Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 201305 |
| ensemblid | ENSG00000182557.8 |
| hgncid | 28433 |
| symbol | SPNS3 |
| name | SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative) |
| refseq_nuc | NM_182538.5 |
| refseq_prot | NP_872344.3 |
| ensembl_nuc | ENST00000355530.7 |
| ensembl_prot | ENSP00000347721.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 4433940 |
| end | 4488204 |
| strand | + |
| ver | v1.2 |
| region | chr17:4433940-4488204 |
| region5000 | chr17:4428940-4493204 |
| regionname0 | SPNS3_chr17_4433940_4488204 |
| regionname5000 | SPNS3_chr17_4428940_4493204 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 512 | 252 | 88 | 28 | 113 | 6 | 16 | 79 | SPNS3_chr17_4428940_4493204 | SPNS3 | MAGGM others(507): Show |
chr17 | 4428940 | 4493204 |
| a0002 | 0/1 | 512 | 59 | 2 | 28 | 11 | 2 | 15 | 6 | SPNS3_chr17_4428940_4493204 | SPNS3 | MAGGM others(507): Show |
chr17 | 4428940 | 4493204 |
| a0003 | 0/0 | 512 | 35 | 2 | 9 | 9 | 5 | 10 | 5 | SPNS3_chr17_4428940_4493204 | SPNS3 | MAGGM others(507): Show |
chr17 | 4428940 | 4493204 |
| a0004 | 0/0 | 512 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | MAGGM others(507): Show |
chr17 | 4428940 | 4493204 |
| a0005 | 0/0 | 512 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | MAGGM others(507): Show |
chr17 | 4428940 | 4493204 |
| a0006 | 0/0 | 512 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | MVGGM others(507): Show |
chr17 | 4428940 | 4493204 |
| a0007 | 0/0 | 512 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | MAGGM others(507): Show |
chr17 | 4428940 | 4493204 |
| a0008 | 0/0 | 512 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | MAGGM others(507): Show |
chr17 | 4428940 | 4493204 |
| a0009 | 0/0 | 512 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | MAGGM others(507): Show |
chr17 | 4428940 | 4493204 |
| a0010 | 0/0 | 512 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | MAGGM others(507): Show |
chr17 | 4428940 | 4493204 |
| a0011 | 0/0 | 512 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | MARGM others(507): Show |
chr17 | 4428940 | 4493204 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1536 | 127 | 29 | 8 | 82 | 1 | 6 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0003 | 0/0 | 1536 | 29 | 14 | 5 | 7 | 2 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0004 | 0/0 | 1536 | 18 | 2 | 0 | 16 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0006 | 0/0 | 1536 | 13 | 11 | 0 | 0 | 0 | 2 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0007 | 0/0 | 1536 | 13 | 5 | 5 | 1 | 1 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0009 | 0/0 | 1536 | 11 | 6 | 1 | 3 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0010 | 0/0 | 1536 | 9 | 1 | 4 | 0 | 1 | 3 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0012 | 0/0 | 1536 | 5 | 5 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0013 | 0/0 | 1536 | 4 | 1 | 0 | 3 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0014 | 0/0 | 1536 | 4 | 1 | 2 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0018 | 0/0 | 1536 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0023 | 0/0 | 1536 | 2 | 1 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0024 | 0/0 | 1536 | 2 | 0 | 1 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0028 | 0/0 | 1536 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0031 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0034 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0035 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0036 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0038 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0042 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0044 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0045 | 0/0 | 1536 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0046 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0047 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0049 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0001c0052 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0002c0002 | 0/0 | 1536 | 43 | 1 | 25 | 9 | 0 | 8 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0002c0011 | 0/0 | 1536 | 8 | 0 | 2 | 1 | 2 | 3 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0002c0022 | 0/0 | 1536 | 2 | 0 | 1 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0002c0032 | 0/0 | 1536 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0002c0033 | 0/0 | 1536 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0002c0037 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0002c0039 | 0/1 | 1536 | 1 | 0 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0002c0040 | 0/0 | 1536 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0002c0043 | 0/0 | 1536 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0003c0005 | 0/0 | 1536 | 16 | 1 | 2 | 6 | 1 | 6 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0003c0008 | 0/0 | 1536 | 11 | 0 | 6 | 0 | 3 | 2 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0003c0016 | 0/0 | 1536 | 2 | 0 | 0 | 0 | 0 | 2 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0003c0020 | 0/0 | 1536 | 2 | 0 | 1 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0003c0021 | 0/0 | 1536 | 2 | 0 | 0 | 1 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0003c0029 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0003c0051 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0004c0017 | 0/0 | 1536 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0004c0030 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0004c0048 | 0/0 | 1536 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0005c0015 | 0/0 | 1536 | 3 | 0 | 2 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0006c0026 | 0/0 | 1536 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGT others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0007c0025 | 0/0 | 1536 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0008c0019 | 0/0 | 1536 | 2 | 0 | 0 | 0 | 0 | 2 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0009c0050 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0010c0041 | 0/0 | 1536 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 | ||
| a0011c0027 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | ATGGC others(1531): Show |
chr17 | 4428940 | 4493204 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1877 | 101 | 14 | 4 | 76 | 1 | 5 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0001t0002 | 0/0 | 1877 | 26 | 15 | 4 | 6 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0003t0001 | 0/0 | 1877 | 20 | 11 | 1 | 7 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0003t0002 | 0/0 | 1877 | 9 | 3 | 4 | 0 | 2 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0004t0001 | 0/0 | 1877 | 18 | 2 | 0 | 16 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0006t0001 | 0/0 | 1877 | 7 | 6 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0006t0002 | 0/0 | 1877 | 6 | 5 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0007t0003 | 0/0 | 1877 | 13 | 5 | 5 | 1 | 1 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0009t0001 | 0/0 | 1877 | 4 | 1 | 0 | 2 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0009t0002 | 0/0 | 1877 | 6 | 4 | 1 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0009t0004 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0010t0001 | 0/0 | 1877 | 4 | 1 | 2 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0010t0002 | 0/0 | 1877 | 5 | 0 | 2 | 0 | 0 | 3 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0012t0001 | 0/0 | 1877 | 4 | 4 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0012t0002 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0013t0001 | 0/0 | 1877 | 4 | 1 | 0 | 3 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0014t0001 | 0/0 | 1877 | 2 | 0 | 1 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0014t0002 | 0/0 | 1877 | 2 | 1 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0018t0002 | 0/0 | 1877 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0023t0003 | 0/0 | 1877 | 2 | 1 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0024t0003 | 0/0 | 1877 | 2 | 0 | 1 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0028t0003 | 0/0 | 1877 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0031t0005 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0034t0002 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0035t0002 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0036t0003 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0038t0003 | 0/0 | 1877 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0042t0002 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0044t0002 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0045t0003 | 0/0 | 1877 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0046t0002 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0047t0002 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0049t0002 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0001c0052t0002 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0002c0002t0001 | 0/0 | 1877 | 38 | 1 | 20 | 9 | 0 | 8 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0002c0002t0002 | 0/0 | 1877 | 5 | 0 | 5 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0002c0011t0003 | 0/0 | 1877 | 8 | 0 | 2 | 1 | 2 | 3 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0002c0022t0001 | 0/0 | 1877 | 2 | 0 | 1 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0002c0032t0001 | 0/0 | 1877 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0002c0033t0003 | 0/0 | 1877 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0002c0037t0002 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0002c0039t0001 | 0/1 | 1877 | 1 | 0 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0002c0040t0001 | 0/0 | 1877 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0002c0043t0001 | 0/0 | 1877 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0003c0005t0001 | 0/0 | 1877 | 15 | 1 | 1 | 6 | 1 | 6 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0003c0005t0002 | 0/0 | 1877 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0003c0008t0003 | 0/0 | 1877 | 11 | 0 | 6 | 0 | 3 | 2 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0003c0016t0001 | 0/0 | 1877 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0003c0016t0002 | 0/0 | 1877 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0003c0020t0001 | 0/0 | 1877 | 2 | 0 | 1 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0003c0021t0003 | 0/0 | 1877 | 2 | 0 | 0 | 1 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0003c0029t0003 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0003c0051t0001 | 0/0 | 1877 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0004c0017t0002 | 0/0 | 1877 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0004c0030t0002 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0004c0048t0002 | 0/0 | 1877 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0005c0015t0003 | 0/0 | 1877 | 3 | 0 | 2 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0006c0026t0001 | 0/0 | 1877 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0007c0025t0002 | 0/0 | 1877 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0008c0019t0001 | 0/0 | 1877 | 2 | 0 | 0 | 0 | 0 | 2 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0009c0050t0001 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0010c0041t0003 | 0/0 | 1877 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| a0011c0027t0001 | 0/0 | 1877 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | AGTCT others(1872): Show |
chr17 | 4428940 | 4493204 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0192 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0003t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0006t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0006t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0006t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0006t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0006t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0006t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0006t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0006t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0006t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0006t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0006t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0006t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0007t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0007t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0007t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0007t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0007t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0007t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0007t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0007t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0007t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0007t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0007t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0007t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0007t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0009t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0009t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0009t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0009t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0009t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0009t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0009t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0009t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0009t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0009t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0009t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0010t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0010t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0010t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0010t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0010t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0010t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0010t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0010t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0010t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0012t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0012t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0012t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0012t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0012t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0013t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0013t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0013t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0013t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0014t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0014t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0014t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0014t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0018t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0018t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0023t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0023t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0024t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0024t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0028t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0031t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0034t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0035t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0036t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0038t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0042t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0044t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0045t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0046t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0047t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0049t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0001c0052t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0011t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0011t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0011t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0011t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0011t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0011t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0011t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0011t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0022t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0022t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0032t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0033t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0037t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0039t0001g0356 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0040t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0002c0043t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0005t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0008t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0008t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0008t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0008t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0008t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0008t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0008t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0008t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0008t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0008t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0008t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0016t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0016t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0020t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0020t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0021t0003g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0021t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0029t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0003c0051t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0004c0017t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0004c0017t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0004c0030t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0004c0048t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0005c0015t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0005c0015t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0005c0015t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0006c0026t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0006c0026t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0007c0025t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0007c0025t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0008c0019t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0008c0019t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0009c0050t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0010c0041t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| a0011c0027t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0028 | t0003 | g0173 | EUR | GBR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00099 | hp2 | a0002 | c0011 | t0003 | g0254 | EUR | GBR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00280 | hp1 | a0003 | c0021 | t0003 | g0002 | EUR | FIN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00280 | hp2 | a0001 | c0007 | t0003 | g0248 | EUR | FIN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00323 | hp1 | a0005 | c0015 | t0003 | g0153 | EUR | FIN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00423 | hp1 | a0006 | c0026 | t0001 | g0225 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00438 | hp1 | a0001 | c0004 | t0001 | g0068 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00597 | hp1 | a0001 | c0004 | t0001 | g0074 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00597 | hp2 | a0003 | c0005 | t0001 | g0114 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00639 | hp1 | a0001 | c0007 | t0003 | g0163 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00639 | hp2 | a0001 | c0045 | t0003 | g0150 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00642 | hp1 | a0005 | c0015 | t0003 | g0104 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00642 | hp2 | a0003 | c0005 | t0001 | g0156 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00673 | hp1 | a0001 | c0004 | t0001 | g0093 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00738 | hp1 | a0001 | c0014 | t0001 | g0017 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00738 | hp2 | a0001 | c0010 | t0002 | g0086 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00741 | hp1 | a0001 | c0014 | t0002 | g0018 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG00741 | hp2 | a0001 | c0003 | t0002 | g0139 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0357 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01069 | hp2 | a0001 | c0010 | t0001 | g0080 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0299 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01070 | hp2 | a0001 | c0007 | t0003 | g0172 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0358 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0301 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01074 | hp2 | a0002 | c0022 | t0001 | g0059 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01081 | hp1 | a0001 | c0010 | t0001 | g0078 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01081 | hp2 | a0001 | c0024 | t0003 | g0062 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01099 | hp1 | a0004 | c0048 | t0002 | g0006 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01099 | hp2 | a0003 | c0008 | t0003 | g0128 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01106 | hp1 | a0003 | c0005 | t0002 | g0155 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0126 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01109 | hp1 | a0001 | c0009 | t0002 | g0024 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0264 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0265 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0266 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01169 | hp2 | a0003 | c0008 | t0003 | g0174 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01175 | hp1 | a0001 | c0003 | t0002 | g0256 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01175 | hp2 | a0001 | c0023 | t0003 | g0053 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0142 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01192 | hp2 | a0002 | c0011 | t0003 | g0287 | AMR | PUR | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0274 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01255 | hp2 | a0003 | c0008 | t0003 | g0268 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01256 | hp2 | a0002 | c0011 | t0003 | g0255 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01257 | hp1 | a0005 | c0015 | t0003 | g0159 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01257 | hp2 | a0003 | c0008 | t0003 | g0099 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01258 | hp2 | a0003 | c0008 | t0003 | g0103 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0276 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0354 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0280 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01361 | hp1 | a0003 | c0008 | t0003 | g0101 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0302 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01433 | hp1 | a0001 | c0003 | t0002 | g0136 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01433 | hp2 | a0001 | c0007 | t0003 | g0241 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0277 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0300 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01515 | hp1 | a0001 | c0003 | t0002 | g0138 | EUR | IBS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01515 | hp2 | a0003 | c0008 | t0003 | g0267 | EUR | IBS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01516 | hp1 | a0003 | c0008 | t0003 | g0102 | EUR | IBS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01516 | hp2 | a0001 | c0010 | t0001 | g0084 | EUR | IBS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01517 | hp1 | a0001 | c0003 | t0002 | g0137 | EUR | IBS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01517 | hp2 | a0003 | c0008 | t0003 | g0100 | EUR | IBS | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01884 | hp2 | a0001 | c0007 | t0003 | g0158 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01891 | hp1 | a0001 | c0006 | t0001 | g0047 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01891 | hp2 | a0001 | c0006 | t0002 | g0043 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0278 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0120 