 | 2157/7964 | 1872/4605 | 624/1534 | chr10 | 97043495 | ||
| chr10:97046755
|
G | C | 6 | a0001c0002a0001c0015a0001c0023others(3): Show | 28 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(25): Show |
synonymous_variant | LOW | c.1752C>G | p.Ala584Ala | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/37 | 2037/7964 | 1752/4605 | 584/1534 | chr10 | 97046755 | ||
| chr10:97047698
|
C | T | 1 | a0001c0020 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.1626G>A | p.Thr542Thr | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 16/37 | 1911/7964 | 1626/4605 | 542/1534 | chr10 | 97047698 | ||
| chr10:97047749
|
C | T | 1 | a0001c0010 | 3 | HG03017.hp1 HG03704.hp2 HG04199.hp2 |
synonymous_variant | LOW | c.1575G>A | p.Glu525Glu | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 16/37 | 1860/7964 | 1575/4605 | 525/1534 | chr10 | 97047749 | ||
| chr10:97048989
|
G | T | 4 | a0001c0008a0001c0011a0001c0019others(1): Show | 9 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(6): Show |
synonymous_variant | LOW | c.1431C>A | p.Ile477Ile | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/37 | 1716/7964 | 1431/4605 | 477/1534 | chr10 | 97048989 | ||
| chr10:97049109
|
C | G | 29 | a0001c0001a0001c0002a0001c0003others(26): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
synonymous_variant | LOW | c.1311G>C | p.Ala437Ala | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/37 | 1596/7964 | 1311/4605 | 437/1534 | chr10 | 97049109 | ||
| chr10:97057260
|
G | A | 1 | a0001c0030 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.1107C>T | p.Ile369Ile | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/37 | 1392/7964 | 1107/4605 | 369/1534 | chr10 | 97057260 | ||
| chr10:97060771
|
C | G | 4 | a0001c0003a0001c0017a0001c0018others(1): Show | 26 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(23): Show |
synonymous_variant | LOW | c.810G>C | p.Gly270Gly | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 9/37 | 1095/7964 | 810/4605 | 270/1534 | chr10 | 97060771 | ||
| chr10:97064206
|
G | T | 4 | a0001c0007a0001c0011a0001c0015others(1): Show | 10 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
synonymous_variant | LOW | c.591C>A | p.Pro197Pro | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 7/37 | 876/7964 | 591/4605 | 197/1534 | chr10 | 97064206 | ||
| chr10:97163424
|
T | C | 1 | a0001c0032 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.297A>G | p.Ala99Ala | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/37 | 582/7964 | 297/4605 | 99/1534 | chr10 | 97163424 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:96998066
|
G | A | 2 | a0001c0001t0011a0001c0003t0011 | 2 | HG01884.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3046C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 3046 | chr10 | 96998066 | |||||
| chr10:96998085
|
C | T | 1 | a0006c0027t0025 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3027G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 3027 | chr10 | 96998085 | |||||
| chr10:96998087
|
A | ACAT | 3 | a0001c0017t0008a0001c0019t0008a0001c0021t0008 | 3 | HG02559.hp2 HG02970.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3022_*3024dupATG | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 3024 | chr10 | 96998087 | |||||
| chr10:96998117
|
G | A | 1 | a0001c0001t0018 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2995C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 2995 | chr10 | 96998117 | |||||
| chr10:96998122
|
G | T | 1 | a0001c0006t0007 | 3 | HG01109.hp2 HG02257.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2990C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 2990 | chr10 | 96998122 | |||||
| chr10:96998127
|
C | T | 1 | a0001c0003t0026 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2985G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 2985 | chr10 | 96998127 | |||||
| chr10:96998153
|
C | G | 1 | a0001c0001t0017 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2959G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 2959 | chr10 | 96998153 | |||||
| chr10:96998175
|
C | T | 1 | a0001c0001t0021 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2937G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 2937 | chr10 | 96998175 | |||||
| chr10:96998200
|
G | A | 1 | a0001c0001t0022 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2912C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 2912 | chr10 | 96998200 | |||||
| chr10:96998325
|
A | AGAT | 3 | a0001c0001t0006a0001c0003t0006a0002c0013t0006 | 5 | HG00140.hp1 HG00738.hp2 HG01515.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2784_*2786dupATC | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 2786 | chr10 | 96998325 | |||||
| chr10:96998456
|
C | T | 1 | a0001c0001t0020 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2656G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 2656 | chr10 | 96998456 | |||||
| chr10:96998515
|
G | C | 1 | a0001c0001t0023 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2597C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 2597 | chr10 | 96998515 | |||||
| chr10:96998635
|
G | T | 3 | a0001c0017t0008a0001c0019t0008a0001c0021t0008 | 3 | HG02559.hp2 HG02970.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2477C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 2477 | chr10 | 96998635 | |||||
| chr10:96999196
|
G | A | 17 | a0001c0001t0002a0001c0001t0016a0001c0001t0017others(14): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1916C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 1916 | chr10 | 96999196 | |||||
| chr10:96999397
|
T | C | 2 | a0001c0001t0011a0001c0003t0011 | 2 | HG01884.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1715A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 1715 | chr10 | 96999397 | |||||
| chr10:96999535
|
C | T | 1 | a0001c0001t0016 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1577G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 1577 | chr10 | 96999535 | |||||
| chr10:96999768
|
C | T | 6 | a0001c0001t0004a0001c0003t0026a0001c0005t0004others(3): Show | 11 | HG01109.hp2 HG02257.hp2 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1344G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 1344 | chr10 | 96999768 | |||||
| chr10:96999872
|
C | T | 1 | a0001c0001t0019 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1240G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 1240 | chr10 | 96999872 | |||||
| chr10:96999892
|
G | A | 1 | a0001c0003t0015 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1220C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 1220 | chr10 | 96999892 | |||||
| chr10:96999927
|
G | GTAGA | 10 | a0001c0001t0003a0001c0001t0011a0001c0003t0011others(7): Show | 16 | HG01884.hp1 HG02258.hp2 HG02615.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1181_*1184dupTCTA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 1184 | chr10 | 96999927 | |||||
| chr10:96999933
|
A | AGATAGAT | 14 | a0001c0001t0002a0001c0001t0010a0001c0001t0016others(11): Show | 40 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1172_*1178dupATCT others(3): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 1178 | chr10 | 96999933 | |||||
| chr10:96999984
|
G | C | 1 | a0001c0003t0026 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1128C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 1128 | chr10 | 96999984 | |||||
| chr10:97000255
|
A | G | 2 | a0001c0003t0015a0001c0006t0014 | 2 | HG02896.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*857T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 857 | chr10 | 97000255 | |||||
| chr10:97000525
|
G | C | 1 | a0001c0009t0027 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*587C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 587 | chr10 | 97000525 | |||||
| chr10:97000790
|
G | C | 3 | a0001c0001t0005a0001c0003t0005a0001c0009t0005 | 6 | HG00140.hp2 HG01070.hp1 HG01123.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*322C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 322 | chr10 | 97000790 | |||||
| chr10:97000942
|
G | A | 1 | a0001c0001t0028 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*170C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 170 | chr10 | 97000942 | |||||
| chr10:97001084
|
G | A | 1 | a0001c0001t0029 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 37/37 | 28 | chr10 | 97001084 | |||||
| chr10:97185842
|
C | T | 1 | a0001c0001t0013 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-168G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/37 | 168 | chr10 | 97185842 | |||||
| chr10:97185899
|
C | T | 1 | a0001c0002t0012 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-225G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/37 | 225 | chr10 | 97185899 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:97001465
|
T | A | 28 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0099others(25): Show | 28 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.4367-115A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/36 | chr10 | 97001465 | ||||||
| chr10:97001579
|
C | T | 97 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(94): Show | 97 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.4367-229G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/36 | chr10 | 97001579 | ||||||
| chr10:97001595
|
A | AG | 46 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0116others(43): Show | 46 | HG00544.hp1 HG00558.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.4367-246dupC | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/36 | chr10 | 97001595 | ||||||
| chr10:97001604
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4367-254G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/36 | chr10 | 97001604 | ||||||
| chr10:97001639
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4367-289G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/36 | chr10 | 97001639 | ||||||
| chr10:97001652
|
A | G | 10 | a0001c0001t0001g0009a0001c0001t0002g0189a0001c0001t0006g0038others(7): Show | 10 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.4367-302T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/36 | chr10 | 97001652 | ||||||
| chr10:97001679
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4367-329C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/36 | chr10 | 97001679 | ||||||
| chr10:97001699
|
C | G | 1 | a0001c0008t0003g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4367-349G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/36 | chr10 | 97001699 | ||||||
| chr10:97001942
|
C | T | 1 | a0001c0004t0003g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4366+216G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/36 | chr10 | 97001942 | ||||||
| chr10:97001978
|
G | A | 3 | a0001c0001t0001g0160a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02451.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4366+180C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/36 | chr10 | 97001978 | ||||||
| chr10:97002006
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4366+152C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/36 | chr10 | 97002006 | ||||||
| chr10:97002077
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4366+81C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 36/36 | chr10 | 97002077 | ||||||
| chr10:97002414
|
A | AGCCCCAC others(12): Show |
1 | a0001c0003t0015g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4155-64_4155-46dup others(19): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 35/36 | chr10 | 97002414 | ||||||
| chr10:97002435
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4155-66G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 35/36 | chr10 | 97002435 | ||||||
| chr10:97003096
|
G | A | 15 | a0001c0004t0001g0024a0001c0004t0001g0044a0001c0004t0001g0065others(12): Show | 15 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.3866-104C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 34/36 | chr10 | 97003096 | ||||||
| chr10:97003254
|
G | A | 7 | a0001c0001t0001g0078a0001c0001t0001g0178a0001c0001t0001g0188others(4): Show | 7 | HG01891.hp2 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3866-262C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 34/36 | chr10 | 97003254 | ||||||
| chr10:97003291
|
G | A | 2 | a0001c0005t0001g0005a0001c0005t0001g0006 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3866-299C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 34/36 | chr10 | 97003291 | ||||||
| chr10:97003374
|
C | T | 6 | a0001c0001t0001g0094a0001c0001t0001g0160a0001c0004t0001g0210others(3): Show | 6 | HG02451.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.3866-382G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 34/36 | chr10 | 97003374 | ||||||
| chr10:97003541
|
C | G | 4 | a0001c0001t0001g0124a0001c0001t0001g0156a0001c0005t0001g0005others(1): Show | 4 | HG01243.hp1 HG02970.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3865+527G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 34/36 | chr10 | 97003541 | ||||||
| chr10:97003590
|
C | T | 6 | a0001c0004t0001g0069a0001c0004t0001g0074a0001c0004t0001g0075others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3865+478G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 34/36 | chr10 | 97003590 | ||||||
| chr10:97003768
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3865+300G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 34/36 | chr10 | 97003768 | ||||||
| chr10:97004470
|
C | T | 1 | a0001c0003t0001g0255 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3710+223G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 33/36 | chr10 | 97004470 | ||||||
| chr10:97004486
|
G | T | 78 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(75): Show | 78 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.3710+207C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 33/36 | chr10 | 97004486 | ||||||
| chr10:97004499
|
A | G | 81 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(78): Show | 81 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.3710+194T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 33/36 | chr10 | 97004499 | ||||||
| chr10:97004592
|
G | A | 1 | a0001c0004t0003g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3710+101C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 33/36 | chr10 | 97004592 | ||||||
| chr10:97004639
|
G | T | 1 | a0001c0003t0015g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3710+54C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 33/36 | chr10 | 97004639 | ||||||
| chr10:97004937
|
G | T | 92 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(89): Show | 92 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.3580-114C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 32/36 | chr10 | 97004937 | ||||||
| chr10:97005036
|
G | T | 3 | a0001c0017t0008g0123a0001c0019t0008g0059a0001c0021t0008g0028 | 3 | HG02559.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3580-213C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 32/36 | chr10 | 97005036 | ||||||
| chr10:97005144
|
C | G | 3 | a0001c0017t0008g0123a0001c0019t0008g0059a0001c0021t0008g0028 | 3 | HG02559.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3580-321G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 32/36 | chr10 | 97005144 | ||||||
| chr10:97005335
|
C | A | 1 | a0001c0001t0001g0232 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3580-512G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 32/36 | chr10 | 97005335 | ||||||
| chr10:97005673
|
G | A | 1 | a0001c0002t0001g0021 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3579+810C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 32/36 | chr10 | 97005673 | ||||||
| chr10:97005755
|
G | A | 1 | a0001c0004t0001g0166 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3579+728C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 32/36 | chr10 | 97005755 | ||||||
| chr10:97005760
|
G | A | 1 | a0001c0002t0001g0212 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3579+723C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 32/36 | chr10 | 97005760 | ||||||
| chr10:97005966
|
T | C | 1 | a0001c0005t0001g0045 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3579+517A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 32/36 | chr10 | 97005966 | ||||||
| chr10:97005984
|
T | C | 1 | a0001c0005t0001g0045 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3579+499A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 32/36 | chr10 | 97005984 | ||||||
| chr10:97006192
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3579+291A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 32/36 | chr10 | 97006192 | ||||||
| chr10:97006294
|
T | C | 3 | a0001c0001t0001g0054a0001c0001t0011g0150a0001c0003t0011g0012 | 3 | HG01884.hp1 HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3579+189A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 32/36 | chr10 | 97006294 | ||||||
| chr10:97006464
|
C | T | 9 | a0001c0004t0001g0024a0001c0004t0001g0044a0001c0004t0001g0140others(6): Show | 9 | HG00558.hp1 HG02165.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.3579+19G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 32/36 | chr10 | 97006464 | ||||||
| chr10:97006833
|
C | A | 79 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(76): Show | 79 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.3342-113G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97006833 | ||||||
| chr10:97006865
|
T | A | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3342-145A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97006865 | ||||||
| chr10:97006940
|
C | T | 1 | a0001c0007t0001g0057 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3342-220G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97006940 | ||||||
| chr10:97007409
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3342-689T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97007409 | ||||||
| chr10:97007504
|
A | G | 1 | a0001c0001t0002g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3342-784T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97007504 | ||||||
| chr10:97007506
|
AGACC | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0156a0001c0015t0001g0177 | 3 | HG02970.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3342-790_3342-787d others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97007506 | ||||||
| chr10:97007547
|
C | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0156 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3342-827G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97007547 | ||||||
| chr10:97007553
|
A | G | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3342-833T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97007553 | ||||||
| chr10:97007610
|
C | T | 1 | a0001c0003t0002g0125 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3342-890G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97007610 | ||||||
| chr10:97007780
|
G | A | 3 | a0001c0008t0003g0085a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02451.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3342-1060C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97007780 | ||||||
| chr10:97007983
|
A | AGGAG | 3 | a0001c0017t0008g0123a0001c0019t0008g0059a0001c0021t0008g0028 | 3 | HG02559.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3342-1267_3342-126 others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97007983 | ||||||
| chr10:97008032
|
AGCAG | A | 79 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(76): Show | 79 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.3342-1316_3342-131 others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008032 | ||||||
| chr10:97008085
|
T | G | 171 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(168): Show | 171 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.3342-1365A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008085 | ||||||
| chr10:97008106
|
A | C | 80 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(77): Show | 80 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.3342-1386T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008106 | ||||||
| chr10:97008463
|
G | A | 32 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0078others(29): Show | 32 | HG00558.hp1 HG00639.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.3342-1743C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008463 | ||||||
| chr10:97008656
|
A | G | 6 | a0001c0001t0001g0115a0001c0001t0001g0131a0001c0001t0001g0221others(3): Show | 6 | HG00280.hp2 HG01070.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.3342-1936T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008656 | ||||||
| chr10:97008696
|
C | CA | 12 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0242others(9): Show | 12 | HG01261.hp1 HG01361.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.3342-1977dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008696 | ||||||
| chr10:97008696
|
CA | C | 5 | a0001c0001t0001g0160a0001c0006t0014g0213a0001c0008t0003g0085others(2): Show | 5 | HG02451.hp1 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.3342-1977delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008696 | ||||||
| chr10:97008696
|
CAA | C | 84 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(81): Show | 84 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.3342-1978_3342-197 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008696 | ||||||
| chr10:97008882
|
A | AT | 9 | a0001c0004t0001g0065a0001c0004t0001g0069a0001c0004t0001g0074others(6): Show | 9 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.3341+2110dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008882 | ||||||
| chr10:97008891
|
A | T | 84 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(81): Show | 84 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.3341+2102T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008891 | ||||||
| chr10:97008906
|
G | A | 5 | a0001c0001t0001g0124a0001c0001t0001g0156a0001c0005t0001g0005others(2): Show | 5 | HG01243.hp1 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3341+2087C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008906 | ||||||
| chr10:97008936
|
G | A | 79 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(76): Show | 79 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.3341+2057C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008936 | ||||||
| chr10:97008974
|
G | T | 30 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0121others(27): Show | 30 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.3341+2019C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008974 | ||||||
| chr10:97008984
|
A | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0161others(1): Show | 4 | HG02145.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3341+2009T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97008984 | ||||||
| chr10:97009070
|
G | A | 1 | a0001c0003t0015g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3341+1923C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97009070 | ||||||
| chr10:97009167
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3341+1826C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97009167 | ||||||
| chr10:97009369
|
C | T | 9 | a0001c0001t0003g0017a0001c0001t0003g0169a0001c0001t0013g0002others(6): Show | 9 | HG02615.hp1 HG02809.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.3341+1624G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97009369 | ||||||
| chr10:97010256
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3341+737T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97010256 | ||||||
| chr10:97010617
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3341+376C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 31/36 | chr10 | 97010617 | ||||||
| chr10:97011215
|
C | T | 6 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0008t0003g0085others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3204-85G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97011215 | ||||||
| chr10:97011264
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3204-134T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97011264 | ||||||
| chr10:97011429
|
C | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0078others(23): Show | 26 | HG00558.hp1 HG00639.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.3204-299G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97011429 | ||||||
| chr10:97011459
|
A | T | 1 | a0001c0001t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3204-329T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97011459 | ||||||
| chr10:97011524
|
C | T | 3 | a0001c0010t0002g0003a0001c0010t0002g0107a0001c0010t0002g0253 | 3 | HG03017.hp1 HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3204-394G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97011524 | ||||||
| chr10:97011693
|
C | T | 29 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0121others(26): Show | 29 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.3204-563G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97011693 | ||||||
| chr10:97011814
|
C | T | 3 | a0001c0017t0008g0123a0001c0019t0008g0059a0001c0021t0008g0028 | 3 | HG02559.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3204-684G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97011814 | ||||||
| chr10:97011883
|
C | A | 1 | a0001c0001t0001g0156 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3204-753G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97011883 | ||||||
| chr10:97011883
|
C | T | 6 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0063others(3): Show | 6 | HG02451.hp2 HG03139.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.3204-753G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97011883 | ||||||
| chr10:97012047
|
G | A | 2 | a0001c0005t0001g0005a0001c0005t0001g0006 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3204-917C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012047 | ||||||
| chr10:97012075
|
T | TAC | 3 | a0001c0001t0001g0072a0001c0008t0003g0060a0001c0008t0003g0082 | 3 | HG01109.hp1 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3204-947_3204-946d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012075 | ||||||
| chr10:97012075
|
TAC | T | 22 | a0001c0001t0001g0033a0001c0001t0001g0062a0001c0001t0001g0112others(19): Show | 22 | HG00140.hp1 HG00544.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.3204-947_3204-946d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012075 | ||||||
| chr10:97012075
|
TACAC | T | 21 | a0001c0001t0001g0011a0001c0001t0001g0077a0001c0001t0001g0078others(18): Show | 21 | HG00140.hp2 HG01261.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.3204-949_3204-946d others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012075 | ||||||
| chr10:97012075
|
TACACAC | T | 37 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0068others(34): Show | 37 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.3204-951_3204-946d others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012075 | ||||||
| chr10:97012075
|
TACACACA others(1): Show |
T | 45 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0054others(42): Show | 45 | HG00408.hp1 HG00438.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.3204-953_3204-946d others(10): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012075 | ||||||
| chr10:97012075
|
TACACACA others(3): Show |
T | 46 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0049others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.3204-955_3204-946d others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012075 | ||||||
| chr10:97012075
|
TACACACA others(5): Show |
T | 67 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0043others(64): Show | 67 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.3204-957_3204-946d others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012075 | ||||||
| chr10:97012075
|
TACACACA others(7): Show |
T | 6 | a0001c0001t0001g0102a0001c0001t0001g0124a0001c0001t0002g0222others(3): Show | 6 | HG00621.hp2 HG02027.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3204-959_3204-946d others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012075 | ||||||
| chr10:97012075
|
TACACACA others(9): Show |
T | 6 | a0001c0001t0001g0214a0001c0001t0002g0042a0001c0001t0002g0148others(3): Show | 6 | HG00438.hp2 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.3204-961_3204-946d others(18): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012075 | ||||||
| chr10:97012381
|
T | C | 1 | a0001c0003t0001g0035 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3204-1251A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012381 | ||||||
| chr10:97012436
|
C | T | 2 | a0001c0005t0001g0005a0001c0005t0001g0006 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3203+1305G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012436 | ||||||
| chr10:97012470
|
G | A | 3 | a0001c0003t0015g0087a0001c0005t0001g0005a0001c0005t0001g0006 | 3 | HG01243.hp1 HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3203+1271C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012470 | ||||||
| chr10:97012640
|
C | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0182a0001c0001t0001g0249 | 3 | HG02523.hp2 NA18954.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.3203+1101G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012640 | ||||||
| chr10:97012665
|
A | G | 255 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(252): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.3203+1076T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012665 | ||||||
| chr10:97012682
|
G | A | 4 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3203+1059C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012682 | ||||||
| chr10:97012723
|
T | C | 1 | a0001c0003t0015g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3203+1018A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97012723 | ||||||
| chr10:97013277
|
G | A | 1 | a0001c0002t0001g0021 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3203+464C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97013277 | ||||||
| chr10:97013402
|
G | A | 51 | a0001c0001t0001g0185a0001c0001t0002g0008a0001c0001t0002g0016others(48): Show | 51 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.3203+339C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97013402 | ||||||
| chr10:97013450
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3203+291G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97013450 | ||||||
| chr10:97013487
|
T | C | 1 | a0001c0003t0015g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3203+254A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 30/36 | chr10 | 97013487 | ||||||
| chr10:97013922
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3110-88G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 29/36 | chr10 | 97013922 | ||||||
| chr10:97014161
|
G | T | 2 | a0001c0005t0001g0005a0001c0005t0001g0006 | 2 | HG01243.hp1 NA18522.hp2 |
splice_region_variant&intron_variant | LOW | c.2970-3C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014161 | ||||||
| chr10:97014165
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG00639.hp2 HG02895.hp1 HG02897.hp1 |
splice_region_variant&intron_variant | LOW | c.2970-7C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014165 | ||||||
| chr10:97014226
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2970-68C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014226 | ||||||
| chr10:97014244
|
C | T | 7 | a0001c0001t0001g0094a0001c0001t0001g0160a0001c0001t0001g0214others(4): Show | 7 | HG02109.hp2 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2970-86G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014244 | ||||||
| chr10:97014256
|
C | A | 3 | a0001c0001t0001g0054a0001c0001t0011g0150a0001c0003t0011g0012 | 3 | HG01884.hp1 HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2970-98G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014256 | ||||||
| chr10:97014345
|
T | C | 29 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0121others(26): Show | 29 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2970-187A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014345 | ||||||
| chr10:97014510
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2970-352G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014510 | ||||||
| chr10:97014533
|
C | T | 42 | a0001c0001t0001g0185a0001c0001t0002g0008a0001c0001t0002g0016others(39): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.2970-375G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014533 | ||||||
| chr10:97014566
|
G | A | 1 | a0001c0003t0015g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2970-408C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014566 | ||||||
| chr10:97014665
|
G | A | 2 | a0001c0001t0001g0214a0001c0030t0001g0010 | 2 | HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2970-507C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014665 | ||||||
| chr10:97014692
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0119others(11): Show | 14 | HG00639.hp2 HG02027.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2970-534G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014692 | ||||||
| chr10:97014737
|
G | A | 3 | a0001c0001t0005g0130a0001c0001t0005g0240a0001c0003t0005g0183 | 3 | HG00140.hp2 HG01517.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2970-579C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014737 | ||||||
| chr10:97014751
|
A | G | 1 | a0001c0004t0001g0195 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2970-593T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014751 | ||||||
| chr10:97014759
|
G | A | 2 | a0001c0002t0001g0256a0001c0002t0012g0001 | 2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2970-601C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014759 | ||||||
| chr10:97014865
|
C | CA | 8 | a0001c0001t0004g0063a0001c0002t0001g0108a0001c0006t0014g0213others(5): Show | 8 | HG01515.hp1 HG02559.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.2970-708dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014865 | ||||||
| chr10:97014865
|
CA | C | 36 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(33): Show | 36 | HG00639.hp1 HG00673.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2970-708delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97014865 | ||||||
| chr10:97015070
|
G | C | 1 | a0001c0004t0001g0044 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2970-912C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97015070 | ||||||
| chr10:97015433
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2970-1275C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97015433 | ||||||
| chr10:97016063
|
C | G | 43 | a0001c0001t0001g0185a0001c0001t0002g0008a0001c0001t0002g0016others(40): Show | 43 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.2970-1905G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97016063 | ||||||
| chr10:97016170
|
G | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0026others(44): Show | 47 | HG00558.hp1 HG00639.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2970-2012C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97016170 | ||||||
| chr10:97016258
|
G | A | 2 | a0001c0001t0028g0093a0004c0028t0001g0216 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2970-2100C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97016258 | ||||||
| chr10:97016362
|
T | C | 3 | a0001c0001t0004g0019a0001c0005t0004g0153a0001c0026t0004g0090 | 3 | HG02451.hp2 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2970-2204A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97016362 | ||||||
| chr10:97016461
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2969+2125A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97016461 | ||||||
| chr10:97016518
|
C | T | 17 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0215others(14): Show | 17 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2969+2068G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97016518 | ||||||
| chr10:97016679
|
G | C | 2 | a0001c0001t0022g0254a0001c0009t0027g0223 | 2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2969+1907C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97016679 | ||||||
| chr10:97016921
|
G | A | 42 | a0001c0001t0001g0185a0001c0001t0002g0008a0001c0001t0002g0016others(39): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.2969+1665C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97016921 | ||||||
| chr10:97017002
|
G | C | 1 | a0001c0002t0001g0037 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2969+1584C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97017002 | ||||||
| chr10:97017199
|
C | T | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2969+1387G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97017199 | ||||||
| chr10:97017229
|
G | A | 7 | a0001c0001t0001g0160a0001c0001t0001g0214a0001c0007t0003g0114others(4): Show | 7 | HG02109.hp2 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2969+1357C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97017229 | ||||||
| chr10:97017257
|
G | A | 1 | a0001c0004t0001g0044 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2969+1329C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97017257 | ||||||
| chr10:97017647
|
G | T | 45 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0119others(42): Show | 45 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.2969+939C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97017647 | ||||||
| chr10:97017653
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG00639.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2969+933G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97017653 | ||||||
| chr10:97017848
|
C | CT | 54 | a0001c0001t0001g0009a0001c0001t0001g0094a0001c0001t0001g0118others(51): Show | 54 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2969+737dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97017848 | ||||||
| chr10:97017852
|
T | C | 7 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0247others(4): Show | 7 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2969+734A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97017852 | ||||||
| chr10:97017949
|
A | G | 1 | a0001c0006t0007g0209 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2969+637T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97017949 | ||||||
| chr10:97018099
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG00639.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2969+487C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97018099 | ||||||
| chr10:97018136
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0232 | 2 | NA18952.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.2969+450G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97018136 | ||||||
| chr10:97018386
|
C | G | 88 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(85): Show | 88 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.2969+200G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 28/36 | chr10 | 97018386 | ||||||
| chr10:97018720
|
C | T | 20 | a0001c0001t0001g0078a0001c0003t0001g0064a0001c0003t0026g0170others(17): Show | 20 | HG00558.hp1 HG00741.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.2872-37G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 27/36 | chr10 | 97018720 | ||||||
| chr10:97018811
|
C | T | 2 | a0001c0005t0001g0005a0001c0005t0001g0006 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2872-128G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 27/36 | chr10 | 97018811 | ||||||
| chr10:97018817
|
C | CTTCA | 64 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0119others(61): Show | 64 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2872-138_2872-135d others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 27/36 | chr10 | 97018817 | ||||||
| chr10:97018817
|
CTTCA | C | 13 | a0001c0001t0001g0094a0001c0001t0001g0121a0001c0001t0001g0122others(10): Show | 13 | HG02451.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.2872-138_2872-135d others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 27/36 | chr10 | 97018817 | ||||||
| chr10:97018817
|
CTTCATTC others(1): Show |
C | 7 | a0001c0001t0001g0214a0001c0001t0004g0018a0001c0001t0004g0019others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2872-142_2872-135d others(10): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 27/36 | chr10 | 97018817 | ||||||
| chr10:97018817
|
CTTCATTC others(5): Show |
C | 2 | a0001c0001t0001g0124a0001c0001t0001g0156 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2872-146_2872-135d others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 27/36 | chr10 | 97018817 | ||||||
| chr10:97019184
|
A | G | 27 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(24): Show | 27 | HG01261.hp1 HG01361.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.2747-77T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97019184 | ||||||
| chr10:97019234
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0156 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2747-127C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97019234 | ||||||
| chr10:97019380
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2747-273G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97019380 | ||||||
| chr10:97019464
|
C | A | 2 | a0001c0004t0001g0024a0001c0004t0001g0140 | 2 | NA18943.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2747-357G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97019464 | ||||||
| chr10:97019525
|
G | T | 1 | a0001c0001t0001g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2747-418C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97019525 | ||||||
| chr10:97019533
|
G | T | 36 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(33): Show | 36 | HG00639.hp1 HG00673.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.2747-426C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97019533 | ||||||
| chr10:97019543
|
C | T | 1 | a0001c0003t0015g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2747-436G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97019543 | ||||||
| chr10:97019557
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2747-450G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97019557 | ||||||
| chr10:97019576
|
G | A | 2 | a0001c0004t0001g0165a0001c0004t0001g0166 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.2747-469C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97019576 | ||||||
| chr10:97019744
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2747-637C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97019744 | ||||||
| chr10:97019907
|
C | T | 11 | a0001c0003t0026g0170a0001c0004t0001g0024a0001c0004t0001g0044others(8): Show | 11 | HG00558.hp1 HG02165.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2747-800G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97019907 | ||||||
| chr10:97019927
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2747-820G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97019927 | ||||||
| chr10:97019982
|
AT | A | 42 | a0001c0001t0001g0185a0001c0001t0002g0008a0001c0001t0002g0016others(39): Show | 42 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.2747-876delA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97019982 | ||||||
| chr10:97020520
|
C | A | 9 | a0001c0001t0001g0094a0001c0001t0001g0160a0001c0001t0001g0214others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2746+730G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97020520 | ||||||
| chr10:97020600
|
A | G | 1 | a0001c0005t0001g0045 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2746+650T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97020600 | ||||||
| chr10:97020621
|
G | A | 1 | a0001c0002t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2746+629C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97020621 | ||||||
| chr10:97020813
|
G | A | 2 | a0001c0001t0001g0004a0001c0003t0001g0250 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2746+437C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97020813 | ||||||
| chr10:97020860
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2746+390C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97020860 | ||||||
| chr10:97020869
|
G | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(22): Show | 25 | HG01261.hp1 HG01361.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.2746+381C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97020869 | ||||||
| chr10:97020910
|
A | G | 3 | a0001c0001t0005g0130a0001c0001t0005g0240a0001c0003t0005g0183 | 3 | HG00140.hp2 HG01517.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2746+340T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97020910 | ||||||
| chr10:97020967
|
C | T | 5 | a0001c0001t0001g0160a0001c0007t0003g0114a0001c0008t0003g0085others(2): Show | 5 | HG02451.hp1 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2746+283G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97020967 | ||||||
| chr10:97021036
|
C | T | 4 | a0001c0003t0015g0087a0001c0005t0001g0005a0001c0005t0001g0006others(1): Show | 4 | HG01243.hp1 HG02896.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2746+214G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97021036 | ||||||
| chr10:97021121
|
G | GCCTTGTT others(1): Show |
45 | a0001c0001t0001g0124a0001c0001t0001g0185a0001c0001t0002g0008others(42): Show | 45 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.2746+121_2746+128d others(10): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97021121 | ||||||
| chr10:97021146
|
C | T | 1 | a0001c0009t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2746+104G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97021146 | ||||||
| chr10:97021147
|
G | A | 2 | a0001c0004t0001g0147a0001c0004t0001g0195 | 2 | NA18960.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.2746+103C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97021147 | ||||||
| chr10:97021176
|
T | C | 44 | a0001c0001t0001g0185a0001c0001t0002g0008a0001c0001t0002g0016others(41): Show | 44 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2746+74A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97021176 | ||||||
| chr10:97021211
|
T | C | 2 | a0001c0005t0001g0005a0001c0005t0001g0006 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2746+39A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 26/36 | chr10 | 97021211 | ||||||
| chr10:97021426
|
C | A | 6 | a0001c0001t0001g0094a0001c0001t0001g0160a0001c0007t0003g0114others(3): Show | 6 | HG02451.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2583-13G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97021426 | ||||||
| chr10:97021551
|
A | T | 1 | a0001c0001t0001g0106 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2583-138T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97021551 | ||||||
| chr10:97021558
|
CT | C | 67 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(64): Show | 67 | HG00558.hp1 HG00639.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.2583-146delA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97021558 | ||||||
| chr10:97021575
|
T | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0119others(5): Show | 8 | HG00639.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.2583-162A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97021575 | ||||||
| chr10:97021623
|
C | T | 26 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(23): Show | 26 | HG00639.hp1 HG00673.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.2583-210G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97021623 | ||||||
| chr10:97021674
|
T | C | 6 | a0001c0001t0001g0050a0001c0001t0001g0182a0001c0001t0001g0249others(3): Show | 6 | HG02523.hp2 NA18954.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.2583-261A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97021674 | ||||||
| chr10:97021843
|
G | A | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2583-430C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97021843 | ||||||
| chr10:97021851
|
C | T | 10 | a0001c0003t0026g0170a0001c0004t0001g0024a0001c0004t0001g0044others(7): Show | 10 | HG00558.hp1 HG02165.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.2583-438G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97021851 | ||||||
| chr10:97022039
|
A | G | 9 | a0001c0001t0001g0094a0001c0001t0001g0160a0001c0001t0001g0214others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2583-626T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022039 | ||||||
| chr10:97022051
|
C | T | 44 | a0001c0001t0001g0185a0001c0001t0002g0008a0001c0001t0002g0016others(41): Show | 44 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2583-638G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022051 | ||||||
| chr10:97022233
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2583-820A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022233 | ||||||
| chr10:97022381
|
G | A | 1 | a0001c0021t0008g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2583-968C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022381 | ||||||
| chr10:97022478
|
T | G | 1 | a0001c0003t0002g0125 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2583-1065A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022478 | ||||||
| chr10:97022525
|
G | T | 1 | a0001c0016t0001g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2583-1112C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022525 | ||||||
| chr10:97022602
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2583-1189C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022602 | ||||||
| chr10:97022637
|
A | G | 11 | a0001c0001t0001g0094a0001c0001t0001g0160a0001c0001t0001g0214others(8): Show | 11 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2583-1224T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022637 | ||||||
| chr10:97022666
|
A | G | 1 | a0001c0002t0001g0021 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2583-1253T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022666 | ||||||
| chr10:97022668
|
C | A | 1 | a0001c0001t0002g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2583-1255G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022668 | ||||||
| chr10:97022722
|
G | A | 4 | a0001c0001t0001g0078a0001c0001t0001g0188a0001c0001t0023g0046others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2583-1309C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022722 | ||||||
| chr10:97022805
|
C | T | 2 | a0001c0006t0014g0213a0001c0015t0001g0177 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2583-1392G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022805 | ||||||
| chr10:97022812
|
G | GGCCTTTC others(72): Show |
1 | a0001c0005t0002g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2583-1478_2583-140 others(83): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022812 | ||||||
| chr10:97022821
|
C | T | 1 | a0001c0003t0011g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2583-1408G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022821 | ||||||
| chr10:97022901
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2583-1488C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022901 | ||||||
| chr10:97022955
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2583-1542C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97022955 | ||||||
| chr10:97023056
|
T | G | 47 | a0001c0001t0001g0156a0001c0001t0001g0185a0001c0001t0002g0016others(44): Show | 47 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.2583-1643A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97023056 | ||||||
| chr10:97023057
|
T | G | 1 | a0001c0001t0002g0008 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2583-1644A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97023057 | ||||||
| chr10:97023129
|
G | A | 2 | a0001c0005t0001g0005a0001c0005t0001g0006 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2583-1716C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97023129 | ||||||
| chr10:97023217
|
A | AT | 12 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0156others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2583-1805dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97023217 | ||||||
| chr10:97023217
|
AT | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG00639.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2583-1805delA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97023217 | ||||||
| chr10:97023263
|
G | A | 1 | a0001c0005t0009g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2583-1850C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97023263 | ||||||
| chr10:97023329
|
G | A | 1 | a0001c0003t0006g0036 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2583-1916C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97023329 | ||||||
| chr10:97023360
|
C | G | 9 | a0001c0001t0001g0094a0001c0001t0001g0160a0001c0001t0001g0214others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2583-1947G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97023360 | ||||||
| chr10:97023660
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0161 | 3 | HG02622.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2583-2247G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97023660 | ||||||
| chr10:97023836
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2583-2423C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97023836 | ||||||
| chr10:97023868
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0011g0150a0001c0017t0008g0123others(1): Show | 4 | HG01884.hp2 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2583-2455C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97023868 | ||||||
| chr10:97023967
|
G | C | 44 | a0001c0001t0001g0185a0001c0001t0002g0008a0001c0001t0002g0016others(41): Show | 44 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2583-2554C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97023967 | ||||||
| chr10:97023998
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2583-2585G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97023998 | ||||||
| chr10:97024236
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG00639.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2583-2823C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97024236 | ||||||
| chr10:97024344
|
C | T | 1 | a0001c0006t0007g0088 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2583-2931G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97024344 | ||||||
| chr10:97024362
|
