Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 124976 |
| ensemblid | ENSG00000183018.9 |
| hgncid | 26992 |
| symbol | SPNS2 |
| name | SPNS lysolipid transporter 2, sphingosine-1-phosphate |
| refseq_nuc | NM_001124758.3 |
| refseq_prot | NP_001118230.1 |
| ensembl_nuc | ENST00000329078.8 |
| ensembl_prot | ENSP00000333292.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 4498881 |
| end | 4539035 |
| strand | + |
| ver | v1.2 |
| region | chr17:4498881-4539035 |
| region5000 | chr17:4493881-4544035 |
| regionname0 | SPNS2_chr17_4498881_4539035 |
| regionname5000 | SPNS2_chr17_4493881_4544035 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 549 | 403 | 95 | 88 | 158 | 14 | 46 | 118 | SPNS2_chr17_4493881_4544035 | SPNS2 | MMCLE others(544): Show |
chr17 | 4493881 | 4544035 |
| a0002 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | MMCLE others(544): Show |
chr17 | 4493881 | 4544035 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1647 | 362 | 72 | 87 | 142 | 13 | 46 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0002 | 0/0 | 1647 | 9 | 9 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0003 | 0/0 | 1647 | 8 | 8 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0004 | 0/0 | 1647 | 7 | 0 | 0 | 7 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0005 | 0/0 | 1647 | 5 | 0 | 0 | 5 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0006 | 0/0 | 1647 | 3 | 2 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0007 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0008 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0009 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0010 | 0/0 | 1647 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0012 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0013 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0014 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0015 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0001c0016 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 | ||
| a0002c0011 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | ATGAT others(1642): Show |
chr17 | 4493881 | 4544035 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3400 | 132 | 10 | 38 | 65 | 4 | 14 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0002 | 0/0 | 3400 | 83 | 0 | 17 | 57 | 0 | 9 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0003 | 1/0 | 3404 | 40 | 6 | 19 | 1 | 5 | 8 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3399): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0004 | 0/0 | 3400 | 17 | 13 | 4 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0005 | 0/0 | 3400 | 9 | 1 | 2 | 1 | 0 | 5 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0006 | 0/0 | 3400 | 8 | 8 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0007 | 0/0 | 3400 | 5 | 4 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0008 | 0/0 | 3400 | 5 | 0 | 0 | 4 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0009 | 0/0 | 3404 | 5 | 4 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3399): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0010 | 0/0 | 3400 | 5 | 0 | 3 | 0 | 1 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0011 | 0/0 | 3400 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0012 | 0/0 | 3400 | 4 | 0 | 0 | 4 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0013 | 0/0 | 3400 | 4 | 0 | 2 | 0 | 2 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0014 | 0/0 | 3404 | 4 | 1 | 1 | 0 | 0 | 2 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3399): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0015 | 0/0 | 3400 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0016 | 0/0 | 3404 | 3 | 2 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3399): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0017 | 0/0 | 3404 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3399): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0018 | 0/0 | 3389 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3384): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0019 | 0/0 | 3400 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0020 | 0/0 | 3400 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0021 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3399): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0022 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0023 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0025 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0026 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3399): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0028 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0029 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0030 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0031 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3399): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0033 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3399): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0034 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0035 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0036 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0037 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0038 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0039 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0040 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0042 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0043 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0046 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0047 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0048 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0049 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0050 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0051 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0001t0052 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0002t0004 | 0/0 | 3400 | 5 | 5 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0002t0006 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0002t0011 | 0/0 | 3400 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0002t0044 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0003t0004 | 0/0 | 3400 | 3 | 3 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0003t0005 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0003t0006 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0003t0007 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0003t0024 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0003t0041 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0004t0001 | 0/0 | 3400 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0004t0002 | 0/0 | 3400 | 5 | 0 | 0 | 5 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0005t0002 | 0/0 | 3400 | 5 | 0 | 0 | 5 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0006t0002 | 0/0 | 3400 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0006t0027 | 0/0 | 3400 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0007t0004 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0008t0004 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0009t0015 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0010t0001 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0012t0002 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0013t0045 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3399): Show |
chr17 | 4493881 | 4544035 |
| a0001c0014t0002 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0015t0002 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0001c0016t0001 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| a0002c0011t0032 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | GCAGC others(3395): Show |
chr17 | 4493881 | 4544035 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0003g0353 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0005g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0005g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0005g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0006g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0008g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0008g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0009g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0009g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0010g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0010g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0010g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0010g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0010g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0011g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0011g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0012g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0012g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0012g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0012g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0013g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0013g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0014g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0014g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0014g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0014g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0015g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0015g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0016g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0016g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0016g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0017g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0017g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0018g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0018g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0019g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0019g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0020g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0020g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0021g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0022g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0023g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0025g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0026g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0028g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0029g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0030g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0031g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0033g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0034g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0035g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0036g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0037g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0038g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0039g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0040g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0042g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0043g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0046g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0047g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0048g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0049g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0050g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0051g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0001t0052g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0002t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0002t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0002t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0002t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0002t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0002t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0002t0011g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0002t0011g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0002t0044g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0003t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0003t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0003t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0003t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0003t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0003t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0003t0024g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0003t0041g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0004t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0004t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0004t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0004t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0004t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0004t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0005t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0005t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0005t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0005t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0005t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0006t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0006t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0006t0027g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0007t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0008t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0009t0015g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0010t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0012t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0013t0045g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0014t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0015t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0001c0016t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| a0002c0011t0032g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0074 | EUR | GBR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00099 | hp2 | a0001 | c0010 | t0001 | g0150 | EUR | GBR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0050 | EUR | FIN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00323 | hp1 | a0001 | c0001 | t0009 | g0186 | EUR | FIN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0153 | EUR | FIN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00423 | hp1 | a0001 | c0001 | t0043 | g0317 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00423 | hp2 | a0001 | c0004 | t0002 | g0267 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00438 | hp2 | a0001 | c0014 | t0002 | g0140 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00639 | hp1 | a0001 | c0001 | t0014 | g0079 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0102 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00673 | hp1 | a0001 | c0005 | t0002 | g0077 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00673 | hp2 | a0001 | c0015 | t0002 | g0065 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00735 | hp2 | a0001 | c0001 | t0010 | g0041 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0151 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG00741 | hp2 | a0001 | c0001 | t0013 | g0003 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01081 | hp2 | a0001 | c0001 | t0010 | g0211 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0352 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01167 | hp1 | a0001 | c0006 | t0027 | g0192 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0056 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0187 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01256 | hp1 | a0001 | c0001 | t0010 | g0216 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0185 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0360 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01433 | hp2 | a0001 | c0001 | t0013 | g0003 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01515 | hp2 | a0001 | c0001 | t0013 | g0044 | EUR | IBS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0200 | EUR | IBS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0008 | EUR | IBS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | IBS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01517 | hp2 | a0001 | c0001 | t0013 | g0003 | EUR | IBS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0178 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01884 | hp2 | a0001 | c0001 | t0051 | g0193 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01891 | hp1 | a0001 | c0001 | t0022 | g0365 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0173 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0254 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0252 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02015 | hp1 | a0001 | c0001 | t0042 | g0155 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02055 | hp2 | a0001 | c0006 | t0002 | g0046 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02145 | hp1 | a0001 | c0009 | t0015 | g0165 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | CDX | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | CDX | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02257 | hp1 | a0001 | c0001 | t0016 | g0261 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02257 | hp2 | a0001 | c0002 | t0004 | g0072 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02258 | hp1 | a0001 | c0003 | t0041 | g0068 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0166 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0276 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02451 | hp2 | a0001 | c0006 | t0002 | g0195 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02572 | hp1 | a0001 | c0002 | t0011 | g0366 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02572 | hp2 | a0001 | c0001 | t0025 | g0174 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02622 | hp1 | a0002 | c0011 | t0032 | g0162 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02622 | hp2 | a0001 | c0001 | t0033 | g0030 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02630 | hp1 | a0001 | c0001 | t0021 | g0367 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02630 | hp2 | a0001 | c0003 | t0004 | g0069 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0237 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02698 | hp1 | a0001 | c0001 | t0049 | g0108 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0341 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0238 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0330 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02723 | hp1 | a0001 | c0002 | t0006 | g0159 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0202 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0167 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02809 | hp2 | a0001 | c0001 | t0016 | g0057 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02818 | hp2 | a0001 | c0007 | t0004 | g0194 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02886 | hp1 | a0001 | c0001 | t0034 | g0028 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0347 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02896 | hp2 | a0001 | c0001 | t0038 | g0221 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0348 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02922 | hp2 | a0001 | c0001 | t0019 | g0228 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0169 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0070 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02970 | hp2 | a0001 | c0001 | t0015 | g0176 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02976 | hp1 | a0001 | c0001 | t0014 | g0141 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0350 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0326 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03041 | hp1 | a0001 | c0001 | t0017 | g0368 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03041 | hp2 | a0001 | c0001 | t0035 | g0032 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03098 | hp1 | a0001 | c0001 | t0050 | g0131 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03098 | hp2 | a0001 | c0003 | t0004 | g0351 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03130 | hp1 | a0001 | c0003 | t0024 | g0171 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03130 | hp2 | a0001 | c0001 | t0017 | g0363 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03139 | hp1 | a0001 | c0003 | t0007 | g0168 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0163 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03195 | hp2 | a0001 | c0002 | t0011 | g0364 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0172 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03209 | hp2 | a0001 | c0001 | t0028 | g0179 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0034 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03225 | hp2 | a0001 | c0001 | t0031 | g0031 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03239 | hp1 | a0001 | c0001 | t0052 | g0181 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03453 | hp1 | a0001 | c0001 | t0026 | g0189 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0164 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0355 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0158 