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01952 | hp1 | a0001 | c0007 | t0003 | g0169 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0289 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0312 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0228 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01981 | hp1 | a0001 | c0003 | t0002 | g0148 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0298 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02015 | hp1 | a0001 | c0004 | t0001 | g0069 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0318 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02071 | hp1 | a0001 | c0013 | t0001 | g0359 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02129 | hp1 | a0003 | c0005 | t0001 | g0176 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0146 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02145 | hp2 | a0001 | c0009 | t0002 | g0031 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0293 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02148 | hp2 | a0001 | c0010 | t0002 | g0081 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CDX | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02155 | hp2 | a0003 | c0051 | t0001 | g0013 | EAS | CDX | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02165 | hp1 | a0003 | c0005 | t0001 | g0118 | EAS | CDX | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02165 | hp2 | a0001 | c0004 | t0001 | g0092 | EAS | CDX | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02257 | hp2 | a0001 | c0006 | t0002 | g0048 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02258 | hp2 | a0001 | c0012 | t0001 | g0039 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02273 | hp1 | a0003 | c0020 | t0001 | g0117 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0330 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02280 | hp2 | a0001 | c0012 | t0001 | g0038 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0121 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02451 | hp2 | a0001 | c0009 | t0001 | g0008 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02572 | hp1 | a0001 | c0049 | t0002 | g0003 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02572 | hp2 | a0007 | c0025 | t0002 | g0041 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0253 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02602 | hp2 | a0001 | c0006 | t0001 | g0077 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02615 | hp1 | a0001 | c0047 | t0002 | g0321 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02615 | hp2 | a0001 | c0052 | t0002 | g0063 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02622 | hp1 | a0001 | c0006 | t0001 | g0010 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02622 | hp2 | a0001 | c0006 | t0001 | g0051 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02630 | hp2 | a0007 | c0025 | t0002 | g0040 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02647 | hp1 | a0001 | c0007 | t0003 | g0249 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02647 | hp2 | a0001 | c0042 | t0002 | g0339 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02683 | hp1 | a0003 | c0005 | t0001 | g0175 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02683 | hp2 | a0003 | c0005 | t0001 | g0180 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02698 | hp1 | a0003 | c0008 | t0003 | g0119 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02698 | hp2 | a0003 | c0005 | t0001 | g0310 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02717 | hp1 | a0001 | c0034 | t0002 | g0045 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02717 | hp2 | a0001 | c0006 | t0002 | g0052 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02723 | hp1 | a0001 | c0010 | t0001 | g0044 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02723 | hp2 | a0003 | c0005 | t0001 | g0140 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02735 | hp1 | a0010 | c0041 | t0003 | g0314 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0307 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02738 | hp1 | a0002 | c0032 | t0001 | g0079 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02738 | hp2 | a0008 | c0019 | t0001 | g0340 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02809 | hp1 | a0001 | c0007 | t0003 | g0319 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0127 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02818 | hp1 | a0004 | c0017 | t0002 | g0331 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0327 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02895 | hp2 | a0001 | c0006 | t0002 | g0011 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0112 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02896 | hp2 | a0001 | c0018 | t0002 | g0349 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02897 | hp1 | a0001 | c0018 | t0002 | g0350 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02897 | hp2 | a0001 | c0006 | t0002 | g0012 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02922 | hp1 | a0001 | c0031 | t0005 | g0033 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0320 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0125 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02976 | hp2 | a0001 | c0009 | t0004 | g0061 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03041 | hp1 | a0001 | c0009 | t0002 | g0022 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03041 | hp2 | a0001 | c0009 | t0002 | g0025 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0027 | AFR | MSL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03098 | hp2 | a0004 | c0017 | t0002 | g0029 | AFR | MSL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0342 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03139 | hp1 | a0001 | c0023 | t0003 | g0014 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0124 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03195 | hp1 | a0001 | c0009 | t0002 | g0023 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03195 | hp2 | a0002 | c0037 | t0002 | g0323 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0333 | AFR | MSL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0344 | AFR | MSL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | MSL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | MSL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03239 | hp1 | a0001 | c0014 | t0001 | g0019 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03239 | hp2 | a0003 | c0005 | t0001 | g0106 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03453 | hp2 | a0001 | c0007 | t0003 | g0325 | AFR | MSL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03490 | hp1 | a0001 | c0010 | t0002 | g0088 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0279 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03492 | hp2 | a0001 | c0010 | t0002 | g0087 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03516 | hp1 | a0004 | c0030 | t0002 | g0009 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0315 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03540 | hp2 | a0001 | c0007 | t0003 | g0337 | AFR | GWD | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0346 | AFR | MSL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03579 | hp2 | a0001 | c0035 | t0002 | g0034 | AFR | MSL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03654 | hp2 | a0001 | c0006 | t0002 | g0089 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03669 | hp1 | a0002 | c0040 | t0001 | g0313 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03669 | hp2 | a0003 | c0005 | t0001 | g0107 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03688 | hp1 | a0002 | c0011 | t0003 | g0281 | SAS | STU | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03688 | hp2 | a0002 | c0011 | t0003 | g0252 | SAS | STU | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0355 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0273 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0292 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03710 | hp2 | a0003 | c0016 | t0001 | g0083 | SAS | PJL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03834 | hp1 | a0003 | c0008 | t0003 | g0141 | SAS | BEB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03834 | hp2 | a0002 | c0033 | t0003 | g0091 | SAS | BEB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03927 | hp1 | a0001 | c0024 | t0003 | g0057 | SAS | BEB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03927 | hp2 | a0002 | c0011 | t0003 | g0308 | SAS | BEB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03942 | hp1 | a0001 | c0010 | t0002 | g0090 | SAS | BEB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0157 | SAS | BEB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0309 | SAS | STU | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG04115 | hp2 | a0003 | c0016 | t0002 | g0082 | SAS | STU | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0285 | SAS | BEB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG04184 | hp2 | a0003 | c0005 | t0001 | g0108 | SAS | BEB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | STU | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG04204 | hp2 | a0008 | c0019 | t0001 | g0341 | SAS | STU | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG04228 | hp1 | a0002 | c0043 | t0001 | g0226 | SAS | STU | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | STU | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18522 | hp1 | a0001 | c0012 | t0002 | g0042 | AFR | YRI | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | YRI | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | CHB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | CHB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18747 | hp2 | a0001 | c0004 | t0001 | g0064 | EAS | CHB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0145 | AFR | YRI | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18906 | hp2 | a0001 | c0046 | t0002 | g0316 | AFR | YRI | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18943 | hp1 | a0001 | c0003 | t0001 | g0351 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18943 | hp2 | a0001 | c0009 | t0001 | g0005 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0072 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18954 | hp1 | a0003 | c0020 | t0001 | g0115 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18960 | hp1 | a0001 | c0004 | t0001 | g0067 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18960 | hp2 | a0001 | c0004 | t0001 | g0066 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18961 | hp2 | a0001 | c0038 | t0003 | g0291 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18962 | hp1 | a0001 | c0004 | t0001 | g0071 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18962 | hp2 | a0001 | c0013 | t0001 | g0178 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18965 | hp2 | a0001 | c0004 | t0001 | g0056 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18966 | hp2 | a0002 | c0011 | t0003 | g0258 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18971 | hp1 | a0003 | c0021 | t0003 | g0188 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18982 | hp2 | a0006 | c0026 | t0001 | g0240 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18983 | hp2 | a0001 | c0004 | t0001 | g0075 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0170 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0152 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19009 | hp2 | a0001 | c0004 | t0001 | g0065 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19011 | hp1 | a0003 | c0005 | t0001 | g0234 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19011 | hp2 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19012 | hp1 | a0002 | c0022 | t0001 | g0055 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19012 | hp2 | a0001 | c0007 | t0003 | g0296 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19030 | hp1 | a0001 | c0036 | t0003 | g0144 | AFR | LWK | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19030 | hp2 | a0001 | c0012 | t0001 | g0036 | AFR | LWK | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19043 | hp1 | a0001 | c0014 | t0002 | g0007 | AFR | LWK | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19043 | hp2 | a0003 | c0029 | t0003 | g0085 | AFR | LWK | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0239 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19060 | hp2 | a0001 | c0009 | t0002 | g0076 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19063 | hp1 | a0001 | c0013 | t0001 | g0259 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19064 | hp2 | a0003 | c0005 | t0001 | g0235 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19067 | hp1 | a0011 | c0027 | t0001 | g0232 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19068 | hp2 | a0001 | c0004 | t0001 | g0073 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19070 | hp1 | a0003 | c0005 | t0001 | g0171 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0177 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19079 | hp1 | a0001 | c0004 | t0001 | g0054 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19081 | hp1 | a0001 | c0009 | t0001 | g0004 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0132 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19088 | hp1 | a0001 | c0004 | t0001 | g0070 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | YRI | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA19240 | hp2 | a0001 | c0006 | t0001 | g0050 | AFR | YRI | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0122 | AFR | ASW | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA20129 | hp2 | a0001 | c0044 | t0002 | g0236 | AFR | ASW | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA20805 | hp1 | a0003 | c0005 | t0001 | g0116 | EUR | TSI | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA20805 | hp2 | a0002 | c0011 | t0003 | g0149 | EUR | TSI | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA20905 | hp1 | a0001 | c0007 | t0003 | g0247 | SAS | GIH | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA20905 | hp2 | a0001 | c0009 | t0001 | g0058 | SAS | GIH | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0304 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG01123 | hp2 | a0001 | c0007 | t0003 | g0161 | AMR | CLM | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02109 | hp1 | a0009 | c0050 | t0001 | g0060 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0049 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0026 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0123 | AFR | MSL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | MSL | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG06807 | hp1 | a0001 | c0012 | t0001 | g0037 | AFR | USA | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0345 | AFR | USA | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0286 | AFR | USA | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0336 | AFR | USA | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA21309 | hp1 | a0001 | c0013 | t0001 | g0113 | AFR | LWK | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| NA21309 | hp2 | a0001 | c0006 | t0001 | g0032 | AFR | LWK | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| homoSapiens | chm13v2 | a0002 | c0039 | t0001 | g0356 | REF | REF | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0192 | REF | REF | SPNS3_chr17_4428940_4493204 | SPNS3 | chr17 | 4428940 | 4493204 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4433972 | C | T | 1 | a0006 | 2 | HG00423.hp1 NA18982.hp2 |
missense_variant | MODERATE | c.5C>T | p.Ala2Val | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/12 | 33/1877 | 5/1539 | 2/512 | chr17 | 4433972 | |||
| chr17:4433974 | G | A | 1 | a0011 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.7G>A | p.Gly3Arg | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/12 | 35/1877 | 7/1539 | 3/512 | chr17 | 4433974 | |||
| chr17:4434107 | C | G | 1 | a0007 | 2 | HG02572.hp2 HG02630.hp2 |
missense_variant | MODERATE | c.140C>G | p.Ala47Gly | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/12 | 168/1877 | 140/1539 | 47/512 | chr17 | 4434107 | |||
| chr17:4448239 | G | C | 1 | a0004 | 4 | HG01099.hp1 HG02818.hp1 HG03098.hp2 others(1): Show |
missense_variant | MODERATE | c.706G>C | p.Gly236Arg | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/12 | 734/1877 | 706/1539 | 236/512 | chr17 | 4448239 | |||
| chr17:4449297 | G | C | 1 | a0008 | 2 | HG02738.hp2 HG04204.hp2 |
missense_variant | MODERATE | c.833G>C | p.Gly278Ala | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/12 | 861/1877 | 833/1539 | 278/512 | chr17 | 4449297 | |||
| chr17:4449341 | G | A | 2 | a0003 a0010 |
36 | HG00280.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
missense_variant | MODERATE | c.877G>A | p.Gly293Arg | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/12 | 905/1877 | 877/1539 | 293/512 | chr17 | 4449341 | |||
| chr17:4453080 | G | T | 3 | a0002 a0009 a0010 |
60 | HG00099.hp2 HG00621.hp1 HG01070.hp1 others(57): Show |
missense_variant | MODERATE | c.988G>T | p.Ala330Ser | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/12 | 1016/1877 | 988/1539 | 330/512 | chr17 | 4453080 | |||
| chr17:4486313 | A | G | 1 | a0009 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1265A>G | p.Tyr422Cys | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 10/12 | 1293/1877 | 1265/1539 | 422/512 | chr17 | 4486313 | |||
| chr17:4487890 | C | G | 1 | a0005 | 3 | HG00323.hp1 HG00642.hp1 HG01257.hp1 |
missense_variant | MODERATE | c.1535C>G | p.Pro512Arg | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 12/12 | 1563/1877 | 1535/1539 | 512/512 | chr17 | 4487890 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4433988 | G | A | 11 | a0001c0006 a0001c0010 a0001c0028 others(8): Show |
32 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(29): Show |
synonymous_variant | LOW | c.21G>A | p.Ala7Ala | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/12 | 49/1877 | 21/1539 | 7/512 | chr17 | 4433988 | |||
| chr17:4434117 | C | G | 23 | a0001c0004 a0001c0006 a0001c0009 others(20): Show |
82 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(79): Show |
synonymous_variant | LOW | c.150C>G | p.Val50Val | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/12 | 178/1877 | 150/1539 | 50/512 | chr17 | 4434117 | |||
| chr17:4445117 | T | C | 1 | a0003c0029 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.351T>C | p.Gly117Gly | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/12 | 379/1877 | 351/1539 | 117/512 | chr17 | 4445117 | |||
| chr17:4448265 | G | A | 16 | a0001c0013 a0001c0014 a0001c0018 others(13): Show |
74 | HG00099.hp2 HG00621.hp1 HG00738.hp1 others(71): Show |
synonymous_variant | LOW | c.732G>A | p.Arg244Arg | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/12 | 760/1877 | 732/1539 | 244/512 | chr17 | 4448265 | |||
| chr17:4449244 | C | T | 28 | a0001c0003 a0001c0009 a0001c0010 others(25): Show |
136 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(133): Show |
synonymous_variant | LOW | c.780C>T | p.Phe260Phe | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/12 | 808/1877 | 780/1539 | 260/512 | chr17 | 4449244 | |||
| chr17:4449370 | G | A | 2 | a0003c0020 a0003c0021 |
4 | HG00280.hp1 HG02273.hp1 NA18954.hp1 others(1): Show |
synonymous_variant | LOW | c.906G>A | p.Pro302Pro | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/12 | 934/1877 | 906/1539 | 302/512 | chr17 | 4449370 | |||
| chr17:4453046 | C | T | 4 | a0001c0012 a0001c0044 a0001c0047 others(1): Show |
9 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(6): Show |
synonymous_variant | LOW | c.954C>T | p.Thr318Thr | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/12 | 982/1877 | 954/1539 | 318/512 | chr17 | 4453046 | |||
| chr17:4486504 | C | T | 4 | a0001c0035 a0001c0042 a0001c0046 others(1): Show |
4 | HG02615.hp2 HG02647.hp2 HG03579.hp2 others(1): Show |
synonymous_variant | LOW | c.1371C>T | p.Ile457Ile | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/12 | 1399/1877 | 1371/1539 | 457/512 | chr17 | 4486504 | |||
| chr17:4486582 | A | T | 1 | a0002c0040 | 1 | HG03669.hp1 | splice_region_variant&synonymous_variant | LOW | c.1449A>T | p.Thr483Thr | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/12 | 1477/1877 | 1449/1539 | 483/512 | chr17 | 4486582 | |||
| chr17:4487837 | C | T | 15 | a0001c0007 a0001c0023 a0001c0024 others(12): Show |
49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
synonymous_variant | LOW | c.1482C>T | p.Asn494Asn | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 12/12 | 1510/1877 | 1482/1539 | 494/512 | chr17 | 4487837 | |||
| chr17:4487858 | A | G | 21 | a0001c0007 a0001c0018 a0001c0023 others(18): Show |
56 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(53): Show |
synonymous_variant | LOW | c.1503A>G | p.Leu501Leu | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 12/12 | 1531/1877 | 1503/1539 | 501/512 | chr17 | 4487858 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4487906 | A | G | 15 | a0001c0007t0003 a0001c0023t0003 a0001c0024t0003 others(12): Show |
49 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*12A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 12/12 | 12 | chr17 | 4487906 | ||||||
| chr17:4487922 | C | G | 1 | a0001c0031t0005 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 12/12 | 28 | chr17 | 4487922 | ||||||
| chr17:4487957 | C | T | 1 | a0001c0009t0004 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*63C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 12/12 | 63 | chr17 | 4487957 | ||||||
| chr17:4488135 | T | C | 39 | a0001c0001t0002 a0001c0003t0002 a0001c0006t0002 others(36): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*241T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 12/12 | 241 | chr17 | 4488135 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:4434322 | G | A | 1 | a0003c0021t0003g0002 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.199+156G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434322 | |||||||
| chr17:4434503 | A | AT | 6 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0002g0357 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+348dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4434503 | ||||||
| chr17:4434503 | A | T | 3 | a0001c0001t0001g0360 a0001c0001t0001g0361 a0001c0013t0001g0359 |
3 | HG00544.hp2 HG02071.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.199+337A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434503 | |||||||
| chr17:4434507 | T | A | 91 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(88): Show |
91 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.199+341T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434507 | |||||||
| chr17:4434527 | C | T | 1 | a0001c0003t0001g0351 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.199+361C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434527 | |||||||
| chr17:4434536 | G | A | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199+370G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434536 | |||||||
| chr17:4434537 | C | A | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199+371C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434537 | |||||||
| chr17:4434589 | C | T | 2 | a0001c0018t0002g0349 a0001c0018t0002g0350 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.199+423C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434589 | |||||||
| chr17:4434621 | C | T | 2 | a0001c0004t0001g0092 a0001c0004t0001g0093 |
2 | HG00673.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.199+455C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434621 | |||||||
| chr17:4434621 | CGAGTAGC others(3283): Show |
C | 1 | a0002c0002t0001g0094 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.199+468_200-1735de others(1): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4434621 | ||||||
| chr17:4434645 | C | T | 15 | a0001c0006t0001g0077 a0001c0006t0002g0089 a0001c0010t0001g0078 others(12): Show |
15 | HG00738.hp2 HG01069.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.199+479C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434645 | |||||||
| chr17:4434646 | A | G | 15 | a0001c0006t0001g0077 a0001c0006t0002g0089 a0001c0010t0001g0078 others(12): Show |
15 | HG00738.hp2 HG01069.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.199+480A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434646 | |||||||
| chr17:4434654 | A | G | 15 | a0001c0006t0001g0077 a0001c0006t0002g0089 a0001c0010t0001g0078 others(12): Show |
15 | HG00738.hp2 HG01069.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.199+488A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434654 | |||||||
| chr17:4434655 | T | C | 15 | a0001c0006t0001g0077 a0001c0006t0002g0089 a0001c0010t0001g0078 others(12): Show |
15 | HG00738.hp2 HG01069.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.199+489T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434655 | |||||||
| chr17:4434658 | G | A | 2 | a0001c0009t0001g0004 a0001c0009t0001g0005 |