T | C | 1 | a0001c0003t0002g0125 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2583-2949A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97024362 | ||||||
| chr10:97024487
|
G | A | 1 | a0001c0003t0005g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2583-3074C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97024487 | ||||||
| chr10:97024623
|
T | A | 155 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(152): Show | 155 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.2583-3210A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97024623 | ||||||
| chr10:97024737
|
T | A | 117 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(114): Show | 117 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.2583-3324A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97024737 | ||||||
| chr10:97024840
|
G | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0242a0001c0002t0001g0120others(3): Show | 6 | HG01261.hp1 HG01361.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.2583-3427C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97024840 | ||||||
| chr10:97024955
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2583-3542G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97024955 | ||||||
| chr10:97025257
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG00639.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2583-3844A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97025257 | ||||||
| chr10:97025345
|
G | A | 1 | a0001c0007t0003g0114 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2583-3932C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97025345 | ||||||
| chr10:97025507
|
G | C | 5 | a0001c0001t0001g0054a0001c0001t0011g0150a0001c0001t0013g0002others(2): Show | 5 | HG01884.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2583-4094C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97025507 | ||||||
| chr10:97025552
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0174 | 2 | NA18963.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2583-4139G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97025552 | ||||||
| chr10:97026019
|
T | C | 111 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(108): Show | 111 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.2583-4606A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026019 | ||||||
| chr10:97026035
|
C | CAAAAAGA others(300): Show |
2 | a0001c0003t0026g0170a0001c0005t0009g0091 | 2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2583-4623_2583-462 others(311): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026035 | ||||||
| chr10:97026096
|
C | T | 2 | a0001c0001t0002g0196a0001c0002t0002g0164 | 2 | NA19003.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2582+4661G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026096 | ||||||
| chr10:97026204
|
C | T | 5 | a0001c0006t0004g0204a0001c0006t0007g0013a0001c0006t0007g0088others(2): Show | 5 | HG01109.hp2 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2582+4553G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026204 | ||||||
| chr10:97026358
|
G | A | 4 | a0001c0001t0001g0078a0001c0001t0001g0188a0001c0001t0023g0046others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2582+4399C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026358 | ||||||
| chr10:97026464
|
C | CTAAA | 90 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0026others(87): Show | 90 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.2582+4289_2582+429 others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026464 | ||||||
| chr10:97026464
|
C | CTAAATAA others(1): Show |
13 | a0001c0001t0001g0054a0001c0001t0001g0118a0001c0001t0001g0119others(10): Show | 13 | HG00558.hp2 HG00621.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.2582+4285_2582+429 others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026464 | ||||||
| chr10:97026464
|
C | CTAAATAA others(5): Show |
2 | a0001c0002t0001g0151a0001c0006t0009g0055 | 2 | HG02809.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2582+4281_2582+429 others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026464 | ||||||
| chr10:97026464
|
C | CTAAATAA others(9): Show |
1 | a0001c0002t0001g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2582+4277_2582+429 others(20): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026464 | ||||||
| chr10:97026464
|
CTAAA | C | 16 | a0001c0001t0001g0073a0001c0001t0001g0115a0001c0001t0001g0124others(13): Show | 16 | HG00639.hp1 HG01358.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2582+4289_2582+429 others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026464 | ||||||
| chr10:97026464
|
CTAAATAA others(1): Show |
C | 29 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(26): Show | 29 | HG01261.hp1 HG01361.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.2582+4285_2582+429 others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026464 | ||||||
| chr10:97026489
|
TAAATA | T | 8 | a0001c0004t0001g0065a0001c0004t0001g0074a0001c0004t0001g0075others(5): Show | 8 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2582+4263_2582+426 others(9): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026489 | ||||||
| chr10:97026507
|
G | A | 9 | a0001c0001t0001g0124a0001c0001t0001g0160a0001c0001t0001g0214others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2582+4250C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026507 | ||||||
| chr10:97026515
|
C | A | 1 | a0001c0001t0003g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2582+4242G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026515 | ||||||
| chr10:97026527
|
G | A | 4 | a0001c0004t0001g0024a0001c0004t0001g0140a0001c0004t0001g0147others(1): Show | 4 | NA18943.hp2 NA18960.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2582+4230C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026527 | ||||||
| chr10:97026547
|
T | C | 18 | a0001c0003t0026g0170a0001c0004t0001g0024a0001c0004t0001g0044others(15): Show | 18 | HG00558.hp1 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.2582+4210A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026547 | ||||||
| chr10:97026829
|
ATCATTAC others(21): Show |
A | 1 | a0001c0004t0001g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2582+3900_2582+392 others(32): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026829 | ||||||
| chr10:97026852
|
T | C | 10 | a0001c0001t0001g0094a0001c0001t0001g0124a0001c0001t0001g0160others(7): Show | 10 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2582+3905A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026852 | ||||||
| chr10:97026855
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2582+3902C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026855 | ||||||
| chr10:97026901
|
G | A | 44 | a0001c0001t0001g0185a0001c0001t0002g0008a0001c0001t0002g0016others(41): Show | 44 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2582+3856C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97026901 | ||||||
| chr10:97027058
|
C | T | 2 | a0001c0006t0014g0213a0001c0015t0001g0177 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2582+3699G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97027058 | ||||||
| chr10:97027099
|
A | C | 36 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(33): Show | 36 | HG00639.hp1 HG00673.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.2582+3658T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97027099 | ||||||
| chr10:97027151
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2582+3606G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97027151 | ||||||
| chr10:97027279
|
C | G | 1 | a0001c0005t0009g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2582+3478G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97027279 | ||||||
| chr10:97027436
|
A | G | 1 | a0001c0005t0002g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2582+3321T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97027436 | ||||||
| chr10:97027488
|
A | G | 4 | a0001c0006t0004g0204a0001c0006t0007g0013a0001c0006t0007g0088others(1): Show | 4 | HG01109.hp2 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2582+3269T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97027488 | ||||||
| chr10:97027597
|
T | C | 171 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(168): Show | 171 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.2582+3160A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97027597 | ||||||
| chr10:97027752
|
C | T | 1 | a0001c0001t0005g0240 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2582+3005G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97027752 | ||||||
| chr10:97027805
|
C | G | 11 | a0001c0001t0001g0178a0001c0001t0001g0247a0001c0001t0003g0017others(8): Show | 11 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2582+2952G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97027805 | ||||||
| chr10:97027905
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2582+2852T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97027905 | ||||||
| chr10:97028007
|
T | C | 1 | a0001c0001t0011g0150 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2582+2750A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97028007 | ||||||
| chr10:97028125
|
A | G | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2582+2632T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97028125 | ||||||
| chr10:97028190
|
T | C | 11 | a0001c0001t0001g0094a0001c0001t0001g0215a0001c0001t0001g0246others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2582+2567A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97028190 | ||||||
| chr10:97028249
|
C | G | 40 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(37): Show | 40 | HG00558.hp1 HG00639.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.2582+2508G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97028249 | ||||||
| chr10:97028378
|
C | A | 3 | a0001c0001t0004g0019a0001c0001t0017g0015a0003c0029t0002g0014 | 3 | HG02109.hp1 HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2582+2379G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97028378 | ||||||
| chr10:97028497
|
G | A | 4 | a0001c0005t0001g0005a0001c0005t0001g0006a0001c0005t0004g0153others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2582+2260C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97028497 | ||||||
| chr10:97028744
|
T | G | 7 | a0001c0001t0001g0160a0001c0001t0001g0188a0001c0001t0013g0002others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2582+2013A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97028744 | ||||||
| chr10:97029073
|
C | T | 12 | a0001c0001t0001g0131a0001c0001t0002g0224a0001c0001t0004g0200others(9): Show | 12 | HG02165.hp2 HG02602.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.2582+1684G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97029073 | ||||||
| chr10:97029170
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2582+1587T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97029170 | ||||||
| chr10:97029466
|
A | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(22): Show | 25 | HG00639.hp2 HG01123.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.2582+1291T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97029466 | ||||||
| chr10:97029674
|
C | T | 1 | a0001c0003t0001g0255 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2582+1083G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97029674 | ||||||
| chr10:97030023
|
G | C | 1 | a0001c0003t0001g0179 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2582+734C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97030023 | ||||||
| chr10:97030030
|
T | C | 9 | a0001c0001t0001g0054a0001c0001t0001g0214a0001c0001t0004g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2582+727A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97030030 | ||||||
| chr10:97030163
|
C | T | 1 | a0001c0003t0001g0126 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2582+594G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97030163 | ||||||
| chr10:97030396
|
T | C | 97 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(94): Show | 97 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.2582+361A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97030396 | ||||||
| chr10:97030397
|
G | A | 1 | a0006c0027t0025g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2582+360C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97030397 | ||||||
| chr10:97030483
|
G | A | 2 | a0001c0002t0001g0025a0001c0002t0001g0149 | 2 | NA18939.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.2582+274C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97030483 | ||||||
| chr10:97030495
|
A | G | 3 | a0001c0008t0003g0085a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02451.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2582+262T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 25/36 | chr10 | 97030495 | ||||||
| chr10:97030917
|
G | C | 77 | a0001c0001t0001g0078a0001c0001t0001g0121a0001c0001t0001g0122others(74): Show | 77 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.2511-89C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 24/36 | chr10 | 97030917 | ||||||
| chr10:97031049
|
A | G | 6 | a0001c0001t0001g0054a0001c0001t0001g0214a0001c0001t0011g0150others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2511-221T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 24/36 | chr10 | 97031049 | ||||||
| chr10:97031050
|
CTG | C | 59 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0185others(56): Show | 59 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2511-224_2511-223d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 24/36 | chr10 | 97031050 | ||||||
| chr10:97031202
|
C | CT | 89 | a0001c0001t0001g0078a0001c0001t0001g0121a0001c0001t0001g0122others(86): Show | 89 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.2511-375dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 24/36 | chr10 | 97031202 | ||||||
| chr10:97031221
|
T | G | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2510+385A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 24/36 | chr10 | 97031221 | ||||||
| chr10:97031270
|
C | T | 41 | a0001c0001t0001g0156a0001c0001t0001g0185a0001c0001t0002g0016others(38): Show | 41 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.2510+336G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 24/36 | chr10 | 97031270 | ||||||
| chr10:97031326
|
T | C | 6 | a0001c0001t0001g0160a0001c0001t0001g0188a0001c0007t0003g0114others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2510+280A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 24/36 | chr10 | 97031326 | ||||||
| chr10:97031368
|
C | G | 41 | a0001c0001t0001g0156a0001c0001t0001g0185a0001c0001t0002g0016others(38): Show | 41 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.2510+238G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 24/36 | chr10 | 97031368 | ||||||
| chr10:97031508
|
G | A | 36 | a0001c0001t0001g0156a0001c0001t0001g0185a0001c0001t0002g0016others(33): Show | 36 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.2510+98C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 24/36 | chr10 | 97031508 | ||||||
| chr10:97031682
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01243.hp2 | splice_region_variant&intron_variant | LOW | c.2439-5C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97031682 | ||||||
| chr10:97031739
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2439-62G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97031739 | ||||||
| chr10:97031810
|
C | T | 1 | a0001c0003t0011g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2439-133G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97031810 | ||||||
| chr10:97031821
|
T | G | 77 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(74): Show | 77 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.2439-144A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97031821 | ||||||
| chr10:97031824
|
G | A | 77 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(74): Show | 77 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.2439-147C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97031824 | ||||||
| chr10:97031833
|
C | T | 1 | a0001c0005t0002g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2439-156G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97031833 | ||||||
| chr10:97032005
|
A | G | 4 | a0001c0001t0005g0130a0001c0001t0005g0240a0001c0001t0021g0031others(1): Show | 4 | HG00140.hp2 HG01433.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.2439-328T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032005 | ||||||
| chr10:97032188
|
A | G | 12 | a0001c0001t0001g0094a0001c0001t0001g0215a0001c0001t0001g0246others(9): Show | 12 | HG01081.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2439-511T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032188 | ||||||
| chr10:97032382
|
G | A | 125 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0033others(122): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2439-705C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032382 | ||||||
| chr10:97032398
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0242others(6): Show | 9 | HG01123.hp2 HG01261.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.2439-721C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032398 | ||||||
| chr10:97032570
|
C | A | 1 | a0001c0001t0001g0211 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2439-893G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032570 | ||||||
| chr10:97032570
|
C | CA | 13 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0022g0254others(10): Show | 13 | HG00280.hp1 HG00735.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.2439-894dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032570 | ||||||
| chr10:97032570
|
CA | C | 16 | a0001c0001t0001g0100a0001c0001t0001g0135a0001c0001t0001g0160others(13): Show | 16 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.2439-894delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032570 | ||||||
| chr10:97032668
|
A | G | 75 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(72): Show | 75 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.2439-991T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032668 | ||||||
| chr10:97032702
|
C | T | 3 | a0001c0001t0006g0038a0002c0013t0006g0029a0002c0013t0006g0030 | 3 | HG01515.hp1 HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2439-1025G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032702 | ||||||
| chr10:97032724
|
A | G | 45 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0033others(42): Show | 45 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.2439-1047T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032724 | ||||||
| chr10:97032744
|
C | T | 10 | a0001c0001t0001g0160a0001c0001t0001g0188a0001c0001t0001g0215others(7): Show | 10 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2439-1067G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032744 | ||||||
| chr10:97032750
|
GT | G | 102 | a0001c0001t0001g0022a0001c0001t0001g0043a0001c0001t0001g0048others(99): Show | 102 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.2439-1074delA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032750 | ||||||
| chr10:97032752
|
T | C | 10 | a0001c0001t0001g0160a0001c0001t0001g0188a0001c0001t0001g0215others(7): Show | 10 | HG01891.hp2 HG02451.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2439-1075A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032752 | ||||||
| chr10:97032763
|
C | T | 121 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0034others(118): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.2439-1086G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032763 | ||||||
| chr10:97032802
|
A | G | 118 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0023others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.2439-1125T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032802 | ||||||
| chr10:97032825
|
G | A | 21 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0099others(18): Show | 21 | HG01243.hp1 HG01891.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2439-1148C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032825 | ||||||
| chr10:97032992
|
G | A | 3 | a0001c0001t0001g0242a0002c0014t0001g0202a0002c0014t0001g0227 | 3 | HG01261.hp1 HG01361.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.2439-1315C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97032992 | ||||||
| chr10:97033050
|
C | CT | 58 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0001g0156others(55): Show | 58 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.2439-1374dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033050 | ||||||
| chr10:97033050
|
C | T | 2 | a0001c0015t0001g0177a0001c0026t0004g0090 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2439-1373G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033050 | ||||||
| chr10:97033050
|
CT | C | 15 | a0001c0001t0001g0160a0001c0001t0001g0188a0001c0001t0004g0200others(12): Show | 15 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2439-1374delA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033050 | ||||||
| chr10:97033078
|
C | T | 14 | a0001c0001t0001g0160a0001c0001t0001g0188a0001c0001t0004g0200others(11): Show | 14 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2438+1393G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033078 | ||||||
| chr10:97033453
|
C | CA | 4 | a0001c0005t0001g0005a0001c0005t0001g0006a0001c0005t0004g0153others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2438+1017dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033453 | ||||||
| chr10:97033547
|
C | T | 4 | a0001c0008t0003g0060a0001c0008t0003g0082a0001c0008t0003g0084others(1): Show | 4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2438+924G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033547 | ||||||
| chr10:97033768
|
T | C | 1 | a0001c0003t0006g0036 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2438+703A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033768 | ||||||
| chr10:97033800
|
T | C | 25 | a0001c0001t0001g0007a0001c0001t0006g0038a0001c0003t0001g0035others(22): Show | 25 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.2438+671A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033800 | ||||||
| chr10:97033817
|
C | T | 3 | a0001c0004t0003g0176a0001c0015t0001g0177a0001c0026t0004g0090 | 3 | HG02258.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2438+654G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033817 | ||||||
| chr10:97033848
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2438+623A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033848 | ||||||
| chr10:97033860
|
A | AT | 63 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(60): Show | 63 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.2438+610dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033860 | ||||||
| chr10:97033860
|
A | ATT | 24 | a0001c0001t0001g0051a0001c0002t0001g0021a0001c0002t0001g0025others(21): Show | 24 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.2438+609_2438+610d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033860 | ||||||
| chr10:97033860
|
AT | A | 37 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0054others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.2438+610delA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033860 | ||||||
| chr10:97033958
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0118others(3): Show | 6 | HG00639.hp2 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2438+513T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97033958 | ||||||
| chr10:97034006
|
A | G | 75 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(72): Show | 75 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.2438+465T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97034006 | ||||||
| chr10:97034019
|
C | T | 3 | a0001c0008t0003g0085a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02451.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2438+452G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97034019 | ||||||
| chr10:97034077
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2438+394C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97034077 | ||||||
| chr10:97034107
|
C | T | 3 | a0001c0001t0001g0214a0001c0005t0001g0052a0001c0030t0001g0010 | 3 | HG02109.hp2 HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2438+364G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97034107 | ||||||
| chr10:97034144
|
C | T | 6 | a0001c0001t0001g0246a0001c0007t0001g0057a0001c0007t0001g0058others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2438+327G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97034144 | ||||||
| chr10:97034302
|
A | G | 22 | a0001c0001t0006g0038a0001c0003t0001g0035a0001c0003t0001g0064others(19): Show | 22 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2438+169T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97034302 | ||||||
| chr10:97034321
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2438+150T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97034321 | ||||||
| chr10:97034364
|
G | A | 5 | a0001c0001t0001g0160a0001c0007t0003g0114a0001c0008t0003g0085others(2): Show | 5 | HG02451.hp1 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2438+107C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97034364 | ||||||
| chr10:97034365
|
G | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0118others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2438+106C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97034365 | ||||||
| chr10:97034438
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2438+33C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 23/36 | chr10 | 97034438 | ||||||
| chr10:97034690
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2367-148C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97034690 | ||||||
| chr10:97034750
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0005g0136a0001c0009t0005g0238 | 3 | HG00280.hp2 HG01123.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2367-208C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97034750 | ||||||
| chr10:97034765
|
A | G | 1 | a0001c0003t0011g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2367-223T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97034765 | ||||||
| chr10:97034858
|
C | T | 139 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(136): Show | 139 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.2367-316G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97034858 | ||||||
| chr10:97034914
|
G | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0099a0001c0004t0001g0074others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2367-372C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97034914 | ||||||
| chr10:97034932
|
C | T | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2367-390G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97034932 | ||||||
| chr10:97035120
|
T | C | 139 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(136): Show | 139 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.2367-578A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97035120 | ||||||
| chr10:97035121
|
C | T | 70 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(67): Show | 70 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.2367-579G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97035121 | ||||||
| chr10:97035122
|
T | G | 139 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(136): Show | 139 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.2367-580A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97035122 | ||||||
| chr10:97035127
|
T | TCTC | 139 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(136): Show | 139 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.2367-588_2367-586d others(5): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97035127 | ||||||
| chr10:97035136
|
A | C | 4 | a0001c0005t0001g0005a0001c0005t0001g0006a0001c0005t0004g0153others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2367-594T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97035136 | ||||||
| chr10:97035148
|
A | AC | 3 | a0001c0001t0001g0214a0001c0001t0001g0241a0001c0009t0001g0239 | 3 | HG02055.hp2 HG02109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2367-607dupG | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97035148 | ||||||
| chr10:97035277
|
G | T | 1 | a0001c0002t0002g0095 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2367-735C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97035277 | ||||||
| chr10:97035342
|
C | T | 1 | a0001c0005t0009g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2367-800G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97035342 | ||||||
| chr10:97035710
|
C | G | 77 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(74): Show | 77 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.2367-1168G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97035710 | ||||||
| chr10:97035989
|
C | A | 1 | a0001c0001t0002g0201 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2367-1447G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97035989 | ||||||
| chr10:97036020
|
C | T | 1 | a0001c0002t0002g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2367-1478G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97036020 | ||||||
| chr10:97036173
|
G | A | 3 | a0001c0005t0001g0045a0001c0005t0001g0192a0001c0005t0002g0020 | 3 | HG01081.hp1 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2366+1525C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97036173 | ||||||
| chr10:97036429
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2366+1269C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97036429 | ||||||
| chr10:97036668
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2366+1030C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97036668 | ||||||
| chr10:97036716
|
G | A | 92 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0094others(89): Show | 92 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.2366+982C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97036716 | ||||||
| chr10:97036753
|
G | A | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2366+945C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97036753 | ||||||
| chr10:97036884
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2366+814A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97036884 | ||||||
| chr10:97036956
|
T | C | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2366+742A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97036956 | ||||||
| chr10:97037048
|
T | TTG | 37 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0071others(34): Show | 37 | HG00621.hp1 HG00621.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.2366+648_2366+649d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037048 | ||||||
| chr10:97037048
|
T | TTGTG | 4 | a0001c0001t0001g0103a0001c0001t0001g0198a0001c0001t0001g0242others(1): Show | 4 | HG00558.hp1 HG01515.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.2366+646_2366+649d others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037048 | ||||||
| chr10:97037048
|
T | TTGTGTGT others(3): Show |
1 | a0001c0006t0007g0013 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2366+640_2366+649d others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037048 | ||||||
| chr10:97037048
|
TTG | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0072others(52): Show | 55 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.2366+648_2366+649d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037048 | ||||||
| chr10:97037048
|
TTGTG | T | 34 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0041others(31): Show | 34 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.2366+646_2366+649d others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037048 | ||||||
| chr10:97037048
|
TTGTGTG | T | 15 | a0001c0001t0001g0245a0001c0001t0022g0254a0001c0002t0001g0181others(12): Show | 15 | HG00597.hp2 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.2366+644_2366+649d others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037048 | ||||||
| chr10:97037048
|
TTGTGTGT others(1): Show |
T | 14 | a0001c0001t0001g0054a0001c0001t0004g0018a0001c0001t0006g0038others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.2366+642_2366+649d others(10): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037048 | ||||||
| chr10:97037048
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0003t0001g0126 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2366+640_2366+649d others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037048 | ||||||
| chr10:97037098
|
G | A | 10 | a0001c0001t0001g0054a0001c0001t0001g0214a0001c0001t0003g0169others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2366+600C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037098 | ||||||
| chr10:97037100
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0214 | 2 | HG00438.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2366+598T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037100 | ||||||
| chr10:97037113
|
T | A | 1 | a0001c0001t0001g0214 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2366+585A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037113 | ||||||
| chr10:97037348
|
G | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0198a0001c0012t0002g0047 | 3 | HG00639.hp1 HG02071.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2366+350C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037348 | ||||||
| chr10:97037397
|
G | T | 3 | a0001c0003t0001g0064a0001c0003t0002g0219a0001c0003t0015g0087 | 3 | HG02723.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2366+301C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037397 | ||||||
| chr10:97037461
|
C | T | 1 | a0001c0004t0003g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2366+237G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037461 | ||||||
| chr10:97037493
|
A | G | 10 | a0001c0001t0003g0169a0001c0005t0001g0005a0001c0005t0001g0006others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2366+205T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037493 | ||||||
| chr10:97037594
|
A | G | 254 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(251): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.2366+104T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037594 | ||||||
| chr10:97037603
|
C | T | 22 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0099others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2366+95G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037603 | ||||||
| chr10:97037683
|
G | A | 1 | a0001c0002t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2366+15C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 22/36 | chr10 | 97037683 | ||||||
| chr10:97037890
|
G | T | 20 | a0001c0001t0006g0038a0001c0003t0001g0035a0001c0003t0001g0089others(17): Show | 20 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.2298-124C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97037890 | ||||||
| chr10:97037929
|
C | T | 5 | a0001c0003t0001g0064a0001c0003t0001g0179a0001c0003t0002g0219others(2): Show | 5 | HG02723.hp1 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2298-163G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97037929 | ||||||
| chr10:97038001
|
C | T | 1 | a0001c0007t0001g0218 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2298-235G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97038001 | ||||||
| chr10:97038013
|
C | T | 1 | a0001c0002t0001g0070 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2298-247G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97038013 | ||||||
| chr10:97039002
|
T | C | 23 | a0001c0002t0001g0021a0001c0002t0001g0025a0001c0002t0001g0067others(20): Show | 23 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.2297+986A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97039002 | ||||||
| chr10:97039011
|
T | C | 3 | a0001c0008t0003g0085a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02451.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2297+977A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97039011 | ||||||
| chr10:97039149
|
A | T | 1 | a0001c0003t0001g0255 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2297+839T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97039149 | ||||||
| chr10:97039170
|
G | A | 3 | a0001c0008t0003g0085a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02451.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2297+818C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97039170 | ||||||
| chr10:97039501
|
C | G | 1 | a0001c0001t0002g0251 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2297+487G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97039501 | ||||||
| chr10:97039559
|
T | TA | 25 | a0001c0002t0001g0021a0001c0002t0001g0025a0001c0002t0001g0067others(22): Show | 25 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.2297+428dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97039559 | ||||||
| chr10:97039684
|
C | T | 4 | a0001c0001t0002g0008a0001c0001t0002g0142a0001c0001t0002g0196others(1): Show | 4 | NA18952.hp2 NA18960.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.2297+304G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97039684 | ||||||
| chr10:97039718
|
C | T | 3 | a0001c0008t0003g0085a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02451.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2297+270G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97039718 | ||||||
| chr10:97039892
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2297+96G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97039892 | ||||||
| chr10:97039958
|
G | A | 2 | a0001c0001t0001g0205a0001c0012t0001g0053 | 2 | HG00408.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2297+30C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 21/36 | chr10 | 97039958 | ||||||
| chr10:97040342
|
G | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0041others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.2165-222C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97040342 | ||||||
| chr10:97040397
|
C | T | 1 | a0001c0018t0009g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2165-277G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97040397 | ||||||
| chr10:97040612
|
A | G | 233 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(230): Show | 233 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.2165-492T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97040612 | ||||||
| chr10:97040719
|
C | T | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2165-599G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97040719 | ||||||
| chr10:97040745
|
C | G | 34 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0078others(31): Show | 34 | HG01109.hp2 HG01123.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.2165-625G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97040745 | ||||||
| chr10:97040881
|
A | T | 2 | a0001c0006t0001g0056a0001c0006t0009g0055 | 2 | HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2165-761T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97040881 | ||||||
| chr10:97040904
|
G | A | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2165-784C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97040904 | ||||||
| chr10:97041168
|
G | C | 2 | a0001c0006t0014g0213a0006c0027t0025g0220 | 2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2165-1048C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97041168 | ||||||
| chr10:97041306
|
G | A | 1 | a0001c0011t0001g0187 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2165-1186C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97041306 | ||||||
| chr10:97041473
|
A | AT | 21 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(18): Show | 21 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2165-1354dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97041473 | ||||||
| chr10:97041473
|
AT | A | 21 | a0001c0001t0001g0050a0001c0003t0001g0035a0001c0003t0001g0089others(18): Show | 21 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2165-1354delA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97041473 | ||||||
| chr10:97041521
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2164+1380C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97041521 | ||||||
| chr10:97041529
|
C | T | 1 | a0001c0005t0001g0192 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2164+1372G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97041529 | ||||||
| chr10:97041552
|
A | G | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2164+1349T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97041552 | ||||||
| chr10:97041697
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2164+1204G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97041697 | ||||||
| chr10:97041853
|
AAAG | A | 22 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0051others(19): Show | 22 | HG00558.hp1 HG00597.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.2164+1045_2164+104 others(7): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97041853 | ||||||
| chr10:97042057
|
C | G | 17 | a0001c0003t0001g0035a0001c0003t0001g0089a0001c0003t0001g0096others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.2164+844G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97042057 | ||||||
| chr10:97042124
|
A | T | 5 | a0001c0008t0003g0060a0001c0008t0003g0082a0001c0008t0003g0084others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2164+777T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97042124 | ||||||
| chr10:97042336
|
G | A | 1 | a0001c0001t0010g0197 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2164+565C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97042336 | ||||||
| chr10:97042738
|
C | G | 64 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(61): Show | 64 | HG00558.hp1 HG00597.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.2164+163G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97042738 | ||||||
| chr10:97042832
|
T | C | 6 | a0001c0001t0003g0169a0001c0008t0003g0060a0001c0008t0003g0082others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2164+69A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 20/36 | chr10 | 97042832 | ||||||
| chr10:97043346
|
G | T | 1 | a0001c0004t0001g0228 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1997+24C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 19/36 | chr10 | 97043346 | ||||||
| chr10:97043361
|
C | T | 4 | a0001c0003t0001g0064a0001c0003t0002g0219a0001c0003t0015g0087others(1): Show | 4 | HG02723.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1997+9G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 19/36 | chr10 | 97043361 | ||||||
| chr10:97043542
|
G | C | 1 | a0001c0005t0001g0192 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1854-29C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97043542 | ||||||
| chr10:97043550
|
C | T | 2 | a0001c0015t0001g0177a0001c0026t0004g0090 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1854-37G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97043550 | ||||||
| chr10:97043760
|
C | T | 2 | a0001c0015t0001g0177a0001c0026t0004g0090 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1854-247G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97043760 | ||||||
| chr10:97043816
|
G | A | 4 | a0001c0005t0001g0005a0001c0005t0001g0006a0001c0005t0004g0153others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1854-303C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97043816 | ||||||
| chr10:97043824
|
G | A | 26 | a0001c0002t0001g0021a0001c0002t0001g0025a0001c0002t0001g0037others(23): Show | 26 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1854-311C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97043824 | ||||||
| chr10:97043921
|
C | T | 40 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(37): Show | 40 | HG00558.hp1 HG00597.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1854-408G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97043921 | ||||||
| chr10:97043933
|
G | A | 26 | a0001c0002t0001g0021a0001c0002t0001g0025a0001c0002t0001g0037others(23): Show | 26 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1854-420C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97043933 | ||||||
| chr10:97043966
|
C | T | 1 | a0006c0027t0025g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1854-453G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97043966 | ||||||
| chr10:97044039
|
C | T | 1 | a0001c0005t0009g0091 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1854-526G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97044039 | ||||||
| chr10:97044186
|
G | A | 2 | a0001c0015t0001g0177a0001c0026t0004g0090 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1854-673C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97044186 | ||||||
| chr10:97044233
|
A | G | 1 | a0001c0003t0001g0230 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1854-720T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97044233 | ||||||
| chr10:97044240
|
T | G | 44 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(41): Show | 44 | HG00558.hp1 HG00597.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1854-727A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97044240 | ||||||
| chr10:97044263
|
G | C | 2 | a0001c0004t0001g0165a0001c0004t0001g0166 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1854-750C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97044263 | ||||||
| chr10:97044289
|
G | T | 28 | a0001c0001t0001g0214a0001c0002t0001g0021a0001c0002t0001g0025others(25): Show | 28 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1854-776C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97044289 | ||||||
| chr10:97044568
|
T | C | 250 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(247): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1854-1055A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97044568 | ||||||
| chr10:97044860
|
C | T | 1 | a0001c0003t0001g0179 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1854-1347G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97044860 | ||||||
| chr10:97045271
|
C | T | 48 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(45): Show | 48 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1853+1383G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97045271 | ||||||
| chr10:97045415
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1853+1239A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97045415 | ||||||
| chr10:97045534
|
A | T | 1 | a0001c0001t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1853+1120T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97045534 | ||||||
| chr10:97045559
|
C | T | 1 | a0001c0003t0011g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1853+1095G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97045559 | ||||||
| chr10:97045620
|
A | G | 1 | a0001c0003t0001g0126 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1853+1034T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97045620 | ||||||
| chr10:97045674
|
A | G | 2 | a0001c0015t0001g0177a0001c0026t0004g0090 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1853+980T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97045674 | ||||||
| chr10:97045855
|
T | C | 226 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(223): Show | 226 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1853+799A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97045855 | ||||||
| chr10:97046025
|
G | A | 4 | a0001c0004t0001g0065a0001c0004t0001g0165a0001c0004t0001g0166others(1): Show | 4 | HG00741.hp1 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.1853+629C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 18/36 | chr10 | 97046025 | ||||||
| chr10:97046812
|
G | A | 2 | a0001c0015t0001g0177a0001c0026t0004g0090 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1710-15C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 17/36 | chr10 | 97046812 | ||||||
| chr10:97046920
|
A | T | 26 | a0001c0002t0001g0021a0001c0002t0001g0025a0001c0002t0001g0037others(23): Show | 26 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1709+71T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 17/36 | chr10 | 97046920 | ||||||
| chr10:97047139
|
T | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1635-74A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 16/36 | chr10 | 97047139 | ||||||
| chr10:97047338
|
A | C | 1 | a0001c0009t0001g0039 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1635-273T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 16/36 | chr10 | 97047338 | ||||||
| chr10:97047511
|
G | A | 2 | a0001c0015t0001g0177a0001c0026t0004g0090 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1634+179C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 16/36 | chr10 | 97047511 | ||||||
| chr10:97047647
|
C | T | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1634+43G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 16/36 | chr10 | 97047647 | ||||||
| chr10:97047670
|
G | C | 1 | a0001c0004t0001g0210 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1634+20C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 16/36 | chr10 | 97047670 | ||||||
| chr10:97047878
|
G | A | 26 | a0001c0002t0001g0021a0001c0002t0001g0025a0001c0002t0001g0037others(23): Show | 26 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1490-44C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 15/36 | chr10 | 97047878 | ||||||
| chr10:97048172
|
G | A | 9 | a0001c0008t0003g0060a0001c0008t0003g0082a0001c0008t0003g0084others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1466-176C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048172 | ||||||
| chr10:97048264
|
G | A | 4 | a0001c0005t0001g0005a0001c0005t0001g0006a0001c0005t0004g0153others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1466-268C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048264 | ||||||
| chr10:97048286
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1466-290G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048286 | ||||||
| chr10:97048308
|
C | A | 24 | a0001c0001t0001g0214a0001c0003t0001g0035a0001c0003t0001g0064others(21): Show | 24 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.1466-312G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048308 | ||||||
| chr10:97048350
|
C | T | 1 | a0001c0018t0009g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1466-354G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048350 | ||||||
| chr10:97048388
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1466-392A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048388 | ||||||
| chr10:97048421
|
T | C | 9 | a0001c0008t0003g0060a0001c0008t0003g0082a0001c0008t0003g0084others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1466-425A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048421 | ||||||
| chr10:97048453
|
T | C | 6 | a0001c0001t0001g0041a0001c0001t0001g0099a0001c0004t0001g0074others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1466-457A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048453 | ||||||
| chr10:97048756
|
T | C | 5 | a0001c0008t0003g0060a0001c0008t0003g0082a0001c0008t0003g0084others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1465+199A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048756 | ||||||
| chr10:97048759
|
G | A | 5 | a0001c0001t0001g0097a0001c0001t0002g0251a0001c0010t0002g0003others(2): Show | 5 | HG03017.hp1 HG03490.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.1465+196C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048759 | ||||||
| chr10:97048849
|
G | A | 1 | a0001c0002t0001g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1465+106C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048849 | ||||||
| chr10:97048852
|
T | TAGGTGGA others(1): Show |
217 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1465+102_1465+103i others(10): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048852 | ||||||
| chr10:97048852
|
T | TAGGTGGA others(9): Show |
19 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0099others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1465+102_1465+103i others(18): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048852 | ||||||
| chr10:97048864
|
T | C | 26 | a0001c0001t0001g0124a0001c0001t0001g0214a0001c0001t0013g0002others(23): Show | 26 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1465+91A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048864 | ||||||
| chr10:97048945
|
G | A | 2 | a0001c0001t0001g0214a0001c0030t0001g0010 | 2 | HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1465+10C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 14/36 | chr10 | 97048945 | ||||||
| chr10:97049237
|
A | G | 1 | a0001c0003t0001g0184 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1302-119T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97049237 | ||||||
| chr10:97049437
|
C | T | 2 | a0001c0001t0001g0214a0001c0030t0001g0010 | 2 | HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1302-319G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97049437 | ||||||
| chr10:97049472
|
G | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(36): Show | 39 | HG00558.hp1 HG00639.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1302-354C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97049472 | ||||||
| chr10:97049477
|
G | C | 15 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(12): Show | 15 | HG00639.hp2 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1302-359C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97049477 | ||||||
| chr10:97049520
|
G | C | 2 | a0001c0015t0001g0177a0001c0026t0004g0090 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1302-402C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97049520 | ||||||
| chr10:97049774
|
A | G | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1302-656T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97049774 | ||||||
| chr10:97049857
|
G | A | 3 | a0001c0008t0003g0085a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02451.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1302-739C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97049857 | ||||||
| chr10:97049862
|
T | C | 40 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(37): Show | 40 | HG00558.hp1 HG00639.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1302-744A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97049862 | ||||||