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03540 | hp2 | a0001 | c0013 | t0045 | g0223 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0361 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03579 | hp2 | a0001 | c0001 | t0019 | g0071 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03704 | hp2 | a0001 | c0001 | t0014 | g0337 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03831 | hp1 | a0001 | c0001 | t0046 | g0105 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0180 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03834 | hp2 | a0001 | c0001 | t0008 | g0183 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0004 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0359 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0321 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG04184 | hp2 | a0001 | c0001 | t0048 | g0137 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG04204 | hp1 | a0001 | c0001 | t0030 | g0184 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0217 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG04228 | hp2 | a0001 | c0001 | t0016 | g0314 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0362 | AFR | YRI | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | CHB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18747 | hp2 | a0001 | c0016 | t0001 | g0332 | EAS | CHB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18906 | hp1 | a0001 | c0003 | t0004 | g0232 | AFR | YRI | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0236 | AFR | YRI | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18945 | hp1 | a0001 | c0001 | t0040 | g0264 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18945 | hp2 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18957 | hp2 | a0001 | c0001 | t0012 | g0139 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18960 | hp2 | a0001 | c0001 | t0012 | g0323 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18963 | hp1 | a0001 | c0005 | t0002 | g0148 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18965 | hp1 | a0001 | c0005 | t0002 | g0048 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18970 | hp2 | a0001 | c0012 | t0002 | g0243 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18977 | hp1 | a0001 | c0001 | t0012 | g0120 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18984 | hp1 | a0001 | c0001 | t0047 | g0343 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18986 | hp2 | a0001 | c0001 | t0039 | g0324 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18990 | hp1 | a0001 | c0001 | t0008 | g0182 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18991 | hp1 | a0001 | c0004 | t0001 | g0023 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18994 | hp1 | a0001 | c0001 | t0020 | g0263 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18994 | hp2 | a0001 | c0005 | t0002 | g0053 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18995 | hp2 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19003 | hp2 | a0001 | c0004 | t0002 | g0290 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19004 | hp2 | a0001 | c0004 | t0002 | g0124 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19005 | hp2 | a0001 | c0001 | t0018 | g0112 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19010 | hp1 | a0001 | c0004 | t0002 | g0292 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19012 | hp1 | a0001 | c0004 | t0002 | g0291 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19030 | hp1 | a0001 | c0008 | t0004 | g0073 | AFR | LWK | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | LWK | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19043 | hp1 | a0001 | c0001 | t0036 | g0225 | AFR | LWK | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0170 | AFR | LWK | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19057 | hp2 | a0001 | c0001 | t0018 | g0111 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19068 | hp2 | a0001 | c0004 | t0001 | g0023 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19074 | hp2 | a0001 | c0001 | t0020 | g0273 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19083 | hp2 | a0001 | c0005 | t0002 | g0121 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19085 | hp2 | a0001 | c0001 | t0037 | g0002 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19089 | hp2 | a0001 | c0001 | t0012 | g0086 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA19091 | hp2 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ASW | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA20129 | hp2 | a0001 | c0002 | t0044 | g0233 | AFR | ASW | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | TSI | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0334 | SAS | GIH | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA20905 | hp2 | a0001 | c0001 | t0014 | g0333 | SAS | GIH | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0191 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0161 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG02559 | hp2 | a0001 | c0001 | t0015 | g0188 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03471 | hp1 | a0001 | c0001 | t0023 | g0369 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0227 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG06807 | hp1 | a0001 | c0001 | t0029 | g0175 | AFR | USA | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| HG06807 | hp2 | a0001 | c0003 | t0006 | g0160 | AFR | USA | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | USA | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA21309 | hp1 | a0001 | c0003 | t0005 | g0177 | AFR | LWK | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | LWK | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0027 | REF | REF | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0353 | REF | REF | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4536344 | C | T | 1 | a0002 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1525C>T | p.Pro509Ser | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/13 | 1692/3404 | 1525/1650 | 509/549 | chr17 | 4536344 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4499263 | C | T | 2 | a0001c0001 a0001c0006 |
2 | HG02055.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.216C>T | p.Pro72Pro | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | 383/3404 | 216/1650 | 72/549 | chr17 | 4499263 | |||
| chr17:4513248 | C | T | 1 | a0001c0016 | 1 | NA18747.hp2 | splice_region_variant&synonymous_variant | LOW | c.372C>T | p.Gly124Gly | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/13 | 539/3404 | 372/1650 | 124/549 | chr17 | 4513248 | |||
| chr17:4530634 | C | T | 1 | a0001c0015 | 1 | HG00673.hp2 | splice_region_variant&synonymous_variant | LOW | c.576C>T | p.Tyr192Tyr | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/13 | 743/3404 | 576/1650 | 192/549 | chr17 | 4530634 | |||
| chr17:4530667 | G | A | 1 | a0001c0002 | 9 | HG02257.hp2 HG02572.hp1 HG02723.hp1 others(6): Show |
synonymous_variant | LOW | c.609G>A | p.Val203Val | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/13 | 776/3404 | 609/1650 | 203/549 | chr17 | 4530667 | |||
| chr17:4530673 | C | T | 1 | a0001c0014 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.615C>T | p.Ile205Ile | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/13 | 782/3404 | 615/1650 | 205/549 | chr17 | 4530673 | |||
| chr17:4532550 | T | G | 1 | a0001c0007 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.801T>G | p.Pro267Pro | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 6/13 | 968/3404 | 801/1650 | 267/549 | chr17 | 4532550 | |||
| chr17:4533007 | G | A | 1 | a0001c0006 | 3 | HG01167.hp1 HG02055.hp2 HG02451.hp2 |
synonymous_variant | LOW | c.966G>A | p.Thr322Thr | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 7/13 | 1133/3404 | 966/1650 | 322/549 | chr17 | 4533007 | |||
| chr17:4533010 | G | A | 1 | a0001c0008 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.969G>A | p.Ser323Ser | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 7/13 | 1136/3404 | 969/1650 | 323/549 | chr17 | 4533010 | |||
| chr17:4533025 | C | T | 1 | a0001c0013 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.984C>T | p.Ala328Ala | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 7/13 | 1151/3404 | 984/1650 | 328/549 | chr17 | 4533025 | |||
| chr17:4533059 | C | T | 1 | a0001c0003 | 8 | HG02258.hp1 HG02630.hp2 HG03098.hp2 others(5): Show |
synonymous_variant | LOW | c.1018C>T | p.Leu340Leu | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 7/13 | 1185/3404 | 1018/1650 | 340/549 | chr17 | 4533059 | |||
| chr17:4533288 | G | A | 1 | a0001c0009 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.1134G>A | p.Val378Val | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/13 | 1301/3404 | 1134/1650 | 378/549 | chr17 | 4533288 | |||
| chr17:4536108 | C | A | 1 | a0001c0005 | 5 | HG00673.hp1 NA18963.hp1 NA18965.hp1 others(2): Show |
synonymous_variant | LOW | c.1377C>A | p.Ala459Ala | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/13 | 1544/3404 | 1377/1650 | 459/549 | chr17 | 4536108 | |||
| chr17:4536153 | G | T | 1 | a0001c0012 | 1 | NA18970.hp2 | synonymous_variant | LOW | c.1422G>T | p.Gly474Gly | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/13 | 1589/3404 | 1422/1650 | 474/549 | chr17 | 4536153 | |||
| chr17:4536328 | C | T | 1 | a0001c0004 | 7 | HG00423.hp2 NA18991.hp1 NA19003.hp2 others(4): Show |
synonymous_variant | LOW | c.1509C>T | p.Tyr503Tyr | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/13 | 1676/3404 | 1509/1650 | 503/549 | chr17 | 4536328 | |||
| chr17:4536388 | G | C | 1 | a0001c0010 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.1569G>C | p.Ala523Ala | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/13 | 1736/3404 | 1569/1650 | 523/549 | chr17 | 4536388 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4498886 | G | T | 1 | a0001c0001t0052 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-162G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | 162 | chr17 | 4498886 | ||||||
| chr17:4498895 | G | C | 30 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(27): Show |
61 | HG00323.hp1 HG01167.hp1 HG01243.hp2 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-153G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | 153 | chr17 | 4498895 | ||||||
| chr17:4498919 | G | C | 6 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0021 others(3): Show |
9 | HG01891.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-129G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | 129 | chr17 | 4498919 | ||||||
| chr17:4499000 | C | T | 8 | a0001c0001t0006 a0001c0001t0031 a0001c0001t0033 others(5): Show |
15 | HG02486.hp1 HG02486.hp2 HG02622.hp1 others(12): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-48C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | chr17 | 4499000 | |||||||
| chr17:4499006 | C | A | 1 | a0001c0001t0036 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | 42 | chr17 | 4499006 | ||||||
| chr17:4499027 | G | C | 1 | a0001c0001t0037 | 1 | NA19085.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | 21 | chr17 | 4499027 | ||||||
| chr17:4537516 | G | A | 1 | a0001c0001t0038 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*68G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 574 | chr17 | 4537516 | ||||||
| chr17:4537612 | A | G | 21 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0014 others(18): Show |
164 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*164A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 670 | chr17 | 4537612 | ||||||
| chr17:4537663 | G | A | 1 | a0001c0001t0039 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*215G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 721 | chr17 | 4537663 | ||||||
| chr17:4537696 | G | A | 1 | a0001c0001t0040 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 754 | chr17 | 4537696 | ||||||
| chr17:4537706 | T | C | 1 | a0001c0001t0020 | 2 | NA18994.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*258T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 764 | chr17 | 4537706 | ||||||
| chr17:4537742 | C | T | 1 | a0001c0001t0030 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 800 | chr17 | 4537742 | ||||||
| chr17:4537743 | G | A | 1 | a0001c0001t0046 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*295G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 801 | chr17 | 4537743 | ||||||
| chr17:4537835 | C | A | 1 | a0001c0001t0047 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*387C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 893 | chr17 | 4537835 | ||||||
| chr17:4537855 | G | A | 1 | a0001c0001t0048 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*407G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 913 | chr17 | 4537855 | ||||||
| chr17:4537895 | G | A | 2 | a0001c0001t0021 a0001c0001t0031 |
2 | HG02630.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*447G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 953 | chr17 | 4537895 | ||||||
| chr17:4537923 | G | A | 2 | a0001c0003t0024 a0001c0003t0041 |
2 | HG02258.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*475G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 981 | chr17 | 4537923 | ||||||
| chr17:4538000 | A | C | 1 | a0001c0001t0035 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1058 | chr17 | 4538000 | ||||||
| chr17:4538014 | C | A | 13 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0018 others(10): Show |
109 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*566C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1072 | chr17 | 4538014 | ||||||
| chr17:4538142 | G | A | 4 | a0001c0001t0015 a0001c0002t0044 a0001c0009t0015 others(1): Show |
5 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*694G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1200 | chr17 | 4538142 | ||||||
| chr17:4538224 | A | C | 1 | a0001c0001t0034 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*776A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1282 | chr17 | 4538224 | ||||||
| chr17:4538241 | C | T | 1 | a0001c0001t0013 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*793C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1299 | chr17 | 4538241 | ||||||
| chr17:4538246 | C | T | 1 | a0001c0001t0029 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*798C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1304 | chr17 | 4538246 | ||||||
| chr17:4538380 | A | C | 6 | a0001c0001t0012 a0001c0001t0015 a0001c0002t0044 others(3): Show |
10 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*932A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1438 | chr17 | 4538380 | ||||||
| chr17:4538423 | C | T | 3 | a0001c0001t0012 a0001c0001t0015 a0001c0009t0015 |
7 | HG02145.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*975C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1481 | chr17 | 4538423 | ||||||
| chr17:4538466 | C | A | 1 | a0001c0001t0035 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1018C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1524 | chr17 | 4538466 | ||||||
| chr17:4538470 | AGGGG | A | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(58): Show |
344 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(341): Show |
3_prime_UTR_variant | MODIFIER | c.*1027_*1030delGGGG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1533 | INFO_REALIGN_3_PRIME | chr17 | 4538470 | |||||
| chr17:4538590 | C | G | 24 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0012 others(21): Show |
170 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1142C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1648 | chr17 | 4538590 | ||||||
| chr17:4538591 | CCTGCACT others(4): Show |
C | 1 | a0001c0001t0018 | 2 | NA19005.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1149_*1159delCTTC others(7): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1655 | INFO_REALIGN_3_PRIME | chr17 | 4538591 | |||||
| chr17:4538626 | C | T | 2 | a0001c0001t0019 a0001c0001t0022 |
3 | HG01891.hp1 HG02922.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1178C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1684 | chr17 | 4538626 | ||||||
| chr17:4538638 | G | A | 1 | a0001c0001t0042 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1190G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1696 | chr17 | 4538638 | ||||||
| chr17:4538748 | G | A | 1 | a0001c0001t0043 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1300G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1806 | chr17 | 4538748 | ||||||
| chr17:4538783 | G | A | 2 | a0001c0001t0049 a0001c0006t0027 |
2 | HG01167.hp1 HG02698.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1335G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1841 | chr17 | 4538783 | ||||||
| chr17:4538793 | C | A | 3 | a0001c0001t0010 a0001c0001t0036 a0001c0001t0052 |
7 | HG00735.hp2 HG01081.hp2 HG01256.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1345C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1851 | chr17 | 4538793 | ||||||
| chr17:4538840 | C | T | 1 | a0001c0001t0051 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1392C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1898 | chr17 | 4538840 | ||||||
| chr17:4538899 | G | C | 1 | a0001c0001t0025 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1451G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1957 | chr17 | 4538899 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4499701 | C | T | 9 | a0001c0001t0011g0361 a0001c0001t0011g0362 a0001c0001t0017g0363 others(6): Show |
9 | HG01891.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.370+284C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4499701 | |||||||
| chr17:4499725 | CCTCTGCG others(1): Show |
C | 7 | a0001c0001t0006g0029 a0001c0001t0006g0033 a0001c0001t0006g0034 others(4): Show |
7 | HG02486.hp1 HG02622.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.370+313_370+320del others(8): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4499725 | ||||||
| chr17:4499757 | C | A | 1 | a0001c0001t0003g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.370+340C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4499757 | |||||||
| chr17:4499839 | G | A | 1 | a0001c0001t0003g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.370+422G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4499839 | |||||||
| chr17:4499873 | C | G | 2 | a0001c0001t0005g0359 a0001c0001t0005g0360 |
2 | HG01346.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.370+456C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4499873 | |||||||
| chr17:4500104 | T | C | 130 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(127): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.370+687T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500104 | |||||||
| chr17:4500576 | A | G | 1 | a0001c0001t0006g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.370+1159A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500576 | |||||||
| chr17:4500580 | AACAC | A | 20 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(17): Show |
23 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.370+1171_370+1174d others(6): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4500580 | ||||||
| chr17:4500707 | T | C | 8 | a0001c0001t0003g0035 a0001c0001t0006g0015 a0001c0001t0006g0158 others(5): Show |
9 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.370+1290T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500707 | |||||||
| chr17:4500708 | G | GC | 68 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(65): Show |
75 | HG00323.hp1 HG00735.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.370+1293dupC | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4500708 | ||||||
| chr17:4500770 | G | T | 1 | a0001c0001t0003g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.370+1353G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500770 | |||||||
| chr17:4500775 | C | T | 42 | a0001c0001t0005g0004 a0001c0001t0005g0170 a0001c0001t0005g0180 others(39): Show |
46 | HG00323.hp1 HG01167.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.370+1358C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500775 | |||||||
| chr17:4500824 | C | T | 6 | a0001c0001t0006g0029 a0001c0001t0006g0034 a0001c0001t0031g0031 others(3): Show |
6 | HG02486.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.370+1407C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500824 | |||||||
| chr17:4500838 | G | T | 1 | a0001c0001t0001g0358 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.370+1421G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500838 | |||||||
| chr17:4500846 | G | A | 236 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(233): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.370+1429G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500846 | |||||||
| chr17:4500964 | C | T | 26 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(23): Show |
29 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.370+1547C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500964 | |||||||
| chr17:4501039 | A | G | 2 | a0001c0001t0004g0045 a0001c0006t0002g0046 |
2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.370+1622A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501039 | |||||||
| chr17:4501087 | G | A | 9 | a0001c0001t0011g0361 a0001c0001t0011g0362 a0001c0001t0017g0363 others(6): Show |