2 | NA18943.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.199+492G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434658 | |||||||
| chr17:4434728 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | NA18969.hp2 NA18983.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.199+562G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434728 | |||||||
| chr17:4434750 | C | T | 1 | a0001c0001t0001g0348 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.199+584C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434750 | |||||||
| chr17:4434803 | C | T | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199+637C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434803 | |||||||
| chr17:4434807 | C | CT | 28 | a0001c0001t0001g0347 a0001c0004t0001g0054 a0001c0004t0001g0056 others(25): Show |
28 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.199+653dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4434807 | ||||||
| chr17:4434809 | T | C | 2 | a0001c0014t0002g0007 a0004c0048t0002g0006 |
2 | HG01099.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.199+643T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434809 | |||||||
| chr17:4434992 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.199+826G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434992 | |||||||
| chr17:4434995 | G | T | 3 | a0001c0001t0001g0360 a0001c0001t0001g0361 a0001c0013t0001g0359 |
3 | HG00544.hp2 HG02071.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.199+829G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4434995 | |||||||
| chr17:4435053 | C | T | 1 | a0001c0003t0001g0346 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.199+887C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435053 | |||||||
| chr17:4435089 | C | G | 1 | a0001c0003t0001g0345 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.199+923C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435089 | |||||||
| chr17:4435094 | G | A | 11 | a0001c0001t0001g0105 a0001c0001t0001g0109 a0003c0005t0001g0106 others(8): Show |
11 | HG00642.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.199+928G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435094 | |||||||
| chr17:4435161 | GC | G | 26 | a0001c0004t0001g0056 a0001c0004t0001g0064 a0001c0004t0001g0065 others(23): Show |
26 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.199+997delC | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4435161 | ||||||
| chr17:4435197 | C | T | 50 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0035 others(47): Show |
50 | HG00738.hp2 HG01069.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.199+1031C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435197 | |||||||
| chr17:4435219 | T | C | 26 | a0001c0003t0001g0110 a0001c0004t0001g0056 a0001c0004t0001g0064 others(23): Show |
26 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.199+1053T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435219 | |||||||
| chr17:4435279 | C | T | 1 | a0001c0003t0001g0351 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.199+1113C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435279 | |||||||
| chr17:4435291 | C | T | 16 | a0001c0001t0001g0332 a0001c0001t0001g0334 a0001c0001t0001g0335 others(13): Show |
16 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.199+1125C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435291 | |||||||
| chr17:4435334 | A | G | 2 | a0001c0018t0002g0349 a0001c0018t0002g0350 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.199+1168A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435334 | |||||||
| chr17:4435338 | C | G | 27 | a0001c0003t0001g0110 a0001c0004t0001g0056 a0001c0004t0001g0064 others(24): Show |
27 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.199+1172C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435338 | |||||||
| chr17:4435339 | T | G | 27 | a0001c0003t0001g0110 a0001c0004t0001g0056 a0001c0004t0001g0064 others(24): Show |
27 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.199+1173T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435339 | |||||||
| chr17:4435343 | A | G | 24 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0338 others(21): Show |
24 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.199+1177A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435343 | |||||||
| chr17:4435440 | C | CA | 25 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0105 others(22): Show |
25 | HG00642.hp1 HG01257.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.199+1287dupA | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4435440 | ||||||
| chr17:4435440 | CAA | C | 27 | a0001c0003t0001g0110 a0001c0004t0001g0064 a0001c0004t0001g0065 others(24): Show |
27 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.199+1286_199+1287d others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4435440 | ||||||
| chr17:4435448 | A | T | 1 | a0010c0041t0003g0314 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.199+1282A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435448 | |||||||
| chr17:4435454 | T | A | 25 | a0001c0001t0001g0111 a0001c0001t0001g0294 a0001c0001t0001g0311 others(22): Show |
25 | HG00558.hp2 HG01109.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.199+1288T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435454 | |||||||
| chr17:4435455 | A | AT | 10 | a0001c0004t0001g0026 a0001c0004t0001g0027 a0001c0006t0002g0043 others(7): Show |
10 | HG01109.hp1 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.199+1289_199+1290i others(3): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435455 | |||||||
| chr17:4435455 | A | T | 6 | a0001c0001t0002g0046 a0001c0006t0001g0047 a0001c0006t0001g0049 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+1289A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435455 | |||||||
| chr17:4435456 | A | T | 2 | a0001c0018t0002g0349 a0001c0018t0002g0350 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.199+1290A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435456 | |||||||
| chr17:4435457 | A | AT | 4 | a0001c0001t0001g0311 a0001c0001t0002g0342 a0001c0001t0002g0343 others(1): Show |
4 | HG03130.hp2 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1291_199+1292i others(3): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435457 | |||||||
| chr17:4435457 | A | T | 1 | a0002c0002t0001g0312 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.199+1291A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435457 | |||||||
| chr17:4435458 | A | T | 2 | a0001c0014t0002g0007 a0004c0048t0002g0006 |
2 | HG01099.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.199+1292A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435458 | |||||||
| chr17:4435468 | T | A | 28 | a0001c0003t0001g0110 a0001c0004t0001g0056 a0001c0004t0001g0064 others(25): Show |
28 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.199+1302T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435468 | |||||||
| chr17:4435496 | A | G | 2 | a0001c0006t0001g0032 a0001c0031t0005g0033 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.199+1330A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435496 | |||||||
| chr17:4435537 | G | A | 16 | a0001c0006t0001g0077 a0001c0006t0002g0089 a0001c0010t0001g0078 others(13): Show |
16 | HG00738.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.199+1371G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435537 | |||||||
| chr17:4435669 | C | T | 79 | a0001c0001t0001g0098 a0001c0001t0001g0251 a0001c0001t0001g0257 others(76): Show |
79 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.199+1503C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435669 | |||||||
| chr17:4435747 | AACTC | A | 16 | a0001c0006t0001g0077 a0001c0006t0002g0089 a0001c0010t0001g0078 others(13): Show |
16 | HG00738.hp2 HG01069.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.199+1591_199+1594d others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4435747 | ||||||
| chr17:4435792 | C | T | 2 | a0001c0012t0002g0042 a0002c0033t0003g0091 |
2 | HG03834.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.199+1626C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435792 | |||||||
| chr17:4435801 | T | G | 224 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(221): Show |
224 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.199+1635T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435801 | |||||||
| chr17:4435802 | C | G | 224 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(221): Show |
224 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.199+1636C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435802 | |||||||
| chr17:4435803 | A | G | 227 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(224): Show |
227 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.199+1637A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435803 | |||||||
| chr17:4435847 | G | A | 1 | a0002c0002t0001g0354 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.199+1681G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435847 | |||||||
| chr17:4435857 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.199+1691G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435857 | |||||||
| chr17:4435918 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.199+1752C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435918 | |||||||
| chr17:4435926 | C | T | 176 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(173): Show |
176 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(173): Show |
intron_variant | MODIFIER | c.199+1760C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435926 | |||||||
| chr17:4435952 | A | G | 2 | a0007c0025t0002g0040 a0007c0025t0002g0041 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.199+1786A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435952 | |||||||
| chr17:4435976 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.199+1810T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4435976 | |||||||
| chr17:4436020 | A | ACC | 90 | a0001c0001t0001g0098 a0001c0001t0001g0164 a0001c0001t0001g0165 others(87): Show |
90 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.199+1855_199+1856i others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4436020 | ||||||
| chr17:4436022 | T | C | 90 | a0001c0001t0001g0098 a0001c0001t0001g0164 a0001c0001t0001g0165 others(87): Show |
90 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.199+1856T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436022 | |||||||
| chr17:4436023 | A | AACC | 4 | a0001c0001t0001g0030 a0001c0006t0001g0032 a0001c0031t0005g0033 others(1): Show |
4 | HG02630.hp1 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1859_199+1860i others(5): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4436023 | ||||||
| chr17:4436023 | A | AACTG | 4 | a0001c0001t0001g0111 a0001c0009t0002g0031 a0007c0025t0002g0040 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+1858_199+1861d others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4436023 | ||||||
| chr17:4436023 | A | AACTGTGG others(12): Show |
1 | a0001c0003t0001g0320 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.199+1871_199+1872i others(21): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4436023 | ||||||
| chr17:4436023 | A | C | 90 | a0001c0001t0001g0098 a0001c0001t0001g0164 a0001c0001t0001g0165 others(87): Show |
90 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.199+1857A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436023 | |||||||
| chr17:4436044 | C | G | 92 | a0001c0001t0001g0030 a0001c0001t0001g0098 a0001c0001t0001g0111 others(89): Show |
92 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.199+1878C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436044 | |||||||
| chr17:4436226 | A | G | 11 | a0001c0001t0001g0251 a0001c0001t0001g0297 a0001c0001t0001g0305 others(8): Show |
11 | HG00621.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.199+2060A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436226 | |||||||
| chr17:4436237 | C | A | 1 | a0001c0013t0001g0259 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.199+2071C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436237 | |||||||
| chr17:4436259 | C | G | 17 | a0001c0006t0002g0089 a0001c0007t0003g0248 a0001c0007t0003g0249 others(14): Show |
17 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.199+2093C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436259 | |||||||
| chr17:4436478 | G | GGAGGCTG others(17): Show |
1 | a0001c0003t0001g0320 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.199+2348_199+2371d others(26): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4436478 | ||||||
| chr17:4436478 | G | GGAGGCTG others(65): Show |
1 | a0001c0013t0001g0359 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.199+2320_199+2391d others(74): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4436478 | ||||||
| chr17:4436478 | GGAGGCTG others(17): Show |
G | 3 | a0001c0006t0001g0032 a0001c0031t0005g0033 a0003c0005t0002g0155 |
3 | HG01106.hp1 HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.199+2348_199+2371d others(26): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4436478 | ||||||
| chr17:4436490 | A | AGGAGGAT others(17): Show |
1 | a0001c0001t0002g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.199+2347_199+2348i others(26): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4436490 | ||||||
| chr17:4436514 | A | G | 11 | a0001c0001t0001g0030 a0001c0001t0001g0154 a0001c0001t0001g0311 others(8): Show |
11 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.199+2348A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436514 | |||||||
| chr17:4436514 | AGGAGGAT others(17): Show |
A | 18 | a0001c0001t0001g0111 a0001c0006t0002g0089 a0001c0007t0003g0248 others(15): Show |
18 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.199+2368_199+2391d others(26): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4436514 | ||||||
| chr17:4436537 | C | CGGGAGGA others(66): Show |
1 | a0001c0013t0001g0259 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.199+2391_199+2392i others(75): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4436537 | ||||||
| chr17:4436538 | G | A | 1 | a0002c0002t0001g0290 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.199+2372G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436538 | |||||||
| chr17:4436559 | G | A | 8 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0344 others(5): Show |
8 | HG02738.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.199+2393G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436559 | |||||||
| chr17:4436621 | C | G | 5 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(2): Show |
5 | HG02258.hp2 HG02280.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.199+2455C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436621 | |||||||
| chr17:4436661 | A | G | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.199+2495A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436661 | |||||||
| chr17:4436804 | G | T | 2 | a0001c0007t0003g0158 a0001c0007t0003g0319 |
2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.199+2638G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436804 | |||||||
| chr17:4436846 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.199+2680G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436846 | |||||||
| chr17:4436886 | G | A | 1 | a0001c0013t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.199+2720G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436886 | |||||||
| chr17:4436936 | C | A | 1 | a0001c0007t0003g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.200-2722C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436936 | |||||||
| chr17:4436984 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.200-2674C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4436984 | |||||||
| chr17:4437035 | C | T | 12 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(9): Show |
12 | HG01891.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.200-2623C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437035 | |||||||
| chr17:4437124 | G | A | 2 | a0001c0018t0002g0349 a0001c0018t0002g0350 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.200-2534G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437124 | |||||||
| chr17:4437382 | G | A | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-2276G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437382 | |||||||
| chr17:4437522 | C | G | 10 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0001t0002g0160 others(7): Show |
10 | HG02055.hp2 HG02622.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.200-2136C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437522 | |||||||
| chr17:4437540 | A | G | 150 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0001c0001t0001g0154 others(147): Show |
150 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.200-2118A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437540 | |||||||
| chr17:4437559 | T | C | 168 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0001c0001t0001g0154 others(165): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.200-2099T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437559 | |||||||
| chr17:4437591 | C | G | 23 | a0001c0001t0001g0111 a0001c0006t0001g0032 a0001c0006t0002g0089 others(20): Show |
23 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.200-2067C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437591 | |||||||
| chr17:4437661 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.200-1997A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437661 | |||||||
| chr17:4437676 | T | TAAATA | 185 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(182): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.200-1973_200-1969d others(7): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4437676 | ||||||
| chr17:4437723 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.200-1935A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437723 | |||||||
| chr17:4437788 | C | CTT | 17 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(14): Show |
17 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.200-1856_200-1855d others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4437788 | ||||||
| chr17:4437788 | CTT | C | 146 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0001c0001t0001g0246 others(143): Show |
146 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.200-1856_200-1855d others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4437788 | ||||||
| chr17:4437809 | C | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.200-1849C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437809 | |||||||
| chr17:4437856 | A | T | 18 | a0001c0001t0002g0160 a0001c0001t0002g0317 a0001c0003t0001g0318 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-1802A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437856 | |||||||
| chr17:4437890 | G | A | 2 | a0001c0001t0002g0046 a0001c0006t0002g0043 |
2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.200-1768G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437890 | |||||||
| chr17:4437924 | C | T | 1 | a0001c0009t0001g0005 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.200-1734C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437924 | |||||||
| chr17:4437927 | C | T | 2 | a0007c0025t0002g0040 a0007c0025t0002g0041 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.200-1731C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4437927 | |||||||
| chr17:4438000 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.200-1658G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438000 | |||||||
| chr17:4438032 | C | T | 1 | a0001c0003t0001g0318 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.200-1626C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438032 | |||||||
| chr17:4438053 | C | T | 2 | a0001c0001t0002g0162 a0001c0007t0003g0161 |
2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.200-1605C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438053 | |||||||
| chr17:4438082 | C | T | 1 | a0001c0007t0003g0241 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.200-1576C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438082 | |||||||
| chr17:4438092 | C | A | 141 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0001c0001t0001g0246 others(138): Show |
141 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.200-1566C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438092 | |||||||
| chr17:4438475 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.200-1183T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438475 | |||||||
| chr17:4438478 | C | T | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-1180C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438478 | |||||||
| chr17:4438504 | C | A | 164 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0001c0001t0001g0246 others(161): Show |
164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.200-1154C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438504 | |||||||
| chr17:4438609 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | NA18969.hp2 NA18983.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.200-1049G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438609 | |||||||
| chr17:4438681 | A | G | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-977A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438681 | |||||||
| chr17:4438719 | G | A | 3 | a0001c0009t0002g0022 a0001c0009t0002g0023 a0001c0009t0002g0024 |
3 | HG01109.hp1 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.200-939G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438719 | |||||||
| chr17:4438726 | A | G | 1 | a0006c0026t0001g0240 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.200-932A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438726 | |||||||
| chr17:4438752 | T | C | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-906T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438752 | |||||||
| chr17:4438766 | G | A | 2 | a0008c0019t0001g0340 a0008c0019t0001g0341 |
2 | HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.200-892G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438766 | |||||||
| chr17:4438797 | C | T | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-861C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438797 | |||||||
| chr17:4438799 | C | T | 24 | a0001c0001t0001g0332 a0001c0001t0001g0334 a0001c0001t0001g0335 others(21): Show |
24 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.200-859C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438799 | |||||||
| chr17:4438800 | T | C | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-858T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4438800 | |||||||
| chr17:4438940 | C | CTG | 13 | a0001c0001t0001g0035 a0001c0001t0001g0147 a0001c0001t0001g0238 others(10): Show |
13 | HG00639.hp2 HG01074.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.200-694_200-693dup others(2): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4438940 | ||||||
| chr17:4438940 | CTG | C | 93 | a0001c0001t0001g0098 a0001c0001t0001g0246 a0001c0001t0001g0251 others(90): Show |
93 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.200-694_200-693del others(2): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4438940 | ||||||
| chr17:4438940 | CTGTG | C | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-696_200-693del others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4438940 | ||||||
| chr17:4439012 | C | A | 1 | a0001c0013t0001g0259 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.200-646C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4439012 | |||||||
| chr17:4439014 | A | C | 1 | a0001c0013t0001g0259 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.200-644A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4439014 | |||||||
| chr17:4439061 | G | A | 10 | a0001c0001t0002g0317 a0001c0003t0001g0318 a0001c0003t0001g0320 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.200-597G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4439061 | |||||||
| chr17:4439097 | G | T | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-561G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4439097 | |||||||
| chr17:4439130 | C | CTTT | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-520_200-518dup others(3): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 4439130 | ||||||
| chr17:4439151 | G | A | 23 | a0001c0001t0001g0332 a0001c0001t0001g0334 a0001c0001t0001g0335 others(20): Show |
23 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.200-507G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4439151 | |||||||
| chr17:4439153 | G | A | 75 | a0001c0001t0001g0098 a0001c0001t0001g0246 a0001c0001t0001g0251 others(72): Show |
75 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.200-505G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4439153 | |||||||
| chr17:4439273 | G | A | 2 | a0001c0012t0001g0036 a0001c0012t0001g0037 |