| chr10:97049869
|
G | T | 26 | a0001c0002t0001g0021a0001c0002t0001g0025a0001c0002t0001g0037others(23): Show | 26 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1302-751C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97049869 | ||||||
| chr10:97049902
|
C | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1302-784G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97049902 | ||||||
| chr10:97049924
|
C | A | 44 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(41): Show | 44 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.1302-806G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97049924 | ||||||
| chr10:97049946
|
A | G | 72 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1302-828T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97049946 | ||||||
| chr10:97050088
|
C | T | 5 | a0001c0001t0001g0246a0001c0007t0001g0057a0001c0007t0001g0058others(2): Show | 5 | HG02055.hp1 HG02615.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302-970G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97050088 | ||||||
| chr10:97050216
|
A | G | 8 | a0001c0001t0001g0215a0001c0001t0001g0246a0001c0001t0028g0093others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302-1098T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97050216 | ||||||
| chr10:97050353
|
C | G | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1302-1235G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97050353 | ||||||
| chr10:97050415
|
C | T | 1 | a0001c0001t0005g0240 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1302-1297G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97050415 | ||||||
| chr10:97050489
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1302-1371G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97050489 | ||||||
| chr10:97050570
|
T | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(37): Show | 40 | HG00558.hp1 HG00639.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1302-1452A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97050570 | ||||||
| chr10:97050614
|
T | C | 53 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0054others(50): Show | 53 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1302-1496A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97050614 | ||||||
| chr10:97050808
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1302-1690C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97050808 | ||||||
| chr10:97050983
|
GA | G | 31 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0078others(28): Show | 31 | HG01123.hp2 HG01891.hp2 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1302-1866delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97050983 | ||||||
| chr10:97051059
|
C | A | 2 | a0001c0015t0001g0177a0001c0026t0004g0090 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1302-1941G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051059 | ||||||
| chr10:97051124
|
T | C | 154 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(151): Show | 154 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1302-2006A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051124 | ||||||
| chr10:97051135
|
A | G | 31 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0078others(28): Show | 31 | HG01123.hp2 HG01891.hp2 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1302-2017T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051135 | ||||||
| chr10:97051261
|
C | CA | 28 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0099others(25): Show | 28 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302-2144dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051261 | ||||||
| chr10:97051261
|
C | CAA | 11 | a0001c0001t0001g0124a0001c0001t0001g0214a0001c0003t0001g0064others(8): Show | 11 | HG01884.hp1 HG02109.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1302-2145_1302-214 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051261 | ||||||
| chr10:97051261
|
C | CAAA | 16 | a0001c0003t0001g0035a0001c0003t0001g0089a0001c0003t0001g0096others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1302-2146_1302-214 others(7): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051261 | ||||||
| chr10:97051261
|
CA | C | 153 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(150): Show | 153 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1302-2144delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051261 | ||||||
| chr10:97051296
|
T | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0105 | 2 | HG02027.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1302-2178A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051296 | ||||||
| chr10:97051530
|
T | TGTTG | 92 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0054others(89): Show | 92 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1302-2413_1302-241 others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051530 | ||||||
| chr10:97051539
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(35): Show | 38 | HG00558.hp1 HG00639.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1302-2421G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051539 | ||||||
| chr10:97051597
|
G | A | 18 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0099others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302-2479C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051597 | ||||||
| chr10:97051621
|
T | C | 91 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0054others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1302-2503A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051621 | ||||||
| chr10:97051655
|
C | T | 1 | a0001c0026t0004g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1302-2537G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051655 | ||||||
| chr10:97051760
|
C | T | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1302-2642G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051760 | ||||||
| chr10:97051766
|
C | T | 39 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(36): Show | 39 | HG00558.hp1 HG00639.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1302-2648G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051766 | ||||||
| chr10:97051811
|
C | CA | 88 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0033others(85): Show | 88 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1302-2694dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051811 | ||||||
| chr10:97051811
|
CA | C | 76 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(73): Show | 76 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1302-2694delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051811 | ||||||
| chr10:97051957
|
T | C | 53 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0054others(50): Show | 53 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1302-2839A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051957 | ||||||
| chr10:97051983
|
G | A | 35 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(32): Show | 35 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1302-2865C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97051983 | ||||||
| chr10:97052090
|
G | GT | 6 | a0001c0001t0001g0124a0001c0001t0013g0002a0001c0003t0011g0012others(3): Show | 6 | HG01884.hp1 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1302-2973dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052090 | ||||||
| chr10:97052090
|
G | GTT | 5 | a0001c0008t0003g0060a0001c0008t0003g0082a0001c0008t0003g0084others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302-2974_1302-297 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052090 | ||||||
| chr10:97052090
|
G | T | 35 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(32): Show | 35 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1302-2972C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052090 | ||||||
| chr10:97052099
|
T | G | 35 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(32): Show | 35 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1302-2981A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052099 | ||||||
| chr10:97052100
|
G | T | 41 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0097others(38): Show | 41 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1302-2982C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052100 | ||||||
| chr10:97052104
|
G | GT | 62 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0078others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.1302-2987dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052104 | ||||||
| chr10:97052104
|
G | GTT | 84 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0033others(81): Show | 84 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1302-2988_1302-298 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052104 | ||||||
| chr10:97052108
|
T | G | 2 | a0001c0001t0001g0124a0001c0003t0026g0170 | 2 | HG02895.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1302-2990A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052108 | ||||||
| chr10:97052108
|
T | TG | 35 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(32): Show | 35 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1302-2991_1302-299 others(5): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052108 | ||||||
| chr10:97052113
|
T | G | 35 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(32): Show | 35 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1302-2995A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052113 | ||||||
| chr10:97052286
|
G | A | 238 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(235): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1302-3168C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052286 | ||||||
| chr10:97052349
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(35): Show | 38 | HG00558.hp1 HG00639.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.1302-3231G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052349 | ||||||
| chr10:97052384
|
G | A | 1 | a0001c0030t0001g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1302-3266C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052384 | ||||||
| chr10:97052409
|
C | T | 84 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0033others(81): Show | 84 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1302-3291G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052409 | ||||||
| chr10:97052452
|
G | A | 5 | a0001c0005t0001g0005a0001c0005t0001g0006a0001c0005t0001g0052others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302-3334C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052452 | ||||||
| chr10:97052500
|
G | C | 3 | a0001c0008t0003g0085a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02451.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1302-3382C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052500 | ||||||
| chr10:97052526
|
C | T | 200 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(197): Show | 200 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1302-3408G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052526 | ||||||
| chr10:97052540
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1302-3422T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052540 | ||||||
| chr10:97052564
|
A | G | 2 | a0001c0015t0001g0177a0001c0026t0004g0090 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1302-3446T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052564 | ||||||
| chr10:97052597
|
G | C | 68 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0043others(65): Show | 68 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.1302-3479C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052597 | ||||||
| chr10:97052611
|
T | C | 2 | a0001c0001t0013g0002a0001c0003t0011g0012 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1302-3493A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052611 | ||||||
| chr10:97052770
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1301+3551T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052770 | ||||||
| chr10:97052838
|
C | T | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1301+3483G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052838 | ||||||
| chr10:97052879
|
C | T | 123 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0022others(120): Show | 123 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1301+3442G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052879 | ||||||
| chr10:97052943
|
C | T | 26 | a0001c0002t0001g0021a0001c0002t0001g0025a0001c0002t0001g0037others(23): Show | 26 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1301+3378G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97052943 | ||||||
| chr10:97053494
|
C | T | 1 | a0001c0001t0011g0150 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1301+2827G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97053494 | ||||||
| chr10:97053495
|
G | A | 32 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0078others(29): Show | 32 | HG01123.hp2 HG01891.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1301+2826C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97053495 | ||||||
| chr10:97053614
|
A | C | 116 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1301+2707T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97053614 | ||||||
| chr10:97053798
|
A | T | 3 | a0001c0005t0001g0045a0001c0005t0001g0192a0001c0005t0002g0020 | 3 | HG01081.hp1 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1301+2523T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97053798 | ||||||
| chr10:97053876
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1301+2445C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97053876 | ||||||
| chr10:97053953
|
T | G | 1 | a0001c0003t0011g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1301+2368A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97053953 | ||||||
| chr10:97053956
|
G | A | 18 | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0099others(15): Show | 18 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1301+2365C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97053956 | ||||||
| chr10:97053966
|
C | T | 240 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(237): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1301+2355G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97053966 | ||||||
| chr10:97054036
|
G | T | 1 | a0001c0001t0001g0049 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1301+2285C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97054036 | ||||||
| chr10:97054099
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0178a0001c0001t0001g0247 | 3 | HG01884.hp2 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1301+2222G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97054099 | ||||||
| chr10:97054327
|
T | C | 3 | a0001c0008t0003g0085a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02451.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1301+1994A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97054327 | ||||||
| chr10:97054391
|
T | C | 200 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1301+1930A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97054391 | ||||||
| chr10:97054418
|
T | C | 4 | a0001c0005t0001g0005a0001c0005t0001g0006a0001c0005t0004g0153others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301+1903A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97054418 | ||||||
| chr10:97054524
|
C | T | 1 | a0001c0020t0001g0079 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1301+1797G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97054524 | ||||||
| chr10:97054614
|
A | G | 1 | a0001c0005t0001g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1301+1707T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97054614 | ||||||
| chr10:97054982
|
C | T | 83 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0033others(80): Show | 83 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1301+1339G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97054982 | ||||||
| chr10:97054989
|
A | G | 254 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(251): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1301+1332T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97054989 | ||||||
| chr10:97055028
|
C | T | 3 | a0001c0005t0001g0045a0001c0005t0001g0192a0001c0005t0002g0020 | 3 | HG01081.hp1 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1301+1293G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97055028 | ||||||
| chr10:97055090
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1301+1231C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97055090 | ||||||
| chr10:97055234
|
C | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0161 | 3 | HG02622.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1301+1087G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97055234 | ||||||
| chr10:97055254
|
T | G | 120 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0041others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1301+1067A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97055254 | ||||||
| chr10:97055283
|
C | T | 247 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(244): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1301+1038G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97055283 | ||||||
| chr10:97055534
|
A | T | 244 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1301+787T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97055534 | ||||||
| chr10:97055554
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1301+767C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97055554 | ||||||
| chr10:97055882
|
T | G | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1301+439A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97055882 | ||||||
| chr10:97056100
|
G | A | 124 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0022others(121): Show | 124 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1301+221C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97056100 | ||||||
| chr10:97056100
|
G | T | 1 | a0001c0030t0001g0010 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1301+221C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97056100 | ||||||
| chr10:97056135
|
A | G | 6 | a0001c0003t0011g0012a0001c0008t0003g0085a0001c0011t0001g0157others(3): Show | 6 | HG01884.hp1 HG02451.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1301+186T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97056135 | ||||||
| chr10:97056227
|
C | T | 1 | a0001c0001t0002g0134 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1301+94G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97056227 | ||||||
| chr10:97056274
|
G | C | 2 | a0001c0001t0001g0033a0001c0001t0006g0038 | 2 | HG00738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1301+47C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 13/36 | chr10 | 97056274 | ||||||
| chr10:97056542
|
C | T | 31 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0078others(28): Show | 31 | HG01123.hp2 HG01891.hp2 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1158-78G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056542 | ||||||
| chr10:97056616
|
C | A | 83 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0033others(80): Show | 83 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1158-152G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056616 | ||||||
| chr10:97056621
|
G | A | 2 | a0001c0004t0001g0165a0001c0004t0001g0166 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1158-157C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056621 | ||||||
| chr10:97056624
|
G | C | 1 | a0001c0004t0001g0117 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1158-160C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056624 | ||||||
| chr10:97056649
|
C | T | 114 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0041others(111): Show | 114 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1158-185G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056649 | ||||||
| chr10:97056686
|
C | T | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1158-222G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056686 | ||||||
| chr10:97056761
|
TG | T | 115 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0041others(112): Show | 115 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1158-298delC | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056761 | ||||||
| chr10:97056762
|
G | A | 42 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0048others(39): Show | 42 | HG00280.hp1 HG00408.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1158-298C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056762 | ||||||
| chr10:97056762
|
G | T | 1 | a0001c0005t0002g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1158-298C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056762 | ||||||
| chr10:97056763
|
G | A | 6 | a0001c0003t0011g0012a0001c0008t0003g0085a0001c0011t0001g0157others(3): Show | 6 | HG01884.hp1 HG02451.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158-299C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056763 | ||||||
| chr10:97056892
|
G | C | 1 | a0001c0002t0001g0021 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1157+318C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056892 | ||||||
| chr10:97056908
|
C | A | 4 | a0001c0001t0002g0148a0001c0001t0002g0222a0001c0001t0020g0109others(1): Show | 4 | HG00438.hp2 HG00621.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1157+302G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056908 | ||||||
| chr10:97056912
|
C | G | 2 | a0001c0015t0001g0177a0001c0026t0004g0090 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1157+298G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056912 | ||||||
| chr10:97056961
|
C | G | 9 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0049others(6): Show | 9 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1157+249G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056961 | ||||||
| chr10:97056961
|
C | T | 3 | a0001c0005t0001g0045a0001c0005t0001g0192a0001c0005t0002g0020 | 3 | HG01081.hp1 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1157+249G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056961 | ||||||
| chr10:97056967
|
G | A | 3 | a0001c0005t0001g0045a0001c0005t0001g0192a0001c0005t0002g0020 | 3 | HG01081.hp1 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1157+243C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97056967 | ||||||
| chr10:97057029
|
T | C | 135 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0022others(132): Show | 135 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1157+181A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97057029 | ||||||
| chr10:97057037
|
C | G | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1157+173G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97057037 | ||||||
| chr10:97057038
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1157+172G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97057038 | ||||||
| chr10:97057101
|
C | T | 2 | a0001c0015t0001g0177a0001c0026t0004g0090 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1157+109G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 12/36 | chr10 | 97057101 | ||||||
| chr10:97057320
|
C | G | 2 | a0001c0006t0004g0204a0001c0021t0008g0028 | 2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1086-39G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 11/36 | chr10 | 97057320 | ||||||
| chr10:97057424
|
A | G | 3 | a0001c0008t0003g0085a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02451.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1086-143T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 11/36 | chr10 | 97057424 | ||||||
| chr10:97057540
|
C | T | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1086-259G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 11/36 | chr10 | 97057540 | ||||||
| chr10:97057590
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG00639.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1086-309G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 11/36 | chr10 | 97057590 | ||||||
| chr10:97057712
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1086-431T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 11/36 | chr10 | 97057712 | ||||||
| chr10:97057905
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(30): Show | 33 | HG00558.hp1 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1086-624C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 11/36 | chr10 | 97057905 | ||||||
| chr10:97057930
|
A | G | 80 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0054others(77): Show | 80 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1086-649T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 11/36 | chr10 | 97057930 | ||||||
| chr10:97058009
|
A | G | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1086-728T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 11/36 | chr10 | 97058009 | ||||||
| chr10:97058317
|
G | A | 16 | a0001c0003t0001g0035a0001c0003t0001g0089a0001c0003t0001g0096others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1086-1036C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 11/36 | chr10 | 97058317 | ||||||
| chr10:97058793
|
C | T | 3 | a0001c0005t0001g0045a0001c0005t0001g0192a0001c0005t0002g0020 | 3 | HG01081.hp1 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1085+667G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 11/36 | chr10 | 97058793 | ||||||
| chr10:97059111
|
T | C | 1 | a0001c0001t0002g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1085+349A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 11/36 | chr10 | 97059111 | ||||||
| chr10:97059144
|
G | T | 1 | a0001c0002t0001g0021 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1085+316C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 11/36 | chr10 | 97059144 | ||||||
| chr10:97059243
|
C | T | 1 | a0001c0007t0003g0114 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1085+217G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 11/36 | chr10 | 97059243 | ||||||
| chr10:97059560
|
A | G | 129 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0022others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1014-29T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 10/36 | chr10 | 97059560 | ||||||
| chr10:97059715
|
G | A | 2 | a0001c0003t0001g0171a0001c0003t0001g0172 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1014-184C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 10/36 | chr10 | 97059715 | ||||||
| chr10:97059838
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG00639.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013+249C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 10/36 | chr10 | 97059838 | ||||||
| chr10:97059940
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0078a0001c0001t0001g0188others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013+147G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 10/36 | chr10 | 97059940 | ||||||
| chr10:97060165
|
G | A | 3 | a0001c0008t0003g0085a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02451.hp1 HG03098.hp2 NA19043.hp2 |
splice_region_variant&intron_variant | LOW | c.942-7C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 9/36 | chr10 | 97060165 | ||||||
| chr10:97060310
|
G | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0049others(3): Show | 6 | HG00280.hp1 HG00738.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.942-152C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 9/36 | chr10 | 97060310 | ||||||
| chr10:97060340
|
C | T | 1 | a0001c0003t0005g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.942-182G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 9/36 | chr10 | 97060340 | ||||||
| chr10:97060352
|
A | G | 64 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(61): Show | 64 | HG00621.hp1 HG01070.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.942-194T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 9/36 | chr10 | 97060352 | ||||||
| chr10:97060379
|
A | G | 65 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0043others(62): Show | 65 | HG00621.hp1 HG01070.hp2 HG01071.hp1 others(62): Show |
intron_variant | MODIFIER | c.942-221T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 9/36 | chr10 | 97060379 | ||||||
| chr10:97060396
|
C | T | 2 | a0001c0006t0007g0088a0001c0006t0007g0209 | 2 | HG01109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.942-238G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 9/36 | chr10 | 97060396 | ||||||
| chr10:97060557
|
G | A | 15 | a0001c0001t0001g0043a0001c0001t0001g0106a0001c0001t0001g0112others(12): Show | 15 | HG00621.hp1 HG01081.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.941+83C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 9/36 | chr10 | 97060557 | ||||||
| chr10:97060604
|
G | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0118others(6): Show | 9 | HG00639.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.941+36C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 9/36 | chr10 | 97060604 | ||||||
| chr10:97060929
|
T | C | 1 | a0001c0002t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.794-142A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97060929 | ||||||
| chr10:97061017
|
A | C | 2 | a0001c0001t0001g0111a0001c0001t0010g0137 | 2 | HG00408.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.794-230T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97061017 | ||||||
| chr10:97061672
|
C | T | 2 | a0001c0006t0004g0204a0001c0021t0008g0028 | 2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.794-885G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97061672 | ||||||
| chr10:97061720
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.794-933A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97061720 | ||||||
| chr10:97061888
|
C | T | 5 | a0001c0008t0003g0060a0001c0008t0003g0082a0001c0008t0003g0084others(2): Show | 5 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-1101G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97061888 | ||||||
| chr10:97062071
|
G | A | 121 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0026others(118): Show | 121 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.794-1284C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97062071 | ||||||
| chr10:97062158
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.793+1297G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97062158 | ||||||
| chr10:97062229
|
G | GCA | 32 | a0001c0001t0013g0002a0001c0003t0001g0035a0001c0003t0001g0064others(29): Show | 32 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.793+1224_793+1225d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97062229 | ||||||
| chr10:97062233
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.793+1222T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97062233 | ||||||
| chr10:97062261
|
G | A | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.793+1194C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97062261 | ||||||
| chr10:97062374
|
C | T | 2 | a0001c0001t0001g0225a0001c0004t0001g0117 | 2 | HG02155.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.793+1081G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97062374 | ||||||
| chr10:97062481
|
T | C | 250 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(247): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.793+974A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97062481 | ||||||
| chr10:97062544
|
A | T | 1 | a0001c0002t0001g0256 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.793+911T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97062544 | ||||||
| chr10:97062589
|
G | C | 4 | a0001c0002t0001g0212a0001c0004t0001g0065a0001c0004t0001g0165others(1): Show | 4 | HG00741.hp1 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+866C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97062589 | ||||||
| chr10:97062597
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.793+858G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97062597 | ||||||
| chr10:97062598
|
G | A | 1 | a0002c0014t0001g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.793+857C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97062598 | ||||||
| chr10:97062732
|
G | A | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.793+723C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97062732 | ||||||
| chr10:97062842
|
G | C | 3 | a0001c0006t0001g0056a0001c0006t0009g0055a0001c0007t0003g0114 | 3 | HG02809.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.793+613C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97062842 | ||||||
| chr10:97063407
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.793+48C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 8/36 | chr10 | 97063407 | ||||||
| chr10:97063760
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.630-142G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 7/36 | chr10 | 97063760 | ||||||
| chr10:97063854
|
C | T | 3 | a0001c0003t0001g0089a0001c0003t0001g0237a0001c0006t0007g0209 | 3 | HG01109.hp2 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630-236G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 7/36 | chr10 | 97063854 | ||||||
| chr10:97064015
|
G | C | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.629+153C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 7/36 | chr10 | 97064015 | ||||||
| chr10:97064127
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0023g0046 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629+41C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 7/36 | chr10 | 97064127 | ||||||
| chr10:97064344
|
C | G | 14 | a0001c0001t0001g0007a0001c0001t0001g0160a0001c0001t0001g0215others(11): Show | 14 | HG01081.hp1 HG02280.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.558-105G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 6/36 | chr10 | 97064344 | ||||||
| chr10:97064425
|
G | A | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.558-186C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 6/36 | chr10 | 97064425 | ||||||
| chr10:97064502
|
C | T | 2 | a0001c0001t0001g0188a0001c0008t0003g0085 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.558-263G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 6/36 | chr10 | 97064502 | ||||||
| chr10:97064549
|
T | C | 12 | a0001c0001t0001g0007a0001c0001t0001g0160a0001c0001t0001g0215others(9): Show | 12 | HG01081.hp1 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.557+256A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 6/36 | chr10 | 97064549 | ||||||
| chr10:97064676
|
C | T | 1 | a0001c0003t0001g0250 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.557+129G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 6/36 | chr10 | 97064676 | ||||||
| chr10:97064753
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.557+52G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 6/36 | chr10 | 97064753 | ||||||
| chr10:97064964
|
C | CAAAAGAG others(342): Show |
1 | a0001c0001t0023g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.486-89_486-88insTT others(347): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97064964 | ||||||
| chr10:97064970
|
A | G | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.486-94T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97064970 | ||||||
| chr10:97065019
|
C | T | 3 | a0001c0001t0001g0131a0001c0001t0001g0158a0001c0003t0006g0190 | 3 | HG00738.hp2 HG02257.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.486-143G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065019 | ||||||
| chr10:97065098
|
A | G | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.486-222T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065098 | ||||||
| chr10:97065107
|
T | C | 2 | a0001c0003t0011g0012a0001c0017t0008g0123 | 2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.486-231A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065107 | ||||||
| chr10:97065137
|
TAC | T | 4 | a0001c0001t0001g0099a0001c0001t0001g0203a0001c0003t0002g0125others(1): Show | 4 | HG02145.hp1 HG03654.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-263_486-262del others(2): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065137 | ||||||
| chr10:97065137
|
TACAC | T | 75 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0072others(72): Show | 75 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.486-265_486-262del others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065137 | ||||||
| chr10:97065137
|
TACACAC | T | 11 | a0001c0001t0023g0046a0001c0002t0001g0243a0001c0005t0009g0091others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-267_486-262del others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065137 | ||||||
| chr10:97065137
|
TACACACA others(1): Show |
T | 18 | a0001c0001t0010g0197a0001c0002t0001g0025a0001c0002t0001g0037others(15): Show | 18 | HG00642.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.486-269_486-262del others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065137 | ||||||
| chr10:97065137
|
TACACACA others(5): Show |
T | 1 | a0001c0002t0012g0001 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.486-273_486-262del others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065137 | ||||||
| chr10:97065137
|
TACACACA others(7): Show |
T | 140 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(137): Show | 140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.486-275_486-262del others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065137 | ||||||
| chr10:97065143
|
C | T | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.486-267G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065143 | ||||||
| chr10:97065145
|
C | T | 1 | a0001c0003t0011g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.486-269G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065145 | ||||||
| chr10:97065381
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.486-505C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065381 | ||||||
| chr10:97065482
|
T | C | 22 | a0001c0001t0001g0007a0001c0001t0001g0118a0001c0001t0001g0119others(19): Show | 22 | HG01081.hp1 HG01884.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.485+533A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065482 | ||||||
| chr10:97065528
|
G | A | 1 | a0001c0001t0005g0136 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.485+487C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065528 | ||||||
| chr10:97065624
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.485+391A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065624 | ||||||
| chr10:97065790
|
T | C | 1 | a0001c0018t0009g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.485+225A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065790 | ||||||
| chr10:97065792
|
C | T | 9 | a0001c0007t0001g0057a0001c0007t0001g0058a0001c0007t0001g0180others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.485+223G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065792 | ||||||
| chr10:97065948
|
C | G | 18 | a0001c0002t0001g0025a0001c0002t0001g0037a0001c0002t0001g0101others(15): Show | 18 | HG00642.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+67G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 5/36 | chr10 | 97065948 | ||||||
| chr10:97066183
|
G | A | 144 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(141): Show | 144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.414-97C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066183 | ||||||
| chr10:97066263
|
T | TTGAA | 15 | a0001c0002t0001g0025a0001c0002t0001g0037a0001c0002t0001g0101others(12): Show | 15 | HG00642.hp1 HG01167.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.414-181_414-178dup others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066263 | ||||||
| chr10:97066348
|
G | A | 1 | a0001c0002t0001g0212 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.414-262C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066348 | ||||||
| chr10:97066365
|
G | T | 2 | a0001c0001t0002g0224a0001c0005t0001g0052 | 2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.414-279C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066365 | ||||||
| chr10:97066386
|
G | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0160a0001c0001t0001g0215others(9): Show | 12 | HG01081.hp1 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.414-300C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066386 | ||||||
| chr10:97066397
|
C | T | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.414-311G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066397 | ||||||
| chr10:97066445
|
G | A | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.414-359C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066445 | ||||||
| chr10:97066556
|
C | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0023g0046 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.414-470G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066556 | ||||||
| chr10:97066566
|
G | C | 2 | a0001c0001t0001g0188a0001c0008t0003g0085 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.414-480C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066566 | ||||||
| chr10:97066745
|
G | C | 18 | a0001c0001t0001g0007a0001c0001t0001g0160a0001c0001t0001g0215others(15): Show | 18 | HG01081.hp1 HG01884.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.414-659C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066745 | ||||||
| chr10:97066875
|
C | T | 8 | a0001c0001t0001g0104a0001c0001t0001g0110a0001c0001t0001g0185others(5): Show | 8 | HG00621.hp1 HG00673.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-789G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066875 | ||||||
| chr10:97066926
|
A | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0141 | 2 | NA19007.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.414-840T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066926 | ||||||
| chr10:97066955
|
T | TGTG | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0023g0046 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.414-872_414-870dup others(3): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066955 | ||||||
| chr10:97066963
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414-877C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97066963 | ||||||
| chr10:97067124
|
G | A | 1 | a0001c0001t0002g0251 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.414-1038C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97067124 | ||||||
| chr10:97067132
|
C | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0118a0001c0001t0001g0119others(12): Show | 15 | HG01081.hp1 HG02280.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.414-1046G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97067132 | ||||||
| chr10:97067133
|
G | A | 1 | a0001c0004t0001g0117 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.414-1047C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97067133 | ||||||
| chr10:97067155
|
C | A | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.414-1069G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97067155 | ||||||
| chr10:97067163
|
C | T | 5 | a0001c0001t0001g0094a0001c0001t0003g0017a0001c0001t0003g0169others(2): Show | 5 | HG02886.hp1 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-1077G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97067163 | ||||||
| chr10:97067554
|
G | C | 21 | a0001c0001t0001g0007a0001c0001t0001g0118a0001c0001t0001g0119others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.414-1468C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97067554 | ||||||
| chr10:97067670
|
T | C | 162 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(159): Show | 162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.414-1584A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97067670 | ||||||
| chr10:97067738
|
G | A | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-1652C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97067738 | ||||||
| chr10:97067799
|
G | A | 144 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(141): Show | 144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.414-1713C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97067799 | ||||||
| chr10:97067912
|
C | T | 1 | a0001c0006t0004g0204 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.414-1826G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97067912 | ||||||
| chr10:97067930
|
G | A | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.414-1844C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97067930 | ||||||
| chr10:97067947
|
G | A | 4 | a0001c0001t0001g0099a0001c0010t0002g0003a0001c0010t0002g0107others(1): Show | 4 | HG03017.hp1 HG03704.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-1861C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97067947 | ||||||
| chr10:97068127
|
C | T | 21 | a0001c0001t0001g0007a0001c0001t0001g0118a0001c0001t0001g0119others(18): Show | 21 | HG01081.hp1 HG01884.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.414-2041G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97068127 | ||||||
| chr10:97068133
|
T | TTGAA | 4 | a0001c0005t0001g0005a0001c0005t0001g0006a0001c0005t0004g0153others(1): Show | 4 | HG01243.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-2051_414-2048d others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97068133 | ||||||
| chr10:97068133
|
T | TTGAATGA others(1): Show |
15 | a0001c0001t0001g0007a0001c0001t0001g0160a0001c0001t0001g0215others(12): Show | 15 | HG01081.hp1 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.414-2055_414-2048d others(10): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97068133 | ||||||
| chr10:97068133
|
T | TTGAATGA others(5): Show |
5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0002g0224others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-2059_414-2048d others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97068133 | ||||||
| chr10:97068224
|
G | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0023g0046 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.414-2138C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97068224 | ||||||
| chr10:97068391
|
G | C | 19 | a0001c0001t0010g0197a0001c0002t0001g0025a0001c0002t0001g0037others(16): Show | 19 | HG00642.hp1 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.414-2305C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97068391 | ||||||
| chr10:97068597
|
A | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0023g0046 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.414-2511T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97068597 | ||||||
| chr10:97068755
|
C | T | 7 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0002g0224others(4): Show | 7 | HG01884.hp1 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-2669G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97068755 | ||||||
| chr10:97068762
|
G | A | 1 | a0001c0001t0019g0155 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.414-2676C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97068762 | ||||||
| chr10:97068874
|
A | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0186 | 3 | HG02027.hp2 HG02071.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.414-2788T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97068874 | ||||||
| chr10:97068912
|
T | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0160a0001c0001t0001g0215others(9): Show | 12 | HG01081.hp1 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.414-2826A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97068912 | ||||||
| chr10:97068912
|
T | G | 167 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(164): Show | 167 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.414-2826A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97068912 | ||||||
| chr10:97068959
|
C | A | 16 | a0001c0001t0001g0131a0001c0001t0001g0156a0001c0001t0001g0158others(13): Show | 16 | HG00738.hp2 HG01123.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.414-2873G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97068959 | ||||||
| chr10:97069025
|
C | G | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0023g0046 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.414-2939G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97069025 | ||||||
| chr10:97069060
|
C | T | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.414-2974G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97069060 | ||||||
| chr10:97069220
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.414-3134C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97069220 | ||||||
| chr10:97069575
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.414-3489A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97069575 | ||||||
| chr10:97069912
|
G | A | 5 | a0001c0002t0001g0025a0001c0002t0001g0101a0001c0002t0001g0108others(2): Show | 5 | NA18939.hp2 NA18961.hp1 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-3826C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97069912 | ||||||
| chr10:97069984
|
A | G | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0002g0224others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-3898T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97069984 | ||||||
| chr10:97070417
|
T | C | 1 | a0001c0002t0001g0067 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.414-4331A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97070417 | ||||||
| chr10:97070702
|
A | G | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0002g0224others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-4616T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97070702 | ||||||
| chr10:97070870
|
C | T | 2 | a0001c0001t0002g0224a0001c0005t0001g0052 | 2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.414-4784G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97070870 | ||||||
| chr10:97071019
|
A | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0023g0046 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.414-4933T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97071019 | ||||||
| chr10:97071184
|
T | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0023g0046 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.414-5098A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97071184 | ||||||
| chr10:97071203
|
G | A | 1 | a0001c0032t0001g0061 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.414-5117C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97071203 | ||||||
| chr10:97071345
|
C | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0023g0046 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.414-5259G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97071345 | ||||||
| chr10:97071358
|
C | T | 2 | a0001c0001t0002g0224a0001c0005t0001g0052 | 2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.414-5272G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97071358 | ||||||
| chr10:97071783
|
G | A | 3 | a0001c0005t0001g0005a0001c0005t0001g0006a0001c0005t0004g0153 | 3 | HG01243.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.414-5697C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97071783 | ||||||
| chr10:97071971
|
A | G | 250 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(247): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.414-5885T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97071971 | ||||||
| chr10:97072503
|
A | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(152): Show | 155 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.414-6417T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97072503 | ||||||
| chr10:97072531
|
G | T | 10 | a0001c0001t0001g0094a0001c0001t0003g0017a0001c0001t0003g0169others(7): Show | 10 | HG02257.hp2 HG02886.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-6445C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97072531 | ||||||
| chr10:97072552
|
C | T | 1 | a0001c0006t0004g0204 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.414-6466G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97072552 | ||||||
| chr10:97072626
|
G | A | 190 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(187): Show | 190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.414-6540C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97072626 | ||||||
| chr10:97072820
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.414-6734A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97072820 | ||||||
| chr10:97072940
|
A | G | 25 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0203others(22): Show | 25 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.414-6854T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97072940 | ||||||
| chr10:97072970
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.414-6884A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97072970 | ||||||
| chr10:97073001
|
C | T | 2 | a0002c0014t0001g0202a0002c0014t0001g0227 | 2 | HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.414-6915G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97073001 | ||||||
| chr10:97073035
|
G | A | 2 | a0002c0013t0006g0029a0002c0013t0006g0030 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.414-6949C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97073035 | ||||||
| chr10:97073141
|
T | G | 1 | a0001c0001t0010g0137 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.414-7055A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97073141 | ||||||
| chr10:97073547
|
G | T | 1 | a0001c0001t0004g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.414-7461C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97073547 | ||||||
| chr10:97074004
|
C | T | 2 | a0001c0001t0011g0150a0001c0001t0024g0027 | 2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.414-7918G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97074004 | ||||||
| chr10:97074022
|
C | A | 1 | a0006c0027t0025g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.414-7936G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97074022 | ||||||
| chr10:97074214
|
A | G | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0002g0224others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-8128T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97074214 | ||||||
| chr10:97074316
|
A | G | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0002g0224others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-8230T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97074316 | ||||||
| chr10:97074386
|