9 | HG01891.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.370+1670G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501087 | |||||||
| chr17:4501113 | G | A | 2 | a0001c0001t0007g0164 a0001c0009t0015g0165 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.370+1696G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501113 | |||||||
| chr17:4501129 | A | G | 2 | a0001c0001t0001g0356 a0001c0001t0002g0357 |
2 | NA18969.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.370+1712A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501129 | |||||||
| chr17:4501263 | T | C | 20 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(17): Show |
23 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.370+1846T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501263 | |||||||
| chr17:4501279 | C | G | 20 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(17): Show |
23 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.370+1862C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501279 | |||||||
| chr17:4501280 | C | T | 2 | a0001c0001t0003g0239 a0001c0001t0003g0240 |
2 | HG01433.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.370+1863C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501280 | |||||||
| chr17:4501322 | CAG | C | 7 | a0001c0001t0001g0014 a0001c0001t0003g0149 a0001c0001t0003g0152 others(4): Show |
8 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.370+1910_370+1911d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4501322 | ||||||
| chr17:4501527 | G | A | 9 | a0001c0001t0011g0361 a0001c0001t0011g0362 a0001c0001t0017g0363 others(6): Show |
9 | HG01891.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.370+2110G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501527 | |||||||
| chr17:4501528 | C | T | 9 | a0001c0001t0011g0361 a0001c0001t0011g0362 a0001c0001t0017g0363 others(6): Show |
9 | HG01891.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.370+2111C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501528 | |||||||
| chr17:4501636 | T | C | 2 | a0001c0001t0001g0242 a0001c0001t0002g0241 |
2 | NA18948.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.370+2219T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501636 | |||||||
| chr17:4501919 | A | G | 6 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
6 | HG02083.hp1 HG02523.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.370+2502A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501919 | |||||||
| chr17:4502097 | T | C | 358 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(355): Show |
392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.370+2680T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502097 | |||||||
| chr17:4502200 | A | AC | 138 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0022 others(135): Show |
153 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.370+2789dupC | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4502200 | ||||||
| chr17:4502324 | G | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0022 others(136): Show |
154 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.370+2907G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502324 | |||||||
| chr17:4502366 | T | G | 1 | a0001c0001t0002g0047 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.370+2949T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502366 | |||||||
| chr17:4502379 | CA | C | 144 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(141): Show |
154 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.370+2978delA | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4502379 | ||||||
| chr17:4502379 | CAA | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0022 others(149): Show |
168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.370+2977_370+2978d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4502379 | ||||||
| chr17:4502418 | ATGT | A | 3 | a0001c0001t0051g0193 a0001c0006t0002g0195 a0001c0007t0004g0194 |
3 | HG01884.hp2 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.370+3006_370+3008d others(5): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4502418 | ||||||
| chr17:4502428 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0242 a0001c0001t0001g0244 others(27): Show |
34 | HG00423.hp2 HG02004.hp2 HG02071.hp2 others(31): Show |
intron_variant | MODIFIER | c.370+3011T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502428 | |||||||
| chr17:4502510 | C | T | 1 | a0001c0001t0048g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.370+3093C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502510 | |||||||
| chr17:4502569 | C | G | 5 | a0001c0001t0001g0235 a0001c0001t0003g0237 a0001c0001t0004g0234 others(2): Show |
5 | HG02145.hp2 HG02683.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.370+3152C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502569 | |||||||
| chr17:4502775 | C | G | 1 | a0001c0001t0003g0154 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.370+3358C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502775 | |||||||
| chr17:4502775 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | NA18983.hp2 NA19063.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.370+3358C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502775 | |||||||
| chr17:4502854 | A | G | 351 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(348): Show |
383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.370+3437A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502854 | |||||||
| chr17:4502910 | G | A | 9 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): Show |
11 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.370+3493G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502910 | |||||||
| chr17:4502950 | C | T | 1 | a0001c0001t0010g0041 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.370+3533C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502950 | |||||||
| chr17:4502954 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.370+3537C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502954 | |||||||
| chr17:4503161 | G | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(157): Show |
179 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.370+3744G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503161 | |||||||
| chr17:4503166 | C | T | 3 | a0001c0001t0051g0193 a0001c0006t0002g0195 a0001c0007t0004g0194 |
3 | HG01884.hp2 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.370+3749C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503166 | |||||||
| chr17:4503175 | G | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(157): Show |
179 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.370+3758G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503175 | |||||||
| chr17:4503212 | G | A | 1 | a0001c0001t0016g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.370+3795G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503212 | |||||||
| chr17:4503678 | G | A | 27 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0066 others(24): Show |
31 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.370+4261G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503678 | |||||||
| chr17:4503795 | C | T | 2 | a0001c0001t0009g0191 a0001c0006t0027g0192 |
2 | HG01167.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.370+4378C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503795 | |||||||
| chr17:4503924 | G | A | 6 | a0001c0001t0006g0029 a0001c0001t0006g0034 a0001c0001t0031g0031 others(3): Show |
6 | HG02486.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.370+4507G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503924 | |||||||
| chr17:4503982 | C | CT | 85 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0026 others(82): Show |
92 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.370+4580dupT | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4503982 | ||||||
| chr17:4503982 | C | CTT | 119 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(116): Show |
128 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.370+4579_370+4580d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4503982 | ||||||
| chr17:4503982 | C | CTTT | 53 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(50): Show |
61 | HG00323.hp1 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.370+4578_370+4580d others(5): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4503982 | ||||||
| chr17:4504080 | G | C | 1 | a0001c0001t0001g0265 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.370+4663G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504080 | |||||||
| chr17:4504210 | C | T | 1 | a0001c0001t0040g0264 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.370+4793C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504210 | |||||||
| chr17:4504299 | T | C | 360 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(357): Show |
394 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.370+4882T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504299 | |||||||
| chr17:4504379 | C | A | 1 | a0001c0001t0003g0197 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.370+4962C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504379 | |||||||
| chr17:4504417 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0022 others(146): Show |
163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.370+5000A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504417 | |||||||
| chr17:4504435 | CAT | C | 2 | a0001c0001t0003g0008 a0001c0001t0003g0059 |
3 | HG01361.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.370+5020_370+5021d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4504435 | ||||||
| chr17:4504464 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.370+5047G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504464 | |||||||
| chr17:4504709 | C | T | 1 | a0001c0001t0004g0224 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.370+5292C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504709 | |||||||
| chr17:4504711 | C | T | 140 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(137): Show |
150 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.370+5294C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504711 | |||||||
| chr17:4505046 | C | T | 2 | a0001c0001t0006g0033 a0001c0001t0036g0225 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.370+5629C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505046 | |||||||
| chr17:4505146 | C | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0248 a0001c0001t0001g0256 others(9): Show |
15 | HG00558.hp2 HG00642.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.370+5729C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505146 | |||||||
| chr17:4505201 | C | A | 2 | a0001c0001t0009g0166 a0001c0001t0009g0167 |
2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.370+5784C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505201 | |||||||
| chr17:4505404 | G | A | 1 | a0001c0008t0004g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.370+5987G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505404 | |||||||
| chr17:4505415 | C | G | 4 | a0001c0001t0001g0230 a0001c0001t0003g0231 a0001c0002t0044g0233 others(1): Show |
4 | HG01243.hp1 HG02647.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.370+5998C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505415 | |||||||
| chr17:4505431 | A | G | 2 | a0001c0001t0005g0190 a0001c0001t0008g0005 |
4 | NA18945.hp2 NA18980.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.370+6014A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505431 | |||||||
| chr17:4505482 | G | A | 1 | a0001c0001t0029g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.370+6065G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505482 | |||||||
| chr17:4505516 | A | G | 1 | a0001c0001t0004g0224 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.370+6099A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505516 | |||||||
| chr17:4505526 | G | C | 35 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0196 others(32): Show |
37 | HG00099.hp1 HG00280.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.370+6109G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505526 | |||||||
| chr17:4505549 | G | A | 4 | a0001c0001t0007g0178 a0001c0001t0015g0176 a0001c0001t0028g0179 others(1): Show |
4 | HG01884.hp1 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.370+6132G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505549 | |||||||
| chr17:4505736 | G | T | 160 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(157): Show |
174 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.370+6319G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505736 | |||||||
| chr17:4505793 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0288 a0001c0001t0002g0287 |
4 | NA18946.hp2 NA18948.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.370+6376G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505793 | |||||||
| chr17:4505918 | G | A | 1 | a0001c0001t0040g0264 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.370+6501G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505918 | |||||||
| chr17:4506078 | C | A | 1 | a0001c0001t0002g0198 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.370+6661C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506078 | |||||||
| chr17:4506158 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.370+6741C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506158 | |||||||
| chr17:4506171 | T | C | 2 | a0001c0001t0003g0051 a0001c0001t0003g0052 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.370+6754T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506171 | |||||||
| chr17:4506236 | G | A | 2 | a0001c0001t0006g0033 a0001c0001t0036g0225 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.370+6819G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506236 | |||||||
| chr17:4506251 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0004g0224 a0001c0013t0045g0223 |
3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.370+6834C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506251 | |||||||
| chr17:4506362 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.371-6885T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506362 | |||||||
| chr17:4506442 | G | C | 2 | a0001c0001t0011g0362 a0001c0001t0017g0363 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.371-6805G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506442 | |||||||
| chr17:4506471 | G | T | 1 | a0001c0001t0001g0344 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.371-6776G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506471 | |||||||
| chr17:4506581 | C | T | 1 | a0001c0002t0004g0236 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.371-6666C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506581 | |||||||
| chr17:4506774 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.371-6473T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506774 | |||||||
| chr17:4506961 | G | A | 3 | a0001c0001t0003g0208 a0001c0001t0009g0191 a0001c0006t0027g0192 |
3 | HG01167.hp1 HG02109.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.371-6286G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506961 | |||||||
| chr17:4507187 | C | T | 95 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0055 others(92): Show |
101 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.371-6060C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507187 | |||||||
| chr17:4507188 | G | A | 17 | a0001c0001t0003g0035 a0001c0001t0005g0170 a0001c0001t0007g0172 others(14): Show |
17 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.371-6059G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507188 | |||||||
| chr17:4507212 | G | A | 3 | a0001c0004t0002g0290 a0001c0004t0002g0291 a0001c0004t0002g0292 |
3 | NA19003.hp2 NA19010.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.371-6035G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507212 | |||||||
| chr17:4507331 | A | C | 2 | a0001c0001t0001g0289 a0001c0001t0002g0341 |
2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.371-5916A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507331 | |||||||
| chr17:4507364 | C | T | 6 | a0001c0001t0005g0170 a0001c0001t0007g0172 a0001c0001t0007g0173 others(3): Show |
6 | HG01891.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.371-5883C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507364 | |||||||
| chr17:4507398 | C | A | 5 | a0001c0001t0001g0199 a0001c0001t0001g0210 a0001c0001t0002g0075 others(2): Show |
5 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.371-5849C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507398 | |||||||
| chr17:4507418 | A | C | 3 | a0001c0001t0001g0222 a0001c0001t0004g0224 a0001c0013t0045g0223 |
3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5829A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507418 | |||||||
| chr17:4507420 | A | G | 3 | a0001c0001t0001g0222 a0001c0001t0004g0224 a0001c0013t0045g0223 |
3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5827A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507420 | |||||||
| chr17:4507461 | C | T | 12 | a0001c0001t0003g0237 a0001c0001t0004g0045 a0001c0001t0004g0238 others(9): Show |
13 | HG02055.hp2 HG02486.hp2 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.371-5786C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507461 | |||||||
| chr17:4507552 | T | G | 1 | a0001c0001t0002g0293 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.371-5695T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507552 | |||||||
| chr17:4507561 | A | C | 15 | a0001c0001t0001g0262 a0001c0001t0003g0237 a0001c0001t0004g0045 others(12): Show |
16 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.371-5686A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507561 | |||||||
| chr17:4507628 | G | A | 2 | a0001c0001t0006g0033 a0001c0001t0036g0225 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.371-5619G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507628 | |||||||
| chr17:4507670 | G | A | 2 | a0001c0001t0006g0033 a0001c0001t0036g0225 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.371-5577G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507670 | |||||||
| chr17:4507766 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.371-5481G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507766 | |||||||
| chr17:4507831 | C | T | 6 | a0001c0001t0006g0029 a0001c0001t0006g0034 a0001c0001t0031g0031 others(3): Show |
6 | HG02486.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.371-5416C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507831 | |||||||
| chr17:4508022 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0004g0224 a0001c0013t0045g0223 |
3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5225C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508022 | |||||||
| chr17:4508118 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0004g0224 a0001c0013t0045g0223 |
3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5129C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508118 | |||||||
| chr17:4508139 | A | G | 3 | a0001c0001t0001g0222 a0001c0001t0004g0224 a0001c0013t0045g0223 |
3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5108A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508139 | |||||||
| chr17:4508210 | A | T | 95 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0055 others(92): Show |
101 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.371-5037A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508210 | |||||||
| chr17:4508211 | T | C | 3 | a0001c0001t0001g0222 a0001c0001t0004g0224 a0001c0013t0045g0223 |
3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5036T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508211 | |||||||
| chr17:4508230 | T | C | 3 | a0001c0001t0001g0222 a0001c0001t0004g0224 a0001c0013t0045g0223 |
3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5017T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508230 | |||||||
| chr17:4508534 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(270): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.371-4713A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508534 | |||||||
| chr17:4508561 | G | T | 1 | a0001c0008t0004g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.371-4686G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508561 | |||||||
| chr17:4508575 | C | T | 1 | a0001c0001t0003g0017 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.371-4672C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508575 | |||||||
| chr17:4508586 | G | C | 22 | a0001c0001t0001g0142 a0001c0001t0001g0226 a0001c0001t0001g0230 others(19): Show |
23 | HG00558.hp1 HG01243.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.371-4661G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508586 | |||||||
| chr17:4508649 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.371-4598C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508649 | |||||||
| chr17:4508683 | G | A | 4 | a0001c0001t0009g0166 a0001c0001t0009g0167 a0001c0001t0009g0169 others(1): Show |
4 | HG02258.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.371-4564G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508683 | |||||||
| chr17:4508760 | C | T | 1 | a0001c0005t0002g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.371-4487C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508760 | |||||||