2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.200-385G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4439273 | |||||||
| chr17:4439326 | C | T | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-332C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4439326 | |||||||
| chr17:4439389 | C | G | 175 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0001c0001t0001g0147 others(172): Show |
175 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.200-269C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4439389 | |||||||
| chr17:4439416 | G | A | 36 | a0001c0001t0001g0332 a0001c0001t0001g0334 a0001c0001t0001g0335 others(33): Show |
36 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.200-242G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4439416 | |||||||
| chr17:4439417 | T | C | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.200-241T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4439417 | |||||||
| chr17:4439428 | G | A | 24 | a0001c0001t0001g0332 a0001c0001t0001g0334 a0001c0001t0001g0335 others(21): Show |
24 | HG01109.hp1 HG01884.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.200-230G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 1/11 | chr17 | 4439428 | |||||||
| chr17:4439793 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.265+70A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4439793 | |||||||
| chr17:4439818 | A | T | 1 | a0001c0001t0001g0246 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.265+95A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4439818 | |||||||
| chr17:4439855 | G | A | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.265+132G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4439855 | |||||||
| chr17:4439858 | T | G | 8 | a0001c0001t0002g0160 a0001c0006t0001g0010 a0001c0006t0002g0011 others(5): Show |
8 | HG02055.hp2 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.265+135T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4439858 | |||||||
| chr17:4439892 | T | C | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.265+169T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4439892 | |||||||
| chr17:4439902 | C | T | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.265+179C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4439902 | |||||||
| chr17:4439932 | C | T | 2 | a0001c0001t0001g0035 a0001c0044t0002g0236 |
2 | HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.265+209C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4439932 | |||||||
| chr17:4439937 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.265+214G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4439937 | |||||||
| chr17:4439970 | C | G | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.265+247C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4439970 | |||||||
| chr17:4440090 | A | C | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.265+367A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4440090 | |||||||
| chr17:4440156 | A | G | 18 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.265+433A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4440156 | |||||||
| chr17:4440230 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.265+507G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4440230 | |||||||
| chr17:4440260 | G | A | 17 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(14): Show |
17 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.265+537G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4440260 | |||||||
| chr17:4440381 | G | A | 17 | a0001c0001t0002g0162 a0001c0003t0001g0110 a0001c0003t0001g0152 others(14): Show |
17 | HG00323.hp1 HG01074.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.265+658G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4440381 | |||||||
| chr17:4440404 | C | T | 27 | a0001c0001t0001g0111 a0001c0001t0001g0332 a0001c0001t0001g0334 others(24): Show |
27 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.265+681C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4440404 | |||||||
| chr17:4440426 | C | G | 27 | a0001c0001t0002g0143 a0001c0001t0002g0162 a0001c0003t0001g0110 others(24): Show |
27 | HG00323.hp1 HG00741.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.265+703C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4440426 | |||||||
| chr17:4440461 | T | C | 1 | a0003c0005t0001g0171 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.265+738T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4440461 | |||||||
| chr17:4440651 | A | G | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+928A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4440651 | |||||||
| chr17:4440730 | T | C | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+1007T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4440730 | |||||||
| chr17:4440753 | A | G | 42 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(39): Show |
42 | HG00323.hp1 HG00609.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.265+1030A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4440753 | |||||||
| chr17:4441016 | G | T | 1 | a0001c0013t0001g0259 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.265+1293G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441016 | |||||||
| chr17:4441034 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.265+1311C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441034 | |||||||
| chr17:4441150 | G | A | 1 | a0004c0048t0002g0006 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.265+1427G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441150 | |||||||
| chr17:4441171 | C | T | 2 | a0001c0007t0003g0337 a0001c0023t0003g0014 |
2 | HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.265+1448C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441171 | |||||||
| chr17:4441244 | C | T | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+1521C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441244 | |||||||
| chr17:4441245 | A | G | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+1522A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441245 | |||||||
| chr17:4441372 | A | T | 23 | a0001c0001t0001g0111 a0001c0001t0001g0332 a0001c0001t0001g0334 others(20): Show |
23 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.265+1649A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441372 | |||||||
| chr17:4441399 | A | G | 1 | a0002c0011t0003g0258 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.265+1676A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441399 | |||||||
| chr17:4441421 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.265+1698A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441421 | |||||||
| chr17:4441451 | A | G | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.265+1728A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441451 | |||||||
| chr17:4441467 | A | G | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+1744A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441467 | |||||||
| chr17:4441545 | G | A | 1 | a0001c0001t0001g0360 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.265+1822G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441545 | |||||||
| chr17:4441591 | T | C | 1 | a0002c0002t0001g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.265+1868T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441591 | |||||||
| chr17:4441650 | G | A | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+1927G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441650 | |||||||
| chr17:4441740 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.265+2017G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441740 | |||||||
| chr17:4441744 | C | A | 1 | a0001c0013t0001g0259 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.265+2021C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441744 | |||||||
| chr17:4441757 | A | G | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.265+2034A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441757 | |||||||
| chr17:4441778 | A | G | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+2055A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441778 | |||||||
| chr17:4441798 | T | C | 2 | a0002c0002t0001g0265 a0002c0002t0001g0266 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.265+2075T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441798 | |||||||
| chr17:4441799 | T | TG | 63 | a0001c0001t0001g0035 a0001c0001t0001g0147 a0001c0001t0001g0233 others(60): Show |
63 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.265+2084dupG | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441799 | ||||||
| chr17:4441893 | A | G | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+2170A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441893 | |||||||
| chr17:4441981 | G | GGTGTGTG others(3): Show |
2 | a0001c0003t0001g0177 a0001c0003t0002g0127 |
2 | HG02809.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.265+2258_265+2259i others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441981 | |||||||
| chr17:4441981 | G | GGTGTGTG others(5): Show |
8 | a0001c0003t0001g0126 a0001c0003t0001g0145 a0001c0003t0001g0146 others(5): Show |
8 | HG00642.hp1 HG01106.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.265+2258_265+2259i others(14): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441981 | |||||||
| chr17:4441981 | G | GGTGTGTG others(7): Show |
30 | a0001c0001t0001g0147 a0001c0003t0001g0121 a0001c0003t0001g0122 others(27): Show |
30 | HG00280.hp1 HG01074.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.265+2258_265+2259i others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441981 | |||||||
| chr17:4441981 | G | GGTGTGTG others(9): Show |
8 | a0001c0001t0002g0160 a0001c0001t0002g0342 a0001c0001t0002g0343 others(5): Show |
8 | HG01106.hp1 HG01255.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.265+2258_265+2259i others(18): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441981 | |||||||
| chr17:4441981 | G | GGTGTGTG others(11): Show |
8 | a0001c0001t0001g0035 a0001c0003t0002g0137 a0001c0003t0002g0138 others(5): Show |
8 | HG00642.hp2 HG00741.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.265+2258_265+2259i others(20): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441981 | |||||||
| chr17:4441981 | G | GGTGTGTG others(13): Show |
3 | a0001c0003t0002g0136 a0003c0005t0001g0310 a0003c0008t0003g0174 |
3 | HG01169.hp2 HG01433.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.265+2258_265+2259i others(22): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441981 | |||||||
| chr17:4441981 | G | GGTGTGTG others(15): Show |
1 | a0010c0041t0003g0314 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.265+2258_265+2259i others(24): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441981 | |||||||
| chr17:4441982 | A | G | 61 | a0001c0001t0001g0035 a0001c0001t0001g0147 a0001c0001t0002g0160 others(58): Show |
61 | HG00280.hp1 HG00597.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.265+2259A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441982 | |||||||
| chr17:4441983 | A | AGT | 16 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0179 others(13): Show |
16 | HG01175.hp1 HG01257.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.265+2293_265+2294d others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441983 | ||||||
| chr17:4441983 | A | AGTGT | 8 | a0001c0010t0001g0078 a0001c0010t0001g0080 a0001c0010t0002g0081 others(5): Show |
8 | HG01069.hp2 HG01081.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.265+2291_265+2294d others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441983 | ||||||
| chr17:4441983 | A | AGTGTGT | 3 | a0001c0006t0001g0010 a0001c0006t0002g0011 a0001c0006t0002g0012 |
3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.265+2289_265+2294d others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441983 | ||||||
| chr17:4441983 | A | AGTGTGTG others(3): Show |
16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0317 others(13): Show |
16 | HG00099.hp2 HG01256.hp2 HG02148.hp1 others(13): Show |
intron_variant | MODIFIER | c.265+2285_265+2294d others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441983 | ||||||
| chr17:4441983 | A | AGTGTGTG others(5): Show |
3 | a0001c0006t0002g0048 a0001c0038t0003g0291 a0002c0002t0001g0303 |
3 | HG00621.hp1 HG02257.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.265+2283_265+2294d others(14): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441983 | ||||||
| chr17:4441983 | A | AGTGTGTG others(7): Show |
51 | a0001c0001t0001g0030 a0001c0001t0001g0129 a0001c0001t0001g0130 others(48): Show |
51 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.265+2281_265+2294d others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441983 | ||||||
| chr17:4441983 | A | AGTGTGTG others(9): Show |
27 | a0001c0001t0001g0154 a0001c0001t0001g0238 a0001c0001t0001g0271 others(24): Show |
27 | HG00323.hp1 HG01099.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.265+2279_265+2294d others(18): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441983 | ||||||
| chr17:4441983 | A | AGTGTGTG others(11): Show |
13 | a0001c0003t0001g0152 a0001c0003t0001g0346 a0001c0006t0002g0052 others(10): Show |
13 | HG01081.hp2 HG01099.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.265+2277_265+2294d others(20): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441983 | ||||||
| chr17:4441983 | A | AGTGTGTG others(13): Show |
6 | a0001c0009t0001g0005 a0001c0009t0001g0058 a0001c0045t0003g0150 others(3): Show |
6 | HG00639.hp2 HG01074.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+2275_265+2294d others(22): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441983 | ||||||
| chr17:4441983 | A | AGTGTGTG others(15): Show |
2 | a0001c0001t0001g0263 a0001c0024t0003g0057 |
2 | HG00609.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.265+2273_265+2294d others(24): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441983 | ||||||
| chr17:4441983 | A | AGTGTGTG others(17): Show |
1 | a0001c0007t0003g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.265+2271_265+2294d others(26): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441983 | ||||||
| chr17:4441983 | A | T | 61 | a0001c0001t0001g0035 a0001c0001t0001g0147 a0001c0001t0002g0160 others(58): Show |
61 | HG00280.hp1 HG00597.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.265+2260A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4441983 | |||||||
| chr17:4441983 | AGT | A | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | NA18955.hp1 NA18969.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+2293_265+2294d others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441983 | ||||||
| chr17:4441983 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0028 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.265+2285_265+2294d others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4441983 | ||||||
| chr17:4442017 | T | TGTGTGTG others(6): Show |
1 | a0002c0002t0001g0354 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.265+2294_265+2295i others(15): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442017 | |||||||
| chr17:4442017 | T | TGTGTGTG others(8): Show |
1 | a0002c0002t0001g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.265+2294_265+2295i others(17): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442017 | |||||||
| chr17:4442017 | T | TGTGTGTG others(10): Show |
2 | a0001c0001t0001g0297 a0003c0005t0001g0114 |
2 | HG00597.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.265+2294_265+2295i others(19): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442017 | |||||||
| chr17:4442017 | T | TGTGTGTG others(12): Show |
1 | a0001c0003t0001g0309 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.265+2294_265+2295i others(21): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442017 | |||||||
| chr17:4442028 | G | A | 3 | a0001c0001t0001g0275 a0001c0013t0001g0178 a0002c0011t0003g0258 |
3 | NA18747.hp1 NA18962.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.265+2305G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442028 | |||||||
| chr17:4442039 | G | T | 3 | a0001c0001t0002g0160 a0001c0001t0002g0342 a0001c0001t0002g0343 |
3 | HG02055.hp2 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.265+2316G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442039 | |||||||
| chr17:4442148 | C | T | 2 | a0003c0005t0001g0234 a0003c0005t0001g0235 |
2 | NA19011.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.265+2425C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442148 | |||||||
| chr17:4442155 | C | T | 2 | a0001c0003t0001g0152 a0001c0009t0002g0076 |
2 | NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.265+2432C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442155 | |||||||
| chr17:4442156 | G | A | 2 | a0001c0007t0003g0337 a0001c0023t0003g0014 |
2 | HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.265+2433G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442156 | |||||||
| chr17:4442253 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.265+2530T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442253 | |||||||
| chr17:4442303 | T | TGAGGC | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+2581_265+2582i others(7): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4442303 | ||||||
| chr17:4442323 | G | A | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+2600G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442323 | |||||||
| chr17:4442325 | G | A | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+2602G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442325 | |||||||
| chr17:4442330 | T | C | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+2607T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442330 | |||||||
| chr17:4442343 | G | A | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.265+2620G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442343 | |||||||
| chr17:4442393 | T | C | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.266-2639T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442393 | |||||||
| chr17:4442443 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.266-2589G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442443 | |||||||
| chr17:4442488 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | NA18952.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.266-2544G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442488 | |||||||
| chr17:4442492 | C | T | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.266-2540C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442492 | |||||||
| chr17:4442530 | C | CA | 14 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(11): Show |
14 | HG00738.hp1 HG00741.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.266-2492dupA | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4442530 | ||||||
| chr17:4442530 | C | CAA | 42 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(39): Show |
42 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.266-2493_266-2492d others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4442530 | ||||||
| chr17:4442598 | C | A | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.266-2434C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442598 | |||||||
| chr17:4442626 | G | A | 3 | a0001c0004t0001g0056 a0001c0004t0001g0065 a0001c0004t0001g0066 |
3 | NA18960.hp2 NA18965.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.266-2406G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442626 | |||||||
| chr17:4442690 | C | T | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.266-2342C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442690 | |||||||
| chr17:4442917 | G | C | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.266-2115G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442917 | |||||||
| chr17:4442932 | G | T | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.266-2100G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442932 | |||||||
| chr17:4442934 | G | A | 1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.266-2098G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442934 | |||||||
| chr17:4442979 | G | A | 1 | a0001c0006t0002g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.266-2053G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4442979 | |||||||
| chr17:4443077 | G | GT | 13 | a0001c0001t0001g0168 a0001c0001t0001g0231 a0001c0001t0001g0353 others(10): Show |
13 | HG00099.hp1 HG00323.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.266-1944dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4443077 | ||||||
| chr17:4443077 | GT | G | 104 | a0001c0001t0001g0035 a0001c0001t0001g0111 a0001c0001t0001g0147 others(101): Show |
104 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.266-1944delT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4443077 | ||||||
| chr17:4443093 | G | A | 2 | a0008c0019t0001g0340 a0008c0019t0001g0341 |
2 | HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.266-1939G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443093 | |||||||
| chr17:4443097 | C | G | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-1935C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443097 | |||||||
| chr17:4443126 | A | C | 2 | a0001c0001t0002g0162 a0001c0007t0003g0161 |
2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.266-1906A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443126 | |||||||
| chr17:4443133 | C | T | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.266-1899C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443133 | |||||||
| chr17:4443220 | G | A | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.266-1812G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443220 | |||||||
| chr17:4443238 | C | T | 43 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(40): Show |
43 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.266-1794C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443238 | |||||||
| chr17:4443243 | G | C | 1 | a0001c0014t0002g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.266-1789G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443243 | |||||||
| chr17:4443305 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.266-1727G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443305 | |||||||
| chr17:4443362 | C | T | 1 | a0001c0014t0002g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.266-1670C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443362 | |||||||
| chr17:4443364 | T | C | 42 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(39): Show |
42 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.266-1668T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443364 | |||||||
| chr17:4443512 | T | C | 42 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(39): Show |
42 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.266-1520T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443512 | |||||||
| chr17:4443541 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.266-1491T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443541 | |||||||
| chr17:4443616 | G | A | 1 | a0001c0003t0002g0315 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.266-1416G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443616 | |||||||
| chr17:4443660 | A | C | 40 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(37): Show |
40 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.266-1372A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443660 | |||||||
| chr17:4443684 | T | C | 226 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(223): Show |
226 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.266-1348T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443684 | |||||||
| chr17:4443826 | C | A | 40 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(37): Show |
40 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.266-1206C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443826 | |||||||
| chr17:4443838 | C | T | 1 | a0001c0003t0001g0346 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.266-1194C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443838 | |||||||
| chr17:4443849 | C | G | 1 | a0001c0006t0001g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.266-1183C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443849 | |||||||
| chr17:4443867 | G | A | 62 | a0001c0001t0001g0238 a0001c0001t0001g0260 a0001c0001t0001g0271 others(59): Show |
62 | HG00099.hp2 HG00621.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.266-1165G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443867 | |||||||
| chr17:4443875 | C | T | 40 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(37): Show |
40 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.266-1157C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443875 | |||||||
| chr17:4443952 | T | G | 1 | a0001c0001t0001g0347 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.266-1080T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4443952 | |||||||
| chr17:4444005 | A | G | 40 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(37): Show |