G | A | 4 | a0001c0001t0001g0051a0001c0001t0001g0138a0001c0002t0001g0181others(1): Show | 4 | HG00544.hp1 HG00597.hp2 HG00673.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-8300C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97074386 | ||||||
| chr10:97074602
|
A | G | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0002g0224others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-8516T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97074602 | ||||||
| chr10:97074627
|
A | C | 19 | a0001c0001t0010g0197a0001c0002t0001g0025a0001c0002t0001g0037others(16): Show | 19 | HG00642.hp1 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.414-8541T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97074627 | ||||||
| chr10:97074638
|
T | C | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0002g0224others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-8552A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97074638 | ||||||
| chr10:97074660
|
A | G | 2 | a0001c0001t0002g0224a0001c0005t0001g0052 | 2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.414-8574T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97074660 | ||||||
| chr10:97074697
|
G | T | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.414-8611C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97074697 | ||||||
| chr10:97074705
|
G | A | 1 | a0001c0003t0006g0036 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.414-8619C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97074705 | ||||||
| chr10:97074748
|
G | A | 1 | a0001c0003t0005g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.414-8662C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97074748 | ||||||
| chr10:97074789
|
T | C | 29 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0100others(26): Show | 29 | HG00544.hp1 HG00597.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.414-8703A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97074789 | ||||||
| chr10:97075193
|
A | C | 1 | a0001c0003t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.414-9107T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97075193 | ||||||
| chr10:97075224
|
G | T | 1 | a0001c0003t0015g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.414-9138C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97075224 | ||||||
| chr10:97075307
|
T | C | 2 | a0001c0003t0011g0012a0001c0017t0008g0123 | 2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.414-9221A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97075307 | ||||||
| chr10:97075393
|
C | T | 236 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(233): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.414-9307G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97075393 | ||||||
| chr10:97075401
|
G | C | 1 | a0001c0009t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.414-9315C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97075401 | ||||||
| chr10:97075624
|
C | T | 2 | a0001c0001t0002g0224a0001c0005t0001g0052 | 2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.414-9538G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97075624 | ||||||
| chr10:97075625
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.414-9539C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97075625 | ||||||
| chr10:97075788
|
G | C | 1 | a0001c0001t0018g0168 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.414-9702C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97075788 | ||||||
| chr10:97075887
|
C | T | 2 | a0001c0001t0002g0224a0001c0005t0001g0052 | 2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.414-9801G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97075887 | ||||||
| chr10:97076037
|
C | T | 1 | a0001c0002t0002g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.414-9951G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97076037 | ||||||
| chr10:97076492
|
A | G | 1 | a0001c0003t0011g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.414-10406T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97076492 | ||||||
| chr10:97076560
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.414-10474C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97076560 | ||||||
| chr10:97076988
|
G | A | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.414-10902C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97076988 | ||||||
| chr10:97077020
|
C | T | 4 | a0001c0003t0001g0096a0001c0003t0002g0125a0002c0013t0006g0029others(1): Show | 4 | HG01515.hp1 HG01517.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-10934G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97077020 | ||||||
| chr10:97077044
|
T | C | 1 | a0001c0001t0023g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414-10958A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97077044 | ||||||
| chr10:97077300
|
C | T | 1 | a0001c0004t0001g0210 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.414-11214G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97077300 | ||||||
| chr10:97077324
|
C | G | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.414-11238G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97077324 | ||||||
| chr10:97077436
|
A | G | 3 | a0001c0001t0002g0224a0001c0001t0023g0046a0001c0005t0001g0052 | 3 | HG02280.hp1 HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.414-11350T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97077436 | ||||||
| chr10:97077620
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.414-11534A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97077620 | ||||||
| chr10:97077687
|
G | A | 1 | a0001c0002t0002g0164 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.414-11601C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97077687 | ||||||
| chr10:97077763
|
G | A | 9 | a0001c0001t0001g0160a0001c0005t0001g0045a0001c0005t0001g0192others(6): Show | 9 | HG01081.hp1 HG02280.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-11677C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97077763 | ||||||
| chr10:97077824
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.414-11738T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97077824 | ||||||
| chr10:97078115
|
A | T | 1 | a0001c0001t0023g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414-12029T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97078115 | ||||||
| chr10:97078209
|
C | T | 26 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0043others(23): Show | 26 | HG00639.hp2 HG01891.hp2 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.414-12123G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97078209 | ||||||
| chr10:97078225
|
G | A | 1 | a0001c0005t0001g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.414-12139C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97078225 | ||||||
| chr10:97078248
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.414-12162G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97078248 | ||||||
| chr10:97078457
|
A | G | 18 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0002t0001g0025others(15): Show | 18 | HG00735.hp1 HG02258.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.414-12371T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97078457 | ||||||
| chr10:97078476
|
C | T | 2 | a0001c0004t0001g0165a0001c0004t0001g0166 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.414-12390G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97078476 | ||||||
| chr10:97078529
|
C | T | 1 | a0002c0014t0001g0227 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.414-12443G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97078529 | ||||||
| chr10:97078657
|
CCT | C | 77 | a0001c0001t0001g0041a0001c0001t0001g0051a0001c0001t0001g0072others(74): Show | 77 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.414-12573_414-1257 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97078657 | ||||||
| chr10:97078731
|
C | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(3): Show | 6 | HG00639.hp2 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-12645G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97078731 | ||||||
| chr10:97078731
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.414-12645G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97078731 | ||||||
| chr10:97078798
|
G | A | 2 | a0001c0001t0013g0002a0001c0007t0001g0218 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.414-12712C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97078798 | ||||||
| chr10:97078937
|
C | T | 136 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(133): Show | 136 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.414-12851G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97078937 | ||||||
| chr10:97078978
|
C | A | 90 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(87): Show | 90 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.414-12892G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97078978 | ||||||
| chr10:97079008
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.414-12922A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97079008 | ||||||
| chr10:97079107
|
T | C | 2 | a0001c0002t0002g0199a0001c0004t0001g0044 | 2 | HG00558.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.414-13021A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97079107 | ||||||
| chr10:97079176
|
G | A | 3 | a0001c0001t0001g0214a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02109.hp2 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.414-13090C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97079176 | ||||||
| chr10:97079200
|
C | T | 8 | a0001c0001t0001g0160a0001c0003t0002g0219a0001c0005t0001g0192others(5): Show | 8 | HG01081.hp1 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-13114G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97079200 | ||||||
| chr10:97079551
|
C | T | 1 | a0001c0003t0001g0255 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.414-13465G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97079551 | ||||||
| chr10:97079678
|
A | G | 8 | a0001c0007t0001g0057a0001c0007t0001g0058a0001c0007t0001g0180others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-13592T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97079678 | ||||||
| chr10:97079853
|
C | T | 2 | a0001c0003t0001g0064a0001c0003t0015g0087 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.414-13767G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97079853 | ||||||
| chr10:97079920
|
G | A | 1 | a0006c0027t0025g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.414-13834C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97079920 | ||||||
| chr10:97080286
|
A | T | 1 | a0001c0003t0001g0179 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.414-14200T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97080286 | ||||||
| chr10:97080319
|
C | T | 35 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(32): Show | 35 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.414-14233G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97080319 | ||||||
| chr10:97080590
|
C | T | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-14504G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97080590 | ||||||
| chr10:97080651
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.414-14565C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97080651 | ||||||
| chr10:97080652
|
G | C | 14 | a0001c0001t0001g0124a0001c0001t0001g0160a0001c0001t0001g0203others(11): Show | 14 | HG01081.hp1 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.414-14566C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97080652 | ||||||
| chr10:97080772
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0235 | 2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.414-14686C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97080772 | ||||||
| chr10:97080922
|
T | C | 111 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(108): Show | 111 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.414-14836A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97080922 | ||||||
| chr10:97080933
|
G | A | 1 | a0001c0003t0001g0244 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.414-14847C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97080933 | ||||||
| chr10:97080939
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.414-14853C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97080939 | ||||||
| chr10:97080992
|
C | A | 1 | a0001c0002t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.414-14906G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97080992 | ||||||
| chr10:97081032
|
T | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(95): Show | 98 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.414-14946A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97081032 | ||||||
| chr10:97081093
|
C | T | 95 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(92): Show | 95 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.414-15007G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97081093 | ||||||
| chr10:97081133
|
C | A | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.414-15047G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97081133 | ||||||
| chr10:97081242
|
G | A | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-15156C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97081242 | ||||||
| chr10:97081286
|
T | C | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-15200A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97081286 | ||||||
| chr10:97081380
|
G | A | 45 | a0001c0001t0001g0043a0001c0001t0001g0106a0001c0001t0001g0118others(42): Show | 45 | HG00597.hp2 HG00735.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.414-15294C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97081380 | ||||||
| chr10:97081448
|
A | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(78): Show | 81 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.414-15362T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97081448 | ||||||
| chr10:97081465
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(93): Show | 96 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.414-15379G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97081465 | ||||||
| chr10:97081801
|
C | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0004t0001g0024 | 3 | NA18943.hp2 NA18998.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.414-15715G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97081801 | ||||||
| chr10:97081816
|
G | C | 1 | a0001c0001t0002g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.414-15730C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97081816 | ||||||
| chr10:97081948
|
C | T | 6 | a0001c0001t0001g0004a0001c0005t0001g0005a0001c0005t0001g0006others(3): Show | 6 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-15862G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97081948 | ||||||
| chr10:97082012
|
C | T | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-15926G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97082012 | ||||||
| chr10:97082045
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.414-15959T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97082045 | ||||||
| chr10:97082103
|
G | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0178a0001c0001t0001g0247 | 3 | HG01884.hp2 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.414-16017C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97082103 | ||||||
| chr10:97082262
|
A | G | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-16176T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97082262 | ||||||
| chr10:97082728
|
C | T | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-16642G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97082728 | ||||||
| chr10:97082770
|
C | T | 1 | a0001c0001t0023g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414-16684G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97082770 | ||||||
| chr10:97082783
|
G | A | 6 | a0001c0001t0001g0004a0001c0005t0001g0005a0001c0005t0001g0006others(3): Show | 6 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-16697C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97082783 | ||||||
| chr10:97082917
|
G | A | 1 | a0001c0001t0023g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414-16831C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97082917 | ||||||
| chr10:97082917
|
G | C | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-16831C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97082917 | ||||||
| chr10:97083068
|
C | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(34): Show | 37 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.414-16982G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97083068 | ||||||
| chr10:97083105
|
T | A | 1 | a0001c0002t0002g0199 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.414-17019A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97083105 | ||||||
| chr10:97083416
|
T | C | 2 | a0001c0001t0001g0188a0001c0008t0003g0085 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.414-17330A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97083416 | ||||||
| chr10:97083543
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.414-17457C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97083543 | ||||||
| chr10:97083716
|
A | G | 235 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(232): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.414-17630T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97083716 | ||||||
| chr10:97084011
|
G | GTCT | 136 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(133): Show | 136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.414-17928_414-1792 others(7): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97084011 | ||||||
| chr10:97084048
|
A | C | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-17962T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97084048 | ||||||
| chr10:97084216
|
C | T | 2 | a0001c0001t0002g0224a0006c0027t0025g0220 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.414-18130G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97084216 | ||||||
| chr10:97084273
|
T | C | 136 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(133): Show | 136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.414-18187A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97084273 | ||||||
| chr10:97084573
|
C | T | 2 | a0001c0001t0001g0188a0001c0008t0003g0085 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.414-18487G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97084573 | ||||||
| chr10:97084584
|
A | C | 1 | a0001c0001t0001g0033 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.414-18498T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97084584 | ||||||
| chr10:97084597
|
CTCTTT | C | 191 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(188): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.414-18516_414-1851 others(9): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97084597 | ||||||
| chr10:97084701
|
G | T | 3 | a0001c0001t0002g0142a0001c0001t0002g0201a0001c0004t0001g0147 | 3 | NA18952.hp2 NA18960.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.414-18615C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97084701 | ||||||
| chr10:97084916
|
T | G | 1 | a0001c0001t0001g0232 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.414-18830A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97084916 | ||||||
| chr10:97084924
|
C | CT | 7 | a0001c0001t0001g0124a0001c0001t0001g0131a0001c0001t0002g0189others(4): Show | 7 | HG00738.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-18839dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97084924 | ||||||
| chr10:97084924
|
C | CTT | 119 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(116): Show | 119 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.414-18840_414-1883 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97084924 | ||||||
| chr10:97085386
|
CT | C | 14 | a0001c0001t0001g0160a0001c0001t0001g0203a0001c0003t0001g0064others(11): Show | 14 | HG01081.hp1 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.414-19301delA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97085386 | ||||||
| chr10:97085396
|
T | G | 88 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0026others(85): Show | 88 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.414-19310A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97085396 | ||||||
| chr10:97085397
|
T | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0207 | 2 | NA18994.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.414-19311A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97085397 | ||||||
| chr10:97085400
|
G | T | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-19314C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97085400 | ||||||
| chr10:97085467
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.414-19381T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97085467 | ||||||
| chr10:97085628
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.414-19542G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97085628 | ||||||
| chr10:97085666
|
G | A | 11 | a0001c0001t0001g0043a0001c0001t0001g0106a0001c0001t0001g0135others(8): Show | 11 | HG02071.hp1 HG02155.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-19580C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97085666 | ||||||
| chr10:97085779
|
G | A | 134 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(131): Show | 134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.414-19693C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97085779 | ||||||
| chr10:97086081
|
T | C | 2 | a0001c0011t0001g0157a0001c0011t0001g0187 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.414-19995A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97086081 | ||||||
| chr10:97086137
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.414-20051T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97086137 | ||||||
| chr10:97086254
|
T | C | 11 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0007t0001g0057others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-20168A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97086254 | ||||||
| chr10:97086394
|
A | C | 1 | a0001c0001t0023g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414-20308T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97086394 | ||||||
| chr10:97086457
|
A | T | 23 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0141others(20): Show | 23 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.414-20371T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97086457 | ||||||
| chr10:97086566
|
A | G | 10 | a0001c0002t0001g0037a0001c0002t0001g0120a0001c0002t0001g0193others(7): Show | 10 | HG00558.hp1 HG02602.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-20480T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97086566 | ||||||
| chr10:97086681
|
T | A | 138 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(135): Show | 138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.414-20595A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97086681 | ||||||
| chr10:97086798
|
G | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.414-20712C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97086798 | ||||||
| chr10:97086826
|
T | C | 1 | a0001c0001t0023g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414-20740A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97086826 | ||||||
| chr10:97086910
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.414-20824C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97086910 | ||||||
| chr10:97086934
|
T | C | 1 | a0001c0004t0001g0044 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.414-20848A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97086934 | ||||||
| chr10:97086957
|
G | A | 140 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(137): Show | 140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.414-20871C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97086957 | ||||||
| chr10:97087078
|
A | C | 2 | a0001c0001t0002g0113a0001c0002t0002g0095 | 2 | NA18942.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.414-20992T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087078 | ||||||
| chr10:97087099
|
T | TA | 151 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0022others(148): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.414-21014dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087099 | ||||||
| chr10:97087171
|
G | A | 136 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(133): Show | 136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.414-21085C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087171 | ||||||
| chr10:97087205
|
G | C | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-21119C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087205 | ||||||
| chr10:97087215
|
C | A | 1 | a0001c0001t0001g0092 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.414-21129G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087215 | ||||||
| chr10:97087370
|
C | T | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-21284G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087370 | ||||||
| chr10:97087487
|
G | C | 137 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(134): Show | 137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.414-21401C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087487 | ||||||
| chr10:97087547
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.414-21461T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087547 | ||||||
| chr10:97087637
|
C | T | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.414-21551G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087637 | ||||||
| chr10:97087693
|
G | C | 2 | a0001c0001t0001g0215a0001c0001t0028g0093 | 2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.414-21607C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087693 | ||||||
| chr10:97087720
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.414-21634G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087720 | ||||||
| chr10:97087806
|
G | C | 1 | a0001c0001t0023g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414-21720C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087806 | ||||||
| chr10:97087884
|
A | C | 1 | a0001c0008t0003g0084 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.414-21798T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087884 | ||||||
| chr10:97087896
|
C | G | 1 | a0001c0019t0008g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.414-21810G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087896 | ||||||
| chr10:97087907
|
T | C | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.414-21821A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087907 | ||||||
| chr10:97087910
|
C | G | 188 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(185): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.414-21824G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087910 | ||||||
| chr10:97087988
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.414-21902C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97087988 | ||||||
| chr10:97088011
|
G | A | 1 | a0003c0029t0002g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.414-21925C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97088011 | ||||||
| chr10:97088019
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0005t0001g0005others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-21933C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97088019 | ||||||
| chr10:97088228
|
GATCTCTA others(5): Show |
G | 7 | a0001c0007t0001g0057a0001c0007t0001g0058a0001c0007t0001g0180others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-22154_414-2214 others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97088228 | ||||||
| chr10:97088472
|
G | A | 10 | a0001c0001t0001g0092a0001c0001t0001g0103a0001c0001t0001g0111others(7): Show | 10 | HG00408.hp2 HG00438.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-22386C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97088472 | ||||||
| chr10:97088521
|
T | C | 1 | a0001c0005t0001g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.414-22435A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97088521 | ||||||
| chr10:97088577
|
C | T | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-22491G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97088577 | ||||||
| chr10:97088635
|
A | C | 1 | a0001c0001t0001g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.414-22549T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97088635 | ||||||
| chr10:97088802
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.414-22716G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97088802 | ||||||
| chr10:97089088
|
C | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0174 | 2 | NA18963.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.414-23002G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97089088 | ||||||
| chr10:97089110
|
C | T | 1 | a0001c0002t0001g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.414-23024G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97089110 | ||||||
| chr10:97089178
|
A | G | 245 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.414-23092T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97089178 | ||||||
| chr10:97089584
|
G | A | 137 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(134): Show | 137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.414-23498C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97089584 | ||||||
| chr10:97089673
|
G | C | 126 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(123): Show | 126 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.414-23587C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97089673 | ||||||
| chr10:97089786
|
G | A | 4 | a0001c0003t0001g0089a0001c0003t0001g0237a0001c0003t0001g0250others(1): Show | 4 | HG01109.hp2 HG02622.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-23700C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97089786 | ||||||
| chr10:97090008
|
A | G | 23 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0154others(20): Show | 23 | HG00438.hp1 HG00597.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.414-23922T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090008 | ||||||
| chr10:97090050
|
T | A | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-23964A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090050 | ||||||
| chr10:97090057
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-23971G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090057 | ||||||
| chr10:97090101
|
C | T | 144 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(141): Show | 144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.414-24015G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090101 | ||||||
| chr10:97090112
|
A | G | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-24026T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090112 | ||||||
| chr10:97090156
|
G | T | 1 | a0001c0002t0001g0108 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.414-24070C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090156 | ||||||
| chr10:97090264
|
C | T | 126 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(123): Show | 126 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.414-24178G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090264 | ||||||
| chr10:97090289
|
T | C | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-24203A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090289 | ||||||
| chr10:97090348
|
G | A | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-24262C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090348 | ||||||
| chr10:97090437
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.414-24351C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090437 | ||||||
| chr10:97090492
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.414-24406A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090492 | ||||||
| chr10:97090556
|
A | G | 1 | a0001c0002t0001g0067 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.414-24470T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090556 | ||||||
| chr10:97090585
|
A | G | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.414-24499T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090585 | ||||||
| chr10:97090597
|
TG | T | 255 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(252): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.414-24512delC | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090597 | ||||||
| chr10:97090720
|
T | A | 1 | a0001c0001t0023g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414-24634A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97090720 | ||||||
| chr10:97091043
|
G | A | 187 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(184): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.414-24957C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97091043 | ||||||
| chr10:97091202
|
A | G | 1 | a0001c0004t0001g0069 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.414-25116T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97091202 | ||||||
| chr10:97091214
|
A | G | 1 | a0001c0002t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.414-25128T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97091214 | ||||||
| chr10:97091238
|
G | A | 13 | a0001c0001t0001g0160a0001c0001t0001g0203a0001c0003t0001g0064others(10): Show | 13 | HG01081.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-25152C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97091238 | ||||||
| chr10:97091293
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.414-25207G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97091293 | ||||||
| chr10:97091669
|
G | T | 21 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0072others(18): Show | 21 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.414-25583C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97091669 | ||||||
| chr10:97091698
|
A | G | 2 | a0002c0013t0006g0029a0002c0013t0006g0030 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.414-25612T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97091698 | ||||||
| chr10:97091742
|
G | A | 3 | a0001c0001t0002g0189a0001c0002t0002g0040a0001c0003t0006g0190 | 3 | HG00738.hp2 HG01123.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.414-25656C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97091742 | ||||||
| chr10:97091891
|
C | A | 1 | a0001c0007t0001g0058 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.414-25805G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97091891 | ||||||
| chr10:97091993
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.414-25907G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97091993 | ||||||
| chr10:97092078
|
C | T | 13 | a0001c0001t0001g0160a0001c0001t0001g0203a0001c0003t0001g0064others(10): Show | 13 | HG01081.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-25992G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97092078 | ||||||
| chr10:97092288
|
T | C | 1 | a0001c0021t0008g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.414-26202A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97092288 | ||||||
| chr10:97092343
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.414-26257C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97092343 | ||||||
| chr10:97092371
|
T | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.414-26285A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97092371 | ||||||
| chr10:97092397
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.414-26311T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97092397 | ||||||
| chr10:97092590
|
A | G | 10 | a0001c0001t0001g0214a0001c0007t0001g0057a0001c0007t0001g0058others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.414-26504T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97092590 | ||||||
| chr10:97092682
|
G | T | 1 | a0001c0001t0020g0109 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.414-26596C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97092682 | ||||||
| chr10:97092859
|
G | A | 3 | a0001c0001t0001g0094a0001c0001t0018g0168a0004c0028t0001g0216 | 3 | HG02976.hp2 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.414-26773C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97092859 | ||||||
| chr10:97092943
|
A | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0186 | 2 | HG00438.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.414-26857T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97092943 | ||||||
| chr10:97093051
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.414-26965T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97093051 | ||||||
| chr10:97093136
|
T | C | 50 | a0001c0001t0001g0043a0001c0001t0001g0106a0001c0001t0001g0118others(47): Show | 50 | HG00438.hp1 HG00597.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.414-27050A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97093136 | ||||||
| chr10:97093148
|
G | T | 19 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0072others(16): Show | 19 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.414-27062C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97093148 | ||||||
| chr10:97093177
|
T | C | 1 | a0001c0005t0001g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.414-27091A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97093177 | ||||||
| chr10:97093348
|
C | T | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-27262G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97093348 | ||||||
| chr10:97093679
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0005t0001g0005others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-27593C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97093679 | ||||||
| chr10:97093891
|
T | G | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.414-27805A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97093891 | ||||||
| chr10:97093991
|
C | T | 13 | a0001c0001t0001g0160a0001c0001t0001g0203a0001c0003t0001g0064others(10): Show | 13 | HG01081.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-27905G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97093991 | ||||||
| chr10:97094051
|
G | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(100): Show | 103 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.414-27965C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97094051 | ||||||
| chr10:97094207
|
G | C | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.414-28121C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97094207 | ||||||
| chr10:97094210
|
C | T | 2 | a0001c0001t0002g0129a0001c0004t0001g0140 | 2 | NA18984.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.414-28124G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97094210 | ||||||
| chr10:97094328
|
T | C | 11 | a0001c0001t0001g0043a0001c0001t0001g0106a0001c0001t0001g0135others(8): Show | 11 | HG02071.hp1 HG02155.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-28242A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97094328 | ||||||
| chr10:97094596
|
C | T | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.414-28510G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97094596 | ||||||
| chr10:97094645
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0005t0001g0005others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-28559C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97094645 | ||||||
| chr10:97094653
|
A | G | 94 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0043others(91): Show | 94 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.414-28567T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97094653 | ||||||
| chr10:97094697
|
A | G | 13 | a0001c0001t0001g0160a0001c0001t0001g0203a0001c0003t0001g0064others(10): Show | 13 | HG01081.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-28611T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97094697 | ||||||
| chr10:97094894
|
G | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0232 | 2 | NA18952.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.414-28808C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97094894 | ||||||
| chr10:97094921
|
G | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(100): Show | 103 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.414-28835C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97094921 | ||||||
| chr10:97095026
|
T | C | 51 | a0001c0001t0001g0043a0001c0001t0001g0106a0001c0001t0001g0118others(48): Show | 51 | HG00438.hp1 HG00597.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.414-28940A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97095026 | ||||||
| chr10:97095177
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.414-29091C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97095177 | ||||||
| chr10:97095275
|
T | G | 1 | a0001c0003t0001g0035 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.414-29189A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97095275 | ||||||
| chr10:97095350
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.414-29264C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97095350 | ||||||
| chr10:97095550
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.414-29464G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97095550 | ||||||
| chr10:97095601
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.414-29515A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97095601 | ||||||
| chr10:97095624
|
T | G | 46 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(43): Show | 46 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.414-29538A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97095624 | ||||||
| chr10:97095708
|
G | A | 48 | a0001c0001t0001g0043a0001c0001t0001g0106a0001c0001t0001g0118others(45): Show | 48 | HG00438.hp1 HG00597.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.414-29622C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97095708 | ||||||
| chr10:97095933
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.414-29847C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97095933 | ||||||
| chr10:97095946
|
C | T | 3 | a0001c0001t0001g0214a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02109.hp2 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.414-29860G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97095946 | ||||||
| chr10:97096172
|
C | T | 29 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0072others(26): Show | 29 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.414-30086G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97096172 | ||||||
| chr10:97096198
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.414-30112T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97096198 | ||||||
| chr10:97096241
|
A | G | 1 | a0001c0009t0005g0238 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.414-30155T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97096241 | ||||||
| chr10:97096362
|
C | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0175 | 2 | HG00408.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.414-30276G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97096362 | ||||||
| chr10:97096386
|
C | G | 1 | a0001c0003t0001g0255 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.414-30300G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97096386 | ||||||
| chr10:97096392
|
C | T | 1 | a0001c0005t0001g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.414-30306G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97096392 | ||||||
| chr10:97096426
|
C | G | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-30340G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97096426 | ||||||
| chr10:97096439
|
G | A | 1 | a0001c0024t0001g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.414-30353C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97096439 | ||||||
| chr10:97096582
|
A | G | 1 | a0001c0005t0001g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.414-30496T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97096582 | ||||||
| chr10:97096623
|
A | T | 1 | a0001c0004t0001g0228 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.414-30537T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97096623 | ||||||
| chr10:97096700
|
G | A | 16 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0049others(13): Show | 16 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.414-30614C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97096700 | ||||||
| chr10:97096746
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.414-30660G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97096746 | ||||||
| chr10:97096905
|
T | C | 14 | a0001c0001t0001g0043a0001c0001t0001g0106a0001c0001t0001g0135others(11): Show | 14 | HG00408.hp1 HG02027.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.414-30819A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97096905 | ||||||
| chr10:97097106
|
C | T | 7 | a0001c0001t0001g0156a0001c0001t0004g0019a0001c0001t0011g0150others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-31020G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097106 | ||||||
| chr10:97097130
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.414-31044G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097130 | ||||||
| chr10:97097136
|
C | G | 15 | a0001c0001t0001g0097a0001c0001t0001g0241a0001c0001t0002g0251others(12): Show | 15 | HG00558.hp1 HG02602.hp1 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.414-31050G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097136 | ||||||
| chr10:97097144
|
C | T | 1 | a0001c0003t0001g0179 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.414-31058G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097144 | ||||||
| chr10:97097190
|
T | A | 1 | a0001c0004t0001g0024 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.414-31104A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097190 | ||||||
| chr10:97097205
|
C | T | 4 | a0001c0001t0001g0054a0001c0005t0001g0052a0001c0005t0009g0091others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-31119G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097205 | ||||||
| chr10:97097206
|
G | A | 2 | a0001c0003t0001g0171a0001c0003t0001g0172 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.414-31120C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097206 | ||||||
| chr10:97097312
|
G | A | 1 | a0001c0007t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.414-31226C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097312 | ||||||
| chr10:97097399
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.414-31313C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097399 | ||||||
| chr10:97097599
|
A | C | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.414-31513T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097599 | ||||||
| chr10:97097827
|
C | T | 1 | a0001c0002t0001g0151 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.414-31741G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097827 | ||||||
| chr10:97097836
|
T | C | 1 | a0006c0027t0025g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.414-31750A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097836 | ||||||
| chr10:97097855
|
G | T | 1 | a0001c0002t0001g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.414-31769C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097855 | ||||||
| chr10:97097883
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.414-31797T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097883 | ||||||
| chr10:97097934
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.414-31848G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97097934 | ||||||
| chr10:97098166
|
C | T | 141 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(138): Show | 141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.414-32080G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97098166 | ||||||
| chr10:97098224
|
C | T | 11 | a0001c0001t0001g0124a0001c0001t0001g0214a0001c0007t0001g0057others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-32138G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97098224 | ||||||
| chr10:97098252
|
C | T | 3 | a0001c0001t0001g0188a0001c0008t0003g0085a0001c0018t0009g0217 | 3 | HG01891.hp2 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.414-32166G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97098252 | ||||||
| chr10:97098347
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.414-32261A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97098347 | ||||||
| chr10:97098457
|
G | A | 3 | a0001c0001t0001g0214a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02109.hp2 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.414-32371C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97098457 | ||||||
| chr10:97098463
|
C | T | 15 | a0001c0001t0001g0097a0001c0001t0001g0241a0001c0001t0002g0251others(12): Show | 15 | HG00558.hp1 HG02602.hp1 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.414-32377G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97098463 | ||||||
| chr10:97098464
|
G | A | 2 | a0001c0002t0001g0212a0001c0003t0001g0244 | 2 | HG01167.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.414-32378C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97098464 | ||||||
| chr10:97098513
|
C | T | 7 | a0001c0007t0001g0057a0001c0007t0001g0058a0001c0007t0001g0180others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-32427G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97098513 | ||||||
| chr10:97098767
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.414-32681C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97098767 | ||||||
| chr10:97099006
|
G | A | 119 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.414-32920C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099006 | ||||||
| chr10:97099135
|
C | T | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.414-33049G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099135 | ||||||
| chr10:97099151
|
T | TG | 119 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.414-33066dupC | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099151 | ||||||
| chr10:97099193
|
C | T | 3 | a0001c0002t0001g0067a0001c0006t0001g0056a0001c0006t0009g0055 | 3 | HG02647.hp2 HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.414-33107G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099193 | ||||||
| chr10:97099228
|
T | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-33142A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099228 | ||||||
| chr10:97099327
|
C | T | 3 | a0001c0001t0001g0188a0001c0008t0003g0085a0001c0018t0009g0217 | 3 | HG01891.hp2 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.414-33241G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099327 | ||||||
| chr10:97099346
|
T | C | 177 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.414-33260A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099346 | ||||||
| chr10:97099405
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.414-33319C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099405 | ||||||
| chr10:97099421
|
A | C | 143 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.414-33335T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099421 | ||||||
| chr10:97099434
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.414-33348C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099434 | ||||||
| chr10:97099585
|
G | T | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-33499C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099585 | ||||||
| chr10:97099611
|
C | T | 10 | a0001c0001t0001g0124a0001c0001t0001g0214a0001c0007t0001g0057others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.414-33525G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099611 | ||||||
| chr10:97099635
|
C | T | 1 | a0001c0009t0005g0032 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.414-33549G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099635 | ||||||
| chr10:97099784
|
G | A | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.414-33698C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099784 | ||||||
| chr10:97099851
|
C | T | 1 | a0001c0011t0001g0157 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.414-33765G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97099851 | ||||||
| chr10:97100230
|
C | G | 48 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0094others(45): Show | 48 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.414-34144G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97100230 | ||||||
| chr10:97100460
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0174 | 2 | NA18963.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.414-34374G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97100460 | ||||||
| chr10:97100632
|
C | CAA | 144 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.414-34548_414-3454 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97100632 | ||||||
| chr10:97100646
|
T | A | 1 | a0001c0006t0007g0013 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.414-34560A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97100646 | ||||||
| chr10:97100717
|
C | T | 20 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0078others(17): Show | 20 | HG01109.hp1 HG01257.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.414-34631G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97100717 | ||||||
| chr10:97100828
|
C | A | 122 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.414-34742G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97100828 | ||||||
| chr10:97100862
|
C | T | 145 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.414-34776G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97100862 | ||||||
| chr10:97100901
|
G | C | 17 | a0001c0001t0001g0054a0001c0001t0001g0241a0001c0002t0001g0037others(14): Show | 17 | HG00558.hp1 HG01884.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.414-34815C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97100901 | ||||||
| chr10:97101003
|
C | A | 142 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(139): Show | 142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.414-34917G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97101003 | ||||||
| chr10:97101035
|
C | T | 7 | a0001c0001t0001g0124a0001c0007t0001g0057a0001c0007t0001g0058others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-34949G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97101035 | ||||||
| chr10:97101270