| chr17:4508984 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0002g0340 a0001c0004t0002g0124 |
3 | HG02165.hp2 NA19004.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.371-4263C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508984 | |||||||
| chr17:4508996 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.371-4251G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508996 | |||||||
| chr17:4508997 | A | G | 1 | a0001c0001t0002g0058 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.371-4250A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508997 | |||||||
| chr17:4508998 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.371-4249G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508998 | |||||||
| chr17:4509038 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.371-4209G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4509038 | |||||||
| chr17:4509425 | G | A | 12 | a0001c0001t0005g0004 a0001c0001t0005g0180 a0001c0001t0005g0185 others(9): Show |
16 | HG00323.hp1 HG01257.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.371-3822G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4509425 | |||||||
| chr17:4509575 | G | A | 1 | a0001c0001t0009g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.371-3672G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4509575 | |||||||
| chr17:4509602 | GGCCCAA | G | 8 | a0001c0001t0007g0178 a0001c0001t0009g0166 a0001c0001t0009g0167 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.371-3641_371-3636d others(8): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4509602 | ||||||
| chr17:4509720 | C | T | 3 | a0001c0001t0007g0178 a0001c0001t0028g0179 a0001c0003t0005g0177 |
3 | HG01884.hp1 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.371-3527C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4509720 | |||||||
| chr17:4509729 | T | C | 4 | a0001c0001t0009g0166 a0001c0001t0009g0167 a0001c0001t0009g0169 others(1): Show |
4 | HG02258.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.371-3518T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4509729 | |||||||
| chr17:4510037 | G | A | 2 | a0001c0001t0003g0051 a0001c0001t0003g0052 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.371-3210G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510037 | |||||||
| chr17:4510093 | G | A | 1 | a0001c0001t0002g0266 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.371-3154G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510093 | |||||||
| chr17:4510096 | C | T | 1 | a0001c0001t0004g0056 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.371-3151C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510096 | |||||||
| chr17:4510135 | C | A | 2 | a0001c0001t0006g0158 a0001c0002t0011g0364 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.371-3112C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510135 | |||||||
| chr17:4510147 | C | T | 2 | a0001c0001t0005g0185 a0001c0001t0009g0186 |
2 | HG00323.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.371-3100C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510147 | |||||||
| chr17:4510187 | C | T | 17 | a0001c0001t0003g0035 a0001c0001t0005g0170 a0001c0001t0007g0172 others(14): Show |
17 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.371-3060C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510187 | |||||||
| chr17:4510248 | C | A | 9 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0003g0231 others(6): Show |
10 | HG01243.hp1 HG02451.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.371-2999C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510248 | |||||||
| chr17:4510581 | T | C | 2 | a0001c0001t0002g0083 a0001c0014t0002g0140 |
2 | HG00438.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.371-2666T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510581 | |||||||
| chr17:4510594 | C | T | 2 | a0001c0001t0006g0033 a0001c0001t0036g0225 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.371-2653C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510594 | |||||||
| chr17:4510732 | A | G | 222 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(219): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.371-2515A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510732 | |||||||
| chr17:4510840 | C | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0066 a0001c0001t0001g0067 others(18): Show |
23 | HG00099.hp1 HG00673.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.371-2407C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510840 | |||||||
| chr17:4510874 | C | T | 6 | a0001c0001t0001g0282 a0001c0001t0001g0339 a0001c0001t0002g0021 others(3): Show |
7 | HG00597.hp1 NA18941.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.371-2373C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510874 | |||||||
| chr17:4510944 | T | C | 1 | a0001c0001t0002g0294 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.371-2303T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510944 | |||||||
| chr17:4511047 | T | C | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0004t0002g0267 |
3 | HG00423.hp2 HG02071.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.371-2200T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511047 | |||||||
| chr17:4511154 | A | G | 1 | a0001c0001t0004g0229 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.371-2093A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511154 | |||||||
| chr17:4511293 | C | T | 2 | a0001c0001t0003g0051 a0001c0001t0003g0052 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.371-1954C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511293 | |||||||
| chr17:4511395 | G | A | 16 | a0001c0001t0003g0035 a0001c0001t0005g0170 a0001c0001t0007g0172 others(13): Show |
16 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.371-1852G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511395 | |||||||
| chr17:4511499 | A | C | 1 | a0001c0001t0009g0166 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.371-1748A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511499 | |||||||
| chr17:4511753 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.371-1494G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511753 | |||||||
| chr17:4511793 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.371-1454G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511793 | |||||||
| chr17:4511796 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.371-1451C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511796 | |||||||
| chr17:4511808 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0003g0208 |
2 | HG03710.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.371-1439A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511808 | |||||||
| chr17:4511812 | C | T | 1 | a0001c0001t0047g0343 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.371-1435C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511812 | |||||||
| chr17:4511883 | A | AACACCCT others(3): Show |
1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.371-1364_371-1363i others(12): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511883 | |||||||
| chr17:4511885 | A | C | 1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.371-1362A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511885 | |||||||
| chr17:4511893 | T | C | 1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.371-1354T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511893 | |||||||
| chr17:4511922 | C | T | 1 | a0001c0001t0002g0281 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.371-1325C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511922 | |||||||
| chr17:4511976 | G | A | 2 | a0001c0001t0001g0268 a0001c0004t0002g0267 |
2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.371-1271G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511976 | |||||||
| chr17:4512020 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0004g0224 a0001c0013t0045g0223 |
3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-1227C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512020 | |||||||
| chr17:4512041 | C | T | 1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.371-1206C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512041 | |||||||
| chr17:4512064 | T | C | 1 | a0001c0014t0002g0140 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.371-1183T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512064 | |||||||
| chr17:4512099 | T | A | 2 | a0001c0002t0004g0347 a0001c0002t0004g0348 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.371-1148T>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512099 | |||||||
| chr17:4512176 | A | G | 1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.371-1071A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512176 | |||||||
| chr17:4512177 | G | A | 1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.371-1070G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512177 | |||||||
| chr17:4512422 | G | A | 19 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0129 others(16): Show |
22 | HG01109.hp1 HG01123.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.371-825G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512422 | |||||||
| chr17:4512462 | G | A | 2 | a0001c0001t0003g0051 a0001c0001t0003g0052 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.371-785G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512462 | |||||||
| chr17:4512531 | A | C | 98 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(95): Show |
106 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.371-716A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512531 | |||||||
| chr17:4512636 | G | GTGTGTGT others(19): Show |
2 | a0001c0001t0007g0178 a0001c0001t0028g0179 |
2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.371-600_371-575dup others(26): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4512636 | ||||||
| chr17:4512640 | GTGTGCGT others(15): Show |
G | 1 | a0001c0001t0014g0337 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.371-602_371-581del others(22): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4512640 | ||||||
| chr17:4512647 | T | C | 19 | a0001c0001t0001g0235 a0001c0001t0004g0234 a0001c0001t0005g0004 others(16): Show |
23 | HG00323.hp1 HG01167.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.371-600T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512647 | |||||||
| chr17:4512649 | C | T | 1 | a0001c0006t0002g0046 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.371-598C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512649 | |||||||
| chr17:4512673 | C | CGAGCGGG others(13): Show |
3 | a0001c0001t0001g0222 a0001c0001t0004g0224 a0001c0013t0045g0223 |
3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-573_371-572ins others(20): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4512673 | ||||||
| chr17:4512675 | C | CGCGGGTG others(13): Show |
2 | a0001c0001t0006g0033 a0001c0001t0036g0225 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.371-571_371-570ins others(20): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4512675 | ||||||
| chr17:4512675 | C | T | 4 | a0001c0001t0001g0222 a0001c0001t0003g0052 a0001c0001t0004g0224 others(1): Show |
4 | HG02559.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.371-572C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512675 | |||||||
| chr17:4512677 | T | C | 143 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(140): Show |
152 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.371-570T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512677 | |||||||
| chr17:4512708 | A | G | 1 | a0001c0001t0049g0108 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.371-539A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512708 | |||||||
| chr17:4512742 | A | G | 23 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0129 others(20): Show |
25 | HG01081.hp2 HG01123.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.371-505A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512742 | |||||||
| chr17:4512758 | G | A | 1 | a0001c0001t0012g0086 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.371-489G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512758 | |||||||
| chr17:4512808 | G | A | 9 | a0001c0001t0001g0226 a0001c0001t0001g0230 a0001c0001t0003g0231 others(6): Show |
10 | HG01243.hp1 HG02451.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.371-439G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512808 | |||||||
| chr17:4512825 | C | G | 11 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0002g0012 others(8): Show |
12 | HG01257.hp1 HG01258.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.371-422C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512825 | |||||||
| chr17:4512833 | TC | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0196 a0001c0001t0001g0214 others(21): Show |
27 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.371-410delC | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4512833 | ||||||
| chr17:4512862 | C | T | 7 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(4): Show |
7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.371-385C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512862 | |||||||
| chr17:4512925 | G | A | 1 | a0001c0001t0003g0094 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.371-322G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512925 | |||||||
| chr17:4512929 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(133): Show |
152 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.371-318T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512929 | |||||||
| chr17:4512961 | C | G | 1 | a0001c0006t0002g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.371-286C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512961 | |||||||
| chr17:4512968 | G | A | 2 | a0001c0001t0005g0180 a0001c0001t0052g0181 |
2 | HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.371-279G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512968 | |||||||
| chr17:4512999 | G | A | 141 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(138): Show |
150 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.371-248G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512999 | |||||||
| chr17:4513121 | C | A | 3 | a0001c0001t0001g0262 a0001c0001t0004g0260 a0001c0001t0016g0261 |
3 | HG01109.hp2 HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.371-126C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4513121 | |||||||
| chr17:4513340 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.436+28C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513340 | |||||||
| chr17:4513343 | G | A | 120 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0016 others(117): Show |
127 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.436+31G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513343 | |||||||
| chr17:4513357 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.436+45G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513357 | |||||||
| chr17:4513379 | T | C | 142 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(139): Show |
151 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.436+67T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513379 | |||||||
| chr17:4513574 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.436+262G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513574 | |||||||
| chr17:4513685 | G | A | 141 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(138): Show |
150 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.436+373G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513685 | |||||||
| chr17:4513766 | T | G | 1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.436+454T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513766 | |||||||
| chr17:4513800 | C | T | 1 | a0001c0001t0040g0264 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.436+488C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513800 | |||||||
| chr17:4513821 | G | A | 27 | a0001c0001t0001g0142 a0001c0001t0001g0226 a0001c0001t0001g0230 others(24): Show |
28 | HG01243.hp1 HG02074.hp2 HG02165.hp2 others(25): Show |
intron_variant | MODIFIER | c.436+509G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513821 | |||||||
| chr17:4513956 | C | T | 78 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0055 others(75): Show |
84 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.436+644C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513956 | |||||||
| chr17:4513963 | G | C | 86 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(83): Show |
94 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.436+651G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513963 | |||||||
| chr17:4513997 | C | G | 10 | a0001c0001t0003g0035 a0001c0001t0011g0361 a0001c0001t0011g0362 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+685C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513997 | |||||||
| chr17:4514186 | A | C | 10 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(7): Show |
10 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+874A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514186 | |||||||
| chr17:4514238 | C | G | 5 | a0001c0001t0001g0222 a0001c0001t0004g0224 a0001c0001t0006g0033 others(2): Show |
5 | HG02559.hp1 HG02818.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+926C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514238 | |||||||
| chr17:4514274 | G | T | 2 | a0001c0001t0007g0178 a0001c0001t0028g0179 |
2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.436+962G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514274 | |||||||
| chr17:4514283 | C | T | 1 | a0001c0008t0004g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.436+971C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514283 | |||||||
| chr17:4514414 | C | A | 1 | a0001c0001t0003g0040 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.436+1102C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514414 | |||||||
| chr17:4514601 | C | T | 1 | a0001c0008t0004g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.436+1289C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514601 | |||||||
| chr17:4514892 | C | T | 20 | a0001c0001t0001g0142 a0001c0001t0001g0226 a0001c0001t0001g0230 others(17): Show |
21 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.436+1580C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514892 | |||||||
| chr17:4515044 | G | T | 76 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0016 others(73): Show |
82 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.436+1732G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515044 | |||||||
| chr17:4515051 | C | T | 2 | a0001c0001t0003g0153 a0001c0001t0025g0174 |
2 | HG00323.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.436+1739C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515051 | |||||||
| chr17:4515104 | G | A | 1 | a0001c0001t0002g0338 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.436+1792G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515104 | |||||||
| chr17:4515189 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.436+1877T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515189 | |||||||
| chr17:4515256 | G | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(246): Show |
272 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.436+1944G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515256 | |||||||
| chr17:4515328 | A | T | 1 | a0001c0001t0001g0288 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.436+2016A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515328 | |||||||
| chr17:4515410 | C | T | 1 | a0001c0001t0009g0186 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.436+2098C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515410 | |||||||
| chr17:4515630 | T | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(243): Show |
269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2318T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515630 | |||||||
| chr17:4515726 | G | A | 10 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(7): Show |
10 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+2414G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515726 | |||||||
| chr17:4515729 | A | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(243): Show |
269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2417A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515729 | |||||||
| chr17:4515795 | T | TG | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(243): Show |
269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2485dupG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4515795 | ||||||
| chr17:4515834 | G | A | 5 | a0001c0001t0005g0170 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+2522G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515834 | |||||||
| chr17:4515834 | G | T | 1 | a0001c0001t0029g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.436+2522G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515834 | |||||||
| chr17:4515986 | A | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(243): Show |
269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2674A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515986 | |||||||
| chr17:4515995 | G | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(243): Show |