40 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.266-1027A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4444005 | |||||||
| chr17:4444083 | A | G | 40 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(37): Show |
40 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.266-949A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4444083 | |||||||
| chr17:4444175 | C | T | 40 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(37): Show |
40 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.266-857C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4444175 | |||||||
| chr17:4444220 | C | CT | 41 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(38): Show |
41 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.266-800dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 4444220 | ||||||
| chr17:4444317 | C | T | 12 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(9): Show |
12 | HG01167.hp2 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.266-715C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4444317 | |||||||
| chr17:4444337 | C | T | 1 | a0001c0003t0001g0152 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.266-695C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4444337 | |||||||
| chr17:4444355 | C | T | 40 | a0001c0001t0001g0111 a0001c0001t0001g0263 a0001c0001t0001g0332 others(37): Show |
40 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.266-677C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4444355 | |||||||
| chr17:4444411 | T | G | 2 | a0001c0001t0001g0035 a0001c0044t0002g0236 |
2 | HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.266-621T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4444411 | |||||||
| chr17:4444434 | G | A | 1 | a0001c0009t0004g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.266-598G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4444434 | |||||||
| chr17:4444515 | G | A | 38 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(35): Show |
38 | HG01074.hp1 HG01891.hp1 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.266-517G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4444515 | |||||||
| chr17:4444592 | T | C | 17 | a0001c0001t0001g0263 a0001c0001t0002g0143 a0001c0003t0001g0110 others(14): Show |
17 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.266-440T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4444592 | |||||||
| chr17:4444607 | C | A | 5 | a0001c0009t0002g0031 a0004c0017t0002g0029 a0004c0017t0002g0331 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-425C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4444607 | |||||||
| chr17:4444609 | G | C | 5 | a0001c0009t0002g0031 a0004c0017t0002g0029 a0004c0017t0002g0331 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-423G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4444609 | |||||||
| chr17:4444922 | A | G | 8 | a0001c0003t0001g0121 a0001c0003t0001g0122 a0001c0003t0001g0123 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.266-110A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 2/11 | chr17 | 4444922 | |||||||
| chr17:4445191 | A | G | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG01167.hp2 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+23A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | chr17 | 4445191 | |||||||
| chr17:4445238 | C | T | 22 | a0001c0001t0001g0111 a0001c0001t0001g0332 a0001c0001t0001g0334 others(19): Show |
22 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.402+70C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | chr17 | 4445238 | |||||||
| chr17:4445375 | C | CT | 41 | a0001c0001t0001g0030 a0001c0001t0001g0129 a0001c0001t0001g0130 others(38): Show |
41 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.402+224dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 4445375 | ||||||
| chr17:4445375 | CTT | C | 73 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0003t0001g0121 others(70): Show |
73 | HG00280.hp1 HG00597.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.402+223_402+224del others(2): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 4445375 | ||||||
| chr17:4445375 | CTTT | C | 28 | a0001c0001t0001g0111 a0001c0001t0001g0332 a0001c0001t0001g0334 others(25): Show |
28 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.402+222_402+224del others(3): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 4445375 | ||||||
| chr17:4445568 | G | A | 100 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0111 others(97): Show |
100 | HG00280.hp1 HG00597.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.402+400G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | chr17 | 4445568 | |||||||
| chr17:4445593 | T | C | 13 | a0001c0001t0001g0028 a0001c0003t0002g0256 a0001c0010t0001g0078 others(10): Show |
13 | HG00738.hp2 HG01069.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.402+425T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | chr17 | 4445593 | |||||||
| chr17:4445727 | G | A | 54 | a0001c0001t0001g0035 a0001c0003t0001g0121 a0001c0003t0001g0122 others(51): Show |
54 | HG00280.hp1 HG00597.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.403-321G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | chr17 | 4445727 | |||||||
| chr17:4445737 | C | T | 6 | a0001c0003t0001g0320 a0001c0003t0001g0346 a0001c0003t0002g0315 others(3): Show |
6 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.403-311C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | chr17 | 4445737 | |||||||
| chr17:4445750 | C | T | 11 | a0001c0001t0001g0028 a0001c0003t0002g0256 a0001c0010t0001g0078 others(8): Show |
11 | HG00738.hp2 HG01069.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.403-298C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | chr17 | 4445750 | |||||||
| chr17:4445837 | T | C | 98 | a0001c0001t0001g0035 a0001c0001t0001g0129 a0001c0001t0001g0130 others(95): Show |
98 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.403-211T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | chr17 | 4445837 | |||||||
| chr17:4445878 | C | G | 11 | a0001c0003t0002g0256 a0001c0010t0001g0078 a0001c0010t0001g0080 others(8): Show |
11 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.403-170C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | chr17 | 4445878 | |||||||
| chr17:4445879 | G | C | 3 | a0001c0018t0002g0349 a0001c0018t0002g0350 a0001c0049t0002g0003 |
3 | HG02572.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.403-169G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | chr17 | 4445879 | |||||||
| chr17:4445905 | G | A | 10 | a0001c0003t0002g0256 a0001c0010t0001g0078 a0001c0010t0001g0080 others(7): Show |
10 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-143G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 3/11 | chr17 | 4445905 | |||||||
| chr17:4446213 | G | A | 46 | a0001c0001t0001g0030 a0001c0001t0001g0147 a0001c0001t0002g0046 others(43): Show |
46 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.554+14G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446213 | |||||||
| chr17:4446273 | C | T | 2 | a0001c0003t0001g0126 a0005c0015t0003g0104 |
2 | HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.554+74C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446273 | |||||||
| chr17:4446286 | G | A | 1 | a0001c0001t0001g0348 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.554+87G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446286 | |||||||
| chr17:4446396 | A | T | 1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.554+197A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446396 | |||||||
| chr17:4446427 | T | G | 1 | a0001c0007t0003g0158 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.554+228T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446427 | |||||||
| chr17:4446676 | C | T | 1 | a0002c0002t0001g0293 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.555-220C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446676 | |||||||
| chr17:4446706 | C | T | 22 | a0001c0001t0001g0111 a0001c0001t0001g0332 a0001c0001t0001g0334 others(19): Show |
22 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.555-190C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446706 | |||||||
| chr17:4446719 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.555-177C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446719 | |||||||
| chr17:4446746 | G | A | 1 | a0001c0012t0001g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.555-150G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446746 | |||||||
| chr17:4446804 | C | T | 10 | a0001c0004t0001g0075 a0001c0009t0002g0022 a0001c0009t0002g0023 others(7): Show |
10 | HG01099.hp1 HG01109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.555-92C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446804 | |||||||
| chr17:4446807 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.555-89G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446807 | |||||||
| chr17:4446807 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.555-89G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446807 | |||||||
| chr17:4446809 | G | T | 23 | a0001c0001t0001g0111 a0001c0001t0001g0332 a0001c0001t0001g0334 others(20): Show |
23 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.555-87G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446809 | |||||||
| chr17:4446840 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.555-56G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446840 | |||||||
| chr17:4446875 | G | A | 1 | a0003c0005t0002g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.555-21G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446875 | |||||||
| chr17:4446887 | T | C | 234 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(231): Show |
234 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.555-9T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 4/11 | chr17 | 4446887 | |||||||
| chr17:4447033 | C | T | 1 | a0002c0002t0001g0230 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.621+71C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447033 | |||||||
| chr17:4447072 | A | G | 230 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(227): Show |
230 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.621+110A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447072 | |||||||
| chr17:4447078 | GGT | G | 204 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(201): Show |
204 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.621+118_621+119del others(2): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 4447078 | ||||||
| chr17:4447079 | GT | G | 21 | a0001c0001t0001g0111 a0001c0001t0001g0332 a0001c0001t0001g0334 others(18): Show |
21 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.621+118delT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447079 | |||||||
| chr17:4447112 | G | C | 206 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(203): Show |
206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.621+150G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447112 | |||||||
| chr17:4447324 | G | A | 17 | a0001c0001t0001g0111 a0001c0001t0001g0332 a0001c0001t0001g0334 others(14): Show |
17 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.621+362G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447324 | |||||||
| chr17:4447345 | T | A | 1 | a0001c0006t0002g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.621+383T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447345 | |||||||
| chr17:4447345 | T | G | 70 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(67): Show |
70 | HG00280.hp1 HG00597.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.621+383T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447345 | |||||||
| chr17:4447370 | C | G | 227 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(224): Show |
227 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.621+408C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447370 | |||||||
| chr17:4447476 | T | C | 1 | a0002c0002t0001g0288 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.621+514T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447476 | |||||||
| chr17:4447536 | C | G | 1 | a0001c0009t0001g0005 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.621+574C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447536 | |||||||
| chr17:4447564 | G | A | 1 | a0003c0005t0001g0175 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.622-591G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447564 | |||||||
| chr17:4447695 | T | G | 104 | a0001c0003t0001g0110 a0001c0003t0001g0121 a0001c0003t0001g0122 others(101): Show |
104 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.622-460T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447695 | |||||||
| chr17:4447699 | T | C | 8 | a0001c0001t0001g0035 a0001c0012t0001g0036 a0001c0012t0001g0037 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.622-456T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447699 | |||||||
| chr17:4447735 | G | T | 3 | a0001c0003t0001g0320 a0001c0003t0001g0346 a0001c0034t0002g0045 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.622-420G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447735 | |||||||
| chr17:4447752 | C | T | 5 | a0001c0006t0001g0010 a0001c0006t0002g0011 a0001c0006t0002g0012 others(2): Show |
5 | HG01884.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.622-403C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447752 | |||||||
| chr17:4447819 | C | T | 5 | a0001c0006t0001g0010 a0001c0006t0002g0011 a0001c0006t0002g0012 others(2): Show |
5 | HG01884.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.622-336C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447819 | |||||||
| chr17:4447955 | C | G | 1 | a0001c0009t0004g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.622-200C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4447955 | |||||||
| chr17:4448017 | A | G | 142 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(139): Show |
142 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.622-138A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4448017 | |||||||
| chr17:4448050 | A | C | 210 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(207): Show |
210 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.622-105A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4448050 | |||||||
| chr17:4448101 | C | T | 210 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(207): Show |
210 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.622-54C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 5/11 | chr17 | 4448101 | |||||||
| chr17:4448342 | C | A | 1 | a0004c0017t0002g0331 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.770+39C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4448342 | |||||||
| chr17:4448345 | G | A | 210 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(207): Show |
210 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.770+42G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4448345 | |||||||
| chr17:4448377 | C | G | 9 | a0001c0009t0002g0022 a0001c0009t0002g0023 a0001c0009t0002g0024 others(6): Show |
9 | HG01099.hp1 HG01109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.770+74C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4448377 | |||||||
| chr17:4448492 | A | T | 210 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(207): Show |
210 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.770+189A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4448492 | |||||||
| chr17:4448518 | C | T | 2 | a0003c0005t0001g0106 a0003c0016t0001g0083 |
2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.770+215C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4448518 | |||||||
| chr17:4448555 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.770+252C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4448555 | |||||||
| chr17:4448624 | C | A | 2 | a0003c0005t0001g0106 a0003c0016t0001g0083 |
2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.770+321C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4448624 | |||||||
| chr17:4448638 | C | T | 5 | a0001c0003t0001g0121 a0001c0003t0001g0122 a0001c0003t0001g0123 others(2): Show |
5 | HG02451.hp1 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+335C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4448638 | |||||||
| chr17:4448703 | C | T | 34 | a0003c0005t0001g0106 a0003c0005t0001g0107 a0003c0005t0001g0114 others(31): Show |
34 | HG00280.hp1 HG00597.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.770+400C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4448703 | |||||||
| chr17:4448864 | G | C | 6 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.771-371G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4448864 | |||||||
| chr17:4448964 | G | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0311 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.771-271G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4448964 | |||||||
| chr17:4448970 | T | A | 17 | a0001c0001t0001g0111 a0001c0001t0001g0332 a0001c0001t0001g0334 others(14): Show |
17 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.771-265T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4448970 | |||||||
| chr17:4449046 | A | C | 38 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(35): Show |
38 | HG01074.hp1 HG01167.hp2 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.771-189A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4449046 | |||||||
| chr17:4449087 | G | A | 1 | a0002c0022t0001g0055 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.771-148G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 6/11 | chr17 | 4449087 | |||||||
| chr17:4449504 | T | G | 204 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0111 others(201): Show |
204 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.923+117T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4449504 | |||||||
| chr17:4449594 | A | G | 195 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0111 others(192): Show |
195 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.923+207A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4449594 | |||||||
| chr17:4449620 | T | TC | 36 | a0001c0010t0001g0084 a0003c0005t0001g0106 a0003c0005t0001g0107 others(33): Show |
36 | HG00280.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.923+237dupC | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 4449620 | ||||||
| chr17:4449652 | G | A | 1 | a0001c0014t0002g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.923+265G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4449652 | |||||||
| chr17:4449701 | T | C | 4 | a0001c0001t0002g0162 a0001c0007t0003g0161 a0001c0007t0003g0172 others(1): Show |
4 | HG00099.hp1 HG01070.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+314T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4449701 | |||||||
| chr17:4449766 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(150): Show |
154 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.923+379C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4449766 | |||||||
| chr17:4449827 | T | G | 8 | a0001c0001t0002g0160 a0001c0006t0001g0010 a0001c0006t0002g0011 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.923+440T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4449827 | |||||||
| chr17:4449862 | G | A | 7 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0194 others(4): Show |
7 | HG01099.hp1 HG01167.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.923+475G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4449862 | |||||||
| chr17:4449864 | G | T | 1 | a0001c0001t0002g0330 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.923+477G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4449864 | |||||||
| chr17:4449885 | C | T | 7 | a0001c0001t0001g0028 a0001c0001t0002g0330 a0001c0003t0001g0346 others(4): Show |
7 | HG02280.hp1 HG02717.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.923+498C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4449885 | |||||||
| chr17:4449886 | G | A | 1 | a0001c0004t0001g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.923+499G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4449886 | |||||||
| chr17:4450026 | C | G | 1 | a0004c0048t0002g0006 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.923+639C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450026 | |||||||
| chr17:4450060 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.923+673C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450060 | |||||||
| chr17:4450064 | T | G | 2 | a0001c0001t0002g0143 a0001c0007t0003g0163 |
2 | HG00639.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.923+677T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450064 | |||||||
| chr17:4450124 | G | A | 19 | a0001c0001t0001g0332 a0001c0001t0001g0334 a0001c0003t0001g0121 others(16): Show |
19 | HG00741.hp2 HG01433.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.923+737G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450124 | |||||||
| chr17:4450155 | G | A | 4 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 others(1): Show |
4 | HG02809.hp2 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+768G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450155 | |||||||
| chr17:4450278 | C | T | 1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.923+891C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450278 | |||||||
| chr17:4450305 | CTCTCTTT others(8): Show |
C | 4 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 others(1): Show |
4 | HG02809.hp2 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+919_923+933del others(15): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450305 | |||||||
| chr17:4450338 | C | A | 5 | a0001c0001t0001g0028 a0001c0003t0001g0346 a0001c0003t0002g0315 others(2): Show |
5 | HG02717.hp1 HG02965.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.923+951C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450338 | |||||||
| chr17:4450351 | C | T | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.923+964C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450351 | |||||||
| chr17:4450353 | T | TTCTC | 61 | a0001c0001t0001g0030 a0001c0001t0001g0154 a0001c0001t0001g0311 others(58): Show |
61 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.923+966_923+967ins others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450353 | |||||||
| chr17:4450354 | C | CCTCT | 145 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(142): Show |
145 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.923+979_923+982dup others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 4450354 | ||||||
| chr17:4450354 | C | CCTCTCT | 25 | a0001c0001t0001g0111 a0001c0001t0001g0335 a0001c0001t0001g0338 others(22): Show |
25 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.923+977_923+982dup others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 4450354 | ||||||
| chr17:4450354 | C | T | 61 | a0001c0001t0001g0030 a0001c0001t0001g0154 a0001c0001t0001g0311 others(58): Show |
61 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.923+967C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450354 | |||||||
| chr17:4450557 | G | A | 4 | a0002c0002t0001g0142 a0002c0002t0001g0228 a0002c0002t0001g0273 others(1): Show |
4 | HG01192.hp1 HG01346.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+1170G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450557 | |||||||
| chr17:4450562 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0105 others(125): Show |
129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.923+1175C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450562 | |||||||
| chr17:4450604 | A | AC | 5 | a0001c0001t0001g0028 a0001c0003t0001g0346 a0001c0003t0002g0315 others(2): Show |
5 | HG02717.hp1 HG02965.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.923+1217_923+1218i others(3): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450604 | |||||||
| chr17:4450608 | T | A | 7 | a0001c0023t0003g0014 a0001c0031t0005g0033 a0002c0002t0001g0094 others(4): Show |
7 | HG01346.hp1 HG01496.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.923+1221T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450608 | |||||||
| chr17:4450679 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0105 others(130): Show |
134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.923+1292T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450679 | |||||||
| chr17:4450760 | C | T | 3 | a0003c0005t0002g0155 a0003c0008t0003g0119 a0003c0016t0002g0082 |
3 | HG01106.hp1 HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.923+1373C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450760 | |||||||
| chr17:4450762 | A | AT | 136 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0035 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.923+1392dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 4450762 | ||||||
| chr17:4450762 | A | ATT | 54 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.923+1391_923+1392d others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 4450762 | ||||||