|
A | C | 1 | a0001c0001t0003g0169 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.414-35184T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97101270 | ||||||
| chr10:97101305
|
A | C | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-35219T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97101305 | ||||||
| chr10:97101310
|
C | T | 1 | a0001c0004t0001g0173 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.414-35224G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97101310 | ||||||
| chr10:97101327
|
C | T | 20 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0078others(17): Show | 20 | HG01109.hp1 HG01257.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.414-35241G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97101327 | ||||||
| chr10:97101464
|
A | G | 1 | a0001c0003t0001g0035 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.414-35378T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97101464 | ||||||
| chr10:97101514
|
G | C | 9 | a0001c0001t0002g0042a0001c0001t0002g0128a0001c0001t0002g0222others(6): Show | 9 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-35428C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97101514 | ||||||
| chr10:97101809
|
C | T | 3 | a0001c0001t0001g0214a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02109.hp2 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.414-35723G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97101809 | ||||||
| chr10:97101923
|
A | G | 1 | a0001c0032t0001g0061 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.414-35837T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97101923 | ||||||
| chr10:97102046
|
A | G | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-35960T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97102046 | ||||||
| chr10:97102123
|
G | A | 20 | a0001c0001t0001g0054a0001c0001t0001g0214a0001c0001t0001g0241others(17): Show | 20 | HG00558.hp1 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-36037C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97102123 | ||||||
| chr10:97102159
|
C | T | 145 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.414-36073G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97102159 | ||||||
| chr10:97102329
|
G | A | 79 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0034others(76): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.414-36243C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97102329 | ||||||
| chr10:97102422
|
C | CA | 56 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0071others(53): Show | 56 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.414-36337dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97102422 | ||||||
| chr10:97102422
|
C | CAA | 10 | a0001c0001t0001g0160a0001c0001t0010g0137a0001c0003t0002g0219others(7): Show | 10 | HG01081.hp1 HG02723.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-36338_414-3633 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97102422 | ||||||
| chr10:97102436
|
AAAG | A | 138 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(135): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.414-36353_414-3635 others(7): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97102436 | ||||||
| chr10:97102438
|
AG | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0178a0001c0001t0001g0247 | 3 | HG02258.hp1 HG02559.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.414-36353delC | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97102438 | ||||||
| chr10:97102439
|
G | A | 36 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0071others(33): Show | 36 | HG00639.hp2 HG01081.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.414-36353C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97102439 | ||||||
| chr10:97102458
|
G | GA | 13 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0049others(10): Show | 13 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.414-36373dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97102458 | ||||||
| chr10:97102628
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.414-36542C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97102628 | ||||||
| chr10:97102979
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0110 | 2 | HG00673.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.414-36893C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97102979 | ||||||
| chr10:97102984
|
A | G | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-36898T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97102984 | ||||||
| chr10:97103060
|
C | A | 13 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0078others(10): Show | 13 | HG01109.hp1 HG01257.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-36974G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97103060 | ||||||
| chr10:97103079
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.414-36993C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97103079 | ||||||
| chr10:97103183
|
A | G | 2 | a0001c0001t0001g0242a0002c0014t0001g0202 | 2 | HG01261.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.414-37097T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97103183 | ||||||
| chr10:97103267
|
A | G | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-37181T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97103267 | ||||||
| chr10:97103432
|
C | T | 20 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0078others(17): Show | 20 | HG01109.hp1 HG01257.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.414-37346G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97103432 | ||||||
| chr10:97103803
|
C | T | 1 | a0001c0001t0023g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414-37717G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97103803 | ||||||
| chr10:97103804
|
G | A | 13 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0078others(10): Show | 13 | HG01109.hp1 HG01257.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-37718C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97103804 | ||||||
| chr10:97104181
|
T | A | 1 | a0001c0001t0010g0137 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.414-38095A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97104181 | ||||||
| chr10:97104512
|
G | A | 20 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0078others(17): Show | 20 | HG01109.hp1 HG01257.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.414-38426C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97104512 | ||||||
| chr10:97104555
|
C | T | 57 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(54): Show | 57 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.414-38469G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97104555 | ||||||
| chr10:97104857
|
C | G | 122 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.414-38771G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97104857 | ||||||
| chr10:97104927
|
C | T | 1 | a0001c0001t0010g0197 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.414-38841G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97104927 | ||||||
| chr10:97104992
|
G | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-38906C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97104992 | ||||||
| chr10:97105153
|
A | G | 3 | a0001c0001t0001g0162a0001c0001t0013g0002a0006c0027t0025g0220 | 3 | HG03098.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.414-39067T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105153 | ||||||
| chr10:97105170
|
G | T | 122 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.414-39084C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105170 | ||||||
| chr10:97105235
|
T | C | 7 | a0001c0001t0001g0124a0001c0007t0001g0057a0001c0007t0001g0058others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-39149A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105235 | ||||||
| chr10:97105255
|
T | C | 2 | a0001c0001t0013g0002a0006c0027t0025g0220 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.414-39169A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105255 | ||||||
| chr10:97105428
|
C | A | 9 | a0001c0001t0001g0160a0001c0003t0002g0219a0001c0003t0015g0087others(6): Show | 9 | HG01081.hp1 HG02615.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-39342G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105428 | ||||||
| chr10:97105432
|
T | A | 1 | a0001c0001t0001g0048 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.414-39346A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105432 | ||||||
| chr10:97105450
|
C | T | 20 | a0001c0001t0001g0054a0001c0001t0001g0214a0001c0001t0001g0241others(17): Show | 20 | HG00558.hp1 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-39364G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105450 | ||||||
| chr10:97105529
|
A | G | 223 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.414-39443T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105529 | ||||||
| chr10:97105622
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-39536C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105622 | ||||||
| chr10:97105782
|
AG | A | 6 | a0001c0001t0001g0156a0001c0001t0004g0019a0001c0001t0011g0150others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-39697delC | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105782 | ||||||
| chr10:97105868
|
C | T | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-39782G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105868 | ||||||
| chr10:97105871
|
G | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-39785C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105871 | ||||||
| chr10:97105949
|
G | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-39863C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105949 | ||||||
| chr10:97105960
|
T | C | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-39874A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97105960 | ||||||
| chr10:97106149
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0225 | 2 | NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.414-40063C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106149 | ||||||
| chr10:97106345
|
G | C | 145 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.414-40259C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106345 | ||||||
| chr10:97106387
|
A | AGAAT | 145 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.414-40305_414-4030 others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106387 | ||||||
| chr10:97106403
|
T | TGAAC | 58 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(55): Show | 58 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.414-40321_414-4031 others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106403 | ||||||
| chr10:97106403
|
T | TGAACGAA others(1): Show |
13 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0078others(10): Show | 13 | HG01109.hp1 HG01257.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-40318_414-4031 others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106403 | ||||||
| chr10:97106407
|
C | CGAACGAA others(1): Show |
6 | a0001c0007t0001g0057a0001c0007t0001g0058a0001c0007t0001g0180others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-40322_414-4032 others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106407 | ||||||
| chr10:97106411
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.414-40325A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106411 | ||||||
| chr10:97106417
|
A | AATGAATG others(17): Show |
1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.414-40332_414-4033 others(28): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106417 | ||||||
| chr10:97106484
|
G | C | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-40398C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106484 | ||||||
| chr10:97106538
|
A | G | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-40452T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106538 | ||||||
| chr10:97106641
|
G | GTT | 74 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(71): Show | 74 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.414-40557_414-4055 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106641 | ||||||
| chr10:97106641
|
GT | G | 13 | a0001c0001t0001g0241a0001c0002t0001g0037a0001c0002t0001g0120others(10): Show | 13 | HG00558.hp1 HG02602.hp1 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-40556delA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106641 | ||||||
| chr10:97106742
|
C | T | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-40656G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106742 | ||||||
| chr10:97106765
|
A | G | 122 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.414-40679T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106765 | ||||||
| chr10:97106892
|
G | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-40806C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106892 | ||||||
| chr10:97106952
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.414-40866C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97106952 | ||||||
| chr10:97107053
|
A | G | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-40967T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97107053 | ||||||
| chr10:97107253
|
C | T | 79 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(76): Show | 79 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.414-41167G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97107253 | ||||||
| chr10:97107392
|
G | C | 20 | a0001c0001t0001g0054a0001c0001t0001g0214a0001c0001t0001g0241others(17): Show | 20 | HG00558.hp1 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.414-41306C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97107392 | ||||||
| chr10:97107445
|
G | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0174 | 2 | NA18963.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.414-41359C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97107445 | ||||||
| chr10:97107458
|
T | C | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-41372A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97107458 | ||||||
| chr10:97107468
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.414-41382G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97107468 | ||||||
| chr10:97107482
|
G | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-41396C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97107482 | ||||||
| chr10:97107537
|
G | A | 77 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(74): Show | 77 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.414-41451C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97107537 | ||||||
| chr10:97107566
|
G | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(75): Show | 78 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.414-41480C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97107566 | ||||||
| chr10:97107720
|
G | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(67): Show | 70 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.414-41634C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97107720 | ||||||
| chr10:97107780
|
A | G | 71 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(68): Show | 71 | HG00408.hp1 HG00639.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.414-41694T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97107780 | ||||||
| chr10:97108721
|
T | G | 99 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(96): Show | 99 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.414-42635A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108721 | ||||||
| chr10:97108821
|
G | GAGGTTGC others(1): Show |
13 | a0001c0001t0001g0241a0001c0002t0001g0037a0001c0002t0001g0120others(10): Show | 13 | HG00558.hp1 HG02602.hp1 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-42743_414-4273 others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108821 | ||||||
| chr10:97108852
|
C | T | 7 | a0001c0001t0001g0124a0001c0007t0001g0057a0001c0007t0001g0058others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-42766G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108852 | ||||||
| chr10:97108886
|
C | CA | 25 | a0001c0001t0001g0104a0001c0001t0001g0110a0001c0001t0001g0156others(22): Show | 25 | HG00673.hp1 HG00735.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.414-42801dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108886 | ||||||
| chr10:97108886
|
CA | C | 49 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0054others(46): Show | 49 | HG00408.hp1 HG01071.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.414-42801delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108886 | ||||||
| chr10:97108886
|
CAA | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0051a0001c0001t0001g0080others(35): Show | 38 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.414-42802_414-4280 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108886 | ||||||
| chr10:97108886
|
CAAA | C | 77 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.414-42803_414-4280 others(7): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108886 | ||||||
| chr10:97108886
|
CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-42810_414-4280 others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108886 | ||||||
| chr10:97108886
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.414-42811_414-4280 others(15): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108886 | ||||||
| chr10:97108886
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.414-42815_414-4280 others(19): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108886 | ||||||
| chr10:97108886
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0002g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.414-42816_414-4280 others(20): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108886 | ||||||
| chr10:97108886
|
CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0001g0062a0001c0001t0001g0235 | 2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.414-42818_414-4280 others(22): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108886 | ||||||
| chr10:97108886
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-42819_414-4280 others(23): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108886 | ||||||
| chr10:97108927
|
G | A | 2 | a0001c0001t0001g0094a0004c0028t0001g0216 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.414-42841C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108927 | ||||||
| chr10:97108966
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0002g0224a0001c0005t0001g0005others(2): Show | 5 | HG01243.hp1 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-42880G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97108966 | ||||||
| chr10:97109046
|
A | T | 153 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(150): Show | 153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.414-42960T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97109046 | ||||||
| chr10:97109193
|
C | A | 9 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-43107G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97109193 | ||||||
| chr10:97109198
|
GA | G | 7 | a0001c0001t0001g0124a0001c0007t0001g0057a0001c0007t0001g0058others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-43113delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97109198 | ||||||
| chr10:97109199
|
A | C | 1 | a0001c0002t0002g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.414-43113T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97109199 | ||||||
| chr10:97109374
|
T | A | 13 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0078others(10): Show | 13 | HG01109.hp1 HG01257.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-43288A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97109374 | ||||||
| chr10:97109445
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0002g0224a0001c0005t0001g0005others(2): Show | 5 | HG01243.hp1 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-43359A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97109445 | ||||||
| chr10:97109607
|
A | C | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-43521T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97109607 | ||||||
| chr10:97109626
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.414-43540A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97109626 | ||||||
| chr10:97109631
|
T | A | 202 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(199): Show | 202 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.414-43545A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97109631 | ||||||
| chr10:97109737
|
C | A | 1 | a0001c0021t0008g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.414-43651G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97109737 | ||||||
| chr10:97109837
|
C | T | 13 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0078others(10): Show | 13 | HG01109.hp1 HG01257.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.414-43751G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97109837 | ||||||
| chr10:97109885
|
A | G | 182 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(179): Show | 182 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.414-43799T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97109885 | ||||||
| chr10:97109935
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.414-43849T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97109935 | ||||||
| chr10:97110431
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.414-44345T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97110431 | ||||||
| chr10:97110498
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.414-44412A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97110498 | ||||||
| chr10:97110781
|
T | C | 154 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(151): Show | 154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.414-44695A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97110781 | ||||||
| chr10:97111035
|
C | T | 201 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(198): Show | 201 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.414-44949G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97111035 | ||||||
| chr10:97111281
|
C | T | 154 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(151): Show | 154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.414-45195G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97111281 | ||||||
| chr10:97111452
|
A | C | 154 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(151): Show | 154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.414-45366T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97111452 | ||||||
| chr10:97111454
|
G | A | 105 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(102): Show | 105 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.414-45368C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97111454 | ||||||
| chr10:97111500
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.414-45414C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97111500 | ||||||
| chr10:97111511
|
A | T | 1 | a0001c0004t0001g0228 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.414-45425T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97111511 | ||||||
| chr10:97111519
|
T | C | 174 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(171): Show | 174 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.414-45433A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97111519 | ||||||
| chr10:97111553
|
T | C | 1 | a0001c0005t0001g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.414-45467A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97111553 | ||||||
| chr10:97111608
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.414-45522G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97111608 | ||||||
| chr10:97111718
|
C | T | 9 | a0001c0001t0002g0042a0001c0001t0002g0128a0001c0001t0002g0222others(6): Show | 9 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-45632G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97111718 | ||||||
| chr10:97111720
|
G | C | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.414-45634C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97111720 | ||||||
| chr10:97111774
|
A | G | 203 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(200): Show | 203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.414-45688T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97111774 | ||||||
| chr10:97111848
|
G | A | 154 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(151): Show | 154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.414-45762C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97111848 | ||||||
| chr10:97112018
|
C | A | 1 | a0001c0002t0001g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.413+45800G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97112018 | ||||||
| chr10:97112100
|
C | T | 2 | a0001c0004t0001g0165a0001c0004t0001g0166 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.413+45718G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97112100 | ||||||
| chr10:97112298
|
C | T | 1 | a0001c0024t0001g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.413+45520G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97112298 | ||||||
| chr10:97112372
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.413+45446G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97112372 | ||||||
| chr10:97112377
|
C | T | 154 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(151): Show | 154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.413+45441G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97112377 | ||||||
| chr10:97112454
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.413+45364C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97112454 | ||||||
| chr10:97112658
|
C | A | 7 | a0001c0001t0001g0124a0001c0007t0001g0057a0001c0007t0001g0058others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+45160G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97112658 | ||||||
| chr10:97112665
|
G | A | 153 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(150): Show | 153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.413+45153C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97112665 | ||||||
| chr10:97113213
|
A | G | 7 | a0001c0001t0001g0124a0001c0007t0001g0057a0001c0007t0001g0058others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+44605T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97113213 | ||||||
| chr10:97113243
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.413+44575A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97113243 | ||||||
| chr10:97113301
|
G | A | 153 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(150): Show | 153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.413+44517C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97113301 | ||||||
| chr10:97113518
|
A | G | 4 | a0001c0004t0001g0074a0001c0004t0001g0075a0001c0004t0001g0076others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+44300T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97113518 | ||||||
| chr10:97113552
|
T | G | 1 | a0001c0023t0002g0146 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.413+44266A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97113552 | ||||||
| chr10:97113557
|
G | GT | 13 | a0001c0001t0001g0080a0001c0001t0001g0099a0001c0001t0001g0124others(10): Show | 13 | HG00280.hp2 HG02055.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+44260dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97113557 | ||||||
| chr10:97113557
|
GT | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(9): Show | 12 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.413+44260delA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97113557 | ||||||
| chr10:97113594
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0004t0001g0024 | 3 | NA18943.hp2 NA18998.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.413+44224G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97113594 | ||||||
| chr10:97113819
|
G | C | 166 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(163): Show | 166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.413+43999C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97113819 | ||||||
| chr10:97113836
|
G | A | 166 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(163): Show | 166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.413+43982C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97113836 | ||||||
| chr10:97113864
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.413+43954T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97113864 | ||||||
| chr10:97113955
|
G | C | 1 | a0001c0001t0023g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.413+43863C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97113955 | ||||||
| chr10:97114081
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.413+43737C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97114081 | ||||||
| chr10:97114133
|
C | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+43685G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97114133 | ||||||
| chr10:97114139
|
A | G | 6 | a0001c0001t0001g0156a0001c0001t0004g0019a0001c0001t0011g0150others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+43679T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97114139 | ||||||
| chr10:97114147
|
A | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+43671T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97114147 | ||||||
| chr10:97114304
|
A | G | 186 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(183): Show | 186 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.413+43514T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97114304 | ||||||
| chr10:97114356
|
G | A | 99 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(96): Show | 99 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.413+43462C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97114356 | ||||||
| chr10:97114887
|
C | G | 1 | a0001c0006t0009g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.413+42931G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97114887 | ||||||
| chr10:97114904
|
T | C | 99 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(96): Show | 99 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.413+42914A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97114904 | ||||||
| chr10:97114937
|
C | G | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.413+42881G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97114937 | ||||||
| chr10:97115372
|
C | T | 204 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(201): Show | 204 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.413+42446G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97115372 | ||||||
| chr10:97115415
|
T | C | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.413+42403A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97115415 | ||||||
| chr10:97115512
|
A | G | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.413+42306T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97115512 | ||||||
| chr10:97115565
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+42253T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97115565 | ||||||
| chr10:97115651
|
G | A | 13 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0078others(10): Show | 13 | HG01109.hp1 HG01257.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+42167C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97115651 | ||||||
| chr10:97115895
|
T | C | 28 | a0001c0001t0001g0054a0001c0001t0001g0124a0001c0001t0001g0214others(25): Show | 28 | HG00558.hp1 HG01884.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.413+41923A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97115895 | ||||||
| chr10:97115973
|
G | A | 2 | a0001c0003t0001g0171a0001c0003t0001g0172 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.413+41845C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97115973 | ||||||
| chr10:97115974
|
A | G | 8 | a0001c0001t0001g0124a0001c0001t0002g0083a0001c0007t0001g0057others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+41844T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97115974 | ||||||
| chr10:97116047
|
C | T | 100 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(97): Show | 100 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.413+41771G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97116047 | ||||||
| chr10:97116179
|
T | A | 200 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(197): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.413+41639A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97116179 | ||||||
| chr10:97116278
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0002g0224a0001c0005t0001g0005others(2): Show | 5 | HG01243.hp1 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+41540G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97116278 | ||||||
| chr10:97116393
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0010g0197a0001c0002t0001g0151 | 3 | NA18954.hp2 NA18963.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.413+41425G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97116393 | ||||||
| chr10:97116683
|
G | A | 100 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(97): Show | 100 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.413+41135C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97116683 | ||||||
| chr10:97116696
|
G | A | 2 | a0001c0001t0002g0128a0001c0001t0003g0098 | 2 | HG00558.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.413+41122C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97116696 | ||||||
| chr10:97116903
|
C | A | 4 | a0001c0002t0001g0025a0001c0002t0001g0101a0001c0002t0001g0149others(1): Show | 4 | NA18939.hp2 NA18961.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+40915G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97116903 | ||||||
| chr10:97116953
|
T | C | 1 | a0002c0014t0001g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.413+40865A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97116953 | ||||||
| chr10:97117024
|
T | A | 1 | a0001c0003t0001g0096 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.413+40794A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97117024 | ||||||
| chr10:97117150
|
G | A | 1 | a0001c0018t0009g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.413+40668C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97117150 | ||||||
| chr10:97117172
|
T | A | 3 | a0001c0001t0001g0162a0001c0001t0013g0002a0006c0027t0025g0220 | 3 | HG03098.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.413+40646A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97117172 | ||||||
| chr10:97117184
|
G | A | 197 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(194): Show | 197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.413+40634C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97117184 | ||||||
| chr10:97117198
|
A | G | 1 | a0001c0005t0001g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.413+40620T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97117198 | ||||||
| chr10:97117246
|
G | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+40572C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97117246 | ||||||
| chr10:97117275
|
G | A | 7 | a0001c0001t0001g0124a0001c0007t0001g0057a0001c0007t0001g0058others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+40543C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97117275 | ||||||
| chr10:97117285
|
T | TA | 97 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(94): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.413+40532dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97117285 | ||||||
| chr10:97117516
|
A | G | 1 | a0001c0003t0006g0036 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.413+40302T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97117516 | ||||||
| chr10:97117637
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+40181G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97117637 | ||||||
| chr10:97117686
|
G | C | 201 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(198): Show | 201 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.413+40132C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97117686 | ||||||
| chr10:97117705
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.413+40113A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97117705 | ||||||
| chr10:97117743
|
C | T | 19 | a0001c0001t0001g0050a0001c0001t0001g0100a0001c0001t0001g0104others(16): Show | 19 | HG00621.hp1 HG00673.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+40075G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97117743 | ||||||
| chr10:97118002
|
T | A | 105 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(102): Show | 105 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.413+39816A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97118002 | ||||||
| chr10:97118105
|
G | GT | 105 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(102): Show | 105 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.413+39712dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97118105 | ||||||
| chr10:97118333
|
C | T | 4 | a0001c0002t0001g0025a0001c0002t0001g0101a0001c0002t0001g0149others(1): Show | 4 | NA18939.hp2 NA18961.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+39485G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97118333 | ||||||
| chr10:97118334
|
T | G | 198 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(195): Show | 198 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.413+39484A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97118334 | ||||||
| chr10:97118369
|
C | T | 98 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(95): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.413+39449G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97118369 | ||||||
| chr10:97118544
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.413+39274C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97118544 | ||||||
| chr10:97118624
|
A | C | 200 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(197): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.413+39194T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97118624 | ||||||
| chr10:97119108
|
T | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(96): Show | 99 | HG00408.hp1 HG00558.hp1 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.413+38710A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119108 | ||||||
| chr10:97119129
|
AAAGTCAA others(45): Show |
A | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.413+38637_413+3868 others(56): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119129 | ||||||
| chr10:97119142
|
G | A | 2 | a0001c0003t0001g0171a0001c0003t0001g0172 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.413+38676C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119142 | ||||||
| chr10:97119618
|
G | A | 2 | a0001c0001t0001g0099a0001c0010t0002g0253 | 2 | HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.413+38200C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119618 | ||||||
| chr10:97119666
|
A | G | 198 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(195): Show | 198 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.413+38152T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119666 | ||||||
| chr10:97119904
|
T | C | 13 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0078others(10): Show | 13 | HG01109.hp1 HG01257.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+37914A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119904 | ||||||
| chr10:97119910
|
G | A | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.413+37908C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119910 | ||||||
| chr10:97119913
|
G | GTATA | 5 | a0001c0001t0001g0174a0001c0003t0001g0064a0001c0003t0001g0237others(2): Show | 5 | HG02622.hp1 HG03471.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+37901_413+3790 others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
G | GTATATA | 3 | a0001c0001t0001g0246a0001c0001t0005g0240a0001c0008t0003g0084 | 3 | HG01517.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.413+37899_413+3790 others(10): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
G | GTATATAT others(1): Show |
31 | a0001c0001t0001g0051a0001c0001t0001g0092a0001c0001t0001g0103others(28): Show | 31 | HG00438.hp2 HG01358.hp1 HG01361.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+37897_413+3790 others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
G | GTATATAT others(3): Show |
40 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0034others(37): Show | 40 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.413+37895_413+3790 others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
G | GTATATAT others(5): Show |
42 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0062others(39): Show | 42 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.413+37893_413+3790 others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
G | GTATATAT others(7): Show |
19 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0049others(16): Show | 19 | HG00280.hp1 HG00558.hp2 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+37891_413+3790 others(18): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
G | GTATATAT others(9): Show |
6 | a0001c0001t0001g0072a0001c0001t0001g0221a0001c0001t0003g0169others(3): Show | 6 | HG00280.hp2 HG01109.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+37889_413+3790 others(20): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
G | GTATATAT others(11): Show |
4 | a0001c0001t0001g0105a0001c0001t0006g0038a0001c0003t0001g0184others(1): Show | 4 | HG02071.hp2 HG02155.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+37887_413+3790 others(22): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
G | GTATATAT others(13): Show |
2 | a0001c0001t0001g0078a0001c0004t0001g0024 | 2 | NA18943.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.413+37885_413+3790 others(24): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
G | GTATATAT others(17): Show |
1 | a0001c0005t0001g0192 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.413+37881_413+3790 others(28): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
G | GTGTATAT others(3): Show |
2 | a0001c0001t0001g0073a0001c0009t0005g0032 | 2 | HG00639.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.413+37904_413+3790 others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
G | GTGTATAT others(5): Show |
1 | a0001c0003t0001g0230 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.413+37904_413+3790 others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
G | GTGTATAT others(7): Show |
2 | a0001c0001t0001g0033a0001c0009t0027g0223 | 2 | HG00738.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.413+37904_413+3790 others(18): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
GTA | G | 20 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0131others(17): Show | 20 | HG00140.hp1 HG01109.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.413+37903_413+3790 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
GTATA | G | 33 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(30): Show | 33 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.413+37901_413+3790 others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
GTATATA | G | 9 | a0001c0001t0001g0124a0001c0001t0001g0241a0001c0002t0001g0037others(6): Show | 9 | HG00558.hp1 HG00741.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+37899_413+3790 others(10): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
GTATATAT others(1): Show |
G | 8 | a0001c0001t0001g0050a0001c0002t0001g0120a0001c0002t0001g0193others(5): Show | 8 | HG02602.hp1 HG02738.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+37897_413+3790 others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119913
|
GTATATAT others(9): Show |
G | 3 | a0001c0001t0001g0214a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02109.hp2 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.413+37889_413+3790 others(20): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119913 | ||||||
| chr10:97119941
|
A | ATATATAT others(17): Show |
2 | a0002c0013t0006g0029a0002c0013t0006g0030 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.413+37876_413+3787 others(28): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119941 | ||||||
| chr10:97119941
|
A | ATATATAT others(9): Show |
1 | a0002c0014t0001g0227 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.413+37876_413+3787 others(20): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119941 | ||||||
| chr10:97119951
|
A | G | 4 | a0001c0001t0001g0054a0001c0005t0001g0052a0001c0005t0009g0091others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+37867T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97119951 | ||||||
| chr10:97120290
|
A | G | 1 | a0001c0001t0023g0046 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.413+37528T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97120290 | ||||||
| chr10:97120402
|
A | G | 5 | a0001c0001t0028g0093a0001c0002t0001g0067a0001c0004t0003g0176others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+37416T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97120402 | ||||||
| chr10:97120454
|
A | G | 8 | a0001c0001t0001g0124a0001c0001t0002g0083a0001c0007t0001g0057others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+37364T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97120454 | ||||||
| chr10:97120479
|
C | G | 1 | a0001c0001t0022g0254 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.413+37339G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97120479 | ||||||
| chr10:97120525
|
A | G | 98 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(95): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.413+37293T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97120525 | ||||||
| chr10:97120578
|
G | A | 1 | a0001c0004t0001g0140 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.413+37240C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97120578 | ||||||
| chr10:97120692
|
C | A | 52 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0043others(49): Show | 52 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.413+37126G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97120692 | ||||||
| chr10:97120717
|
G | C | 101 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(98): Show | 101 | HG00408.hp1 HG00558.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.413+37101C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97120717 | ||||||
| chr10:97120775
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.413+37043G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97120775 | ||||||
| chr10:97120998
|
A | G | 98 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(95): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.413+36820T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97120998 | ||||||
| chr10:97121281
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.413+36537G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97121281 | ||||||
| chr10:97121435
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.413+36383G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97121435 | ||||||
| chr10:97121609
|
C | T | 7 | a0001c0001t0002g0083a0001c0007t0001g0057a0001c0007t0001g0058others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+36209G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97121609 | ||||||
| chr10:97121628
|
C | T | 1 | a0001c0002t0001g0231 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.413+36190G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97121628 | ||||||
| chr10:97121645
|
G | A | 1 | a0001c0002t0001g0243 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.413+36173C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97121645 | ||||||
| chr10:97121902
|
T | C | 7 | a0001c0001t0001g0104a0001c0001t0001g0110a0001c0001t0001g0185others(4): Show | 7 | HG00621.hp1 HG00673.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+35916A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97121902 | ||||||
| chr10:97122020
|
C | T | 3 | a0001c0001t0001g0214a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02109.hp2 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.413+35798G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97122020 | ||||||
| chr10:97122313
|
T | C | 3 | a0001c0001t0002g0189a0001c0002t0002g0040a0001c0003t0006g0190 | 3 | HG00738.hp2 HG01123.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.413+35505A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97122313 | ||||||
| chr10:97122542
|
C | A | 97 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(94): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.413+35276G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97122542 | ||||||
| chr10:97122555
|
A | G | 13 | a0001c0001t0001g0050a0001c0001t0001g0241a0001c0002t0001g0037others(10): Show | 13 | HG00558.hp1 HG02602.hp1 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+35263T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97122555 | ||||||
| chr10:97122617
|
C | G | 98 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(95): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.413+35201G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97122617 | ||||||
| chr10:97122668
|
A | G | 136 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(133): Show | 136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.413+35150T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97122668 | ||||||
| chr10:97122886
|
ATATTTCA others(6): Show |
A | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.413+34919_413+3493 others(17): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97122886 | ||||||
| chr10:97123114
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.413+34704C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97123114 | ||||||
| chr10:97123122
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.413+34696C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97123122 | ||||||
| chr10:97123123
|
G | C | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.413+34695C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97123123 | ||||||
| chr10:97123124
|
C | CCCCCCAC others(54): Show |
1 | a0001c0001t0001g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.413+34693_413+3469 others(65): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97123124 | ||||||
| chr10:97123134
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.413+34684A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97123134 | ||||||
| chr10:97123135
|
G | C | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.413+34683C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97123135 | ||||||
| chr10:97123478
|
A | G | 1 | a0007c0031t0001g0152 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.413+34340T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97123478 | ||||||
| chr10:97123585
|
T | C | 52 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0043others(49): Show | 52 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.413+34233A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97123585 | ||||||
| chr10:97123663
|
G | A | 1 | a0001c0001t0019g0155 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.413+34155C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97123663 | ||||||
| chr10:97123721
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+34097G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97123721 | ||||||
| chr10:97123789
|
G | GA | 50 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0043others(47): Show | 50 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.413+34028dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97123789 | ||||||
| chr10:97123789
|
GA | G | 120 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.413+34028delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97123789 | ||||||
| chr10:97123956
|
C | T | 2 | a0001c0001t0001g0236a0001c0003t0006g0036 | 2 | HG00140.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.413+33862G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97123956 | ||||||
| chr10:97124180
|
C | T | 191 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(188): Show | 191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.413+33638G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97124180 | ||||||
| chr10:97124297
|
T | C | 1 | a0001c0001t0002g0196 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.413+33521A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97124297 | ||||||
| chr10:97124350
|
C | T | 1 | a0001c0002t0001g0181 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.413+33468G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97124350 | ||||||
| chr10:97124427
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.413+33391C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97124427 | ||||||
| chr10:97124556
|
C | T | 97 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(94): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.413+33262G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97124556 | ||||||
| chr10:97124645
|
A | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0043others(42): Show | 45 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.413+33173T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97124645 | ||||||
| chr10:97124721
|
T | A | 2 | a0001c0004t0001g0165a0001c0004t0001g0166 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.413+33097A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97124721 | ||||||
| chr10:97125066
|
G | A | 1 | a0001c0012t0002g0047 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.413+32752C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97125066 | ||||||
| chr10:97125085
|
T | C | 62 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0043others(59): Show | 62 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.413+32733A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97125085 | ||||||
| chr10:97125283
|
T | TAAGAGCA others(2): Show |
108 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(105): Show | 108 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.413+32534_413+3253 others(13): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97125283 | ||||||
| chr10:97125373
|
A | C | 4 | a0001c0001t0001g0054a0001c0005t0001g0052a0001c0005t0009g0091others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+32445T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97125373 | ||||||