269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2683G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515995 | |||||||
| chr17:4516018 | A | C | 1 | a0001c0001t0002g0085 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.436+2706A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516018 | |||||||
| chr17:4516022 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(243): Show |
269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2710C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516022 | |||||||
| chr17:4516051 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(235): Show |
259 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.436+2739C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516051 | |||||||
| chr17:4516058 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(243): Show |
269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2746A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516058 | |||||||
| chr17:4516229 | G | A | 2 | a0001c0001t0006g0033 a0001c0001t0036g0225 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.436+2917G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516229 | |||||||
| chr17:4516288 | TG | T | 10 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(7): Show |
10 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+2979delG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516288 | ||||||
| chr17:4516305 | C | G | 10 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(7): Show |
10 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+2993C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516305 | |||||||
| chr17:4516313 | C | CA | 5 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0010g0041 others(2): Show |
7 | HG00735.hp2 HG00741.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+3001_436+3002i others(3): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516313 | |||||||
| chr17:4516314 | C | A | 363 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(360): Show |
395 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.436+3002C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516314 | |||||||
| chr17:4516316 | C | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0010g0041 others(2): Show |
7 | HG00735.hp2 HG00741.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+3004C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516316 | |||||||
| chr17:4516316 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0004g0224 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.436+3014_436+3031d others(20): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516316 | ||||||
| chr17:4516316 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.436+3012_436+3031d others(22): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516316 | ||||||
| chr17:4516316 | CA | C | 75 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0066 others(72): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.436+3031delA | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516316 | ||||||
| chr17:4516316 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0052g0181 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.436+3018_436+3031d others(16): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516316 | ||||||
| chr17:4516326 | A | C | 5 | a0001c0001t0005g0170 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+3014A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516326 | |||||||
| chr17:4516328 | A | C | 1 | a0001c0001t0003g0037 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.436+3016A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516328 | |||||||
| chr17:4516330 | A | C | 21 | a0001c0001t0001g0235 a0001c0001t0001g0259 a0001c0001t0002g0115 others(18): Show |
21 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.436+3018A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516330 | |||||||
| chr17:4516331 | A | C | 65 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0066 others(62): Show |
74 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.436+3019A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516331 | |||||||
| chr17:4516332 | A | C | 21 | a0001c0001t0001g0142 a0001c0001t0001g0226 a0001c0001t0001g0230 others(18): Show |
22 | HG00558.hp1 HG00597.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.436+3020A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516332 | |||||||
| chr17:4516333 | A | C | 14 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0207 others(11): Show |
14 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.436+3021A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516333 | |||||||
| chr17:4516334 | A | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(207): Show |
232 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.436+3022A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516334 | |||||||
| chr17:4516335 | A | C | 11 | a0001c0001t0001g0129 a0001c0001t0001g0248 a0001c0001t0002g0047 others(8): Show |
11 | HG00544.hp1 HG01978.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.436+3023A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516335 | |||||||
| chr17:4516336 | A | C | 21 | a0001c0001t0001g0142 a0001c0001t0001g0226 a0001c0001t0001g0230 others(18): Show |
22 | HG00558.hp1 HG00597.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.436+3024A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516336 | |||||||
| chr17:4516337 | A | C | 5 | a0001c0001t0001g0207 a0001c0001t0004g0126 a0001c0002t0004g0070 others(2): Show |
5 | HG02258.hp1 HG02280.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+3025A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516337 | |||||||
| chr17:4516338 | A | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(206): Show |
231 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.436+3026A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516338 | |||||||
| chr17:4516339 | A | C | 11 | a0001c0001t0001g0129 a0001c0001t0001g0248 a0001c0001t0002g0047 others(8): Show |
11 | HG00544.hp1 HG01978.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.436+3027A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516339 | |||||||
| chr17:4516340 | A | C | 21 | a0001c0001t0001g0142 a0001c0001t0001g0226 a0001c0001t0001g0230 others(18): Show |
22 | HG00558.hp1 HG00597.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.436+3028A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516340 | |||||||
| chr17:4516340 | AAAAC | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(205): Show |
230 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.436+3032_436+3035d others(6): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516340 | ||||||
| chr17:4516341 | A | C | 13 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(10): Show |
13 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.436+3029A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516341 | |||||||
| chr17:4516341 | AAAC | A | 12 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0248 others(9): Show |
12 | HG00544.hp1 HG01978.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+3032_436+3034d others(5): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516341 | ||||||
| chr17:4516342 | A | C | 1 | a0001c0001t0003g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.436+3030A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516342 | |||||||
| chr17:4516342 | AAC | A | 21 | a0001c0001t0001g0142 a0001c0001t0001g0226 a0001c0001t0001g0230 others(18): Show |
22 | HG00558.hp1 HG00597.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.436+3032_436+3033d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516342 | ||||||
| chr17:4516343 | A | C | 1 | a0001c0001t0001g0259 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.436+3031A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516343 | |||||||
| chr17:4516343 | AC | A | 16 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(13): Show |
16 | HG01081.hp2 HG01099.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.436+3032delC | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516343 | |||||||
| chr17:4516344 | C | A | 9 | a0001c0001t0001g0222 a0001c0001t0001g0259 a0001c0001t0003g0052 others(6): Show |
9 | HG02559.hp1 HG02818.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.436+3032C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516344 | |||||||
| chr17:4516352 | C | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(253): Show |
279 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.436+3040C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516352 | |||||||
| chr17:4516367 | G | T | 1 | a0001c0001t0010g0200 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.436+3055G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516367 | |||||||
| chr17:4516394 | T | A | 10 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(7): Show |
10 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+3082T>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516394 | |||||||
| chr17:4516447 | G | A | 1 | a0001c0001t0005g0360 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.436+3135G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516447 | |||||||
| chr17:4516489 | T | C | 1 | a0001c0001t0025g0174 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.436+3177T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516489 | |||||||
| chr17:4516556 | G | A | 5 | a0001c0001t0005g0170 a0001c0001t0007g0172 a0001c0001t0007g0173 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+3244G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516556 | |||||||
| chr17:4516581 | C | T | 15 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(12): Show |
15 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.436+3269C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516581 | |||||||
| chr17:4516602 | C | CG | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(250): Show |
276 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(273): Show |
intron_variant | MODIFIER | c.436+3291dupG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516602 | ||||||
| chr17:4516646 | T | C | 10 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(7): Show |
10 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+3334T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516646 | |||||||
| chr17:4516653 | T | G | 1 | a0001c0001t0001g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.436+3341T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516653 | |||||||
| chr17:4516691 | A | G | 1 | a0001c0001t0010g0041 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.436+3379A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516691 | |||||||
| chr17:4516702 | C | T | 1 | a0001c0002t0044g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.436+3390C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516702 | |||||||
| chr17:4516757 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(299): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.436+3445A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516757 | |||||||
| chr17:4516885 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.436+3573A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516885 | |||||||
| chr17:4516887 | C | T | 9 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(6): Show |
9 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.436+3575C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516887 | |||||||
| chr17:4516905 | C | T | 1 | a0001c0001t0030g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.436+3593C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516905 | |||||||
| chr17:4516963 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.436+3651G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516963 | |||||||
| chr17:4517023 | C | T | 1 | a0001c0001t0009g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.436+3711C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517023 | |||||||
| chr17:4517262 | T | C | 25 | a0001c0001t0001g0142 a0001c0001t0001g0226 a0001c0001t0001g0230 others(22): Show |
26 | HG00558.hp1 HG00597.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.436+3950T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517262 | |||||||
| chr17:4517308 | C | CT | 9 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(6): Show |
9 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.436+3996_436+3997i others(3): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517308 | |||||||
| chr17:4517383 | C | T | 1 | a0001c0001t0007g0173 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.436+4071C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517383 | |||||||
| chr17:4517386 | G | A | 9 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(6): Show |
9 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.436+4074G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517386 | |||||||
| chr17:4517411 | A | C | 3 | a0001c0001t0001g0262 a0001c0001t0004g0260 a0001c0001t0016g0261 |
3 | HG01109.hp2 HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.436+4099A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517411 | |||||||
| chr17:4517415 | T | C | 1 | a0001c0008t0004g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.436+4103T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517415 | |||||||
| chr17:4517428 | C | T | 2 | a0001c0001t0006g0033 a0001c0001t0036g0225 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.436+4116C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517428 | |||||||
| chr17:4517469 | A | G | 2 | a0001c0001t0006g0033 a0001c0001t0036g0225 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.436+4157A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517469 | |||||||
| chr17:4517478 | G | T | 13 | a0001c0001t0003g0035 a0001c0001t0007g0172 a0001c0001t0007g0173 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.436+4166G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517478 | |||||||
| chr17:4517528 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.436+4216C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517528 | |||||||
| chr17:4517672 | T | C | 5 | a0001c0001t0001g0336 a0001c0001t0002g0089 a0001c0001t0002g0127 others(2): Show |
5 | HG00558.hp1 HG00597.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+4360T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517672 | |||||||
| chr17:4517999 | C | A | 4 | a0001c0001t0001g0080 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
4 | HG00733.hp2 HG01074.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+4687C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517999 | |||||||
| chr17:4518262 | C | T | 66 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0055 others(63): Show |
71 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.436+4950C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518262 | |||||||
| chr17:4518290 | T | C | 356 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(353): Show |
390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.436+4978T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518290 | |||||||
| chr17:4518340 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(148): Show |
166 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.436+5028T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518340 | |||||||
| chr17:4518396 | T | C | 5 | a0001c0001t0001g0222 a0001c0001t0004g0224 a0001c0001t0006g0033 others(2): Show |
5 | HG02559.hp1 HG02818.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+5084T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518396 | |||||||
| chr17:4518501 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.436+5189C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518501 | |||||||
| chr17:4518509 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(138): Show |
156 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.436+5197C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518509 | |||||||
| chr17:4518535 | A | AAAAC | 20 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(17): Show |
20 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.436+5235_436+5238d others(6): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4518535 | ||||||
| chr17:4518637 | T | C | 5 | a0001c0001t0001g0226 a0001c0001t0004g0019 a0001c0001t0004g0227 others(2): Show |
6 | HG02451.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+5325T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518637 | |||||||
| chr17:4518642 | G | T | 7 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(4): Show |
7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.436+5330G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518642 | |||||||
| chr17:4518658 | C | T | 1 | a0001c0009t0015g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.436+5346C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518658 | |||||||
| chr17:4518669 | A | T | 1 | a0001c0001t0002g0280 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.436+5357A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518669 | |||||||
| chr17:4518795 | G | A | 91 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0055 others(88): Show |
96 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.436+5483G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518795 | |||||||
| chr17:4518834 | C | T | 80 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0055 others(77): Show |
86 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.436+5522C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518834 | |||||||
| chr17:4518967 | G | A | 1 | a0001c0001t0038g0221 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.436+5655G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518967 | |||||||
| chr17:4519062 | G | A | 1 | a0001c0001t0004g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.436+5750G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519062 | |||||||
| chr17:4519065 | C | T | 2 | a0001c0001t0001g0334 a0001c0001t0014g0333 |
2 | NA20905.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.436+5753C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519065 | |||||||
| chr17:4519222 | G | A | 3 | a0001c0001t0007g0172 a0001c0001t0007g0173 a0001c0009t0015g0165 |
3 | HG01891.hp2 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.437-5835G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519222 | |||||||
| chr17:4519248 | C | T | 20 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(17): Show |
20 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.437-5809C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519248 | |||||||
| chr17:4519338 | G | A | 5 | a0001c0001t0001g0119 a0001c0001t0002g0012 a0001c0001t0002g0116 others(2): Show |
6 | HG01257.hp1 HG01258.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-5719G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519338 | |||||||
| chr17:4519357 | C | T | 1 | a0001c0004t0002g0292 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.437-5700C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519357 | |||||||
| chr17:4519701 | TCAAA | T | 3 | a0001c0001t0001g0230 a0001c0001t0003g0231 a0001c0003t0004g0232 |
3 | HG01243.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.437-5347_437-5344d others(6): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4519701 | ||||||
| chr17:4519722 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.437-5335G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519722 | |||||||
| chr17:4519727 | C | T | 1 | a0001c0001t0009g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.437-5330C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519727 | |||||||
| chr17:4519924 | C | T | 72 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0055 others(69): Show |
77 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.437-5133C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519924 | |||||||
| chr17:4519972 | T | C | 7 | a0001c0001t0003g0035 a0001c0001t0011g0362 a0001c0001t0017g0363 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-5085T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519972 | |||||||
| chr17:4520020 | C | T | 2 | a0001c0001t0005g0004 a0001c0001t0008g0183 |
4 | HG02735.hp1 HG03239.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-5037C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520020 | |||||||
| chr17:4520093 | G | T | 2 | a0001c0001t0003g0051 a0001c0001t0003g0052 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.437-4964G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520093 | |||||||
| chr17:4520115 | C | T | 1 | a0001c0001t0003g0197 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.437-4942C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520115 | |||||||
| chr17:4520194 | G | A | 1 | a0001c0001t0002g0303 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.437-4863G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520194 | |||||||
| chr17:4520246 | G | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0014 others(76): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.437-4811G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520246 | |||||||
| chr17:4520269 | A | T | 16 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(13): Show |
16 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.437-4788A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520269 | |||||||