| chr17:4450762 | AT | A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0317 others(5): Show |
8 | HG02615.hp2 HG02886.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.923+1392delT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 4450762 | ||||||
| chr17:4450815 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.923+1428G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450815 | |||||||
| chr17:4450852 | C | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(80): Show |
84 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.923+1465C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450852 | |||||||
| chr17:4450867 | C | T | 2 | a0001c0001t0002g0143 a0001c0007t0003g0163 |
2 | HG00639.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.923+1480C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450867 | |||||||
| chr17:4450898 | G | A | 2 | a0001c0003t0001g0346 a0001c0034t0002g0045 |
2 | HG02717.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.923+1511G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450898 | |||||||
| chr17:4450962 | G | A | 146 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(143): Show |
146 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.923+1575G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450962 | |||||||
| chr17:4450998 | G | C | 45 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(42): Show |
45 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.923+1611G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4450998 | |||||||
| chr17:4451053 | A | C | 148 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(145): Show |
148 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.923+1666A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451053 | |||||||
| chr17:4451104 | G | A | 3 | a0001c0006t0001g0010 a0001c0007t0003g0158 a0001c0007t0003g0319 |
3 | HG01884.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.923+1717G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451104 | |||||||
| chr17:4451197 | C | G | 147 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(144): Show |
147 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.923+1810C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451197 | |||||||
| chr17:4451230 | A | ACTT | 147 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(144): Show |
147 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.924-1770_924-1768d others(5): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 4451230 | ||||||
| chr17:4451250 | G | GT | 11 | a0001c0001t0001g0195 a0001c0001t0001g0216 a0001c0001t0001g0306 others(8): Show |
11 | HG00438.hp2 HG01123.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.924-1752dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 4451250 | ||||||
| chr17:4451264 | TC | T | 136 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0129 others(133): Show |
136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.924-1750delC | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 4451264 | ||||||
| chr17:4451265 | C | T | 11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0317 others(8): Show |
11 | HG01361.hp2 HG01928.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.924-1751C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451265 | |||||||
| chr17:4451389 | C | T | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.924-1627C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451389 | |||||||
| chr17:4451413 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 others(1): Show |
4 | HG02809.hp2 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.924-1603A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451413 | |||||||
| chr17:4451459 | A | G | 1 | a0001c0001t0002g0336 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.924-1557A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451459 | |||||||
| chr17:4451661 | A | ATTTGT | 4 | a0001c0003t0001g0346 a0001c0003t0002g0315 a0001c0034t0002g0045 others(1): Show |
4 | HG02717.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.924-1336_924-1332d others(7): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 4451661 | ||||||
| chr17:4451674 | T | A | 3 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 |
3 | HG02809.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.924-1342T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451674 | |||||||
| chr17:4451690 | C | T | 3 | a0001c0018t0002g0349 a0001c0018t0002g0350 a0001c0036t0003g0144 |
3 | HG02896.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.924-1326C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451690 | |||||||
| chr17:4451817 | C | T | 8 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.924-1199C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451817 | |||||||
| chr17:4451833 | T | C | 1 | a0002c0002t0001g0157 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.924-1183T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451833 | |||||||
| chr17:4451841 | G | GT | 3 | a0001c0003t0001g0318 a0001c0003t0002g0139 a0001c0003t0002g0148 |
3 | HG00741.hp2 HG01981.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.924-1174dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 4451841 | ||||||
| chr17:4451843 | A | AT | 75 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(72): Show |
75 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.924-1158dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 4451843 | ||||||
| chr17:4451843 | A | T | 22 | a0001c0001t0001g0332 a0001c0001t0001g0334 a0001c0001t0002g0162 others(19): Show |
22 | HG00099.hp1 HG00741.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.924-1173A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451843 | |||||||
| chr17:4451868 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 |
3 | HG02809.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.924-1148G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451868 | |||||||
| chr17:4451878 | T | C | 161 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(158): Show |
161 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.924-1138T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4451878 | |||||||
| chr17:4452038 | A | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.924-978A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452038 | |||||||
| chr17:4452041 | A | G | 12 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-975A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452041 | |||||||
| chr17:4452067 | C | A | 12 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-949C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452067 | |||||||
| chr17:4452158 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0311 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.924-858A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452158 | |||||||
| chr17:4452178 | C | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0311 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.924-838C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452178 | |||||||
| chr17:4452178 | C | T | 12 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-838C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452178 | |||||||
| chr17:4452200 | G | A | 1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.924-816G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452200 | |||||||
| chr17:4452219 | C | A | 1 | a0001c0044t0002g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.924-797C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452219 | |||||||
| chr17:4452286 | A | G | 12 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-730A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452286 | |||||||
| chr17:4452308 | C | G | 2 | a0001c0018t0002g0349 a0001c0018t0002g0350 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.924-708C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452308 | |||||||
| chr17:4452355 | T | G | 12 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-661T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452355 | |||||||
| chr17:4452446 | G | A | 12 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-570G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452446 | |||||||
| chr17:4452494 | G | A | 3 | a0001c0047t0002g0321 a0007c0025t0002g0040 a0007c0025t0002g0041 |
3 | HG02572.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.924-522G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452494 | |||||||
| chr17:4452562 | A | G | 1 | a0001c0035t0002g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.924-454A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452562 | |||||||
| chr17:4452568 | G | T | 1 | a0002c0002t0001g0245 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.924-448G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452568 | |||||||
| chr17:4452607 | G | A | 1 | a0002c0037t0002g0323 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.924-409G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452607 | |||||||
| chr17:4452631 | G | T | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.924-385G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452631 | |||||||
| chr17:4452784 | A | G | 12 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-232A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452784 | |||||||
| chr17:4452809 | G | A | 2 | a0001c0018t0002g0349 a0001c0018t0002g0350 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.924-207G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452809 | |||||||
| chr17:4452822 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.924-194C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452822 | |||||||
| chr17:4452837 | G | T | 12 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.924-179G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452837 | |||||||
| chr17:4452854 | G | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0002g0046 others(4): Show |
7 | HG02258.hp1 HG02630.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.924-162G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 7/11 | chr17 | 4452854 | |||||||
| chr17:4453418 | G | T | 12 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1113+213G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4453418 | |||||||
| chr17:4453481 | G | C | 4 | a0001c0001t0001g0147 a0001c0006t0001g0032 a0001c0006t0001g0077 others(1): Show |
4 | HG01074.hp1 HG02602.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+276G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4453481 | |||||||
| chr17:4453532 | C | T | 4 | a0002c0002t0001g0269 a0002c0002t0001g0270 a0002c0002t0001g0283 others(1): Show |
4 | HG02027.hp1 NA18612.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+327C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4453532 | |||||||
| chr17:4453541 | G | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(107): Show |
111 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1113+336G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4453541 | |||||||
| chr17:4453543 | G | A | 1 | a0002c0002t0001g0302 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1113+338G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4453543 | |||||||
| chr17:4453553 | G | C | 3 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 |
3 | HG02809.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1113+348G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4453553 | |||||||
| chr17:4453621 | G | GC | 110 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(107): Show |
111 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1113+416_1113+417i others(3): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4453621 | |||||||
| chr17:4453622 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(107): Show |
111 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1113+417G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4453622 | |||||||
| chr17:4453785 | G | T | 4 | a0001c0001t0001g0030 a0001c0001t0002g0046 a0001c0007t0003g0337 others(1): Show |
4 | HG02258.hp1 HG02630.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+580G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4453785 | |||||||
| chr17:4453955 | G | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(82): Show |
86 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.1113+750G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4453955 | |||||||
| chr17:4453986 | C | A | 3 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 |
3 | HG02809.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1113+781C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4453986 | |||||||
| chr17:4454026 | C | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0004t0001g0027 |
3 | HG02970.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1113+821C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454026 | |||||||
| chr17:4454148 | C | A | 12 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0004t0001g0027 others(9): Show |
12 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1113+943C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454148 | |||||||
| chr17:4454189 | T | C | 25 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0003t0001g0132 others(22): Show |
25 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.1113+984T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454189 | |||||||
| chr17:4454201 | G | T | 12 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1113+996G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454201 | |||||||
| chr17:4454270 | C | A | 1 | a0003c0016t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1113+1065C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454270 | |||||||
| chr17:4454349 | C | T | 11 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0004t0001g0027 others(8): Show |
11 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1113+1144C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454349 | |||||||
| chr17:4454418 | C | T | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+1213C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454418 | |||||||
| chr17:4454419 | A | C | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+1214A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454419 | |||||||
| chr17:4454478 | A | G | 161 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(158): Show |
161 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1113+1273A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454478 | |||||||
| chr17:4454529 | T | C | 31 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0154 others(28): Show |
31 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1113+1324T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454529 | |||||||
| chr17:4454610 | C | CT | 13 | a0001c0001t0001g0165 a0001c0001t0001g0211 a0001c0001t0001g0212 others(10): Show |
13 | HG00438.hp1 HG00597.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+1429dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4454610 | ||||||
| chr17:4454610 | CT | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(119): Show |
123 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1113+1429delT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4454610 | ||||||
| chr17:4454610 | CTT | C | 70 | a0001c0001t0001g0147 a0001c0001t0001g0168 a0001c0001t0001g0218 others(67): Show |
70 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1113+1428_1113+142 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4454610 | ||||||
| chr17:4454610 | CTTT | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0002g0046 others(8): Show |
11 | HG01070.hp1 HG01975.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+1427_1113+142 others(7): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4454610 | ||||||
| chr17:4454610 | CTTTT | C | 23 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0003t0001g0132 others(20): Show |
23 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1113+1426_1113+142 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4454610 | ||||||
| chr17:4454645 | C | T | 20 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0002g0046 others(17): Show |
20 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1113+1440C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454645 | |||||||
| chr17:4454679 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | NA18973.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1113+1474C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454679 | |||||||
| chr17:4454782 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 |
3 | HG02809.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1113+1577G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454782 | |||||||
| chr17:4454868 | C | A | 9 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0328 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+1663C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454868 | |||||||
| chr17:4454922 | C | CT | 232 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1113+1726dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4454922 | ||||||
| chr17:4454922 | C | CTT | 18 | a0001c0001t0001g0028 a0001c0003t0001g0132 a0001c0003t0001g0152 others(15): Show |
18 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1113+1725_1113+172 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4454922 | ||||||
| chr17:4454969 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(96): Show |
100 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.1113+1764G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454969 | |||||||
| chr17:4454975 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1113+1770G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454975 | |||||||
| chr17:4454982 | C | T | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1113+1777C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454982 | |||||||
| chr17:4454983 | A | G | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1113+1778A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454983 | |||||||
| chr17:4454990 | G | A | 1 | a0001c0023t0003g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1113+1785G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454990 | |||||||
| chr17:4454990 | G | T | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1113+1785G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454990 | |||||||
| chr17:4454992 | T | C | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1113+1787T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4454992 | |||||||
| chr17:4455000 | G | A | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1113+1795G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455000 | |||||||
| chr17:4455011 | T | G | 1 | a0001c0001t0002g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1113+1806T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455011 | |||||||
| chr17:4455039 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(97): Show |
101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1113+1834A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455039 | |||||||
| chr17:4455205 | C | T | 12 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1113+2000C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455205 | |||||||
| chr17:4455319 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1113+2114T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455319 | |||||||
| chr17:4455381 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1113+2176A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455381 | |||||||
| chr17:4455382 | A | C | 1 | a0001c0001t0001g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1113+2177A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455382 | |||||||
| chr17:4455391 | G | A | 1 | a0003c0005t0001g0171 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1113+2186G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455391 | |||||||
| chr17:4455398 | CTGTGTCC others(6): Show |
C | 1 | a0001c0001t0001g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1113+2194_1113+220 others(17): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455398 | |||||||
| chr17:4455413 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1113+2208T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455413 | |||||||
| chr17:4455414 | T | G | 1 | a0001c0001t0001g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1113+2209T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455414 | |||||||
| chr17:4455427 | C | T | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+2222C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455427 | |||||||
| chr17:4455461 | G | C | 5 | a0001c0009t0002g0031 a0004c0017t0002g0029 a0004c0017t0002g0331 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+2256G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455461 | |||||||
| chr17:4455483 | C | T | 1 | a0001c0003t0002g0315 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1113+2278C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455483 | |||||||
| chr17:4455566 | C | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(81): Show |
85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1113+2361C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455566 | |||||||
| chr17:4455567 | G | A | 36 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(33): Show |
36 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.1113+2362G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455567 | |||||||
| chr17:4455661 | T | TC | 43 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(40): Show |
43 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.1113+2461dupC | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4455661 | ||||||
| chr17:4455665 | C | A | 6 | a0001c0001t0001g0028 a0001c0003t0001g0346 a0001c0003t0002g0315 others(3): Show |
6 | HG02717.hp1 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+2460C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455665 | |||||||
| chr17:4455788 | A | G | 82 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0129 others(79): Show |
82 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1113+2583A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455788 | |||||||
| chr17:4455917 | T | TGGGGGGG others(5): Show |
1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+2722_1113+272 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4455917 | ||||||
| chr17:4455917 | TGG | T | 170 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0035 others(167): Show |
170 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1113+2721_1113+272 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4455917 | ||||||
| chr17:4455918 | G | T | 2 | a0001c0004t0001g0092 a0001c0004t0001g0093 |
2 | HG00673.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1113+2713G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455918 | |||||||
| chr17:4455921 | G | A | 170 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0035 others(167): Show |
170 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1113+2716G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455921 | |||||||
| chr17:4455925 | G | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(12): Show |
15 | HG01074.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113+2720G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4455925 | |||||||
| chr17:4456050 | C | G | 1 | a0003c0005t0001g0310 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1113+2845C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456050 | |||||||
| chr17:4456075 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0210 |
2 | HG02040.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1113+2870C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456075 | |||||||
| chr17:4456112 | A | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(84): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1113+2907A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456112 | |||||||
| chr17:4456155 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(84): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1113+2950T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456155 | |||||||
| chr17:4456213 | A | AAGTGCTG others(39): Show |
1 | a0001c0003t0002g0139 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1113+3010_1113+305 others(50): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4456213 | ||||||
| chr17:4456243 | C | T | 2 | a0001c0009t0001g0004 a0001c0009t0001g0005 |
2 | NA18943.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1113+3038C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456243 | |||||||
| chr17:4456309 | G | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(56): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1113+3104G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456309 | |||||||
| chr17:4456334 | C | T | 5 | a0001c0009t0002g0031 a0004c0017t0002g0029 a0004c0017t0002g0331 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+3129C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456334 | |||||||