| chr10:97125533
|
C | CAA | 92 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0026others(89): Show | 92 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.413+32283_413+3228 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97125533 | ||||||
| chr10:97125533
|
C | CAAA | 7 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0116others(4): Show | 7 | HG00735.hp1 HG00741.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+32282_413+3228 others(7): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97125533 | ||||||
| chr10:97125533
|
CA | C | 68 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0050others(65): Show | 68 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.413+32284delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97125533 | ||||||
| chr10:97125553
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.413+32265T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97125553 | ||||||
| chr10:97125847
|
CA | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(6): Show | 9 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+31970delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97125847 | ||||||
| chr10:97125873
|
C | G | 6 | a0001c0001t0001g0160a0001c0008t0003g0060a0001c0008t0003g0082others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+31945G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97125873 | ||||||
| chr10:97126315
|
C | T | 1 | a0001c0032t0001g0061 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.413+31503G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97126315 | ||||||
| chr10:97126977
|
C | T | 2 | a0001c0004t0001g0165a0001c0004t0001g0166 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.413+30841G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97126977 | ||||||
| chr10:97127126
|
T | TA | 101 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(98): Show | 101 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.413+30691dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97127126 | ||||||
| chr10:97127137
|
C | A | 1 | a0001c0001t0002g0196 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.413+30681G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97127137 | ||||||
| chr10:97127138
|
A | C | 1 | a0001c0001t0002g0196 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.413+30680T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97127138 | ||||||
| chr10:97127221
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.413+30597C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97127221 | ||||||
| chr10:97127241
|
A | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(109): Show | 112 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.413+30577T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97127241 | ||||||
| chr10:97127285
|
CA | C | 102 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(99): Show | 102 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.413+30532delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97127285 | ||||||
| chr10:97127295
|
A | C | 1 | a0001c0001t0002g0196 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.413+30523T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97127295 | ||||||
| chr10:97127410
|
C | T | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.413+30408G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97127410 | ||||||
| chr10:97127680
|
G | A | 8 | a0001c0001t0001g0071a0001c0001t0001g0078a0001c0002t0001g0070others(5): Show | 8 | HG01358.hp1 HG01361.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+30138C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97127680 | ||||||
| chr10:97127772
|
G | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(109): Show | 112 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.413+30046C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97127772 | ||||||
| chr10:97127892
|
A | C | 1 | a0001c0001t0002g0134 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.413+29926T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97127892 | ||||||
| chr10:97127941
|
A | C | 171 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(168): Show | 171 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.413+29877T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97127941 | ||||||
| chr10:97128380
|
C | T | 21 | a0001c0001t0001g0050a0001c0001t0001g0214a0001c0001t0001g0241others(18): Show | 21 | HG00140.hp2 HG00558.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.413+29438G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128380 | ||||||
| chr10:97128381
|
G | A | 36 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0094others(33): Show | 36 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.413+29437C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128381 | ||||||
| chr10:97128407
|
T | A | 149 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(146): Show | 149 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.413+29411A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128407 | ||||||
| chr10:97128434
|
T | G | 1 | a0001c0002t0001g0025 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.413+29384A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128434 | ||||||
| chr10:97128476
|
A | C | 2 | a0001c0003t0002g0219a0001c0003t0015g0087 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.413+29342T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128476 | ||||||
| chr10:97128564
|
C | T | 10 | a0001c0001t0001g0124a0001c0001t0002g0083a0001c0005t0009g0091others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.413+29254G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128564 | ||||||
| chr10:97128574
|
C | A | 1 | a0001c0001t0002g0196 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.413+29244G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128574 | ||||||
| chr10:97128575
|
A | C | 1 | a0001c0001t0002g0196 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.413+29243T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128575 | ||||||
| chr10:97128576
|
C | T | 1 | a0001c0001t0002g0196 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.413+29242G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128576 | ||||||
| chr10:97128585
|
T | C | 1 | a0001c0001t0021g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.413+29233A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128585 | ||||||
| chr10:97128647
|
C | T | 1 | a0001c0009t0005g0238 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.413+29171G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128647 | ||||||
| chr10:97128862
|
G | A | 4 | a0001c0002t0001g0070a0002c0013t0006g0029a0002c0013t0006g0030others(1): Show | 4 | HG01361.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+28956C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128862 | ||||||
| chr10:97128892
|
G | C | 103 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(100): Show | 103 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.413+28926C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128892 | ||||||
| chr10:97128926
|
C | CA | 113 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(110): Show | 113 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.413+28891dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97128926 | ||||||
| chr10:97129010
|
C | T | 11 | a0001c0001t0001g0071a0001c0001t0001g0078a0001c0001t0001g0246others(8): Show | 11 | HG01358.hp1 HG01361.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+28808G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129010 | ||||||
| chr10:97129063
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.413+28755C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129063 | ||||||
| chr10:97129337
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.413+28481C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129337 | ||||||
| chr10:97129383
|
C | CA | 10 | a0001c0001t0001g0124a0001c0001t0002g0083a0001c0005t0009g0091others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.413+28434dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129383 | ||||||
| chr10:97129383
|
CA | C | 17 | a0001c0001t0001g0071a0001c0001t0001g0078a0001c0001t0001g0132others(14): Show | 17 | HG01358.hp1 HG01361.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.413+28434delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129383 | ||||||
| chr10:97129383
|
CAA | C | 135 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(132): Show | 135 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.413+28433_413+2843 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129383 | ||||||
| chr10:97129397
|
A | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+28421T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129397 | ||||||
| chr10:97129627
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.413+28191G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129627 | ||||||
| chr10:97129661
|
C | T | 103 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(100): Show | 103 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.413+28157G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129661 | ||||||
| chr10:97129662
|
G | A | 3 | a0001c0001t0001g0124a0001c0005t0009g0091a0001c0026t0004g0090 | 3 | HG02970.hp2 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.413+28156C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129662 | ||||||
| chr10:97129698
|
C | G | 151 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(148): Show | 151 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.413+28120G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129698 | ||||||
| chr10:97129819
|
C | T | 38 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0094others(35): Show | 38 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.413+27999G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129819 | ||||||
| chr10:97129848
|
T | C | 3 | a0001c0001t0001g0103a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | NA18971.hp2 NA18980.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.413+27970A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129848 | ||||||
| chr10:97129956
|
T | C | 141 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(138): Show | 141 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.413+27862A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97129956 | ||||||
| chr10:97130053
|
C | G | 3 | a0001c0001t0001g0241a0001c0002t0001g0256a0001c0020t0001g0079 | 3 | HG03710.hp2 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.413+27765G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97130053 | ||||||
| chr10:97130063
|
A | G | 1 | a0001c0010t0002g0003 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.413+27755T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97130063 | ||||||
| chr10:97130204
|
T | C | 101 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(98): Show | 101 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.413+27614A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97130204 | ||||||
| chr10:97130232
|
A | G | 141 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(138): Show | 141 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.413+27586T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97130232 | ||||||
| chr10:97130364
|
G | A | 38 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0094others(35): Show | 38 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.413+27454C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97130364 | ||||||
| chr10:97130481
|
T | C | 8 | a0001c0001t0002g0042a0001c0001t0002g0128a0001c0001t0003g0098others(5): Show | 8 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+27337A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97130481 | ||||||
| chr10:97130642
|
T | C | 1 | a0001c0024t0001g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.413+27176A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97130642 | ||||||
| chr10:97130860
|
C | T | 15 | a0001c0001t0001g0050a0001c0001t0001g0194a0001c0001t0001g0241others(12): Show | 15 | HG00140.hp2 HG00558.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+26958G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97130860 | ||||||
| chr10:97130940
|
G | C | 1 | a0001c0021t0008g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413+26878C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97130940 | ||||||
| chr10:97130989
|
A | G | 191 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(188): Show | 191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.413+26829T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97130989 | ||||||
| chr10:97131282
|
C | T | 1 | a0001c0023t0002g0146 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.413+26536G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97131282 | ||||||
| chr10:97131338
|
G | A | 10 | a0001c0001t0001g0124a0001c0001t0002g0083a0001c0005t0009g0091others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.413+26480C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97131338 | ||||||
| chr10:97131582
|
A | G | 141 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(138): Show | 141 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.413+26236T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97131582 | ||||||
| chr10:97131599
|
A | C | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.413+26219T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97131599 | ||||||
| chr10:97131630
|
G | C | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.413+26188C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97131630 | ||||||
| chr10:97131631
|
C | A | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.413+26187G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97131631 | ||||||
| chr10:97131667
|
T | A | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.413+26151A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97131667 | ||||||
| chr10:97131683
|
G | C | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.413+26135C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97131683 | ||||||
| chr10:97131811
|
G | T | 35 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0094others(32): Show | 35 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.413+26007C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97131811 | ||||||
| chr10:97131940
|
T | C | 35 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0094others(32): Show | 35 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.413+25878A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97131940 | ||||||
| chr10:97132474
|
C | T | 3 | a0001c0003t0002g0219a0001c0003t0015g0087a0001c0015t0001g0177 | 3 | HG02723.hp1 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.413+25344G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97132474 | ||||||
| chr10:97132637
|
C | G | 1 | a0001c0001t0002g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.413+25181G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97132637 | ||||||
| chr10:97132686
|
C | CA | 4 | a0001c0001t0023g0046a0001c0003t0002g0219a0001c0003t0015g0087others(1): Show | 4 | HG02630.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+25131dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97132686 | ||||||
| chr10:97132953
|
C | T | 7 | a0001c0001t0002g0083a0001c0007t0001g0057a0001c0007t0001g0058others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+24865G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97132953 | ||||||
| chr10:97133114
|
G | A | 125 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(122): Show | 125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.413+24704C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97133114 | ||||||
| chr10:97133272
|
G | A | 1 | a0001c0010t0002g0107 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.413+24546C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97133272 | ||||||
| chr10:97133595
|
C | A | 10 | a0001c0001t0001g0124a0001c0001t0002g0083a0001c0005t0009g0091others(7): Show | 10 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.413+24223G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97133595 | ||||||
| chr10:97133764
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.413+24054A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97133764 | ||||||
| chr10:97133863
|
A | G | 1 | a0001c0003t0002g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.413+23955T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97133863 | ||||||
| chr10:97134075
|
G | A | 1 | a0001c0001t0018g0168 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.413+23743C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97134075 | ||||||
| chr10:97134091
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.413+23727G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97134091 | ||||||
| chr10:97134109
|
G | A | 48 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0094others(45): Show | 48 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.413+23709C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97134109 | ||||||
| chr10:97134144
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+23674G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97134144 | ||||||
| chr10:97134192
|
A | T | 1 | a0001c0002t0002g0199 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.413+23626T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97134192 | ||||||
| chr10:97134266
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0003t0026g0170 | 3 | HG02895.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.413+23552C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97134266 | ||||||
| chr10:97134554
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.413+23264G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97134554 | ||||||
| chr10:97134687
|
C | A | 55 | a0001c0001t0001g0041a0001c0001t0001g0050a0001c0001t0001g0054others(52): Show | 55 | HG00140.hp2 HG00558.hp1 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.413+23131G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97134687 | ||||||
| chr10:97134883
|
A | C | 15 | a0001c0001t0001g0124a0001c0001t0001g0160a0001c0001t0002g0083others(12): Show | 15 | HG01081.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.413+22935T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97134883 | ||||||
| chr10:97135013
|
A | G | 8 | a0001c0001t0001g0124a0001c0001t0002g0083a0001c0007t0001g0057others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+22805T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97135013 | ||||||
| chr10:97135268
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+22550T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97135268 | ||||||
| chr10:97135371
|
G | A | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.413+22447C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97135371 | ||||||
| chr10:97135436
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.413+22382G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97135436 | ||||||
| chr10:97135602
|
T | C | 15 | a0001c0001t0001g0124a0001c0001t0001g0214a0001c0001t0002g0083others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.413+22216A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97135602 | ||||||
| chr10:97136077
|
G | C | 136 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(133): Show | 136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.413+21741C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97136077 | ||||||
| chr10:97136171
|
C | A | 6 | a0001c0001t0002g0083a0001c0007t0001g0057a0001c0007t0001g0058others(3): Show | 6 | HG02145.hp2 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+21647G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97136171 | ||||||
| chr10:97136248
|
G | A | 166 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(163): Show | 166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.413+21570C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97136248 | ||||||
| chr10:97136320
|
T | C | 1 | a0001c0001t0001g0167 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.413+21498A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97136320 | ||||||
| chr10:97136441
|
A | T | 7 | a0001c0001t0002g0083a0001c0007t0001g0057a0001c0007t0001g0058others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+21377T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97136441 | ||||||
| chr10:97136582
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+21236T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97136582 | ||||||
| chr10:97136592
|
A | C | 4 | a0001c0001t0001g0203a0001c0001t0001g0246a0001c0006t0004g0204others(1): Show | 4 | HG02145.hp1 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+21226T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97136592 | ||||||
| chr10:97136639
|
T | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+21179A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97136639 | ||||||
| chr10:97136963
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+20855G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97136963 | ||||||
| chr10:97137022
|
C | A | 120 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.413+20796G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97137022 | ||||||
| chr10:97137163
|
C | T | 120 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.413+20655G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97137163 | ||||||
| chr10:97137301
|
A | G | 4 | a0001c0001t0023g0046a0001c0003t0002g0219a0001c0003t0015g0087others(1): Show | 4 | HG02630.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+20517T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97137301 | ||||||
| chr10:97137378
|
A | G | 8 | a0001c0001t0001g0124a0001c0001t0002g0083a0001c0007t0001g0057others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+20440T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97137378 | ||||||
| chr10:97137449
|
T | C | 1 | a0001c0001t0022g0254 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.413+20369A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97137449 | ||||||
| chr10:97137477
|
A | G | 10 | a0001c0001t0001g0092a0001c0001t0001g0103a0001c0001t0001g0111others(7): Show | 10 | HG00408.hp2 HG00438.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+20341T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97137477 | ||||||
| chr10:97137479
|
T | C | 7 | a0001c0001t0002g0083a0001c0007t0001g0057a0001c0007t0001g0058others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+20339A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97137479 | ||||||
| chr10:97137480
|
G | A | 120 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.413+20338C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97137480 | ||||||
| chr10:97137540
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+20278G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97137540 | ||||||
| chr10:97137749
|
C | T | 13 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0049others(10): Show | 13 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+20069G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97137749 | ||||||
| chr10:97137783
|
G | T | 10 | a0001c0001t0001g0094a0001c0001t0002g0016a0001c0001t0003g0017others(7): Show | 10 | HG02280.hp2 HG02886.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.413+20035C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97137783 | ||||||
| chr10:97137810
|
T | C | 26 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0094others(23): Show | 26 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.413+20008A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97137810 | ||||||
| chr10:97137928
|
C | G | 7 | a0001c0001t0001g0160a0001c0005t0001g0192a0001c0008t0003g0060others(4): Show | 7 | HG01081.hp1 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+19890G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97137928 | ||||||
| chr10:97138187
|
G | A | 2 | a0001c0008t0003g0060a0001c0019t0008g0059 | 2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.413+19631C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97138187 | ||||||
| chr10:97138218
|
T | C | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.413+19600A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97138218 | ||||||
| chr10:97138380
|
C | T | 1 | a0001c0008t0003g0084 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.413+19438G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97138380 | ||||||
| chr10:97138417
|
G | A | 1 | a0001c0001t0002g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.413+19401C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97138417 | ||||||
| chr10:97138522
|
G | T | 1 | a0001c0001t0001g0106 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.413+19296C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97138522 | ||||||
| chr10:97138648
|
T | TG | 72 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(69): Show | 72 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.413+19169dupC | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97138648 | ||||||
| chr10:97138649
|
G | GT | 13 | a0001c0001t0001g0071a0001c0001t0001g0078a0001c0001t0001g0178others(10): Show | 13 | HG01358.hp1 HG01361.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+19168dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97138649 | ||||||
| chr10:97138649
|
GT | G | 27 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0094others(24): Show | 27 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.413+19168delA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97138649 | ||||||
| chr10:97138656
|
T | C | 1 | a0001c0003t0001g0096 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.413+19162A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97138656 | ||||||
| chr10:97138656
|
T | TC | 131 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(128): Show | 131 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.413+19161_413+1916 others(5): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97138656 | ||||||
| chr10:97138725
|
G | A | 237 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(234): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.413+19093C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97138725 | ||||||
| chr10:97139130
|
C | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+18688G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97139130 | ||||||
| chr10:97139301
|
T | G | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.413+18517A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97139301 | ||||||
| chr10:97139357
|
C | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(110): Show | 113 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.413+18461G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97139357 | ||||||
| chr10:97139366
|
A | G | 9 | a0001c0001t0001g0124a0001c0001t0002g0083a0001c0007t0001g0057others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+18452T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97139366 | ||||||
| chr10:97139398
|
C | T | 239 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.413+18420G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97139398 | ||||||
| chr10:97139409
|
T | G | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.413+18409A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97139409 | ||||||
| chr10:97139543
|
C | A | 124 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(121): Show | 124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.413+18275G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97139543 | ||||||
| chr10:97139549
|
C | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.413+18269G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97139549 | ||||||
| chr10:97139740
|
G | A | 3 | a0001c0001t0001g0214a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02109.hp2 HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.413+18078C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97139740 | ||||||
| chr10:97139800
|
A | G | 255 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(252): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.413+18018T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97139800 | ||||||
| chr10:97139886
|
T | C | 238 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(235): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.413+17932A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97139886 | ||||||
| chr10:97139908
|
G | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0235 | 2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.413+17910C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97139908 | ||||||
| chr10:97140035
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0194 | 2 | NA18954.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.413+17783G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97140035 | ||||||
| chr10:97140045
|
T | C | 255 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(252): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.413+17773A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97140045 | ||||||
| chr10:97140410
|
G | A | 165 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(162): Show | 165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.413+17408C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97140410 | ||||||
| chr10:97140444
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.413+17374T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97140444 | ||||||
| chr10:97140666
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.413+17152G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97140666 | ||||||
| chr10:97140846
|
G | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0110 | 2 | HG00673.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.413+16972C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97140846 | ||||||
| chr10:97141023
|
G | A | 1 | a0001c0005t0001g0005 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.413+16795C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141023 | ||||||
| chr10:97141032
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0105 | 2 | HG02027.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.413+16786C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141032 | ||||||
| chr10:97141060
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+16758G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141060 | ||||||
| chr10:97141121
|
C | G | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+16697G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141121 | ||||||
| chr10:97141125
|
G | A | 188 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(185): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.413+16693C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141125 | ||||||
| chr10:97141155
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.413+16663G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141155 | ||||||
| chr10:97141365
|
A | G | 6 | a0001c0001t0001g0160a0001c0001t0001g0215a0001c0005t0001g0192others(3): Show | 6 | HG01081.hp1 HG02615.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+16453T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141365 | ||||||
| chr10:97141402
|
T | G | 39 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0071others(36): Show | 39 | HG00639.hp2 HG01358.hp1 HG01361.hp2 others(36): Show |
intron_variant | MODIFIER | c.413+16416A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141402 | ||||||
| chr10:97141583
|
A | G | 9 | a0001c0001t0002g0083a0001c0007t0001g0057a0001c0007t0001g0058others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+16235T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141583 | ||||||
| chr10:97141653
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0178a0001c0001t0001g0247others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+16165A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141653 | ||||||
| chr10:97141658
|
T | C | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.413+16160A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141658 | ||||||
| chr10:97141668
|
C | CATTGTAT others(3): Show |
1 | a0001c0001t0001g0241 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.413+16149_413+1615 others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141668 | ||||||
| chr10:97141668
|
C | T | 2 | a0001c0001t0029g0206a0001c0015t0001g0177 | 2 | NA18906.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.413+16150G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141668 | ||||||
| chr10:97141671
|
TGTATC | T | 8 | a0001c0001t0001g0050a0001c0001t0001g0132a0001c0002t0001g0037others(5): Show | 8 | HG02602.hp1 HG02738.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+16142_413+1614 others(9): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141671 | ||||||
| chr10:97141675
|
T | TTGTATTG others(48): Show |
1 | a0001c0004t0001g0044 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.413+16142_413+1614 others(59): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141675 | ||||||
| chr10:97141675
|
TCGTATTG others(48): Show |
T | 12 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0001t0001g0115others(9): Show | 12 | HG01884.hp2 HG02257.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.413+16088_413+1614 others(59): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141675 | ||||||
| chr10:97141676
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(221): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.413+16142G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141676 | ||||||
| chr10:97141676
|
CGTATTGT others(48): Show |
C | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.413+16087_413+1614 others(59): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141676 | ||||||
| chr10:97141677
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.413+16141C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141677 | ||||||
| chr10:97141681
|
T | C | 53 | a0001c0001t0001g0004a0001c0001t0001g0071a0001c0001t0001g0078others(50): Show | 53 | HG00408.hp2 HG01123.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.413+16137A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141681 | ||||||
| chr10:97141681
|
T | TGTATC | 76 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(73): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.413+16132_413+1613 others(9): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141681 | ||||||
| chr10:97141681
|
T | TGTATCGT others(113): Show |
1 | a0001c0001t0001g0100 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.413+16136_413+1613 others(124): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141681 | ||||||
| chr10:97141682
|
G | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0106others(22): Show | 25 | HG01243.hp1 HG02027.hp1 HG02155.hp1 others(22): Show |
intron_variant | MODIFIER | c.413+16136C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141682 | ||||||
| chr10:97141691
|
CGTATCGT others(38): Show |
C | 7 | a0001c0001t0001g0178a0001c0001t0001g0247a0001c0001t0002g0224others(4): Show | 7 | HG02258.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+16082_413+1612 others(49): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141691 | ||||||
| chr10:97141696
|
CGTATCGT others(33): Show |
C | 2 | a0001c0001t0001g0007a0006c0027t0025g0220 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.413+16082_413+1612 others(44): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141696 | ||||||
| chr10:97141701
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.413+16117G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141701 | ||||||
| chr10:97141701
|
CGTATTGT others(28): Show |
C | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.413+16082_413+1611 others(39): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141701 | ||||||
| chr10:97141702
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.413+16116C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141702 | ||||||
| chr10:97141705
|
TTGTATTG others(3): Show |
T | 38 | a0001c0001t0001g0004a0001c0001t0001g0071a0001c0001t0001g0078others(35): Show | 38 | HG00408.hp2 HG01243.hp1 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.413+16103_413+1611 others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141705 | ||||||
| chr10:97141705
|
TTGTATTG others(63): Show |
T | 6 | a0001c0001t0002g0016a0001c0001t0003g0017a0001c0001t0004g0018others(3): Show | 6 | HG02280.hp2 HG02886.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+16043_413+1611 others(74): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141705 | ||||||
| chr10:97141706
|
T | C | 24 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0050others(21): Show | 24 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.413+16112A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141706 | ||||||
| chr10:97141710
|
TTGTAC | T | 15 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(12): Show | 15 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+16103_413+1610 others(9): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141710 | ||||||
| chr10:97141711
|
T | C | 8 | a0001c0001t0001g0050a0001c0001t0001g0132a0001c0002t0001g0037others(5): Show | 8 | HG02602.hp1 HG02738.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+16107A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141711 | ||||||
| chr10:97141711
|
TGTACTGT others(53): Show |
T | 5 | a0001c0001t0002g0113a0001c0001t0002g0144a0001c0001t0002g0145others(2): Show | 5 | HG02258.hp2 HG02280.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+16047_413+1610 others(64): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141711 | ||||||
| chr10:97141712
|
G | A | 8 | a0001c0001t0001g0050a0001c0001t0001g0132a0001c0002t0001g0037others(5): Show | 8 | HG02602.hp1 HG02738.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+16106C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141712 | ||||||
| chr10:97141715
|
C | T | 8 | a0001c0001t0001g0050a0001c0001t0001g0132a0001c0002t0001g0037others(5): Show | 8 | HG02602.hp1 HG02738.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+16103G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141715 | ||||||
| chr10:97141716
|
T | C | 61 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(58): Show | 61 | HG00408.hp2 HG00639.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.413+16102A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141716 | ||||||
| chr10:97141726
|
TGTACTGT others(38): Show |
T | 61 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(58): Show | 61 | HG00408.hp2 HG00639.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.413+16047_413+1609 others(49): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141726 | ||||||
| chr10:97141729
|
A | G | 1 | a0001c0003t0006g0036 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.413+16089T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141729 | ||||||
| chr10:97141736
|
T | C | 6 | a0001c0001t0001g0041a0001c0001t0001g0054a0001c0008t0003g0060others(3): Show | 6 | HG01884.hp2 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+16082A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141736 | ||||||
| chr10:97141736
|
TGTATC | T | 4 | a0001c0001t0003g0098a0001c0002t0001g0025a0001c0002t0001g0149others(1): Show | 4 | NA18939.hp2 NA18984.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+16077_413+1608 others(9): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141736 | ||||||
| chr10:97141737
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0054 | 2 | HG01884.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.413+16081C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141737 | ||||||
| chr10:97141746
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.413+16072G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141746 | ||||||
| chr10:97141756
|
C | T | 1 | a0002c0014t0001g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.413+16062G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141756 | ||||||
| chr10:97141771
|
C | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0115a0001c0001t0001g0178others(9): Show | 12 | HG02258.hp1 HG02523.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.413+16047G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141771 | ||||||
| chr10:97141776
|
T | C | 6 | a0001c0001t0002g0016a0001c0001t0003g0017a0001c0001t0004g0018others(3): Show | 6 | HG02280.hp2 HG02886.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+16042A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141776 | ||||||
| chr10:97141818
|
G | A | 17 | a0001c0001t0001g0071a0001c0001t0001g0078a0001c0001t0001g0111others(14): Show | 17 | HG00408.hp2 HG01515.hp1 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.413+16000C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141818 | ||||||
| chr10:97141915
|
T | C | 43 | a0001c0001t0001g0041a0001c0001t0001g0072a0001c0001t0001g0100others(40): Show | 43 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.413+15903A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141915 | ||||||
| chr10:97141964
|
G | T | 34 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0026others(31): Show | 34 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.413+15854C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97141964 | ||||||
| chr10:97142185
|
T | TA | 104 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0026others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.413+15632dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97142185 | ||||||
| chr10:97142279
|
C | A | 1 | a0001c0001t0002g0008 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.413+15539G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97142279 | ||||||
| chr10:97142540
|
G | T | 88 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0041others(85): Show | 88 | HG00280.hp1 HG00621.hp2 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.413+15278C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97142540 | ||||||
| chr10:97142776
|
A | G | 2 | a0001c0001t0001g0124a0001c0004t0003g0176 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.413+15042T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97142776 | ||||||
| chr10:97142892
|
G | A | 1 | a0001c0001t0011g0150 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.413+14926C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97142892 | ||||||
| chr10:97143146
|
A | G | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.413+14672T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97143146 | ||||||
| chr10:97143260
|
A | G | 100 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(97): Show | 100 | HG00544.hp1 HG00621.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.413+14558T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97143260 | ||||||
| chr10:97143637
|
T | C | 88 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0023others(85): Show | 88 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.413+14181A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97143637 | ||||||
| chr10:97143638
|
T | C | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.413+14180A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97143638 | ||||||
| chr10:97143700
|
G | A | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.413+14118C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97143700 | ||||||
| chr10:97143717
|
A | G | 1 | a0002c0014t0001g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.413+14101T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97143717 | ||||||
| chr10:97143719
|
A | T | 1 | a0001c0001t0002g0129 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.413+14099T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97143719 | ||||||
| chr10:97143764
|
T | C | 252 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(249): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.413+14054A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97143764 | ||||||
| chr10:97143852
|
T | C | 90 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0023others(87): Show | 90 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.413+13966A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97143852 | ||||||
| chr10:97144015
|
T | G | 90 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0023others(87): Show | 90 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.413+13803A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97144015 | ||||||
| chr10:97144058
|
C | T | 33 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(30): Show | 33 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.413+13760G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97144058 | ||||||
| chr10:97144067
|
G | A | 3 | a0001c0001t0001g0205a0001c0004t0001g0147a0001c0004t0001g0210 | 3 | HG00408.hp1 NA18960.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.413+13751C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97144067 | ||||||
| chr10:97144123
|
G | A | 5 | a0001c0001t0002g0189a0001c0003t0001g0171a0001c0003t0001g0172others(2): Show | 5 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+13695C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97144123 | ||||||
| chr10:97144142
|
G | A | 31 | a0001c0001t0001g0143a0001c0001t0001g0154a0001c0001t0001g0182others(28): Show | 31 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+13676C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97144142 | ||||||
| chr10:97144197
|
CA | C | 209 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0026others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.413+13620delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97144197 | ||||||
| chr10:97144308
|
G | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+13510C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97144308 | ||||||
| chr10:97144380
|
T | C | 21 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(18): Show | 21 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.413+13438A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97144380 | ||||||
| chr10:97144484
|
A | T | 1 | a0001c0002t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.413+13334T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97144484 | ||||||
| chr10:97144532
|
G | A | 1 | a0001c0003t0002g0125 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.413+13286C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97144532 | ||||||
| chr10:97144720
|
C | G | 3 | a0001c0001t0002g0113a0001c0001t0002g0144a0001c0001t0002g0145 | 3 | NA18942.hp1 NA18990.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.413+13098G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97144720 | ||||||
| chr10:97144862
|
C | T | 19 | a0001c0001t0001g0050a0001c0001t0001g0162a0001c0001t0001g0194others(16): Show | 19 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.413+12956G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97144862 | ||||||
| chr10:97144976
|
T | C | 1 | a0001c0004t0001g0044 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.413+12842A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97144976 | ||||||
| chr10:97145005
|
A | G | 35 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(32): Show | 35 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.413+12813T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145005 | ||||||
| chr10:97145021
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.413+12797G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145021 | ||||||
| chr10:97145211
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.413+12607C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145211 | ||||||
| chr10:97145251
|
A | G | 240 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(237): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.413+12567T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145251 | ||||||
| chr10:97145270
|
A | G | 153 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(150): Show | 153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.413+12548T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145270 | ||||||
| chr10:97145329
|
G | A | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.413+12489C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145329 | ||||||
| chr10:97145352
|
G | A | 1 | a0001c0004t0003g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.413+12466C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145352 | ||||||
| chr10:97145417
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.413+12401T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145417 | ||||||
| chr10:97145466
|
G | A | 119 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(116): Show | 119 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.413+12352C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145466 | ||||||
| chr10:97145518
|
T | C | 2 | a0001c0005t0009g0091a0001c0026t0004g0090 | 2 | HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.413+12300A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145518 | ||||||
| chr10:97145551
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.413+12267C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145551 | ||||||
| chr10:97145641
|
C | G | 2 | a0001c0001t0013g0002a0006c0027t0025g0220 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.413+12177G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145641 | ||||||
| chr10:97145641
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.413+12177G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145641 | ||||||
| chr10:97145797
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.413+12021T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145797 | ||||||
| chr10:97145799
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+12019C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145799 | ||||||
| chr10:97145811
|
C | T | 2 | a0001c0011t0001g0157a0001c0011t0001g0187 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.413+12007G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145811 | ||||||
| chr10:97145837
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.413+11981G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97145837 | ||||||
| chr10:97146231
|
T | C | 192 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(189): Show | 192 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.413+11587A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146231 | ||||||
| chr10:97146281
|
C | T | 2 | a0001c0001t0001g0124a0001c0004t0003g0176 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.413+11537G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146281 | ||||||
| chr10:97146334
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.413+11484T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146334 | ||||||
| chr10:97146351
|
A | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0121others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+11467T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146351 | ||||||
| chr10:97146491
|
T | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0006t0007g0088 | 3 | HG02895.hp1 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.413+11327A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146491 | ||||||
| chr10:97146559
|
G | GCC | 14 | a0001c0001t0001g0185a0001c0001t0001g0198a0001c0001t0001g0214others(11): Show | 14 | HG00621.hp1 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.413+11257_413+1125 others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146559 | ||||||
| chr10:97146559
|
G | GCCC | 15 | a0001c0001t0001g0154a0001c0001t0001g0182a0001c0001t0001g0186others(12): Show | 15 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+11256_413+1125 others(7): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146559 | ||||||
| chr10:97146565
|
C | A | 19 | a0001c0001t0001g0050a0001c0001t0001g0162a0001c0001t0001g0194others(16): Show | 19 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.413+11253G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146565 | ||||||
| chr10:97146565
|
C | G | 33 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(30): Show | 33 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.413+11253G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146565 | ||||||
| chr10:97146565
|
C | T | 2 | a0001c0001t0001g0124a0001c0004t0003g0176 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.413+11253G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146565 | ||||||
| chr10:97146566
|
C | G | 1 | a0001c0004t0001g0173 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.413+11252G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146566 | ||||||
| chr10:97146568
|
A | C | 31 | a0001c0001t0001g0143a0001c0001t0001g0154a0001c0001t0001g0182others(28): Show | 31 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+11250T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146568 | ||||||
| chr10:97146784
|
G | A | 33 | a0001c0001t0001g0143a0001c0001t0001g0154a0001c0001t0001g0178others(30): Show | 33 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.413+11034C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146784 | ||||||
| chr10:97146895
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.413+10923G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146895 | ||||||
| chr10:97146904
|
ATCTGGTG others(17): Show |
A | 32 | a0001c0001t0001g0143a0001c0001t0001g0154a0001c0001t0001g0182others(29): Show | 32 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.413+10890_413+1091 others(28): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146904 | ||||||
| chr10:97146983
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+10835G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97146983 | ||||||
| chr10:97147129
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+10689G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97147129 | ||||||
| chr10:97147259
|
G | A | 1 | a0001c0003t0001g0237 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.413+10559C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97147259 | ||||||
| chr10:97147288
|
T | C | 123 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(120): Show | 123 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.413+10530A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97147288 | ||||||
| chr10:97147319
|
T | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+10499A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97147319 | ||||||
| chr10:97147437
|
A | G | 2 | a0001c0011t0001g0157a0001c0011t0001g0187 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.413+10381T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97147437 | ||||||
| chr10:97147468
|