| chr17:4520379 | G | A | 1 | a0001c0001t0006g0161 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.437-4678G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520379 | |||||||
| chr17:4520509 | C | T | 1 | a0002c0011t0032g0162 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.437-4548C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520509 | |||||||
| chr17:4520541 | A | G | 1 | a0001c0001t0001g0331 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.437-4516A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520541 | |||||||
| chr17:4520545 | C | G | 3 | a0001c0001t0007g0178 a0001c0001t0028g0179 a0001c0003t0005g0177 |
3 | HG01884.hp1 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.437-4512C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520545 | |||||||
| chr17:4520864 | A | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(117): Show |
134 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.437-4193A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520864 | |||||||
| chr17:4520901 | C | G | 7 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(4): Show |
7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.437-4156C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520901 | |||||||
| chr17:4520955 | C | T | 10 | a0001c0001t0001g0142 a0001c0001t0011g0361 a0001c0001t0014g0141 others(7): Show |
10 | HG02257.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.437-4102C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520955 | |||||||
| chr17:4520956 | G | A | 1 | a0001c0001t0030g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.437-4101G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520956 | |||||||
| chr17:4520967 | T | C | 1 | a0001c0012t0002g0243 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.437-4090T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520967 | |||||||
| chr17:4521387 | A | T | 71 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0055 others(68): Show |
76 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.437-3670A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521387 | |||||||
| chr17:4521489 | G | A | 1 | a0001c0001t0014g0333 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.437-3568G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521489 | |||||||
| chr17:4521557 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(243): Show |
266 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.437-3500C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521557 | |||||||
| chr17:4521570 | G | A | 2 | a0001c0001t0021g0367 a0001c0002t0011g0366 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.437-3487G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521570 | |||||||
| chr17:4521670 | G | A | 230 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(227): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.437-3387G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521670 | |||||||
| chr17:4521772 | G | C | 1 | a0001c0001t0002g0249 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.437-3285G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521772 | |||||||
| chr17:4521820 | C | T | 2 | a0001c0001t0004g0045 a0001c0001t0036g0225 |
2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.437-3237C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521820 | |||||||
| chr17:4521856 | G | A | 9 | a0001c0001t0006g0015 a0001c0001t0006g0158 a0001c0001t0006g0161 others(6): Show |
10 | HG02486.hp2 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.437-3201G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521856 | |||||||
| chr17:4521885 | G | A | 2 | a0001c0001t0021g0367 a0001c0002t0011g0366 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.437-3172G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521885 | |||||||
| chr17:4521921 | G | A | 7 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(4): Show |
7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.437-3136G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521921 | |||||||
| chr17:4522035 | C | T | 3 | a0001c0001t0002g0093 a0001c0001t0018g0111 a0001c0001t0018g0112 |
3 | HG00544.hp1 NA19005.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.437-3022C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522035 | |||||||
| chr17:4522038 | A | C | 6 | a0001c0001t0001g0235 a0001c0001t0006g0033 a0001c0001t0009g0191 others(3): Show |
6 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-3019A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522038 | |||||||
| chr17:4522056 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.437-3001G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522056 | |||||||
| chr17:4522099 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.437-2958C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522099 | |||||||
| chr17:4522123 | C | T | 31 | a0001c0001t0001g0142 a0001c0001t0003g0035 a0001c0001t0004g0045 others(28): Show |
32 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(29): Show |
intron_variant | MODIFIER | c.437-2934C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522123 | |||||||
| chr17:4522131 | A | G | 8 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(5): Show |
8 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-2926A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522131 | |||||||
| chr17:4522135 | A | G | 8 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(5): Show |
8 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-2922A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522135 | |||||||
| chr17:4522138 | G | T | 7 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(4): Show |
7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.437-2919G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522138 | |||||||
| chr17:4522167 | C | G | 1 | a0001c0007t0004g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.437-2890C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522167 | |||||||
| chr17:4522178 | G | A | 109 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0036 others(106): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.437-2879G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522178 | |||||||
| chr17:4522220 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.437-2837A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522220 | |||||||
| chr17:4522315 | G | A | 2 | a0001c0001t0003g0051 a0001c0001t0003g0052 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.437-2742G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522315 | |||||||
| chr17:4522370 | C | T | 7 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(4): Show |
7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.437-2687C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522370 | |||||||
| chr17:4522389 | C | T | 1 | a0001c0009t0015g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.437-2668C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522389 | |||||||
| chr17:4522455 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.437-2602C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522455 | |||||||
| chr17:4522525 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.437-2532G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522525 | |||||||
| chr17:4522543 | G | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0066 a0001c0001t0001g0067 others(41): Show |
50 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.437-2514G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522543 | |||||||
| chr17:4522573 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.437-2484T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522573 | |||||||
| chr17:4522641 | C | T | 1 | a0001c0001t0036g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.437-2416C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522641 | |||||||
| chr17:4522703 | C | T | 3 | a0001c0001t0002g0093 a0001c0001t0018g0111 a0001c0001t0018g0112 |
3 | HG00544.hp1 NA19005.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.437-2354C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522703 | |||||||
| chr17:4522727 | C | T | 2 | a0001c0001t0002g0078 a0001c0001t0002g0283 |
2 | HG04199.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.437-2330C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522727 | |||||||
| chr17:4522741 | C | A | 1 | a0001c0005t0002g0053 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.437-2316C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522741 | |||||||
| chr17:4522757 | G | A | 2 | a0001c0001t0009g0169 a0001c0003t0007g0168 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.437-2300G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522757 | |||||||
| chr17:4522830 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0010g0202 |
2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.437-2227G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522830 | |||||||
| chr17:4522946 | C | T | 1 | a0001c0001t0010g0211 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.437-2111C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522946 | |||||||
| chr17:4523084 | G | A | 209 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(206): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.437-1973G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523084 | |||||||
| chr17:4523192 | C | A | 2 | a0001c0001t0004g0045 a0001c0001t0036g0225 |
2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.437-1865C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523192 | |||||||
| chr17:4523204 | G | A | 6 | a0001c0001t0001g0235 a0001c0001t0006g0033 a0001c0001t0009g0191 others(3): Show |
6 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-1853G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523204 | |||||||
| chr17:4523282 | A | G | 6 | a0001c0001t0001g0235 a0001c0001t0006g0033 a0001c0001t0009g0191 others(3): Show |
6 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-1775A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523282 | |||||||
| chr17:4523311 | G | A | 1 | a0001c0001t0003g0208 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.437-1746G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523311 | |||||||
| chr17:4523366 | A | G | 15 | a0001c0001t0001g0235 a0001c0001t0006g0015 a0001c0001t0006g0033 others(12): Show |
16 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.437-1691A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523366 | |||||||
| chr17:4523370 | G | A | 7 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0210 others(4): Show |
7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.437-1687G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523370 | |||||||
| chr17:4523551 | T | C | 1 | a0001c0001t0003g0096 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.437-1506T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523551 | |||||||
| chr17:4523585 | C | T | 1 | a0001c0005t0002g0048 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.437-1472C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523585 | |||||||
| chr17:4523650 | G | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(163): Show |
182 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.437-1407G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523650 | |||||||
| chr17:4523660 | C | T | 1 | a0001c0015t0002g0065 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.437-1397C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523660 | |||||||
| chr17:4523716 | T | C | 1 | a0001c0001t0002g0127 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.437-1341T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523716 | |||||||
| chr17:4523880 | A | G | 6 | a0001c0001t0001g0235 a0001c0001t0006g0033 a0001c0001t0009g0191 others(3): Show |
6 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-1177A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523880 | |||||||
| chr17:4523938 | T | C | 6 | a0001c0001t0001g0235 a0001c0001t0006g0033 a0001c0001t0009g0191 others(3): Show |
6 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-1119T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523938 | |||||||
| chr17:4523963 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.437-1094G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523963 | |||||||
| chr17:4524069 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(229): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.437-988G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4524069 | |||||||
| chr17:4524515 | T | C | 1 | a0001c0001t0029g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.437-542T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4524515 | |||||||
| chr17:4524556 | T | C | 3 | a0001c0001t0003g0231 a0001c0001t0014g0141 a0001c0001t0016g0057 |
3 | HG02647.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.437-501T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4524556 | |||||||
| chr17:4525009 | C | T | 1 | a0002c0011t0032g0162 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.437-48C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4525009 | |||||||
| chr17:4525034 | C | G | 1 | a0001c0001t0014g0337 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.437-23C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4525034 | |||||||
| chr17:4525034 | C | T | 1 | a0001c0001t0036g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.437-23C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4525034 | |||||||
| chr17:4525245 | G | T | 9 | a0001c0001t0003g0035 a0001c0001t0004g0352 a0001c0001t0004g0355 others(6): Show |
9 | HG01099.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.573+52G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525245 | |||||||
| chr17:4525469 | C | G | 6 | a0001c0001t0001g0235 a0001c0001t0006g0033 a0001c0001t0026g0189 others(3): Show |
6 | HG01167.hp1 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+276C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525469 | |||||||
| chr17:4525469 | C | T | 1 | a0001c0001t0025g0174 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.573+276C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525469 | |||||||
| chr17:4525628 | G | A | 1 | a0001c0001t0029g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.573+435G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525628 | |||||||
| chr17:4525747 | C | A | 27 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(24): Show |
30 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.573+554C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525747 | |||||||
| chr17:4525798 | C | T | 2 | a0001c0001t0009g0169 a0001c0003t0007g0168 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.573+605C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525798 | |||||||
| chr17:4525851 | C | T | 5 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0009g0169 others(2): Show |
5 | HG02886.hp2 HG02895.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+658C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525851 | |||||||
| chr17:4525852 | G | A | 38 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(35): Show |
41 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.573+659G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525852 | |||||||
| chr17:4525970 | C | G | 49 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(46): Show |
52 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.573+777C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525970 | |||||||
| chr17:4525976 | G | C | 5 | a0001c0001t0004g0126 a0001c0001t0028g0179 a0001c0003t0004g0069 others(2): Show |
5 | HG02258.hp1 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+783G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525976 | |||||||
| chr17:4526204 | C | T | 1 | a0001c0001t0004g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.573+1011C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526204 | |||||||
| chr17:4526295 | G | A | 43 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(40): Show |
46 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.573+1102G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526295 | |||||||
| chr17:4526529 | G | A | 2 | a0001c0001t0003g0051 a0001c0001t0003g0052 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.573+1336G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526529 | |||||||
| chr17:4526558 | G | A | 43 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(40): Show |
46 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.573+1365G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526558 | |||||||
| chr17:4526603 | CAA | C | 43 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(40): Show |
46 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.573+1422_573+1423d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 4526603 | ||||||
| chr17:4526617 | G | A | 1 | a0001c0004t0002g0290 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.573+1424G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526617 | |||||||
| chr17:4526618 | A | G | 1 | a0001c0004t0002g0290 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.573+1425A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526618 | |||||||
| chr17:4526726 | A | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(217): Show |
244 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.573+1533A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526726 | |||||||
| chr17:4526761 | C | T | 1 | a0001c0006t0027g0192 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.573+1568C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526761 | |||||||
| chr17:4526914 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(118): Show |
134 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.573+1721T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526914 | |||||||
| chr17:4527112 | AGAAACAG others(12): Show |
A | 3 | a0001c0001t0001g0349 a0001c0001t0004g0234 a0001c0001t0004g0350 |
3 | HG02280.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.573+1923_573+1941d others(21): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 4527112 | ||||||
| chr17:4527156 | C | G | 2 | a0001c0001t0001g0147 a0001c0005t0002g0148 |
2 | NA18960.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.573+1963C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527156 | |||||||
| chr17:4527470 | T | C | 1 | a0001c0001t0002g0312 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.573+2277T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527470 | |||||||
| chr17:4527486 | C | T | 1 | a0001c0004t0002g0124 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.573+2293C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527486 | |||||||
| chr17:4527533 | A | G | 5 | a0001c0001t0004g0126 a0001c0001t0009g0191 a0001c0001t0022g0365 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+2340A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527533 | |||||||
| chr17:4527579 | C | T | 1 | a0001c0001t0028g0179 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.573+2386C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527579 | |||||||
| chr17:4527663 | C | T | 120 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0066 others(117): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.573+2470C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527663 | |||||||
| chr17:4527690 | T | C | 16 | a0001c0001t0004g0126 a0001c0001t0004g0227 a0001c0001t0019g0228 others(13): Show |
16 | HG01167.hp1 HG01891.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.573+2497T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527690 | |||||||
| chr17:4527813 | G | C | 113 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0036 others(110): Show |
122 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(119): Show |
intron_variant | MODIFIER | c.573+2620G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527813 | |||||||
| chr17:4527832 | G | A | 1 | a0001c0001t0009g0186 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.573+2639G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527832 | |||||||
| chr17:4527842 | T | C | 1 | a0001c0001t0038g0221 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.573+2649T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527842 | |||||||
| chr17:4527864 | G | A | 4 | a0001c0001t0001g0080 a0001c0001t0002g0043 a0001c0001t0002g0092 others(1): Show |
4 | HG01255.hp1 HG02683.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+2671G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527864 | |||||||
| chr17:4527886 | G | T | 2 | a0001c0001t0002g0109 a0001c0012t0002g0243 |
2 | NA18970.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.573+2693G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527886 | |||||||
| chr17:4527949 | CA | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(251): Show |
284 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.574-2668delA | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 4527949 | ||||||
| chr17:4527963 | A | AC | 6 | a0001c0001t0001g0271 a0001c0001t0002g0253 a0001c0001t0003g0018 others(3): Show |
7 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-2669_574-2668i others(3): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527963 | |||||||
| chr17:4527963 | A | C | 83 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(80): Show |
91 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.574-2669A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527963 | |||||||
| chr17:4528094 | T | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