| chr17:4456417 | G | A | 50 | a0001c0001t0001g0111 a0001c0001t0001g0129 a0001c0001t0001g0130 others(47): Show |
50 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.1113+3212G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456417 | |||||||
| chr17:4456614 | C | A | 5 | a0001c0009t0002g0031 a0004c0017t0002g0029 a0004c0017t0002g0331 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+3409C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456614 | |||||||
| chr17:4456673 | A | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | NA18952.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1113+3468A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456673 | |||||||
| chr17:4456712 | G | GT | 85 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(82): Show |
86 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.1113+3515dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4456712 | ||||||
| chr17:4456713 | T | G | 1 | a0001c0007t0003g0325 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1113+3508T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456713 | |||||||
| chr17:4456721 | G | T | 53 | a0001c0001t0001g0111 a0001c0001t0001g0129 a0001c0001t0001g0130 others(50): Show |
53 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.1113+3516G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456721 | |||||||
| chr17:4456722 | G | GT | 11 | a0001c0001t0001g0035 a0001c0001t0001g0097 a0001c0001t0001g0185 others(8): Show |
11 | HG00423.hp2 HG01978.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.1113+3527dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4456722 | ||||||
| chr17:4456722 | G | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0334 a0001c0003t0001g0346 others(6): Show |
9 | HG02257.hp1 HG02717.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+3517G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456722 | |||||||
| chr17:4456840 | G | A | 1 | a0001c0004t0001g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1113+3635G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456840 | |||||||
| chr17:4456841 | A | T | 1 | a0001c0004t0001g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1113+3636A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4456841 | |||||||
| chr17:4457021 | G | A | 5 | a0001c0009t0002g0031 a0004c0017t0002g0029 a0004c0017t0002g0331 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+3816G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457021 | |||||||
| chr17:4457023 | T | G | 9 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0328 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+3818T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457023 | |||||||
| chr17:4457049 | G | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0317 |
3 | HG02886.hp2 HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1113+3844G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457049 | |||||||
| chr17:4457129 | C | T | 50 | a0001c0001t0001g0111 a0001c0001t0001g0215 a0001c0001t0001g0335 others(47): Show |
50 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.1113+3924C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457129 | |||||||
| chr17:4457130 | G | A | 1 | a0002c0002t0001g0355 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1113+3925G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457130 | |||||||
| chr17:4457237 | A | T | 100 | a0001c0001t0001g0030 a0001c0001t0001g0238 a0001c0001t0001g0260 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1113+4032A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457237 | |||||||
| chr17:4457274 | C | T | 100 | a0001c0001t0001g0030 a0001c0001t0001g0238 a0001c0001t0001g0260 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1113+4069C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457274 | |||||||
| chr17:4457459 | G | A | 1 | a0002c0002t0001g0273 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1113+4254G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457459 | |||||||
| chr17:4457540 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1113+4335C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457540 | |||||||
| chr17:4457587 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1113+4382A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457587 | |||||||
| chr17:4457600 | G | A | 68 | a0001c0001t0001g0238 a0001c0001t0001g0260 a0001c0001t0001g0263 others(65): Show |
68 | HG00099.hp2 HG00609.hp2 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.1113+4395G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457600 | |||||||
| chr17:4457620 | C | A | 1 | a0003c0008t0003g0128 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1113+4415C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457620 | |||||||
| chr17:4457740 | G | GC | 23 | a0001c0001t0001g0020 a0001c0001t0001g0189 a0001c0001t0001g0211 others(20): Show |
23 | HG00597.hp1 HG00609.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1113+4543dupC | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4457740 | ||||||
| chr17:4457742 | C | G | 8 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+4537C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457742 | |||||||
| chr17:4457748 | C | T | 9 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0328 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+4543C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457748 | |||||||
| chr17:4457748 | CT | C | 44 | a0001c0001t0001g0111 a0001c0001t0001g0335 a0001c0001t0001g0338 others(41): Show |
44 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.1113+4544delT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457748 | |||||||
| chr17:4457749 | T | C | 3 | a0001c0001t0001g0215 a0001c0023t0003g0053 a0003c0008t0003g0268 |
3 | HG01175.hp2 HG01255.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1113+4544T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457749 | |||||||
| chr17:4457869 | G | T | 87 | a0001c0001t0001g0030 a0001c0001t0001g0238 a0001c0001t0001g0260 others(84): Show |
87 | HG00099.hp2 HG00609.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.1113+4664G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457869 | |||||||
| chr17:4457950 | G | T | 8 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+4745G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457950 | |||||||
| chr17:4457974 | C | T | 1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1113+4769C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4457974 | |||||||
| chr17:4458015 | C | T | 1 | a0003c0008t0003g0128 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1113+4810C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458015 | |||||||
| chr17:4458069 | G | A | 2 | a0001c0018t0002g0349 a0001c0018t0002g0350 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1113+4864G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458069 | |||||||
| chr17:4458109 | A | G | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(12): Show |
15 | HG01074.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113+4904A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458109 | |||||||
| chr17:4458148 | G | A | 47 | a0001c0001t0001g0111 a0001c0001t0001g0215 a0001c0001t0001g0335 others(44): Show |
47 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.1113+4943G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458148 | |||||||
| chr17:4458387 | CTTCT | C | 91 | a0001c0001t0001g0030 a0001c0001t0001g0185 a0001c0001t0001g0238 others(88): Show |
91 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.1113+5198_1113+520 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458387 | ||||||
| chr17:4458429 | T | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(12): Show |
15 | HG01074.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113+5224T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458429 | |||||||
| chr17:4458429 | TCCTTCCT others(71): Show |
T | 55 | a0001c0001t0001g0238 a0001c0001t0001g0260 a0001c0001t0001g0263 others(52): Show |
55 | HG00609.hp2 HG00639.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.1113+5239_1113+531 others(82): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458429 | ||||||
| chr17:4458444 | T | A | 32 | a0001c0001t0001g0030 a0001c0001t0002g0143 a0001c0010t0001g0084 others(29): Show |
32 | HG00099.hp2 HG01074.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.1113+5239T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458444 | |||||||
| chr17:4458448 | T | G | 32 | a0001c0001t0001g0030 a0001c0001t0002g0143 a0001c0010t0001g0084 others(29): Show |
32 | HG00099.hp2 HG01074.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.1113+5243T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458448 | |||||||
| chr17:4458449 | T | C | 32 | a0001c0001t0001g0030 a0001c0001t0002g0143 a0001c0010t0001g0084 others(29): Show |
32 | HG00099.hp2 HG01074.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.1113+5244T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458449 | |||||||
| chr17:4458452 | TTCTTCTT others(48): Show |
T | 32 | a0001c0001t0001g0030 a0001c0001t0002g0143 a0001c0010t0001g0084 others(29): Show |
32 | HG00099.hp2 HG01074.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.1113+5248_1113+530 others(59): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458452 | |||||||
| chr17:4458485 | CTTCT | C | 4 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+5298_1113+530 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458485 | ||||||
| chr17:4458506 | TC | T | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(12): Show |
15 | HG01074.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113+5304delC | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458506 | ||||||
| chr17:4458509 | C | T | 5 | a0001c0009t0002g0031 a0004c0017t0002g0029 a0004c0017t0002g0331 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+5304C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458509 | |||||||
| chr17:4458515 | C | T | 32 | a0001c0001t0001g0030 a0001c0001t0002g0143 a0001c0010t0001g0084 others(29): Show |
32 | HG00099.hp2 HG01074.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.1113+5310C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458515 | |||||||
| chr17:4458519 | CCCACCCG | C | 32 | a0001c0001t0001g0030 a0001c0001t0002g0143 a0001c0010t0001g0084 others(29): Show |
32 | HG00099.hp2 HG01074.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.1113+5317_1113+532 others(11): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458519 | ||||||
| chr17:4458526 | G | GCCTT | 5 | a0001c0009t0002g0031 a0004c0017t0002g0029 a0004c0017t0002g0331 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+5338_1113+534 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458526 | ||||||
| chr17:4458536 | C | CT | 32 | a0001c0001t0001g0030 a0001c0001t0002g0143 a0001c0010t0001g0084 others(29): Show |
32 | HG00099.hp2 HG01074.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.1113+5333dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458536 | ||||||
| chr17:4458540 | CT | C | 54 | a0001c0001t0001g0238 a0001c0001t0001g0260 a0001c0001t0001g0263 others(51): Show |
54 | HG00609.hp2 HG00639.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1113+5337delT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458540 | ||||||
| chr17:4458545 | T | C | 54 | a0001c0001t0001g0238 a0001c0001t0001g0260 a0001c0001t0001g0263 others(51): Show |
54 | HG00609.hp2 HG00639.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1113+5340T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458545 | |||||||
| chr17:4458556 | T | TC | 54 | a0001c0001t0001g0238 a0001c0001t0001g0260 a0001c0001t0001g0263 others(51): Show |
54 | HG00609.hp2 HG00639.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1113+5352dupC | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458556 | ||||||
| chr17:4458561 | C | CT | 19 | a0001c0001t0001g0271 a0001c0003t0002g0256 a0001c0010t0002g0086 others(16): Show |
19 | HG00738.hp2 HG01109.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1113+5358dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458561 | ||||||
| chr17:4458563 | TCCC | T | 35 | a0001c0001t0001g0238 a0001c0001t0001g0260 a0001c0001t0001g0263 others(32): Show |
35 | HG00609.hp2 HG00639.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1113+5359_1113+536 others(7): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458563 | |||||||
| chr17:4458566 | C | T | 19 | a0001c0001t0001g0271 a0001c0003t0002g0256 a0001c0010t0002g0086 others(16): Show |
19 | HG00738.hp2 HG01109.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1113+5361C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458566 | |||||||
| chr17:4458568 | C | CCTCTTTC others(3): Show |
1 | a0002c0040t0001g0313 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1113+5365_1113+536 others(14): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458568 | ||||||
| chr17:4458568 | C | T | 2 | a0002c0011t0003g0287 a0003c0029t0003g0085 |
2 | HG01192.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1113+5363C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458568 | |||||||
| chr17:4458570 | TTTCTTTC others(9): Show |
T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1113+5367_1113+538 others(20): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458570 | ||||||
| chr17:4458572 | T | C | 35 | a0001c0001t0001g0238 a0001c0001t0001g0260 a0001c0001t0001g0263 others(32): Show |
35 | HG00609.hp2 HG00639.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1113+5367T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458572 | |||||||
| chr17:4458576 | T | C | 19 | a0001c0001t0001g0271 a0001c0003t0002g0256 a0001c0010t0002g0086 others(16): Show |
19 | HG00738.hp2 HG01109.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1113+5371T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458576 | |||||||
| chr17:4458576 | TCTTCCTT others(5): Show |
T | 17 | a0001c0001t0001g0030 a0001c0010t0002g0081 a0001c0013t0001g0359 others(14): Show |
17 | HG01074.hp2 HG01192.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.1113+5375_1113+538 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458576 | ||||||
| chr17:4458578 | TTCCTTCC others(1): Show |
T | 10 | a0001c0001t0002g0143 a0001c0010t0002g0087 a0001c0010t0002g0088 others(7): Show |
10 | HG00099.hp2 HG01943.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.1113+5379_1113+538 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458578 | ||||||
| chr17:4458580 | C | T | 6 | a0001c0010t0001g0078 a0001c0010t0001g0084 a0002c0002t0001g0230 others(3): Show |
6 | HG01081.hp1 HG01516.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+5375C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458580 | |||||||
| chr17:4458582 | T | C | 19 | a0001c0001t0001g0271 a0001c0003t0002g0256 a0001c0010t0002g0086 others(16): Show |
19 | HG00738.hp2 HG01109.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1113+5377T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458582 | |||||||
| chr17:4458584 | C | T | 5 | a0001c0010t0001g0084 a0002c0002t0001g0230 a0002c0011t0003g0149 others(2): Show |
5 | HG01516.hp2 HG02735.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+5379C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458584 | |||||||
| chr17:4458586 | C | CTCCT | 32 | a0001c0001t0001g0131 a0001c0001t0001g0165 a0001c0001t0001g0182 others(29): Show |
32 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.1113+5383_1113+538 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458586 | ||||||
| chr17:4458586 | C | CTCCTTCC others(1): Show |
3 | a0001c0001t0002g0327 a0001c0003t0001g0320 a0001c0006t0002g0052 |
3 | HG02717.hp2 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1113+5386_1113+538 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458586 | ||||||
| chr17:4458586 | C | CTCCTTCC others(5): Show |
1 | a0001c0006t0001g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1113+5386_1113+538 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458586 | ||||||
| chr17:4458586 | C | T | 24 | a0001c0001t0001g0271 a0001c0003t0002g0256 a0001c0010t0001g0084 others(21): Show |
24 | HG00738.hp2 HG01109.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1113+5381C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458586 | |||||||
| chr17:4458588 | C | CCTTCCTT others(13): Show |
1 | a0001c0012t0001g0039 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1113+5386_1113+538 others(24): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(9): Show |
5 | a0001c0001t0002g0317 a0001c0006t0001g0049 a0001c0009t0002g0022 others(2): Show |
5 | HG02486.hp2 HG03041.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+5386_1113+538 others(20): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(13): Show |
1 | a0001c0009t0002g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1113+5386_1113+538 others(24): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(17): Show |
2 | a0001c0001t0002g0326 a0001c0001t0002g0329 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1113+5386_1113+538 others(28): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(10): Show |
1 | a0001c0004t0001g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1113+5386_1113+538 others(21): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(5): Show |
2 | a0001c0003t0002g0127 a0001c0049t0002g0003 |
2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1113+5386_1113+538 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(9): Show |
4 | a0001c0001t0001g0035 a0001c0001t0001g0105 a0001c0001t0002g0342 others(1): Show |
4 | HG02083.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+5386_1113+538 others(20): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(13): Show |
1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1113+5386_1113+538 others(24): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(17): Show |
2 | a0001c0001t0002g0343 a0001c0006t0002g0048 |
2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1113+5386_1113+538 others(28): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(1): Show |
27 | a0001c0001t0001g0154 a0001c0001t0001g0166 a0001c0001t0001g0181 others(24): Show |
27 | HG00609.hp1 HG00621.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1113+5386_1113+538 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(5): Show |
15 | a0001c0001t0001g0095 a0001c0001t0001g0185 a0001c0001t0001g0199 others(12): Show |
15 | HG00423.hp2 HG00558.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1113+5386_1113+538 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(9): Show |
9 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0129 others(6): Show |
9 | HG00423.hp1 HG01167.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+5386_1113+538 others(20): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(13): Show |
6 | a0001c0001t0001g0201 a0001c0001t0002g0160 a0001c0003t0002g0136 others(3): Show |
6 | HG01169.hp2 HG01433.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+5386_1113+538 others(24): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(17): Show |
2 | a0001c0001t0001g0231 a0001c0014t0002g0007 |
2 | NA19043.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1113+5386_1113+538 others(28): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(21): Show |
1 | a0001c0003t0002g0139 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1113+5386_1113+538 others(32): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTCCTT others(25): Show |
1 | a0001c0001t0002g0336 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1113+5386_1113+538 others(36): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTTCTT others(1): Show |
3 | a0001c0001t0001g0209 a0001c0001t0001g0242 a0001c0001t0001g0244 |
3 | HG00558.hp1 NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1113+5437_1113+544 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTTCTT others(5): Show |
2 | a0001c0003t0001g0146 a0001c0046t0002g0316 |
2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1113+5433_1113+544 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | CCTTTCTT others(9): Show |
1 | a0001c0001t0001g0028 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1113+5429_1113+544 others(20): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | C | T | 35 | a0001c0001t0001g0271 a0001c0001t0002g0143 a0001c0003t0002g0256 others(32): Show |
35 | HG00099.hp2 HG00738.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1113+5383C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458588 | |||||||
| chr17:4458588 | CCTTT | C | 30 | a0001c0001t0001g0098 a0001c0001t0001g0147 a0001c0001t0001g0164 others(27): Show |
30 | HG01070.hp2 HG01074.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1113+5441_1113+544 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | CCTTTCTT others(1): Show |
C | 14 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0238 others(11): Show |
14 | HG02572.hp2 HG02615.hp2 HG02896.hp2 others(11): Show |
intron_variant | MODIFIER | c.1113+5437_1113+544 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | CCTTTCTT others(5): Show |
C | 9 | a0001c0001t0001g0109 a0001c0001t0002g0167 a0001c0001t0002g0328 others(6): Show |
9 | HG00597.hp2 HG02015.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+5433_1113+544 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | CCTTTCTT others(9): Show |
C | 2 | a0002c0002t0001g0290 a0002c0002t0001g0312 |
2 | HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1113+5429_1113+544 others(20): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458588 | CCTTTCTT others(13): Show |
C | 4 | a0001c0003t0001g0121 a0001c0003t0001g0318 a0001c0003t0002g0112 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+5425_1113+544 others(24): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458588 | ||||||
| chr17:4458592 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(95): Show |
99 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1113+5387T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458592 | |||||||
| chr17:4458594 | T | TTTCTTTC others(12): Show |
5 | a0003c0008t0003g0099 a0003c0008t0003g0100 a0003c0008t0003g0101 others(2): Show |
5 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+5392_1113+541 others(23): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458594 | ||||||
| chr17:4458596 | T | C | 25 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0098 others(22): Show |
25 | HG01070.hp2 HG01074.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.1113+5391T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458596 | |||||||
| chr17:4458600 | T | C | 16 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0147 others(13): Show |
16 | HG01074.hp1 HG02280.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.1113+5395T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458600 | |||||||
| chr17:4458604 | T | C | 12 | a0001c0001t0001g0109 a0001c0001t0002g0167 a0001c0001t0002g0328 others(9): Show |
12 | HG00597.hp2 HG02015.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.1113+5399T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458604 | |||||||
| chr17:4458608 | T | C | 5 | a0001c0001t0002g0328 a0001c0012t0001g0037 a0001c0012t0001g0038 others(2): Show |
5 | HG02280.hp2 HG02572.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+5403T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458608 | |||||||
| chr17:4458612 | T | C | 5 | a0001c0001t0002g0328 a0001c0003t0001g0121 a0001c0003t0001g0318 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+5407T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458612 | |||||||
| chr17:4458617 | C | CTTTCTTT others(18): Show |
2 | a0001c0001t0001g0215 a0001c0003t0001g0351 |
2 | NA18943.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1113+5415_1113+543 others(29): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458617 | ||||||
| chr17:4458618 | T | TTTCTTTC others(16): Show |
1 | a0001c0006t0002g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1113+5416_1113+543 others(27): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458618 | ||||||
| chr17:4458619 | T | G | 1 | a0001c0001t0001g0294 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1113+5414T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458619 | |||||||
| chr17:4458621 | C | CT | 5 | a0003c0008t0003g0099 a0003c0008t0003g0100 a0003c0008t0003g0101 others(2): Show |
5 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+5419dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458621 | ||||||
| chr17:4458621 | C | CTTTCTTT others(2): Show |
7 | a0001c0001t0001g0338 a0001c0001t0002g0330 a0001c0003t0001g0152 others(4): Show |
7 | HG00323.hp1 HG02280.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+5419_1113+542 others(13): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458621 | ||||||
| chr17:4458621 | C | CTTTCTTT others(6): Show |
11 | a0001c0001t0001g0111 a0001c0003t0001g0132 a0001c0003t0001g0239 others(8): Show |
11 | HG00642.hp2 HG01081.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.1113+5419_1113+543 others(17): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458621 | ||||||
| chr17:4458621 | C | CTTTCTTT others(10): Show |