A | G | 33 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(30): Show | 33 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.413+10350T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97147468 | ||||||
| chr10:97147635
|
G | C | 6 | a0001c0003t0002g0219a0001c0003t0015g0087a0001c0008t0003g0060others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+10183C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97147635 | ||||||
| chr10:97147656
|
G | C | 123 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(120): Show | 123 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.413+10162C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97147656 | ||||||
| chr10:97147670
|
G | C | 19 | a0001c0001t0001g0050a0001c0001t0001g0162a0001c0001t0001g0194others(16): Show | 19 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.413+10148C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97147670 | ||||||
| chr10:97147689
|
G | A | 244 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.413+10129C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97147689 | ||||||
| chr10:97147729
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.413+10089A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97147729 | ||||||
| chr10:97147857
|
C | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.413+9961G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97147857 | ||||||
| chr10:97147862
|
T | C | 211 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(208): Show | 211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.413+9956A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97147862 | ||||||
| chr10:97148116
|
A | G | 211 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(208): Show | 211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.413+9702T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148116 | ||||||
| chr10:97148120
|
A | G | 176 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0026others(173): Show | 176 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.413+9698T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148120 | ||||||
| chr10:97148121
|
C | T | 174 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0026others(171): Show | 174 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.413+9697G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148121 | ||||||
| chr10:97148289
|
CT | C | 31 | a0001c0001t0001g0143a0001c0001t0001g0154a0001c0001t0001g0182others(28): Show | 31 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+9528delA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148289 | ||||||
| chr10:97148307
|
G | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0247 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+9511C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148307 | ||||||
| chr10:97148320
|
G | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0026others(173): Show | 176 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.413+9498C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148320 | ||||||
| chr10:97148353
|
G | A | 244 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.413+9465C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148353 | ||||||
| chr10:97148366
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.413+9452T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148366 | ||||||
| chr10:97148445
|
T | C | 211 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(208): Show | 211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.413+9373A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148445 | ||||||
| chr10:97148464
|
A | G | 33 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(30): Show | 33 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.413+9354T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148464 | ||||||
| chr10:97148476
|
G | GACGGGGT others(3): Show |
211 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(208): Show | 211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.413+9341_413+9342i others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148476 | ||||||
| chr10:97148477
|
C | G | 211 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(208): Show | 211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.413+9341G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148477 | ||||||
| chr10:97148500
|
G | A | 211 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(208): Show | 211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.413+9318C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148500 | ||||||
| chr10:97148976
|
C | A | 33 | a0001c0001t0001g0143a0001c0001t0001g0154a0001c0001t0001g0182others(30): Show | 33 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.413+8842G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97148976 | ||||||
| chr10:97149017
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(22): Show | 25 | HG00621.hp2 HG01243.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.413+8801G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97149017 | ||||||
| chr10:97149044
|
A | AC | 9 | a0001c0001t0001g0203a0001c0001t0001g0246a0001c0001t0001g0249others(6): Show | 9 | HG00544.hp2 HG01358.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+8773dupG | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97149044 | ||||||
| chr10:97149071
|
C | T | 235 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(232): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.413+8747G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97149071 | ||||||
| chr10:97149220
|
A | T | 1 | a0001c0001t0001g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.413+8598T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97149220 | ||||||
| chr10:97149283
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.413+8535C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97149283 | ||||||
| chr10:97149322
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.413+8496T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97149322 | ||||||
| chr10:97149532
|
G | T | 1 | a0001c0007t0001g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.413+8286C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97149532 | ||||||
| chr10:97149554
|
C | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(23): Show | 26 | HG00621.hp2 HG01243.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.413+8264G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97149554 | ||||||
| chr10:97149603
|
CACTG | C | 32 | a0001c0001t0001g0143a0001c0001t0001g0154a0001c0001t0001g0182others(29): Show | 32 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.413+8211_413+8214d others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97149603 | ||||||
| chr10:97149703
|
G | A | 27 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(24): Show | 27 | HG00621.hp2 HG01243.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.413+8115C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97149703 | ||||||
| chr10:97149740
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.413+8078C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97149740 | ||||||
| chr10:97149987
|
T | C | 250 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(247): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.413+7831A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97149987 | ||||||
| chr10:97149995
|
G | A | 218 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.413+7823C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97149995 | ||||||
| chr10:97150097
|
C | A | 173 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.413+7721G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97150097 | ||||||
| chr10:97150139
|
G | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(25): Show | 28 | HG00621.hp2 HG01243.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.413+7679C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97150139 | ||||||
| chr10:97150158
|
C | T | 1 | a0001c0003t0026g0170 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.413+7660G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97150158 | ||||||
| chr10:97150198
|
A | T | 27 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(24): Show | 27 | HG00621.hp2 HG01243.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.413+7620T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97150198 | ||||||
| chr10:97150359
|
G | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(25): Show | 28 | HG00621.hp2 HG01243.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.413+7459C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97150359 | ||||||
| chr10:97150458
|
G | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(25): Show | 28 | HG00621.hp2 HG01243.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.413+7360C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97150458 | ||||||
| chr10:97150658
|
C | A | 27 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(24): Show | 27 | HG00621.hp2 HG01243.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.413+7160G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97150658 | ||||||
| chr10:97150669
|
C | T | 27 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(24): Show | 27 | HG00621.hp2 HG01243.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.413+7149G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97150669 | ||||||
| chr10:97150843
|
AAG | A | 29 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(26): Show | 29 | HG00621.hp2 HG01243.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.413+6973_413+6974d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97150843 | ||||||
| chr10:97151003
|
C | G | 2 | a0001c0004t0001g0165a0001c0004t0001g0166 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.413+6815G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151003 | ||||||
| chr10:97151006
|
C | T | 143 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(140): Show | 143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.413+6812G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151006 | ||||||
| chr10:97151007
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(28): Show | 31 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+6811C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151007 | ||||||
| chr10:97151269
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(28): Show | 31 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+6549G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151269 | ||||||
| chr10:97151281
|
T | A | 1 | a0001c0003t0001g0035 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.413+6537A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151281 | ||||||
| chr10:97151313
|
A | G | 13 | a0001c0001t0013g0002a0001c0003t0002g0219a0001c0003t0015g0087others(10): Show | 13 | HG02145.hp2 HG02615.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+6505T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151313 | ||||||
| chr10:97151374
|
G | C | 1 | a0001c0007t0001g0248 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.413+6444C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151374 | ||||||
| chr10:97151383
|
G | A | 1 | a0001c0003t0001g0255 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.413+6435C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151383 | ||||||
| chr10:97151449
|
A | G | 32 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(29): Show | 32 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.413+6369T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151449 | ||||||
| chr10:97151588
|
G | T | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(23): Show | 26 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.413+6230C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151588 | ||||||
| chr10:97151593
|
G | A | 32 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(29): Show | 32 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.413+6225C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151593 | ||||||
| chr10:97151720
|
A | G | 32 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(29): Show | 32 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.413+6098T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151720 | ||||||
| chr10:97151799
|
G | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.413+6019C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151799 | ||||||
| chr10:97151864
|
C | T | 2 | a0001c0003t0001g0171a0001c0003t0001g0172 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.413+5954G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151864 | ||||||
| chr10:97151870
|
A | C | 1 | a0001c0001t0001g0156 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.413+5948T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151870 | ||||||
| chr10:97151911
|
G | T | 3 | a0001c0001t0001g0004a0001c0005t0001g0005a0001c0005t0001g0006 | 3 | HG01243.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.413+5907C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97151911 | ||||||
| chr10:97152179
|
G | C | 40 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0022others(37): Show | 40 | HG00544.hp1 HG00639.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.413+5639C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152179 | ||||||
| chr10:97152255
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.413+5563G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152255 | ||||||
| chr10:97152358
|
A | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(28): Show | 31 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+5460T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152358 | ||||||
| chr10:97152419
|
C | T | 24 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(21): Show | 24 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.413+5399G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152419 | ||||||
| chr10:97152442
|
A | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0178others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+5376T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152442 | ||||||
| chr10:97152458
|
GC | G | 123 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(120): Show | 123 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.413+5359delG | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152458 | ||||||
| chr10:97152518
|
A | G | 31 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(28): Show | 31 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+5300T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152518 | ||||||
| chr10:97152586
|
C | T | 1 | a0001c0003t0001g0184 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.413+5232G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152586 | ||||||
| chr10:97152599
|
C | T | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.413+5219G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152599 | ||||||
| chr10:97152633
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0178others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+5185G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152633 | ||||||
| chr10:97152685
|
C | T | 1 | a0001c0001t0029g0206 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.413+5133G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152685 | ||||||
| chr10:97152686
|
C | T | 4 | a0001c0005t0001g0045a0001c0005t0001g0052a0001c0017t0008g0123others(1): Show | 4 | HG02280.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+5132G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152686 | ||||||
| chr10:97152693
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(28): Show | 31 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+5125C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152693 | ||||||
| chr10:97152695
|
A | G | 31 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(28): Show | 31 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+5123T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97152695 | ||||||
| chr10:97153056
|
C | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(28): Show | 31 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+4762G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97153056 | ||||||
| chr10:97153080
|
G | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(28): Show | 31 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+4738C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97153080 | ||||||
| chr10:97153128
|
C | T | 2 | a0001c0004t0003g0176a0001c0021t0008g0028 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.413+4690G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97153128 | ||||||
| chr10:97153171
|
T | C | 32 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(29): Show | 32 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.413+4647A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97153171 | ||||||
| chr10:97153239
|
A | G | 215 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(212): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.413+4579T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97153239 | ||||||
| chr10:97153335
|
T | G | 2 | a0001c0011t0001g0157a0001c0011t0001g0187 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.413+4483A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97153335 | ||||||
| chr10:97153383
|
C | T | 15 | a0001c0001t0001g0214a0001c0001t0002g0083a0001c0003t0002g0219others(12): Show | 15 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.413+4435G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97153383 | ||||||
| chr10:97153544
|
C | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0016t0001g0159 | 3 | HG01891.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.413+4274G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97153544 | ||||||
| chr10:97153560
|
C | CA | 179 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0026others(176): Show | 179 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.413+4257dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97153560 | ||||||
| chr10:97153579
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.413+4239C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97153579 | ||||||
| chr10:97153716
|
G | A | 4 | a0001c0005t0001g0045a0001c0005t0001g0052a0001c0017t0008g0123others(1): Show | 4 | HG02280.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+4102C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97153716 | ||||||
| chr10:97153871
|
G | T | 179 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0026others(176): Show | 179 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.413+3947C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97153871 | ||||||
| chr10:97154244
|
G | C | 1 | a0001c0001t0029g0206 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.413+3574C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97154244 | ||||||
| chr10:97154388
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.413+3430C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97154388 | ||||||
| chr10:97154481
|
C | CT | 24 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(21): Show | 24 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.413+3336dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97154481 | ||||||
| chr10:97154595
|
C | A | 4 | a0001c0001t0013g0002a0001c0003t0005g0183a0001c0004t0001g0147others(1): Show | 4 | HG00140.hp2 HG02055.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+3223G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97154595 | ||||||
| chr10:97154992
|
G | C | 215 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(212): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.413+2826C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97154992 | ||||||
| chr10:97155115
|
C | T | 16 | a0001c0001t0001g0062a0001c0001t0001g0073a0001c0001t0001g0077others(13): Show | 16 | HG00639.hp1 HG00642.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.413+2703G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97155115 | ||||||
| chr10:97155116
|
A | G | 215 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(212): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.413+2702T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97155116 | ||||||
| chr10:97155291
|
T | G | 2 | a0001c0004t0003g0176a0001c0021t0008g0028 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.413+2527A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97155291 | ||||||
| chr10:97155355
|
T | C | 37 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0131others(34): Show | 37 | HG00621.hp2 HG01109.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.413+2463A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97155355 | ||||||
| chr10:97155392
|
T | C | 3 | a0001c0001t0001g0205a0001c0004t0001g0147a0001c0004t0001g0210 | 3 | HG00408.hp1 NA18960.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.413+2426A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97155392 | ||||||
| chr10:97155415
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.413+2403C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97155415 | ||||||
| chr10:97155603
|
G | A | 4 | a0001c0005t0001g0045a0001c0005t0001g0052a0001c0017t0008g0123others(1): Show | 4 | HG02280.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+2215C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97155603 | ||||||
| chr10:97155632
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.413+2186G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97155632 | ||||||
| chr10:97156117
|
A | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0194 | 2 | NA18954.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.413+1701T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97156117 | ||||||
| chr10:97156316
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0002g0134others(1): Show | 4 | NA18943.hp2 NA18998.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+1502C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97156316 | ||||||
| chr10:97156320
|
G | A | 1 | a0001c0002t0001g0243 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.413+1498C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97156320 | ||||||
| chr10:97156595
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.413+1223C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97156595 | ||||||
| chr10:97156827
|
C | G | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.413+991G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97156827 | ||||||
| chr10:97156846
|
T | TA | 178 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0026others(175): Show | 178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.413+971dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97156846 | ||||||
| chr10:97156937
|
G | T | 21 | a0001c0001t0001g0092a0001c0001t0001g0103a0001c0001t0001g0104others(18): Show | 21 | HG00408.hp2 HG00673.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.413+881C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97156937 | ||||||
| chr10:97156976
|
A | T | 4 | a0001c0005t0001g0045a0001c0005t0001g0052a0001c0017t0008g0123others(1): Show | 4 | HG02280.hp1 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+842T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97156976 | ||||||
| chr10:97157025
|
G | A | 215 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(212): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.413+793C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97157025 | ||||||
| chr10:97157331
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.413+487T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97157331 | ||||||
| chr10:97157349
|
C | A | 5 | a0001c0001t0002g0128a0001c0001t0002g0148a0001c0001t0019g0155others(2): Show | 5 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+469G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97157349 | ||||||
| chr10:97157369
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.413+449G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97157369 | ||||||
| chr10:97157601
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.413+217G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97157601 | ||||||
| chr10:97157698
|
G | A | 4 | a0001c0001t0002g0251a0001c0002t0001g0256a0001c0010t0002g0107others(1): Show | 4 | HG02602.hp1 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+120C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 4/36 | chr10 | 97157698 | ||||||
| chr10:97158009
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.342-120G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158009 | ||||||
| chr10:97158086
|
C | T | 24 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(21): Show | 24 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.342-197G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158086 | ||||||
| chr10:97158144
|
A | G | 37 | a0001c0001t0001g0054a0001c0001t0001g0121a0001c0001t0001g0122others(34): Show | 37 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.342-255T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158144 | ||||||
| chr10:97158174
|
C | T | 24 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(21): Show | 24 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.342-285G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158174 | ||||||
| chr10:97158228
|
T | C | 70 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(67): Show | 70 | HG00544.hp1 HG00621.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.342-339A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158228 | ||||||
| chr10:97158331
|
C | CT | 22 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0049others(19): Show | 22 | HG00280.hp1 HG01167.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.342-443dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158331 | ||||||
| chr10:97158369
|
A | G | 139 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0033others(136): Show | 139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.342-480T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158369 | ||||||
| chr10:97158385
|
G | C | 94 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0034others(91): Show | 94 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.342-496C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158385 | ||||||
| chr10:97158487
|
C | T | 24 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(21): Show | 24 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.342-598G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158487 | ||||||
| chr10:97158577
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.342-688C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158577 | ||||||
| chr10:97158629
|
T | C | 24 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(21): Show | 24 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.342-740A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158629 | ||||||
| chr10:97158661
|
C | CA | 171 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0026others(168): Show | 171 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.342-773dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158661 | ||||||
| chr10:97158661
|
C | CAA | 20 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0133others(17): Show | 20 | HG00639.hp2 HG01884.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.342-774_342-773dup others(2): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158661 | ||||||
| chr10:97158661
|
C | CAAA | 22 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0051others(19): Show | 22 | HG00544.hp1 HG00673.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.342-775_342-773dup others(3): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158661 | ||||||
| chr10:97158879
|
G | GA | 4 | a0001c0001t0001g0174a0001c0004t0003g0176a0001c0012t0001g0053others(1): Show | 4 | HG02258.hp2 HG02559.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.342-991dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158879 | ||||||
| chr10:97158882
|
G | A | 215 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(212): Show | 215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.342-993C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97158882 | ||||||
| chr10:97159009
|
C | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0178others(5): Show | 8 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.342-1120G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97159009 | ||||||
| chr10:97159018
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0115others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.342-1129A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97159018 | ||||||
| chr10:97159310
|
C | T | 2 | a0001c0011t0001g0157a0001c0011t0001g0187 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.342-1421G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97159310 | ||||||
| chr10:97159378
|
G | T | 2 | a0001c0001t0001g0242a0001c0009t0005g0238 | 2 | HG01515.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.342-1489C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97159378 | ||||||
| chr10:97159402
|
TC | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0048others(21): Show | 24 | HG00280.hp1 HG01167.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.342-1514delG | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97159402 | ||||||
| chr10:97159717
|
G | A | 3 | a0001c0002t0001g0101a0001c0002t0001g0108a0001c0002t0001g0231 | 3 | NA18961.hp1 NA19066.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.342-1828C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97159717 | ||||||
| chr10:97159878
|
C | T | 3 | a0001c0001t0004g0019a0001c0001t0017g0015a0003c0029t0002g0014 | 3 | HG02109.hp1 HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.342-1989G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97159878 | ||||||
| chr10:97160141
|
G | A | 1 | a0001c0003t0005g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.342-2252C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97160141 | ||||||
| chr10:97160463
|
G | A | 1 | a0001c0002t0001g0067 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.342-2574C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97160463 | ||||||
| chr10:97160474
|
C | T | 2 | a0001c0004t0003g0176a0001c0021t0008g0028 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.342-2585G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97160474 | ||||||
| chr10:97160636
|
G | A | 19 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0080others(16): Show | 19 | HG01123.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.341+2744C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97160636 | ||||||
| chr10:97160867
|
C | T | 2 | a0001c0001t0001g0124a0001c0008t0003g0084 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.341+2513G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97160867 | ||||||
| chr10:97160868
|
G | A | 95 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0043others(92): Show | 95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.341+2512C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97160868 | ||||||
| chr10:97161083
|
G | A | 30 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0080others(27): Show | 30 | HG00738.hp2 HG01123.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.341+2297C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97161083 | ||||||
| chr10:97161307
|
A | C | 172 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.341+2073T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97161307 | ||||||
| chr10:97161639
|
G | C | 1 | a0005c0025t0002g0163 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.341+1741C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97161639 | ||||||
| chr10:97161651
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0178others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.341+1729C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97161651 | ||||||
| chr10:97161685
|
G | A | 1 | a0001c0001t0020g0109 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.341+1695C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97161685 | ||||||
| chr10:97161693
|
G | A | 1 | a0001c0002t0002g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.341+1687C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97161693 | ||||||
| chr10:97161710
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0246a0001c0003t0026g0170 | 3 | HG02895.hp2 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.341+1670C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97161710 | ||||||
| chr10:97161720
|
G | A | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.341+1660C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97161720 | ||||||
| chr10:97161823
|
A | G | 1 | a0001c0004t0001g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.341+1557T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97161823 | ||||||
| chr10:97161957
|
T | C | 5 | a0001c0001t0001g0162a0001c0001t0002g0189a0001c0003t0001g0171others(2): Show | 5 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+1423A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97161957 | ||||||
| chr10:97162034
|
G | C | 1 | a0001c0001t0002g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.341+1346C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97162034 | ||||||
| chr10:97162100
|
A | G | 38 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0049others(35): Show | 38 | HG00280.hp1 HG01167.hp1 HG01258.hp1 others(35): Show |
intron_variant | MODIFIER | c.341+1280T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97162100 | ||||||
| chr10:97162203
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.341+1177G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97162203 | ||||||
| chr10:97162209
|
A | T | 2 | a0001c0008t0003g0085a0001c0018t0009g0217 | 2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.341+1171T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97162209 | ||||||
| chr10:97162217
|
T | C | 2 | a0001c0004t0003g0176a0001c0021t0008g0028 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.341+1163A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97162217 | ||||||
| chr10:97162337
|
C | T | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.341+1043G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97162337 | ||||||
| chr10:97162650
|
A | C | 1 | a0001c0001t0001g0194 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.341+730T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97162650 | ||||||
| chr10:97162776
|
C | T | 54 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0023others(51): Show | 54 | HG00621.hp2 HG01109.hp2 HG01123.hp1 others(51): Show |
intron_variant | MODIFIER | c.341+604G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97162776 | ||||||
| chr10:97162820
|
A | C | 124 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(121): Show | 124 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.341+560T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97162820 | ||||||
| chr10:97163002
|
A | G | 210 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(207): Show | 210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.341+378T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97163002 | ||||||
| chr10:97163297
|
T | C | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.341+83A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 3/36 | chr10 | 97163297 | ||||||
| chr10:97163604
|
T | C | 253 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.270-153A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97163604 | ||||||
| chr10:97163697
|
T | G | 4 | a0001c0001t0002g0189a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.270-246A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97163697 | ||||||
| chr10:97163774
|
G | A | 95 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(92): Show | 95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.270-323C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97163774 | ||||||
| chr10:97163780
|
A | G | 1 | a0001c0001t0002g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.270-329T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97163780 | ||||||
| chr10:97163893
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.270-442C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97163893 | ||||||
| chr10:97163893
|
G | C | 1 | a0001c0004t0003g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270-442C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97163893 | ||||||
| chr10:97163964
|
A | T | 1 | a0001c0002t0001g0070 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.270-513T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97163964 | ||||||
| chr10:97164008
|
C | T | 2 | a0001c0001t0002g0189a0001c0003t0006g0190 | 2 | HG00738.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.270-557G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97164008 | ||||||
| chr10:97164085
|
A | G | 5 | a0001c0001t0001g0054a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.270-634T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97164085 | ||||||
| chr10:97164124
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0002g0224 | 3 | HG02896.hp2 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.270-673G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97164124 | ||||||
| chr10:97164167
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.269+652C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97164167 | ||||||
| chr10:97164283
|
AG | A | 213 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(210): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.269+535delC | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97164283 | ||||||
| chr10:97164289
|
G | A | 1 | a0001c0003t0002g0125 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.269+530C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97164289 | ||||||
| chr10:97164335
|
G | A | 4 | a0001c0001t0002g0189a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.269+484C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97164335 | ||||||
| chr10:97164464
|
T | A | 5 | a0001c0001t0001g0054a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.269+355A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97164464 | ||||||
| chr10:97164464
|
T | G | 33 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0041others(30): Show | 33 | HG00280.hp1 HG00639.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.269+355A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97164464 | ||||||
| chr10:97164465
|
T | G | 5 | a0001c0001t0001g0054a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.269+354A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97164465 | ||||||
| chr10:97164672
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.269+147G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 2/36 | chr10 | 97164672 | ||||||
| chr10:97164900
|
G | A | 5 | a0001c0001t0001g0051a0001c0001t0001g0135a0001c0001t0001g0138others(2): Show | 5 | HG00544.hp1 HG00673.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.198-10C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97164900 | ||||||
| chr10:97164908
|
G | A | 5 | a0001c0007t0001g0248a0002c0013t0006g0029a0002c0013t0006g0030others(2): Show | 5 | HG01261.hp1 HG01361.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-18C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97164908 | ||||||
| chr10:97164991
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0178others(4): Show | 7 | HG00639.hp2 HG01884.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-101C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97164991 | ||||||
| chr10:97165061
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0006g0038others(2): Show | 5 | HG00280.hp1 HG01167.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-171G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97165061 | ||||||
| chr10:97165203
|
G | A | 1 | a0001c0002t0001g0151 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.198-313C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97165203 | ||||||
| chr10:97165275
|
C | T | 5 | a0001c0007t0001g0248a0002c0013t0006g0029a0002c0013t0006g0030others(2): Show | 5 | HG01261.hp1 HG01361.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-385G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97165275 | ||||||
| chr10:97165279
|
C | A | 1 | a0001c0001t0002g0083 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.198-389G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97165279 | ||||||
| chr10:97165568
|
A | T | 1 | a0001c0002t0002g0040 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.198-678T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97165568 | ||||||
| chr10:97165866
|
C | T | 38 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0048others(35): Show | 38 | HG00280.hp1 HG01071.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.198-976G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97165866 | ||||||
| chr10:97166092
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.198-1202G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166092 | ||||||
| chr10:97166148
|
C | T | 1 | a0001c0002t0002g0199 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.198-1258G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166148 | ||||||
| chr10:97166149
|
G | A | 1 | a0001c0003t0001g0255 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.198-1259C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166149 | ||||||
| chr10:97166230
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0246 | 2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.198-1340A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166230 | ||||||
| chr10:97166232
|
C | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0246a0001c0005t0001g0045others(3): Show | 6 | HG02280.hp1 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-1342G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166232 | ||||||
| chr10:97166388
|
C | T | 36 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0068others(33): Show | 36 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.198-1498G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166388 | ||||||
| chr10:97166481
|
A | C | 109 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0072others(106): Show | 109 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.198-1591T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166481 | ||||||
| chr10:97166517
|
C | CA | 127 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(124): Show | 127 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.198-1628dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166517 | ||||||
| chr10:97166523
|
A | AAAAAG | 8 | a0001c0003t0002g0219a0001c0003t0015g0087a0001c0007t0001g0058others(5): Show | 8 | HG02615.hp2 HG02723.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.198-1634_198-1633i others(7): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166523 | ||||||
| chr10:97166530
|
A | AGAAGGAA others(1): Show |
7 | a0001c0001t0001g0051a0001c0001t0001g0135a0001c0001t0001g0143others(4): Show | 7 | HG00597.hp1 HG00621.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.198-1648_198-1641d others(10): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166530 | ||||||
| chr10:97166530
|
A | AGAAGGAA others(9): Show |
3 | a0001c0001t0010g0137a0001c0007t0001g0248a0002c0014t0001g0202 | 3 | HG01261.hp1 HG02055.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.198-1656_198-1641d others(18): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166530 | ||||||
| chr10:97166530
|
A | G | 10 | a0001c0001t0004g0200a0001c0003t0002g0219a0001c0003t0015g0087others(7): Show | 10 | HG02559.hp2 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.198-1640T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166530 | ||||||
| chr10:97166534
|
G | A | 2 | a0001c0002t0012g0001a0001c0003t0001g0126 | 2 | HG01257.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.198-1644C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166534 | ||||||
| chr10:97166540
|
A | AAGG | 89 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0072others(86): Show | 89 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.198-1653_198-1651d others(5): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166540 | ||||||
| chr10:97166550
|
G | A | 5 | a0001c0001t0002g0189a0001c0001t0004g0200a0001c0003t0001g0171others(2): Show | 5 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-1660C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166550 | ||||||
| chr10:97166553
|
A | G | 5 | a0001c0001t0002g0189a0001c0001t0004g0200a0001c0003t0001g0171others(2): Show | 5 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-1663T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166553 | ||||||
| chr10:97166553
|
AGG | A | 5 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0094others(2): Show | 5 | HG01258.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.198-1665_198-1664d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166553 | ||||||
| chr10:97166554
|
G | A | 29 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0049others(26): Show | 29 | HG00280.hp1 HG00738.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.198-1664C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166554 | ||||||
| chr10:97166554
|
GGAAAGAG others(13): Show |
G | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.198-1684_198-1665d others(22): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166554 | ||||||
| chr10:97166557
|
A | AAG | 12 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0116others(9): Show | 12 | HG00735.hp1 HG01243.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.198-1669_198-1668d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AAGAGAG | 9 | a0001c0001t0001g0077a0001c0001t0001g0132a0001c0002t0001g0025others(6): Show | 9 | HG00558.hp1 HG00642.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-1673_198-1668d others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AAGAGAGA others(3): Show |
22 | a0001c0001t0001g0033a0001c0001t0001g0072a0001c0001t0001g0073others(19): Show | 22 | HG00408.hp2 HG00639.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.198-1677_198-1668d others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AAGAGAGA others(5): Show |
1 | a0001c0001t0001g0249 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.198-1679_198-1668d others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AAGAGAGA others(7): Show |
1 | a0001c0009t0005g0238 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.198-1681_198-1668d others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAAGA others(7): Show |
4 | a0001c0007t0001g0057a0001c0007t0001g0218a0001c0008t0003g0084others(1): Show | 4 | HG02145.hp2 HG02886.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-1668_198-1667i others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(3): Show |
4 | a0001c0001t0001g0004a0001c0001t0001g0225a0001c0004t0003g0176others(1): Show | 4 | HG02258.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-1668_198-1667i others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(7): Show |
4 | a0001c0001t0001g0062a0001c0001t0002g0016a0001c0001t0003g0017others(1): Show | 4 | HG01433.hp1 HG02886.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-1668_198-1667i others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(9): Show |
5 | a0001c0001t0001g0162a0001c0001t0017g0015a0001c0001t0018g0168others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-1668_198-1667i others(18): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(11): Show |
6 | a0001c0001t0001g0023a0001c0001t0001g0110a0001c0001t0001g0247others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-1668_198-1667i others(20): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(13): Show |
1 | a0001c0001t0001g0022 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.198-1668_198-1667i others(22): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(15): Show |
4 | a0001c0001t0001g0160a0001c0001t0001g0233a0001c0001t0011g0150others(1): Show | 4 | HG02280.hp2 HG03209.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-1668_198-1667i others(24): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(17): Show |
3 | a0001c0001t0001g0026a0001c0001t0002g0008a0001c0004t0001g0024 | 3 | NA18943.hp2 NA18960.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.198-1668_198-1667i others(26): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(19): Show |
3 | a0001c0001t0001g0234a0001c0001t0001g0245a0001c0002t0001g0243 | 3 | HG03654.hp1 NA18993.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.198-1668_198-1667i others(28): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(21): Show |
1 | a0001c0001t0001g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.198-1668_198-1667i others(30): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(7): Show |
2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.198-1668_198-1667i others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(9): Show |
4 | a0001c0001t0001g0054a0001c0001t0002g0134a0001c0002t0002g0139others(1): Show | 4 | HG00544.hp1 HG01884.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-1668_198-1667i others(18): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(13): Show |
1 | a0001c0001t0001g0138 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.198-1668_198-1667i others(22): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(17): Show |
2 | a0001c0001t0001g0158a0001c0026t0004g0090 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.198-1668_198-1667i others(26): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(21): Show |
2 | a0001c0004t0001g0228a0001c0005t0009g0091 | 2 | HG03041.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.198-1668_198-1667i others(30): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(11): Show |
3 | a0001c0006t0004g0204a0002c0013t0006g0029a0002c0013t0006g0030 | 3 | HG01515.hp1 HG01517.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.198-1668_198-1667i others(20): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(13): Show |
1 | a0002c0014t0001g0227 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.198-1668_198-1667i others(22): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | AGGAAGGA others(17): Show |
1 | a0001c0001t0001g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.198-1668_198-1667i others(26): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166557
|
A | G | 34 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0048others(31): Show | 34 | HG00280.hp1 HG00738.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.198-1667T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166557 | ||||||
| chr10:97166558
|
A | G | 18 | a0001c0001t0001g0051a0001c0001t0001g0103a0001c0001t0001g0133others(15): Show | 18 | HG00597.hp1 HG01123.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.198-1668T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166558 | ||||||
| chr10:97166559
|
G | A | 1 | a0001c0021t0008g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.198-1669C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166559 | ||||||
| chr10:97166560
|
A | AAG | 4 | a0001c0001t0001g0133a0001c0001t0001g0141a0001c0001t0005g0136others(1): Show | 4 | HG01123.hp1 NA18999.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-1671_198-1670i others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166560 | ||||||
| chr10:97166561
|
G | A | 13 | a0001c0001t0001g0051a0001c0001t0001g0103a0001c0001t0001g0135others(10): Show | 13 | HG00597.hp1 HG01261.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.198-1671C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166561 | ||||||
| chr10:97166562
|
A | AAG | 4 | a0001c0001t0001g0133a0001c0001t0001g0141a0001c0001t0005g0136others(1): Show | 4 | HG01123.hp1 NA18999.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-1673_198-1672i others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166562 | ||||||
| chr10:97166562
|
A | G | 2 | a0001c0001t0002g0142a0001c0001t0002g0201 | 2 | NA18952.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.198-1672T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166562 | ||||||
| chr10:97166565
|
G | A | 15 | a0001c0001t0001g0026a0001c0001t0001g0133a0001c0001t0001g0141others(12): Show | 15 | HG01123.hp1 HG02145.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.198-1675C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166565 | ||||||
| chr10:97166565
|
G | GAA | 7 | a0001c0001t0001g0049a0001c0001t0001g0215a0001c0001t0002g0066others(4): Show | 7 | HG00280.hp1 HG01928.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-1676_198-1675i others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166565 | ||||||
| chr10:97166565
|
G | GAAAGAA | 4 | a0001c0001t0001g0034a0001c0001t0006g0038a0001c0003t0001g0179others(1): Show | 4 | HG01071.hp2 HG02738.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-1676_198-1675i others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166565 | ||||||
| chr10:97166565
|
G | GAAAGAAA others(3): Show |
6 | a0001c0001t0001g0041a0001c0001t0001g0078a0001c0001t0001g0124others(3): Show | 6 | HG01167.hp1 HG02970.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-1676_198-1675i others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166565 | ||||||
| chr10:97166565
|
G | GAAAGAAA others(7): Show |
2 | a0001c0001t0001g0194a0001c0003t0001g0230 | 2 | HG01358.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.198-1676_198-1675i others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166565 | ||||||
| chr10:97166565
|
G | GAAAGAAA others(15): Show |
1 | a0001c0001t0001g0071 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.198-1676_198-1675i others(24): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166565 | ||||||
| chr10:97166565
|
G | GAGAAAGA others(5): Show |
1 | a0001c0001t0028g0093 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.198-1676_198-1675i others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166565 | ||||||
| chr10:97166566
|
A | G | 2 | a0001c0001t0002g0142a0001c0001t0002g0201 | 2 | NA18952.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.198-1676T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166566 | ||||||
| chr10:97166567
|
GAGAGAAA others(11): Show |
G | 1 | a0006c0027t0025g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.198-1695_198-1678d others(20): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166567 | ||||||
| chr10:97166569
|
G | A | 59 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0026others(56): Show | 59 | HG00280.hp1 HG01071.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.198-1679C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAAAGAAA others(3): Show |