149 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.574-2538T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528094 | |||||||
| chr17:4528108 | C | T | 2 | a0001c0001t0004g0229 a0001c0001t0004g0330 |
2 | HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.574-2524C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528108 | |||||||
| chr17:4528115 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0129 a0001c0001t0001g0286 others(1): Show |
5 | HG03490.hp1 HG03491.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-2517C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528115 | |||||||
| chr17:4528171 | C | T | 1 | a0001c0001t0004g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-2461C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528171 | |||||||
| chr17:4528318 | G | A | 1 | a0001c0001t0048g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.574-2314G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528318 | |||||||
| chr17:4528459 | A | G | 12 | a0001c0001t0001g0066 a0001c0001t0001g0142 a0001c0001t0001g0230 others(9): Show |
12 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.574-2173A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528459 | |||||||
| chr17:4528503 | C | T | 11 | a0001c0001t0004g0019 a0001c0001t0004g0224 a0001c0001t0004g0227 others(8): Show |
12 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.574-2129C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528503 | |||||||
| chr17:4528531 | C | T | 2 | a0001c0001t0002g0093 a0001c0001t0002g0312 |
2 | HG00544.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.574-2101C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528531 | |||||||
| chr17:4528627 | C | T | 2 | a0001c0001t0004g0045 a0001c0001t0004g0238 |
2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.574-2005C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528627 | |||||||
| chr17:4528645 | T | G | 122 | a0001c0001t0001g0016 a0001c0001t0001g0272 a0001c0001t0001g0306 others(119): Show |
132 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.574-1987T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528645 | |||||||
| chr17:4528805 | G | A | 1 | a0001c0008t0004g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.574-1827G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528805 | |||||||
| chr17:4528942 | C | CT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(85): Show |
97 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.574-1678dupT | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 4528942 | ||||||
| chr17:4529067 | C | A | 1 | a0001c0005t0002g0148 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.574-1565C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529067 | |||||||
| chr17:4529085 | G | A | 1 | a0001c0001t0034g0028 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.574-1547G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529085 | |||||||
| chr17:4529093 | A | G | 15 | a0001c0001t0001g0066 a0001c0001t0001g0142 a0001c0001t0001g0230 others(12): Show |
15 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.574-1539A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529093 | |||||||
| chr17:4529411 | C | A | 1 | a0001c0001t0003g0049 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.574-1221C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529411 | |||||||
| chr17:4529587 | G | A | 7 | a0001c0001t0003g0037 a0001c0001t0003g0237 a0001c0001t0004g0355 others(4): Show |
8 | HG01192.hp1 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.574-1045G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529587 | |||||||
| chr17:4529593 | A | G | 32 | a0001c0001t0002g0078 a0001c0001t0003g0008 a0001c0001t0003g0017 others(29): Show |
35 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.574-1039A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529593 | |||||||
| chr17:4529680 | G | GA | 43 | a0001c0001t0001g0269 a0001c0001t0002g0078 a0001c0001t0003g0008 others(40): Show |
47 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.574-943dupA | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 4529680 | ||||||
| chr17:4529979 | A | G | 4 | a0001c0001t0001g0067 a0001c0001t0001g0322 a0001c0001t0001g0349 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-653A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529979 | |||||||
| chr17:4530004 | G | A | 1 | a0001c0001t0009g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.574-628G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530004 | |||||||
| chr17:4530017 | G | A | 4 | a0001c0001t0001g0103 a0001c0001t0001g0145 a0001c0001t0001g0245 others(1): Show |
4 | HG02056.hp2 HG02083.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-615G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530017 | |||||||
| chr17:4530081 | C | T | 2 | a0001c0001t0005g0004 a0001c0001t0030g0184 |
4 | HG02735.hp1 HG03239.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-551C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530081 | |||||||
| chr17:4530123 | G | T | 1 | a0001c0001t0003g0254 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.574-509G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530123 | |||||||
| chr17:4530152 | C | T | 1 | a0001c0001t0003g0008 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.574-480C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530152 | |||||||
| chr17:4530305 | G | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(109): Show |
131 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.574-327G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530305 | |||||||
| chr17:4530330 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0196 a0001c0001t0001g0278 |
3 | NA18960.hp1 NA18990.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.574-302C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530330 | |||||||
| chr17:4530450 | G | A | 1 | a0001c0001t0007g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.574-182G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530450 | |||||||
| chr17:4530463 | C | T | 9 | a0001c0001t0004g0019 a0001c0001t0004g0224 a0001c0001t0004g0227 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.574-169C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530463 | |||||||
| chr17:4530522 | C | T | 1 | a0001c0001t0003g0208 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.574-110C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530522 | |||||||
| chr17:4530528 | C | G | 18 | a0001c0001t0001g0271 a0001c0001t0002g0085 a0001c0001t0002g0092 others(15): Show |
18 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.574-104C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530528 | |||||||
| chr17:4530819 | C | G | 1 | a0001c0001t0006g0033 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.725+36C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4530819 | |||||||
| chr17:4530882 | G | A | 4 | a0001c0001t0006g0015 a0001c0001t0006g0161 a0001c0001t0025g0174 others(1): Show |
5 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.725+99G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4530882 | |||||||
| chr17:4530908 | G | C | 4 | a0001c0004t0001g0023 a0001c0004t0002g0290 a0001c0004t0002g0291 others(1): Show |
5 | NA18991.hp1 NA19003.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.725+125G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4530908 | |||||||
| chr17:4530974 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.726-79C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4530974 | |||||||
| chr17:4530979 | C | T | 3 | a0001c0005t0002g0048 a0001c0005t0002g0053 a0001c0005t0002g0077 |
3 | HG00673.hp1 NA18965.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.726-74C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4530979 | |||||||
| chr17:4531002 | T | G | 1 | a0001c0001t0006g0161 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.726-51T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4531002 | |||||||
| chr17:4531050 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG01175.hp2 NA20805.hp2 |
splice_region_variant&intron_variant | LOW | c.726-3C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4531050 | |||||||
| chr17:4531155 | C | T | 11 | a0001c0001t0003g0074 a0001c0003t0004g0069 a0001c0003t0004g0232 others(8): Show |
11 | HG00099.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.792+36C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531155 | |||||||
| chr17:4531176 | G | C | 38 | a0001c0001t0001g0066 a0001c0001t0001g0080 a0001c0001t0001g0142 others(35): Show |
38 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.792+57G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531176 | |||||||
| chr17:4531194 | C | T | 6 | a0001c0001t0010g0200 a0001c0001t0010g0202 a0001c0001t0010g0211 others(3): Show |
6 | HG01081.hp2 HG01256.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+75C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531194 | |||||||
| chr17:4531289 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.792+170C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531289 | |||||||
| chr17:4531310 | G | C | 1 | a0001c0001t0029g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.792+191G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531310 | |||||||
| chr17:4531322 | G | A | 6 | a0001c0001t0010g0200 a0001c0001t0010g0202 a0001c0001t0010g0211 others(3): Show |
6 | HG01081.hp2 HG01256.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+203G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531322 | |||||||
| chr17:4531341 | C | CG | 9 | a0001c0002t0004g0070 a0001c0002t0004g0072 a0001c0002t0004g0236 others(6): Show |
9 | HG02257.hp2 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.792+226dupG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 4531341 | ||||||
| chr17:4531342 | G | A | 9 | a0001c0001t0004g0019 a0001c0001t0004g0224 a0001c0001t0004g0227 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.792+223G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531342 | |||||||
| chr17:4531485 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.792+366G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531485 | |||||||
| chr17:4531507 | G | A | 4 | a0001c0004t0001g0023 a0001c0004t0002g0290 a0001c0004t0002g0291 others(1): Show |
5 | NA18991.hp1 NA19003.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+388G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531507 | |||||||
| chr17:4531599 | T | C | 365 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(362): Show |
399 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.792+480T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531599 | |||||||
| chr17:4531703 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.792+584C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531703 | |||||||
| chr17:4531704 | G | A | 11 | a0001c0002t0004g0070 a0001c0002t0004g0072 a0001c0002t0004g0236 others(8): Show |
11 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.792+585G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531704 | |||||||
| chr17:4531744 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.792+625G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531744 | |||||||
| chr17:4531750 | A | C | 14 | a0001c0001t0001g0080 a0001c0001t0004g0234 a0001c0001t0004g0350 others(11): Show |
14 | HG01255.hp1 HG01257.hp2 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.792+631A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531750 | |||||||
| chr17:4531763 | T | TGGGGGAG others(15): Show |
1 | a0001c0001t0001g0256 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.792+645_792+666dup others(22): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 4531763 | ||||||
| chr17:4531768 | G | GA | 6 | a0001c0001t0002g0116 a0001c0001t0002g0130 a0001c0001t0002g0249 others(3): Show |
6 | HG01975.hp2 HG01993.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+650dupA | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 4531768 | ||||||
| chr17:4531780 | C | T | 2 | a0001c0001t0003g0152 a0001c0006t0027g0192 |
2 | HG00639.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.792+661C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531780 | |||||||
| chr17:4531781 | G | C | 1 | a0001c0001t0003g0208 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.792+662G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531781 | |||||||
| chr17:4531826 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.792+707A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531826 | |||||||
| chr17:4531828 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.792+709C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531828 | |||||||
| chr17:4531881 | C | T | 1 | a0001c0005t0002g0148 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.793-661C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531881 | |||||||
| chr17:4531940 | A | G | 25 | a0001c0001t0001g0066 a0001c0001t0001g0142 a0001c0001t0001g0230 others(22): Show |
25 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.793-602A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531940 | |||||||
| chr17:4531970 | G | A | 1 | a0001c0001t0009g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.793-572G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531970 | |||||||
| chr17:4531980 | C | T | 5 | a0001c0001t0004g0260 a0001c0001t0004g0352 a0001c0001t0019g0071 others(2): Show |
5 | HG01099.hp2 HG01891.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-562C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531980 | |||||||
| chr17:4532016 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.793-526C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532016 | |||||||
| chr17:4532051 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.793-491C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532051 | |||||||
| chr17:4532068 | C | T | 4 | a0001c0001t0001g0067 a0001c0001t0001g0322 a0001c0001t0001g0349 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-474C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532068 | |||||||
| chr17:4532120 | G | T | 2 | a0001c0006t0002g0046 a0001c0006t0002g0195 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.793-422G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532120 | |||||||
| chr17:4532135 | C | G | 2 | a0001c0006t0002g0046 a0001c0006t0002g0195 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.793-407C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532135 | |||||||
| chr17:4532135 | C | T | 1 | a0001c0001t0001g0304 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.793-407C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532135 | |||||||
| chr17:4532140 | ATCCATCT others(13): Show |
A | 2 | a0001c0001t0003g0059 a0001c0001t0006g0033 |
2 | HG01361.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.793-387_793-368del others(20): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 4532140 | ||||||
| chr17:4532156 | GTCTGTCC others(1): Show |
G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): Show |
169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.793-374_793-367del others(8): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 4532156 | ||||||
| chr17:4532260 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0214 |
2 | HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.793-282C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532260 | |||||||
| chr17:4532319 | C | T | 1 | a0001c0001t0002g0311 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.793-223C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532319 | |||||||
| chr17:4532358 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0214 |
2 | HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.793-184C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532358 | |||||||
| chr17:4532372 | G | A | 23 | a0001c0001t0010g0200 a0001c0001t0010g0202 a0001c0001t0010g0211 others(20): Show |
23 | HG01081.hp2 HG01256.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.793-170G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532372 | |||||||
| chr17:4532710 | T | C | 365 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(362): Show |
399 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(396): Show |
intron_variant | MODIFIER | c.935+26T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 6/12 | chr17 | 4532710 | |||||||
| chr17:4532719 | A | G | 9 | a0001c0001t0004g0019 a0001c0001t0004g0224 a0001c0001t0004g0227 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.935+35A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 6/12 | chr17 | 4532719 | |||||||
| chr17:4532924 | AG | A | 9 | a0001c0002t0004g0070 a0001c0002t0004g0072 a0001c0002t0004g0236 others(6): Show |
9 | HG02257.hp2 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.936-47delG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr17 | 4532924 | ||||||
| chr17:4532926 | G | A | 5 | a0001c0001t0004g0045 a0001c0001t0004g0126 a0001c0001t0004g0229 others(2): Show |
5 | HG02280.hp1 HG02451.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.936-51G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 6/12 | chr17 | 4532926 | |||||||
| chr17:4533134 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01175.hp1 | splice_region_variant&intron_variant | LOW | c.1088+5G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 7/12 | chr17 | 4533134 | |||||||
| chr17:4533475 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1278+43G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533475 | |||||||
| chr17:4533479 | C | T | 5 | a0001c0003t0004g0351 a0001c0003t0006g0160 a0001c0003t0007g0168 others(2): Show |
5 | HG02258.hp1 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278+47C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533479 | |||||||
| chr17:4533480 | G | T | 1 | a0001c0001t0006g0033 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1278+48G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533480 | |||||||
| chr17:4533528 | C | T | 2 | a0001c0003t0004g0232 a0001c0003t0005g0177 |
2 | NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1278+96C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533528 | |||||||
| chr17:4533568 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1278+136C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533568 | |||||||
| chr17:4533574 | C | T | 111 | a0001c0001t0001g0016 a0001c0001t0001g0087 a0001c0001t0001g0088 others(108): Show |
120 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1278+142C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533574 | |||||||
| chr17:4533602 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(142): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1278+170G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533602 | |||||||
| chr17:4533628 | C | T | 1 | a0001c0001t0043g0317 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1279-160C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533628 | |||||||
| chr17:4533636 | G | A | 9 | a0001c0001t0001g0080 a0001c0001t0004g0234 a0001c0001t0004g0350 others(6): Show |
9 | HG01255.hp1 HG01257.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1279-152G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533636 | |||||||
| chr17:4533666 | G | A | 9 | a0001c0001t0004g0019 a0001c0001t0004g0224 a0001c0001t0004g0227 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1279-122G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533666 | |||||||
| chr17:4533757 | G | A | 3 | a0001c0001t0012g0086 a0001c0001t0012g0120 a0001c0001t0012g0139 |
3 | NA18957.hp2 NA18977.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1279-31G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533757 | |||||||
| chr17:4533870 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0328 |
2 | NA18977.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1344+17G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4533870 | |||||||
| chr17:4533871 | A | C | 1 | a0001c0001t0004g0234 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1344+18A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4533871 | |||||||
| chr17:4533871 | A | G | 1 | a0001c0005t0002g0121 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1344+18A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4533871 | |||||||
| chr17:4533905 | C | A | 5 | a0001c0001t0004g0045 a0001c0001t0004g0126 a0001c0001t0004g0229 others(2): Show |
5 | HG02280.hp1 HG02451.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+52C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4533905 | |||||||
| chr17:4533919 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(144): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1344+66C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4533919 | |||||||
| chr17:4533944 | G | T | 2 | a0001c0006t0002g0046 a0001c0006t0002g0195 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1344+91G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4533944 | |||||||
| chr17:4534177 | C | T | 2 | a0001c0001t0001g0331 a0001c0001t0002g0300 |
2 | HG03927.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1344+324C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534177 | |||||||
| chr17:4534182 | G | C | 17 | a0001c0001t0001g0271 a0001c0001t0002g0085 a0001c0001t0002g0092 others(14): Show |
17 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1344+329G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534182 | |||||||
| chr17:4534240 | C | CGGCTGG | 4 | a0001c0001t0004g0352 a0001c0001t0019g0228 a0001c0001t0022g0365 others(1): Show |
4 | HG01099.hp2 HG01891.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+395_1344+400d others(8): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4534240 | ||||||
| chr17:4534272 | A | T | 10 | a0001c0001t0003g0037 a0001c0001t0003g0237 a0001c0001t0004g0355 others(7): Show |
11 | HG01192.hp1 HG02486.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1344+419A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534272 | |||||||
| chr17:4534294 | G | C | 1 | a0001c0001t0029g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1344+441G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534294 | |||||||
| chr17:4534297 | C | T | 5 | a0001c0001t0001g0097 a0001c0001t0001g0144 a0001c0001t0001g0270 others(2): Show |
5 | NA18941.hp1 NA18980.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+444C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534297 | |||||||
| chr17:4534334 | G | A | 4 | a0001c0001t0004g0045 a0001c0001t0004g0126 a0001c0001t0004g0229 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+481G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534334 | |||||||
| chr17:4534416 | C | T | 4 | a0001c0001t0004g0045 a0001c0001t0004g0126 a0001c0001t0004g0229 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+563C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534416 | |||||||
| chr17:4534417 | G | A | 2 | a0001c0001t0006g0034 a0001c0001t0007g0178 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1344+564G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534417 | |||||||
| chr17:4534479 | G | C | 1 | a0001c0009t0015g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1344+626G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534479 | |||||||
| chr17:4534496 | T | A | 26 | a0001c0001t0001g0271 a0001c0001t0002g0085 a0001c0001t0002g0092 others(23): Show |
26 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1344+643T>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534496 | |||||||
| chr17:4534562 | G | A | 1 | a0001c0001t0002g0280 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1344+709G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534562 | |||||||
| chr17:4534605 | G | GCCAGGC | 5 | a0001c0001t0004g0352 a0001c0001t0019g0071 a0001c0001t0019g0228 others(2): Show |
5 | HG01099.hp2 HG01891.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1344+753_1344+758d others(8): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4534605 | ||||||
| chr17:4534617 | G | A | 1 | a0001c0003t0005g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1344+764G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534617 | |||||||
| chr17:4534630 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(115): Show |
137 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1344+777C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534630 | |||||||
| chr17:4534631 | G | A | 21 | a0001c0001t0001g0066 a0001c0001t0001g0142 a0001c0001t0001g0230 others(18): Show |
21 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1344+778G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534631 | |||||||
| chr17:4534642 | C | G | 20 | a0001c0001t0004g0019 a0001c0001t0004g0224 a0001c0001t0004g0227 others(17): Show |
21 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.1344+789C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534642 | |||||||
| chr17:4534658 | C | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(264): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1344+805C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534658 | |||||||
| chr17:4534665 | G | A | 1 | a0001c0001t0002g0319 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1344+812G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534665 | |||||||
| chr17:4534718 | C | T | 1 | a0001c0001t0004g0234 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1344+865C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534718 | |||||||
| chr17:4534719 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1344+866G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534719 | |||||||
| chr17:4534767 | A | G | 22 | a0001c0001t0001g0142 a0001c0001t0002g0198 a0001c0001t0002g0299 others(19): Show |
23 | HG01099.hp1 HG01167.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1344+914A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534767 | |||||||
| chr17:4534771 | G | A | 5 | a0001c0001t0002g0020 a0001c0001t0002g0241 a0001c0001t0002g0274 others(2): Show |
6 | NA18948.hp1 NA18956.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.1344+918G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534771 | |||||||
| chr17:4534771 | G | C | 6 | a0001c0001t0003g0035 a0001c0001t0003g0231 a0001c0001t0009g0191 others(3): Show |
6 | HG02109.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344+918G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534771 | |||||||
| chr17:4534800 | C | T | 9 | a0001c0001t0004g0019 a0001c0001t0004g0224 a0001c0001t0004g0227 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1344+947C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534800 | |||||||
| chr17:4534805 | CCA | C | 51 | a0001c0001t0004g0019 a0001c0001t0004g0045 a0001c0001t0004g0224 others(48): Show |
52 | HG01081.hp2 HG01099.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.1344+953_1344+954d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534805 | |||||||
| chr17:4534889 | G | C | 355 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(352): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.1344+1036G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534889 | |||||||
| chr17:4534920 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1344+1067G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534920 | |||||||
| chr17:4534928 | C | T | 1 | a0001c0013t0045g0223 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1344+1075C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534928 | |||||||
| chr17:4534992 | G | C | 16 | a0001c0001t0002g0085 a0001c0001t0002g0092 a0001c0001t0003g0049 others(13): Show |
16 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.1345-1084G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534992 | |||||||
| chr17:4535034 | G | A | 1 | a0001c0001t0042g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1345-1042G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535034 | |||||||
| chr17:4535076 | TAAGGCTG others(8): Show |
T | 119 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0087 others(116): Show |
129 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1345-996_1345-982d others(17): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4535076 | ||||||
| chr17:4535114 | C | T | 6 | a0001c0001t0001g0256 a0001c0001t0004g0352 a0001c0001t0019g0071 others(3): Show |
6 | HG01099.hp2 HG01891.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-962C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535114 | |||||||
| chr17:4535194 | T | TGGCCTGC others(72): Show |
1 | a0001c0001t0003g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1345-878_1345-800d others(81): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4535194 | ||||||
| chr17:4535195 | GGCCTGCC others(313): Show |
G | 1 | a0001c0001t0040g0264 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1345-877_1345-558d others(2): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4535195 | ||||||
| chr17:4535261 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1345-815G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535261 | |||||||
| chr17:4535296 | C | G | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1345-780C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535296 | |||||||
| chr17:4535308 | C | T | 1 | a0001c0001t0009g0166 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1345-768C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535308 | |||||||
| chr17:4535309 | G | A | 1 | a0001c0001t0017g0368 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1345-767G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535309 | |||||||
| chr17:4535310 | G | C | 127 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0039 others(124): Show |
136 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1345-766G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535310 | |||||||
| chr17:4535319 | G | C | 4 | a0001c0001t0004g0352 a0001c0001t0019g0071 a0001c0001t0019g0228 others(1): Show |
4 | HG01099.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-757G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535319 | |||||||
| chr17:4535362 | G | T | 7 | a0001c0001t0002g0294 a0001c0001t0002g0311 a0001c0004t0002g0124 others(4): Show |
7 | HG00423.hp2 NA18951.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.1345-714G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535362 | |||||||
| chr17:4535440 | C | T | 2 | a0001c0001t0004g0126 a0001c0001t0004g0229 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1345-636C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535440 | |||||||
| chr17:4535459 | G | A | 2 | a0001c0001t0004g0126 a0001c0001t0004g0229 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1345-617G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535459 | |||||||
| chr17:4535492 | C | T | 1 | a0001c0001t0001g0308 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1345-584C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535492 | |||||||
| chr17:4535586 | TGGCTCGG others(9): Show |
T | 1 | a0001c0001t0004g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1345-482_1345-467d others(18): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4535586 | ||||||
| chr17:4535732 | A | C | 1 | a0001c0001t0002g0280 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1345-344A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535732 | |||||||
| chr17:4535762 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1345-314G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535762 | |||||||
| chr17:4535852 | GGGA | G | 9 | a0001c0001t0004g0234 a0001c0001t0004g0350 a0001c0001t0005g0170 others(6): Show |
9 | HG02922.hp1 HG02976.hp2 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345-219_1345-217d others(5): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4535852 | ||||||
| chr17:4535857 | G | A | 353 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(350): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1345-219G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535857 | |||||||
| chr17:4535909 | G | C | 1 | a0001c0001t0002g0255 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1345-167G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535909 | |||||||
| chr17:4535952 | G | A | 1 | a0001c0001t0046g0105 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1345-124G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535952 | |||||||
| chr17:4535972 | T | C | 1 | a0001c0008t0004g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1345-104T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535972 | |||||||
| chr17:4535987 | G | A | 112 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0087 others(109): Show |
123 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.1345-89G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535987 | |||||||
| chr17:4536006 | C | T | 5 | a0001c0003t0004g0351 a0001c0003t0006g0160 a0001c0003t0007g0168 others(2): Show |
5 | HG02258.hp1 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345-70C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536006 | |||||||
| chr17:4536018 | A | G | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(358): Show |
395 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.1345-58A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536018 | |||||||
| chr17:4536029 | C | T | 1 | a0001c0001t0001g0006 | 3 | NA18953.hp2 NA19060.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1345-47C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536029 | |||||||
| chr17:4536036 | C | G | 1 | a0001c0001t0001g0207 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1345-40C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536036 | |||||||
| chr17:4536051 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0004g0126 |
2 | HG02280.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1345-25G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536051 | |||||||
| chr17:4536061 | C | T | 6 | a0001c0001t0010g0041 a0001c0001t0010g0200 a0001c0001t0010g0202 others(3): Show |
6 | HG00735.hp2 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-15C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536061 | |||||||
| chr17:4536065 | C | T | 2 | a0001c0001t0004g0350 a0001c0001t0006g0158 |
2 | HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1345-11C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536065 | |||||||
| chr17:4536071 | C | T | 9 | a0001c0001t0003g0096 a0001c0001t0010g0041 a0001c0001t0010g0200 others(6): Show |
9 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.1345-5C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536071 | |||||||
| chr17:4536190 | G | T | 1 | a0001c0001t0049g0108 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1443+16G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536190 | |||||||
| chr17:4536201 | C | A | 102 | a0001c0001t0001g0016 a0001c0001t0001g0087 a0001c0001t0001g0088 others(99): Show |
112 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1443+27C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536201 | |||||||
| chr17:4536202 | A | G | 145 | a0001c0001t0001g0016 a0001c0001t0001g0087 a0001c0001t0001g0088 others(142): Show |
158 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1443+28A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536202 | |||||||
| chr17:4536206 | C | G | 361 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(358): Show |
395 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.1443+32C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536206 | |||||||
| chr17:4536217 | A | C | 3 | a0001c0001t0019g0071 a0001c0001t0019g0228 a0001c0001t0022g0365 |
3 | HG01891.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1443+43A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536217 | |||||||
| chr17:4536217 | A | G | 137 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0039 others(134): Show |
148 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.1443+43A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536217 | |||||||
| chr17:4536220 | G | T | 137 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0087 others(134): Show |
148 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1444-43G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536220 | |||||||
| chr17:4536237 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(305): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.1444-26T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536237 | |||||||
| chr17:4536238 | G | A | 1 | a0001c0001t0002g0311 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1444-25G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536238 | |||||||
| chr17:4536431 | G | GT | 12 | a0001c0001t0004g0330 a0001c0001t0015g0188 a0001c0002t0044g0233 others(9): Show |
12 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.1607+6dupT | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 4536431 | ||||||
| chr17:4536432 | T | TG | 42 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(39): Show |
47 | HG00438.hp1 HG01069.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.1607+13dupG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 4536432 | ||||||
| chr17:4536432 | T | TGG | 27 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0002g0054 others(24): Show |
29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1607+12_1607+13dup others(2): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 4536432 | ||||||
| chr17:4536433 | G | T | 10 | a0001c0001t0004g0350 a0001c0001t0006g0158 a0001c0002t0004g0070 others(7): Show |
10 | HG02257.hp2 HG02572.hp1 HG02723.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1607+7G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536433 | |||||||
| chr17:4536436 | G | GA | 73 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0087 others(70): Show |
81 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1607+10_1607+11ins others(1): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536436 | |||||||
| chr17:4536438 | G | C | 2 | a0001c0004t0002g0290 a0001c0004t0002g0291 |
2 | NA19003.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1607+12G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536438 | |||||||
| chr17:4536439 | G | GGA | 16 | a0001c0001t0002g0085 a0001c0001t0002g0092 a0001c0001t0003g0037 others(13): Show |
16 | HG00738.hp1 HG01192.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1607+13_1607+14ins others(2): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536439 | |||||||
| chr17:4536459 | C | T | 1 | a0001c0005t0002g0121 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1607+33C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536459 | |||||||
| chr17:4536463 | G | A | 2 | a0001c0001t0002g0303 a0001c0001t0004g0350 |
2 | HG02976.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1607+37G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536463 | |||||||
| chr17:4536500 | C | G | 14 | a0001c0001t0003g0008 a0001c0001t0003g0017 a0001c0001t0003g0059 others(11): Show |
18 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1607+74C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536500 | |||||||
| chr17:4536514 | G | C | 9 | a0001c0001t0003g0035 a0001c0001t0003g0231 a0001c0001t0009g0191 others(6): Show |
9 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1607+88G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536514 | |||||||
| chr17:4536533 | A | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(93): Show |
111 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1607+107A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536533 | |||||||
| chr17:4536686 | C | A | 1 | a0001c0001t0002g0064 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1608-214C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536686 | |||||||
| chr17:4536689 | C | T | 4 | a0001c0001t0015g0176 a0001c0001t0015g0188 a0001c0001t0021g0367 others(1): Show |
4 | HG02559.hp2 HG02630.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608-211C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536689 | |||||||
| chr17:4536782 | C | G | 1 | a0001c0001t0002g0089 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1608-118C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536782 | |||||||
| chr17:4536847 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1608-53G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536847 | |||||||
| chr17:4536886 | C | T | 6 | a0001c0001t0003g0035 a0001c0001t0003g0231 a0001c0001t0009g0191 others(3): Show |
6 | HG02109.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1608-14C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536886 | |||||||
| chr17:4537163 | C | T | 1 | a0001c0001t0005g0185 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.*4+217C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537163 | |||||||
| chr17:4537187 | G | A | 1 | a0001c0001t0006g0033 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.*4+241G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537187 | |||||||
| chr17:4537197 | G | GGGCCAGG others(3): Show |
3 | a0001c0001t0016g0057 a0001c0001t0016g0261 a0001c0001t0026g0189 |
3 | HG02257.hp1 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.*5-247_*5-238dupCT others(8): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 4537197 | ||||||
| chr17:4537207 | T | A | 2 | a0001c0001t0002g0083 a0001c0014t0002g0140 |
2 | HG00438.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.*5-246T>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537207 | |||||||
| chr17:4537211 | C | T | 103 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0020 others(100): Show |
111 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.*5-242C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537211 | |||||||
| chr17:4537213 | G | C | 1 | a0001c0001t0001g0335 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.*5-240G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537213 | |||||||
| chr17:4537232 | G | A | 4 | a0001c0001t0004g0045 a0001c0001t0004g0126 a0001c0001t0004g0229 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.*5-221G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537232 | |||||||
| chr17:4537236 | T | G | 27 | a0001c0001t0001g0080 a0001c0001t0003g0035 a0001c0001t0003g0231 others(24): Show |
27 | HG01099.hp2 HG01255.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.*5-217T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537236 | |||||||
| chr17:4537259 | G | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(151): Show |
175 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.*5-194G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537259 | |||||||
| chr17:4537342 | G | A | 7 | a0001c0001t0003g0035 a0001c0001t0003g0231 a0001c0001t0009g0191 others(4): Show |
7 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.*5-111G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537342 |