5 | a0001c0001t0001g0007a0001c0004t0003g0176a0001c0006t0004g0204others(2): Show | 5 | HG01515.hp1 HG01517.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.198-1680_198-1679i others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAAAGAAA others(7): Show |
4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0246others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-1680_198-1679i others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAAAGAAA others(15): Show |
1 | a0001c0002t0002g0199 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.198-1680_198-1679i others(24): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAAAGAAA others(19): Show |
1 | a0001c0001t0002g0148 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.198-1680_198-1679i others(28): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAAAGAAA others(23): Show |
1 | a0001c0002t0001g0149 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.198-1680_198-1679i others(32): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAAGAAAG others(6): Show |
1 | a0001c0006t0001g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.198-1680_198-1679i others(15): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAA | 5 | a0001c0001t0001g0011a0001c0001t0001g0178a0001c0003t0001g0064others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-1683_198-1680d others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAAAGA others(1): Show |
4 | a0001c0001t0001g0188a0001c0002t0001g0067a0001c0005t0001g0192others(1): Show | 4 | HG01081.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-1687_198-1680d others(10): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAAAGA others(5): Show |
3 | a0001c0001t0004g0063a0001c0001t0019g0155a0001c0006t0009g0055 | 3 | HG00544.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.198-1691_198-1680d others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAAAGA others(9): Show |
7 | a0001c0001t0001g0068a0001c0001t0001g0198a0001c0001t0001g0221others(4): Show | 7 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.198-1695_198-1680d others(18): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAAAGA others(13): Show |
2 | a0001c0001t0001g0205a0001c0002t0001g0181 | 2 | HG00408.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.198-1699_198-1680d others(22): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAAAGA others(17): Show |
1 | a0001c0004t0001g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.198-1703_198-1680d others(26): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAAAGA others(21): Show |
1 | a0001c0004t0001g0195 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.198-1707_198-1680d others(30): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAAAGA others(25): Show |
2 | a0001c0001t0001g0154a0001c0004t0001g0210 | 2 | HG00438.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.198-1711_198-1680d others(34): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAAA others(3): Show |
1 | a0001c0003t0001g0172 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.198-1680_198-1679i others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAAA others(7): Show |
1 | a0001c0006t0014g0213 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.198-1680_198-1679i others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAAA others(11): Show |
1 | a0001c0003t0006g0190 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.198-1680_198-1679i others(20): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAAA others(15): Show |
1 | a0001c0003t0005g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.198-1680_198-1679i others(24): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAAA others(19): Show |
2 | a0001c0003t0001g0171a0001c0003t0001g0184 | 2 | HG01358.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.198-1680_198-1679i others(28): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(5): Show |
1 | a0001c0009t0027g0223 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.198-1680_198-1679i others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(13): Show |
2 | a0001c0001t0001g0009a0001c0001t0001g0182 | 2 | HG00639.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.198-1680_198-1679i others(22): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(3): Show |
2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.198-1680_198-1679i others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(7): Show |
5 | a0001c0002t0001g0193a0001c0007t0001g0058a0001c0007t0001g0180others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-1680_198-1679i others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(11): Show |
2 | a0001c0001t0001g0043a0001c0008t0003g0060 | 2 | HG02965.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.198-1680_198-1679i others(20): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(15): Show |
3 | a0001c0003t0002g0219a0001c0003t0015g0087a0001c0005t0001g0006 | 3 | HG02723.hp1 HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.198-1680_198-1679i others(24): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(19): Show |
1 | a0001c0001t0001g0185 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.198-1680_198-1679i others(28): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(23): Show |
1 | a0001c0001t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.198-1680_198-1679i others(32): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(5): Show |
3 | a0001c0001t0001g0115a0001c0002t0001g0120a0001c0003t0001g0089 | 3 | HG03017.hp2 HG04228.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.198-1680_198-1679i others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(9): Show |
1 | a0001c0001t0001g0207 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.198-1680_198-1679i others(18): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(13): Show |
2 | a0001c0001t0001g0097a0001c0010t0002g0253 | 2 | HG03490.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.198-1680_198-1679i others(22): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(29): Show |
1 | a0001c0001t0002g0128 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.198-1680_198-1679i others(38): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(8): Show |
1 | a0001c0001t0001g0099 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.198-1680_198-1679i others(17): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(7): Show |
8 | a0001c0001t0001g0092a0001c0001t0001g0112a0001c0001t0001g0174others(5): Show | 8 | HG01361.hp1 HG02083.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.198-1680_198-1679i others(16): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(11): Show |
12 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0167others(9): Show | 12 | HG00741.hp2 HG01109.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.198-1680_198-1679i others(20): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(15): Show |
2 | a0001c0001t0001g0100a0001c0001t0002g0145 | 2 | NA18963.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.198-1680_198-1679i others(24): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(27): Show |
1 | a0001c0001t0002g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.198-1680_198-1679i others(36): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(11): Show |
2 | a0001c0004t0001g0074a0001c0004t0001g0127 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.198-1680_198-1679i others(20): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166569
|
G | GAGAGAGA others(15): Show |
2 | a0001c0004t0001g0075a0001c0004t0001g0076 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.198-1680_198-1679i others(24): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166569 | ||||||
| chr10:97166570
|
A | G | 1 | a0001c0004t0001g0140 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.198-1680T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166570 | ||||||
| chr10:97166571
|
GAA | G | 8 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(5): Show | 8 | HG00673.hp1 HG02071.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-1683_198-1682d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166571 | ||||||
| chr10:97166573
|
A | G | 48 | a0001c0001t0001g0004a0001c0001t0001g0051a0001c0001t0001g0062others(45): Show | 48 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.198-1683T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166573 | ||||||
| chr10:97166577
|
A | G | 34 | a0001c0001t0001g0051a0001c0001t0001g0102a0001c0001t0001g0103others(31): Show | 34 | HG00597.hp1 HG00621.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.198-1687T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166577 | ||||||
| chr10:97166578
|
A | G | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.198-1688T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166578 | ||||||
| chr10:97166581
|
A | G | 21 | a0001c0001t0001g0051a0001c0001t0001g0103a0001c0001t0001g0104others(18): Show | 21 | HG00597.hp1 HG00673.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.198-1691T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166581 | ||||||
| chr10:97166582
|
A | G | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.198-1692T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166582 | ||||||
| chr10:97166585
|
A | G | 9 | a0001c0001t0001g0103a0001c0001t0001g0133a0001c0001t0001g0141others(6): Show | 9 | HG01123.hp1 HG04204.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-1695T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166585 | ||||||
| chr10:97166589
|
A | G | 2 | a0001c0001t0013g0002a0001c0004t0001g0140 | 2 | HG03486.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.198-1699T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166589 | ||||||
| chr10:97166593
|
A | G | 2 | a0001c0001t0013g0002a0001c0004t0001g0140 | 2 | HG03486.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.198-1703T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166593 | ||||||
| chr10:97166597
|
A | G | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.198-1707T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166597 | ||||||
| chr10:97166623
|
G | GAAAGAGA others(3): Show |
1 | a0001c0001t0021g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.198-1734_198-1733i others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166623 | ||||||
| chr10:97166623
|
G | GAGAAA | 203 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0022others(200): Show | 203 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.198-1738_198-1734d others(7): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166623 | ||||||
| chr10:97166623
|
G | GAGAAAAG others(3): Show |
23 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0178others(20): Show | 23 | HG00140.hp1 HG00639.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.198-1743_198-1734d others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166623 | ||||||
| chr10:97166623
|
G | GAGAAAAG others(8): Show |
10 | a0001c0001t0001g0068a0001c0001t0001g0154a0001c0001t0001g0205others(7): Show | 10 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(7): Show |
intron_variant | MODIFIER | c.198-1748_198-1734d others(17): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166623 | ||||||
| chr10:97166623
|
G | GAGAAAAG others(13): Show |
7 | a0001c0001t0001g0182a0001c0001t0001g0185a0001c0001t0001g0186others(4): Show | 7 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-1753_198-1734d others(22): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166623 | ||||||
| chr10:97166639
|
A | AGAAAAGA others(3): Show |
2 | a0001c0001t0001g0221a0001c0009t0027g0223 | 2 | HG00280.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.198-1750_198-1749i others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166639 | ||||||
| chr10:97166644
|
G | A | 6 | a0001c0001t0001g0054a0001c0001t0002g0189a0001c0001t0004g0019others(3): Show | 6 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-1754C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166644 | ||||||
| chr10:97166654
|
A | G | 5 | a0001c0001t0001g0054a0001c0001t0002g0189a0001c0003t0001g0171others(2): Show | 5 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-1764T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166654 | ||||||
| chr10:97166663
|
AAG | A | 5 | a0001c0001t0001g0054a0001c0001t0002g0189a0001c0003t0001g0171others(2): Show | 5 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-1775_198-1774d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166663 | ||||||
| chr10:97166674
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.198-1784T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166674 | ||||||
| chr10:97166694
|
G | A | 3 | a0001c0001t0003g0098a0001c0001t0010g0197a0005c0025t0002g0163 | 3 | NA18954.hp2 NA18984.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.198-1804C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166694 | ||||||
| chr10:97166701
|
A | G | 4 | a0001c0001t0002g0189a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-1811T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166701 | ||||||
| chr10:97166808
|
C | T | 152 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0041others(149): Show | 152 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(149): Show |
intron_variant | MODIFIER | c.198-1918G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166808 | ||||||
| chr10:97166890
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.198-2000A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166890 | ||||||
| chr10:97166916
|
C | T | 8 | a0001c0004t0001g0140a0001c0007t0001g0057a0001c0007t0001g0058others(5): Show | 8 | HG02145.hp2 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-2026G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166916 | ||||||
| chr10:97166979
|
G | A | 4 | a0001c0003t0002g0219a0001c0003t0015g0087a0001c0008t0003g0084others(1): Show | 4 | HG02723.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-2089C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166979 | ||||||
| chr10:97166987
|
C | T | 254 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(251): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.198-2097G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97166987 | ||||||
| chr10:97167081
|
A | G | 34 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0041others(31): Show | 34 | HG00280.hp1 HG01071.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.198-2191T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167081 | ||||||
| chr10:97167158
|
T | C | 6 | a0001c0001t0001g0203a0001c0001t0002g0189a0001c0003t0001g0171others(3): Show | 6 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-2268A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167158 | ||||||
| chr10:97167204
|
A | G | 85 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.198-2314T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167204 | ||||||
| chr10:97167259
|
C | T | 110 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0072others(107): Show | 110 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.198-2369G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167259 | ||||||
| chr10:97167265
|
G | A | 3 | a0001c0001t0001g0004a0001c0005t0001g0005a0001c0005t0001g0006 | 3 | HG01243.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.198-2375C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167265 | ||||||
| chr10:97167296
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.198-2406C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167296 | ||||||
| chr10:97167319
|
T | C | 2 | a0001c0001t0013g0002a0001c0004t0003g0176 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.198-2429A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167319 | ||||||
| chr10:97167327
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0175 | 2 | HG01361.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.198-2437A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167327 | ||||||
| chr10:97167540
|
C | T | 3 | a0001c0001t0002g0083a0001c0011t0001g0157a0001c0011t0001g0187 | 3 | HG02451.hp1 HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.198-2650G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167540 | ||||||
| chr10:97167658
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.198-2768T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167658 | ||||||
| chr10:97167719
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.198-2829A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167719 | ||||||
| chr10:97167757
|
A | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0004t0001g0024 | 3 | NA18943.hp2 NA18998.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.198-2867T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167757 | ||||||
| chr10:97167895
|
G | A | 1 | a0001c0002t0001g0243 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.198-3005C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167895 | ||||||
| chr10:97167906
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.198-3016T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97167906 | ||||||
| chr10:97168011
|
C | T | 5 | a0001c0001t0004g0200a0001c0001t0013g0002a0001c0004t0003g0176others(2): Show | 5 | HG02258.hp2 HG02559.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-3121G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97168011 | ||||||
| chr10:97168114
|
G | A | 1 | a0001c0002t0001g0256 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.198-3224C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97168114 | ||||||
| chr10:97168521
|
C | T | 6 | a0001c0001t0001g0203a0001c0001t0002g0083a0001c0006t0004g0204others(3): Show | 6 | HG02145.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-3631G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97168521 | ||||||
| chr10:97168542
|
A | G | 1 | a0001c0021t0008g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.198-3652T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97168542 | ||||||
| chr10:97168601
|
A | G | 2 | a0001c0001t0004g0200a0001c0015t0001g0177 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.198-3711T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97168601 | ||||||
| chr10:97168814
|
C | T | 30 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0048others(27): Show | 30 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.198-3924G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97168814 | ||||||
| chr10:97169011
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.198-4121A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97169011 | ||||||
| chr10:97169077
|
TA | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0016t0001g0159 | 3 | HG01891.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.198-4188delT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97169077 | ||||||
| chr10:97169157
|
C | G | 156 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(153): Show | 156 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.198-4267G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97169157 | ||||||
| chr10:97169185
|
A | G | 156 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(153): Show | 156 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.198-4295T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97169185 | ||||||
| chr10:97169316
|
C | T | 6 | a0001c0001t0001g0203a0001c0001t0002g0083a0001c0006t0004g0204others(3): Show | 6 | HG02145.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-4426G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97169316 | ||||||
| chr10:97169317
|
G | A | 6 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0001t0002g0196others(3): Show | 6 | HG00280.hp2 HG01106.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-4427C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97169317 | ||||||
| chr10:97169608
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.198-4718G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97169608 | ||||||
| chr10:97169620
|
C | T | 106 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0072others(103): Show | 106 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.198-4730G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97169620 | ||||||
| chr10:97169665
|
G | A | 196 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.198-4775C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97169665 | ||||||
| chr10:97169703
|
G | A | 201 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.198-4813C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97169703 | ||||||
| chr10:97169988
|
C | T | 106 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0072others(103): Show | 106 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.198-5098G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97169988 | ||||||
| chr10:97170118
|
G | A | 37 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0041others(34): Show | 37 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.198-5228C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170118 | ||||||
| chr10:97170121
|
G | A | 2 | a0001c0001t0004g0200a0001c0015t0001g0177 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.198-5231C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170121 | ||||||
| chr10:97170304
|
T | C | 196 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.198-5414A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170304 | ||||||
| chr10:97170365
|
C | T | 29 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0023others(26): Show | 29 | HG00621.hp2 HG01123.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.198-5475G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170365 | ||||||
| chr10:97170492
|
C | T | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.198-5602G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170492 | ||||||
| chr10:97170493
|
G | A | 42 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0054others(39): Show | 42 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.198-5603C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170493 | ||||||
| chr10:97170591
|
G | T | 106 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0072others(103): Show | 106 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.198-5701C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170591 | ||||||
| chr10:97170592
|
C | T | 6 | a0001c0001t0001g0203a0001c0001t0002g0083a0001c0006t0004g0204others(3): Show | 6 | HG02145.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-5702G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170592 | ||||||
| chr10:97170635
|
T | C | 153 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(150): Show | 153 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.198-5745A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170635 | ||||||
| chr10:97170646
|
G | C | 37 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0041others(34): Show | 37 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.198-5756C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170646 | ||||||
| chr10:97170666
|
A | G | 1 | a0006c0027t0025g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.198-5776T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170666 | ||||||
| chr10:97170667
|
T | C | 42 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0054others(39): Show | 42 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.198-5777A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170667 | ||||||
| chr10:97170703
|
C | A | 1 | a0001c0005t0001g0192 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.198-5813G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170703 | ||||||
| chr10:97170774
|
C | G | 17 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0048others(14): Show | 17 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.198-5884G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170774 | ||||||
| chr10:97170902
|
T | C | 154 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(151): Show | 154 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.198-6012A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170902 | ||||||
| chr10:97170994
|
G | A | 1 | a0001c0002t0002g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.198-6104C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97170994 | ||||||
| chr10:97171021
|
G | A | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.198-6131C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171021 | ||||||
| chr10:97171042
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0188a0001c0001t0001g0246others(2): Show | 5 | HG01891.hp2 HG02809.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-6152A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171042 | ||||||
| chr10:97171071
|
A | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0188a0001c0001t0001g0246others(2): Show | 5 | HG01891.hp2 HG02809.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-6181T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171071 | ||||||
| chr10:97171138
|
G | A | 1 | a0001c0002t0001g0208 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.198-6248C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171138 | ||||||
| chr10:97171202
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0016t0001g0159 | 3 | HG01891.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.198-6312G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171202 | ||||||
| chr10:97171256
|
G | A | 2 | a0001c0001t0013g0002a0001c0004t0003g0176 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.198-6366C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171256 | ||||||
| chr10:97171321
|
C | T | 1 | a0001c0003t0001g0179 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.198-6431G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171321 | ||||||
| chr10:97171408
|
T | C | 154 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(151): Show | 154 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.198-6518A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171408 | ||||||
| chr10:97171493
|
A | G | 1 | a0001c0001t0002g0129 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.198-6603T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171493 | ||||||
| chr10:97171647
|
T | C | 154 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(151): Show | 154 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.198-6757A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171647 | ||||||
| chr10:97171718
|
C | T | 2 | a0001c0001t0004g0200a0001c0015t0001g0177 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.198-6828G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171718 | ||||||
| chr10:97171751
|
G | A | 1 | a0001c0021t0008g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.198-6861C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171751 | ||||||
| chr10:97171766
|
G | C | 254 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(251): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.198-6876C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171766 | ||||||
| chr10:97171775
|
T | C | 5 | a0001c0001t0001g0054a0001c0001t0002g0189a0001c0003t0001g0171others(2): Show | 5 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-6885A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171775 | ||||||
| chr10:97171900
|
G | A | 37 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0041others(34): Show | 37 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.198-7010C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171900 | ||||||
| chr10:97171981
|
T | C | 154 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(151): Show | 154 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.198-7091A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97171981 | ||||||
| chr10:97172064
|
C | T | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.198-7174G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97172064 | ||||||
| chr10:97172210
|
A | T | 1 | a0001c0002t0001g0101 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.198-7320T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97172210 | ||||||
| chr10:97172261
|
A | G | 196 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.198-7371T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97172261 | ||||||
| chr10:97172606
|
C | T | 2 | a0001c0001t0013g0002a0001c0004t0003g0176 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.198-7716G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97172606 | ||||||
| chr10:97172877
|
G | C | 154 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(151): Show | 154 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.198-7987C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97172877 | ||||||
| chr10:97172934
|
GGAGA | G | 106 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0072others(103): Show | 106 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.198-8048_198-8045d others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97172934 | ||||||
| chr10:97172936
|
A | G | 4 | a0001c0001t0002g0189a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-8046T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97172936 | ||||||
| chr10:97173287
|
G | T | 145 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(142): Show | 145 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.198-8397C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97173287 | ||||||
| chr10:97173404
|
A | T | 106 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0072others(103): Show | 106 | HG00408.hp2 HG00558.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.198-8514T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97173404 | ||||||
| chr10:97173494
|
C | CT | 19 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0135others(16): Show | 19 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-8605dupA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97173494 | ||||||
| chr10:97173494
|
CT | C | 5 | a0001c0001t0001g0246a0001c0001t0002g0008a0001c0004t0001g0173others(2): Show | 5 | HG02165.hp2 HG02559.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.198-8605delA | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97173494 | ||||||
| chr10:97173494
|
CTT | C | 140 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(137): Show | 140 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.198-8606_198-8605d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97173494 | ||||||
| chr10:97173673
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.198-8783T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97173673 | ||||||
| chr10:97173680
|
A | G | 1 | a0001c0001t0004g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.198-8790T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97173680 | ||||||
| chr10:97173859
|
G | A | 1 | a0006c0027t0025g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.198-8969C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97173859 | ||||||
| chr10:97173945
|
C | T | 24 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0023others(21): Show | 24 | HG00621.hp2 HG01243.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.198-9055G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97173945 | ||||||
| chr10:97174046
|
C | T | 1 | a0001c0003t0001g0171 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.198-9156G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97174046 | ||||||
| chr10:97174096
|
G | A | 99 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0080others(96): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.198-9206C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97174096 | ||||||
| chr10:97174163
|
A | G | 4 | a0001c0001t0002g0189a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-9273T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97174163 | ||||||
| chr10:97174370
|
C | T | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.198-9480G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97174370 | ||||||
| chr10:97174467
|
C | G | 2 | a0001c0001t0001g0054a0001c0021t0008g0028 | 2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.198-9577G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97174467 | ||||||
| chr10:97174863
|
T | A | 1 | a0001c0017t0008g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.198-9973A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97174863 | ||||||
| chr10:97175452
|
T | C | 1 | a0001c0007t0003g0114 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.197+10026A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97175452 | ||||||
| chr10:97175512
|
C | G | 4 | a0001c0001t0002g0189a0001c0003t0001g0171a0001c0003t0001g0172others(1): Show | 4 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+9966G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97175512 | ||||||
| chr10:97175515
|
C | T | 153 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(150): Show | 153 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.197+9963G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97175515 | ||||||
| chr10:97175528
|
G | A | 1 | a0006c0027t0025g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.197+9950C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97175528 | ||||||
| chr10:97175614
|
C | T | 2 | a0001c0001t0013g0002a0001c0004t0003g0176 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.197+9864G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97175614 | ||||||
| chr10:97175873
|
A | G | 4 | a0001c0001t0001g0203a0001c0001t0013g0002a0001c0004t0003g0176others(1): Show | 4 | HG02145.hp1 HG02258.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+9605T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97175873 | ||||||
| chr10:97175880
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.197+9598T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97175880 | ||||||
| chr10:97175886
|
C | G | 1 | a0001c0001t0002g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.197+9592G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97175886 | ||||||
| chr10:97175995
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.197+9483T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97175995 | ||||||
| chr10:97176103
|
G | A | 1 | a0001c0005t0002g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.197+9375C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97176103 | ||||||
| chr10:97176251
|
A | C | 1 | a0001c0001t0018g0168 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.197+9227T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97176251 | ||||||
| chr10:97176401
|
T | C | 109 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0072others(106): Show | 109 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.197+9077A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97176401 | ||||||
| chr10:97176584
|
C | T | 39 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0068others(36): Show | 39 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.197+8894G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97176584 | ||||||
| chr10:97176808
|
A | G | 2 | a0001c0001t0001g0054a0001c0021t0008g0028 | 2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.197+8670T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97176808 | ||||||
| chr10:97176974
|
C | T | 111 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0054others(108): Show | 111 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.197+8504G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97176974 | ||||||
| chr10:97177033
|
C | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0188a0001c0001t0001g0246others(5): Show | 8 | HG01891.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+8445G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97177033 | ||||||
| chr10:97177174
|
C | T | 1 | a0001c0032t0001g0061 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.197+8304G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97177174 | ||||||
| chr10:97177297
|
C | T | 40 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0041others(37): Show | 40 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.197+8181G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97177297 | ||||||
| chr10:97177382
|
T | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0188a0001c0001t0001g0246others(5): Show | 8 | HG01891.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+8096A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97177382 | ||||||
| chr10:97177543
|
A | G | 39 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0068others(36): Show | 39 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.197+7935T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97177543 | ||||||
| chr10:97177554
|
C | T | 1 | a0001c0004t0001g0195 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.197+7924G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97177554 | ||||||
| chr10:97177557
|
G | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0115others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+7921C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97177557 | ||||||
| chr10:97177698
|
G | A | 38 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0041others(35): Show | 38 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.197+7780C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97177698 | ||||||
| chr10:97177727
|
G | T | 2 | a0001c0001t0004g0200a0001c0015t0001g0177 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.197+7751C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97177727 | ||||||
| chr10:97177747
|
G | A | 1 | a0001c0004t0001g0044 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.197+7731C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97177747 | ||||||
| chr10:97177792
|
A | G | 2 | a0001c0001t0001g0124a0001c0017t0008g0123 | 2 | HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.197+7686T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97177792 | ||||||
| chr10:97177935
|
C | T | 2 | a0001c0001t0001g0203a0001c0006t0004g0204 | 2 | HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.197+7543G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97177935 | ||||||
| chr10:97177980
|
A | C | 2 | a0001c0001t0004g0200a0001c0015t0001g0177 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.197+7498T>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97177980 | ||||||
| chr10:97178006
|
A | G | 10 | a0001c0001t0001g0054a0001c0001t0001g0203a0001c0001t0002g0189others(7): Show | 10 | HG00738.hp2 HG01123.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.197+7472T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97178006 | ||||||
| chr10:97178138
|
G | A | 104 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0072others(101): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.197+7340C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97178138 | ||||||
| chr10:97178151
|
G | A | 38 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0041others(35): Show | 38 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.197+7327C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97178151 | ||||||
| chr10:97178501
|
C | A | 1 | a0001c0021t0008g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.197+6977G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97178501 | ||||||
| chr10:97178527
|
T | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0006t0007g0088 | 3 | HG02895.hp1 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.197+6951A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97178527 | ||||||
| chr10:97178555
|
A | T | 1 | a0001c0006t0007g0209 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.197+6923T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97178555 | ||||||
| chr10:97178583
|
A | T | 2 | a0001c0001t0003g0098a0001c0001t0010g0197 | 2 | NA18954.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.197+6895T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97178583 | ||||||
| chr10:97178711
|
C | T | 6 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0001t0002g0196others(3): Show | 6 | HG00280.hp2 HG01106.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.197+6767G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97178711 | ||||||
| chr10:97178790
|
AGT | A | 35 | a0001c0001t0001g0011a0001c0001t0001g0068a0001c0001t0001g0154others(32): Show | 35 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.197+6686_197+6687d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97178790 | ||||||
| chr10:97178790
|
AGTGT | A | 3 | a0001c0003t0001g0179a0001c0005t0001g0192a0001c0017t0008g0123 | 3 | HG01081.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.197+6684_197+6687d others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97178790 | ||||||
| chr10:97178790
|
AGTGTGT | A | 154 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(151): Show | 154 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.197+6682_197+6687d others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97178790 | ||||||
| chr10:97178952
|
G | A | 1 | a0001c0015t0001g0177 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.197+6526C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97178952 | ||||||
| chr10:97178955
|
G | A | 8 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0002g0142others(5): Show | 8 | HG02523.hp1 NA18952.hp2 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.197+6523C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97178955 | ||||||
| chr10:97179046
|
C | T | 6 | a0001c0001t0001g0133a0001c0001t0001g0158a0001c0003t0001g0089others(3): Show | 6 | HG02257.hp1 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+6432G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97179046 | ||||||
| chr10:97179050
|
C | A | 104 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0072others(101): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.197+6428G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97179050 | ||||||
| chr10:97179290
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.197+6188G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97179290 | ||||||
| chr10:97179410
|
T | C | 1 | a0001c0004t0003g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.197+6068A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97179410 | ||||||
| chr10:97179535
|
C | G | 1 | a0006c0027t0025g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.197+5943G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97179535 | ||||||
| chr10:97179610
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.197+5868G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97179610 | ||||||
| chr10:97179640
|
C | A | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.197+5838G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97179640 | ||||||
| chr10:97179791
|
T | C | 28 | a0001c0001t0001g0051a0001c0001t0001g0062a0001c0001t0001g0133others(25): Show | 28 | HG00544.hp1 HG00597.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.197+5687A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97179791 | ||||||
| chr10:97179800
|
T | TC | 78 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0078others(75): Show | 78 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.197+5677dupG | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97179800 | ||||||
| chr10:97179800
|
T | TCC | 12 | a0001c0001t0001g0081a0001c0001t0001g0115a0001c0001t0001g0116others(9): Show | 12 | HG00735.hp1 HG01109.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.197+5676_197+5677d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97179800 | ||||||
| chr10:97179801
|
C | CG | 8 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0002t0001g0120others(5): Show | 8 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+5676_197+5677i others(3): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97179801 | ||||||
| chr10:97179805
|
G | C | 104 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0072others(101): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.197+5673C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97179805 | ||||||
| chr10:97179985
|
C | T | 1 | a0001c0012t0002g0047 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.197+5493G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97179985 | ||||||
| chr10:97180403
|
C | A | 1 | a0001c0010t0002g0253 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.197+5075G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97180403 | ||||||
| chr10:97180491
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0006t0007g0088 | 3 | HG02895.hp1 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.197+4987C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97180491 | ||||||
| chr10:97180768
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.197+4710G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97180768 | ||||||
| chr10:97180848
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.197+4630G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97180848 | ||||||
| chr10:97181119
|
C | T | 16 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0221others(13): Show | 16 | HG00280.hp2 HG00438.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.197+4359G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97181119 | ||||||
| chr10:97181237
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.197+4241G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97181237 | ||||||
| chr10:97181418
|
C | A | 1 | a0006c0027t0025g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.197+4060G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97181418 | ||||||
| chr10:97181557
|
C | T | 1 | a0001c0001t0002g0201 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.197+3921G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97181557 | ||||||
| chr10:97181688
|
A | AAG | 3 | a0001c0001t0001g0124a0001c0017t0008g0123a0001c0021t0008g0028 | 3 | HG02559.hp2 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.197+3789_197+3790i others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97181688 | ||||||
| chr10:97181690
|
G | A | 3 | a0001c0001t0001g0124a0001c0017t0008g0123a0001c0021t0008g0028 | 3 | HG02559.hp2 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.197+3788C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97181690 | ||||||
| chr10:97182256
|
G | A | 54 | a0001c0001t0001g0054a0001c0001t0001g0092a0001c0001t0001g0094others(51): Show | 54 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.197+3222C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97182256 | ||||||
| chr10:97182482
|
G | A | 1 | a0001c0002t0001g0212 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.197+2996C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97182482 | ||||||
| chr10:97182505
|
C | T | 3 | a0001c0001t0004g0200a0001c0001t0013g0002a0001c0015t0001g0177 | 3 | HG03471.hp1 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.197+2973G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97182505 | ||||||
| chr10:97182557
|
G | A | 35 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0097others(32): Show | 35 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.197+2921C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97182557 | ||||||
| chr10:97182947
|
C | T | 230 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0041others(227): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.197+2531G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97182947 | ||||||
| chr10:97182971
|
G | GA | 21 | a0001c0001t0001g0034a0001c0001t0001g0054a0001c0001t0001g0092others(18): Show | 21 | HG00738.hp2 HG01071.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.197+2506dupT | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97182971 | ||||||
| chr10:97182971
|
G | GAA | 35 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0099others(32): Show | 35 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.197+2505_197+2506d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97182971 | ||||||
| chr10:97183021
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.197+2457C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97183021 | ||||||
| chr10:97183075
|
G | C | 43 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0041others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.197+2403C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97183075 | ||||||
| chr10:97183076
|
C | T | 22 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0041others(19): Show | 22 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.197+2402G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97183076 | ||||||
| chr10:97183111
|
T | A | 190 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(187): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.197+2367A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97183111 | ||||||
| chr10:97183123
|
T | G | 43 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0041others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.197+2355A>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97183123 | ||||||
| chr10:97183149
|
A | G | 1 | a0001c0005t0001g0045 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.197+2329T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97183149 | ||||||
| chr10:97183180
|
T | C | 254 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(251): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.197+2298A>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97183180 | ||||||
| chr10:97183222
|
A | G | 6 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0001t0002g0196others(3): Show | 6 | HG00280.hp2 HG03704.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.197+2256T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97183222 | ||||||
| chr10:97183579
|
C | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0004t0003g0176 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.197+1899G>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97183579 | ||||||
| chr10:97183671
|
A | G | 1 | a0001c0001t0013g0002 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.197+1807T>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97183671 | ||||||
| chr10:97183786
|
T | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0002g0008others(2): Show | 5 | NA18939.hp2 NA18943.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.197+1692A>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97183786 | ||||||
| chr10:97184018
|
C | CCA | 37 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0048others(34): Show | 37 | HG00280.hp1 HG00408.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.197+1458_197+1459d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184018 | ||||||
| chr10:97184018
|
C | CCACA | 39 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0221others(36): Show | 39 | HG00280.hp2 HG00621.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.197+1456_197+1459d others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184018 | ||||||
| chr10:97184018
|
C | CCACACA | 9 | a0001c0001t0001g0026a0001c0001t0001g0249a0001c0001t0002g0251others(6): Show | 9 | HG02055.hp1 HG02280.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.197+1454_197+1459d others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184018 | ||||||
| chr10:97184018
|
C | CCACACAC others(3): Show |
3 | a0001c0001t0022g0254a0001c0001t0024g0027a0001c0003t0001g0255 | 3 | HG00642.hp2 HG00735.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.197+1450_197+1459d others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184018 | ||||||
| chr10:97184018
|
CCA | C | 22 | a0001c0001t0001g0054a0001c0001t0001g0178a0001c0001t0001g0182others(19): Show | 22 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.197+1458_197+1459d others(4): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184018 | ||||||
| chr10:97184018
|
CCACA | C | 35 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0154others(32): Show | 35 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.197+1456_197+1459d others(6): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184018 | ||||||
| chr10:97184018
|
CCACACA | C | 28 | a0001c0001t0001g0051a0001c0001t0001g0124a0001c0001t0001g0131others(25): Show | 28 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.197+1454_197+1459d others(8): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184018 | ||||||
| chr10:97184018
|
CCACACAC others(1): Show |
C | 59 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0072others(56): Show | 59 | HG00408.hp2 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.197+1452_197+1459d others(10): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184018 | ||||||
| chr10:97184018
|
CCACACAC others(3): Show |
C | 2 | a0001c0001t0001g0062a0001c0001t0004g0063 | 2 | HG01433.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.197+1450_197+1459d others(12): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184018 | ||||||
| chr10:97184018
|
CCACACAC others(5): Show |
C | 1 | a0001c0032t0001g0061 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.197+1448_197+1459d others(14): Show |
SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184018 | ||||||
| chr10:97184038
|
A | T | 7 | a0001c0001t0001g0054a0001c0006t0001g0056a0001c0006t0009g0055others(4): Show | 7 | HG01884.hp2 HG02809.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.197+1440T>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184038 | ||||||
| chr10:97184453
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(22): Show | 25 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.197+1025G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184453 | ||||||
| chr10:97184555
|
G | A | 1 | a0001c0005t0001g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.197+923C>T | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184555 | ||||||
| chr10:97184710
|
G | T | 1 | a0001c0012t0001g0053 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.197+768C>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184710 | ||||||
| chr10:97184741
|
C | T | 1 | a0001c0005t0001g0052 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.197+737G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184741 | ||||||
| chr10:97184914
|
C | G | 1 | a0001c0001t0001g0051 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.197+564G>C | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97184914 | ||||||
| chr10:97185253
|
G | C | 1 | a0001c0002t0001g0256 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.197+225C>G | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97185253 | ||||||
| chr10:97185306
|
C | T | 49 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0009others(46): Show | 49 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.197+172G>A | SLIT1 | ENSG00000187122.17 | transcript | ENST00000266058.9 | protein_coding | 1/36 | chr10 | 97185306 |