10 | a0001c0001t0001g0335 a0001c0001t0002g0333 a0001c0003t0001g0309 others(7): Show |
10 | HG00099.hp1 HG00280.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1113+5419_1113+543 others(21): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458621 | ||||||
| chr17:4458621 | C | CTTTCTTT others(14): Show |
5 | a0001c0045t0003g0150 a0003c0005t0001g0140 a0003c0005t0001g0235 others(2): Show |
5 | HG00639.hp2 HG02155.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+5419_1113+543 others(25): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458621 | ||||||
| chr17:4458621 | C | CTTTCTTT others(18): Show |
8 | a0001c0006t0002g0011 a0001c0006t0002g0012 a0001c0007t0003g0319 others(5): Show |
8 | HG01175.hp2 HG02698.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+5419_1113+544 others(29): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458621 | ||||||
| chr17:4458621 | C | CTTTCTTT others(22): Show |
4 | a0001c0006t0001g0010 a0003c0005t0002g0155 a0003c0008t0003g0267 others(1): Show |
4 | HG01106.hp1 HG01255.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+5444_1113+544 others(33): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458621 | ||||||
| chr17:4458621 | C | CTTTCTTT others(34): Show |
1 | a0003c0005t0001g0116 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1113+5444_1113+544 others(45): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458621 | ||||||
| chr17:4458627 | T | TTCTTTCT others(26): Show |
1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1113+5444_1113+544 others(37): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458627 | ||||||
| chr17:4458634 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1113+5429T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458634 | |||||||
| chr17:4458642 | T | TTTCTTTC others(16): Show |
1 | a0001c0038t0003g0291 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1113+5444_1113+544 others(27): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458642 | ||||||
| chr17:4458643 | T | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0004t0001g0027 |
3 | HG02970.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1113+5438T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458643 | |||||||
| chr17:4458646 | T | C | 25 | a0001c0001t0001g0211 a0001c0001t0001g0246 a0001c0001t0002g0326 others(22): Show |
25 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1113+5441T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458646 | |||||||
| chr17:4458646 | T | TTTCTTTC others(5): Show |
1 | a0001c0034t0002g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1113+5444_1113+544 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458646 | ||||||
| chr17:4458646 | T | TTTCTTTC others(20): Show |
1 | a0011c0027t0001g0232 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1113+5444_1113+544 others(31): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458646 | ||||||
| chr17:4458646 | T | TTTCTTTC others(21): Show |
1 | a0001c0003t0001g0346 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1113+5444_1113+544 others(32): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4458646 | ||||||
| chr17:4458650 | C | T | 5 | a0001c0009t0002g0031 a0002c0032t0001g0079 a0004c0017t0002g0331 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+5445C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458650 | |||||||
| chr17:4458658 | T | C | 6 | a0001c0009t0002g0031 a0002c0032t0001g0079 a0004c0017t0002g0029 others(3): Show |
6 | HG01099.hp1 HG02145.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+5453T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458658 | |||||||
| chr17:4458761 | CTG | C | 3 | a0001c0006t0001g0010 a0001c0007t0003g0158 a0001c0007t0003g0319 |
3 | HG01884.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1113+5557_1113+555 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458761 | |||||||
| chr17:4458798 | A | G | 1 | a0001c0007t0003g0248 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1113+5593A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458798 | |||||||
| chr17:4458805 | A | G | 159 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0215 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1113+5600A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458805 | |||||||
| chr17:4458869 | A | G | 18 | a0001c0001t0001g0030 a0001c0001t0002g0046 a0001c0001t0002g0143 others(15): Show |
18 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1113+5664A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458869 | |||||||
| chr17:4458989 | T | C | 76 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(73): Show |
76 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1113+5784T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4458989 | |||||||
| chr17:4459354 | T | A | 1 | a0001c0001t0001g0186 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1113+6149T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459354 | |||||||
| chr17:4459396 | G | A | 1 | a0001c0003t0001g0320 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1113+6191G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459396 | |||||||
| chr17:4459485 | G | T | 1 | a0002c0011t0003g0252 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1113+6280G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459485 | |||||||
| chr17:4459574 | A | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0004t0001g0027 |
3 | HG02970.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1113+6369A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459574 | |||||||
| chr17:4459628 | G | A | 4 | a0001c0023t0003g0053 a0003c0005t0001g0116 a0003c0008t0003g0267 others(1): Show |
4 | HG01175.hp2 HG01255.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+6423G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459628 | |||||||
| chr17:4459638 | A | G | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1113+6433A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459638 | |||||||
| chr17:4459654 | G | A | 262 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1113+6449G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459654 | |||||||
| chr17:4459666 | T | C | 26 | a0001c0001t0001g0166 a0001c0001t0001g0186 a0001c0001t0001g0191 others(23): Show |
26 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1113+6461T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459666 | |||||||
| chr17:4459676 | G | A | 1 | a0003c0016t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1113+6471G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459676 | |||||||
| chr17:4459692 | G | A | 1 | a0002c0002t0001g0286 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1113+6487G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459692 | |||||||
| chr17:4459767 | C | T | 61 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(58): Show |
61 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1113+6562C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459767 | |||||||
| chr17:4459812 | G | A | 1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1113+6607G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459812 | |||||||
| chr17:4459814 | T | C | 1 | a0003c0016t0001g0083 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1113+6609T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459814 | |||||||
| chr17:4459820 | A | G | 4 | a0001c0024t0003g0062 a0001c0028t0003g0173 a0001c0045t0003g0150 others(1): Show |
4 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+6615A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459820 | |||||||
| chr17:4459825 | CAAGATAT others(51): Show |
C | 1 | a0001c0001t0001g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1113+6624_1113+668 others(62): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4459825 | ||||||
| chr17:4459954 | A | G | 1 | a0001c0013t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1113+6749A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459954 | |||||||
| chr17:4459983 | T | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(261): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1113+6778T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4459983 | |||||||
| chr17:4460020 | G | A | 8 | a0002c0002t0001g0253 a0002c0011t0003g0149 a0002c0011t0003g0252 others(5): Show |
8 | HG00099.hp2 HG01256.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+6815G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460020 | |||||||
| chr17:4460020 | G | C | 1 | a0001c0004t0001g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1113+6815G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460020 | |||||||
| chr17:4460400 | T | G | 148 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(145): Show |
148 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.1113+7195T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460400 | |||||||
| chr17:4460429 | A | AT | 25 | a0001c0001t0001g0201 a0001c0001t0001g0216 a0001c0001t0001g0218 others(22): Show |
25 | HG01099.hp1 HG01109.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.1113+7244dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4460429 | ||||||
| chr17:4460429 | A | ATT | 27 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(24): Show |
27 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113+7243_1113+724 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4460429 | ||||||
| chr17:4460429 | AT | A | 132 | a0001c0001t0001g0028 a0001c0001t0001g0111 a0001c0001t0001g0134 others(129): Show |
132 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1113+7244delT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4460429 | ||||||
| chr17:4460429 | ATT | A | 12 | a0001c0007t0003g0247 a0001c0038t0003g0291 a0002c0002t0001g0015 others(9): Show |
12 | HG01074.hp2 HG01169.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+7243_1113+724 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4460429 | ||||||
| chr17:4460491 | G | T | 5 | a0001c0009t0002g0031 a0004c0017t0002g0029 a0004c0017t0002g0331 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+7286G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460491 | |||||||
| chr17:4460493 | G | A | 1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1113+7288G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460493 | |||||||
| chr17:4460521 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1113+7316G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460521 | |||||||
| chr17:4460588 | C | T | 1 | a0001c0023t0003g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1113+7383C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460588 | |||||||
| chr17:4460607 | A | AT | 38 | a0001c0001t0001g0130 a0001c0001t0001g0251 a0001c0001t0001g0261 others(35): Show |
38 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1113+7418dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4460607 | ||||||
| chr17:4460607 | AT | A | 12 | a0001c0001t0001g0154 a0001c0001t0001g0218 a0001c0001t0001g0222 others(9): Show |
12 | HG00673.hp2 HG01361.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.1113+7418delT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4460607 | ||||||
| chr17:4460613 | T | A | 1 | a0001c0001t0001g0206 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1113+7408T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460613 | |||||||
| chr17:4460623 | T | C | 8 | a0002c0002t0001g0253 a0002c0011t0003g0149 a0002c0011t0003g0252 others(5): Show |
8 | HG00099.hp2 HG01256.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+7418T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460623 | |||||||
| chr17:4460624 | A | G | 7 | a0001c0009t0002g0031 a0001c0018t0002g0349 a0001c0018t0002g0350 others(4): Show |
7 | HG01099.hp1 HG02145.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+7419A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460624 | |||||||
| chr17:4460644 | T | G | 61 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(58): Show |
61 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1113+7439T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460644 | |||||||
| chr17:4460663 | C | T | 3 | a0001c0003t0001g0346 a0001c0003t0002g0315 a0001c0034t0002g0045 |
3 | HG02717.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1113+7458C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460663 | |||||||
| chr17:4460700 | C | T | 1 | a0001c0013t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1113+7495C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460700 | |||||||
| chr17:4460731 | C | T | 8 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+7526C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460731 | |||||||
| chr17:4460903 | T | C | 1 | a0002c0002t0001g0285 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1113+7698T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4460903 | |||||||
| chr17:4461000 | T | A | 1 | a0001c0014t0002g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1113+7795T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4461000 | |||||||
| chr17:4461139 | T | A | 1 | a0003c0005t0001g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1113+7934T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4461139 | |||||||
| chr17:4461144 | T | A | 8 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+7939T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4461144 | |||||||
| chr17:4461156 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0002g0151 |
3 | NA18977.hp2 NA18982.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1113+7951C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4461156 | |||||||
| chr17:4461295 | C | G | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+8090C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4461295 | |||||||
| chr17:4461361 | C | CT | 32 | a0001c0001t0001g0001 a0001c0001t0001g0133 a0001c0001t0001g0165 others(29): Show |
33 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1113+8182dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4461361 | ||||||
| chr17:4461361 | C | CTTTT | 16 | a0001c0001t0001g0111 a0001c0001t0001g0335 a0001c0001t0001g0338 others(13): Show |
16 | HG00639.hp2 HG01081.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1113+8179_1113+818 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4461361 | ||||||
| chr17:4461361 | C | CTTTTCTT others(4): Show |
1 | a0003c0021t0003g0002 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1113+8160_1113+816 others(15): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4461361 | ||||||
| chr17:4461361 | C | CTTTTT | 9 | a0001c0003t0001g0309 a0001c0006t0001g0010 a0001c0006t0002g0011 others(6): Show |
9 | HG00099.hp1 HG01255.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+8178_1113+818 others(9): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4461361 | ||||||
| chr17:4461361 | C | CTTTTTT | 11 | a0001c0009t0001g0005 a0001c0038t0003g0291 a0003c0005t0001g0116 others(8): Show |
11 | HG01099.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1113+8177_1113+818 others(10): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4461361 | ||||||
| chr17:4461361 | C | CTTTTTTT others(3): Show |
3 | a0003c0005t0001g0140 a0003c0005t0001g0235 a0003c0008t0003g0141 |
3 | HG02723.hp2 HG03834.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1113+8173_1113+818 others(14): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4461361 | ||||||
| chr17:4461361 | C | CTTTTTTT others(6): Show |
1 | a0003c0005t0001g0156 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1113+8170_1113+818 others(17): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4461361 | ||||||
| chr17:4461361 | CT | C | 111 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(108): Show |
111 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.1113+8182delT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4461361 | ||||||
| chr17:4461361 | CTT | C | 16 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0001g0145 others(13): Show |
16 | HG01074.hp2 HG01167.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.1113+8181_1113+818 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4461361 | ||||||
| chr17:4461361 | CTTTTT | C | 29 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(26): Show |
29 | HG01074.hp1 HG01099.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1113+8178_1113+818 others(9): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4461361 | ||||||
| chr17:4461367 | T | C | 2 | a0001c0001t0001g0219 a0001c0001t0002g0217 |
2 | NA18969.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1113+8162T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4461367 | |||||||
| chr17:4461371 | T | C | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(18): Show |
21 | HG01074.hp1 HG01109.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1113+8166T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4461371 | |||||||
| chr17:4461372 | T | C | 2 | a0001c0006t0002g0048 a0001c0052t0002g0063 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1113+8167T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4461372 | |||||||
| chr17:4461373 | T | C | 1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1113+8168T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4461373 | |||||||
| chr17:4461755 | A | G | 3 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0004t0001g0027 |
3 | HG02970.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1113+8550A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4461755 | |||||||
| chr17:4461757 | G | A | 34 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(31): Show |
34 | HG01074.hp1 HG01099.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1113+8552G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4461757 | |||||||
| chr17:4461896 | A | C | 58 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(55): Show |
58 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1113+8691A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4461896 | |||||||
| chr17:4461968 | A | G | 3 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0004t0001g0027 |
3 | HG02970.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1113+8763A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4461968 | |||||||
| chr17:4462052 | A | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | NA18952.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1113+8847A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462052 | |||||||
| chr17:4462136 | T | C | 89 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(86): Show |
89 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1113+8931T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462136 | |||||||
| chr17:4462138 | C | A | 89 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(86): Show |
89 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1113+8933C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462138 | |||||||
| chr17:4462140 | T | C | 94 | a0001c0001t0001g0215 a0001c0001t0001g0223 a0001c0001t0001g0238 others(91): Show |
94 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.1113+8935T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462140 | |||||||
| chr17:4462142 | C | A | 94 | a0001c0001t0001g0215 a0001c0001t0001g0223 a0001c0001t0001g0238 others(91): Show |
94 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.1113+8937C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462142 | |||||||
| chr17:4462144 | T | C | 76 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(73): Show |
76 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1113+8939T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462144 | |||||||
| chr17:4462146 | C | A | 76 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(73): Show |
76 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1113+8941C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462146 | |||||||
| chr17:4462148 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0105 others(73): Show |
77 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.1113+8943T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462148 | |||||||
| chr17:4462150 | C | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0105 others(73): Show |
77 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.1113+8945C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462150 | |||||||
| chr17:4462152 | T | C | 20 | a0001c0001t0001g0035 a0001c0001t0001g0129 a0001c0001t0001g0131 others(17): Show |
20 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1113+8947T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462152 | |||||||
| chr17:4462154 | C | A | 20 | a0001c0001t0001g0035 a0001c0001t0001g0129 a0001c0001t0001g0131 others(17): Show |
20 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1113+8949C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462154 | |||||||
| chr17:4462156 | T | C | 2 | a0001c0001t0001g0130 a0001c0012t0002g0042 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1113+8951T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462156 | |||||||
| chr17:4462158 | C | A | 2 | a0001c0001t0001g0130 a0001c0012t0002g0042 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1113+8953C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462158 | |||||||
| chr17:4462158 | C | T | 1 | a0001c0014t0002g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1113+8953C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462158 | |||||||
| chr17:4462170 | C | T | 1 | a0001c0014t0002g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1113+8965C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462170 | |||||||
| chr17:4462180 | T | C | 26 | a0001c0001t0001g0166 a0001c0001t0001g0186 a0001c0001t0001g0191 others(23): Show |
26 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1113+8975T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462180 | |||||||
| chr17:4462182 | C | A | 26 | a0001c0001t0001g0166 a0001c0001t0001g0186 a0001c0001t0001g0191 others(23): Show |
26 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1113+8977C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462182 | |||||||
| chr17:4462182 | C | CACCAATC others(1): Show |
4 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(1): Show |
4 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+8978_1113+897 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462182 | ||||||
| chr17:4462184 | T | C | 116 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(113): Show |
116 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1113+8979T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462184 | |||||||
| chr17:4462186 | C | A | 116 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(113): Show |
116 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1113+8981C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462186 | |||||||
| chr17:4462186 | C | T | 26 | a0001c0001t0001g0166 a0001c0001t0001g0186 a0001c0001t0001g0191 others(23): Show |
26 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1113+8981C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462186 | |||||||
| chr17:4462188 | T | C | 56 | a0001c0001t0001g0028 a0001c0001t0001g0215 a0001c0001t0001g0223 others(53): Show |
56 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.1113+8983T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462188 | |||||||
| chr17:4462190 | C | A | 56 | a0001c0001t0001g0028 a0001c0001t0001g0215 a0001c0001t0001g0223 others(53): Show |
56 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.1113+8985C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462190 | |||||||
| chr17:4462190 | C | T | 116 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(113): Show |
116 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1113+8985C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462190 | |||||||
| chr17:4462192 | T | C | 51 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(48): Show |
51 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1113+8987T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462192 | |||||||
| chr17:4462194 | C | A | 51 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(48): Show |
51 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1113+8989C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462194 | |||||||
| chr17:4462194 | C | T | 60 | a0001c0001t0001g0028 a0001c0001t0001g0215 a0001c0001t0001g0223 others(57): Show |
60 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.1113+8989C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462194 | |||||||
| chr17:4462196 | T | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0095 others(78): Show |
82 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1113+8991T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462196 | |||||||
| chr17:4462198 | C | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0095 others(78): Show |
82 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1113+8993C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462198 | |||||||
| chr17:4462198 | C | T | 76 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(73): Show |
76 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1113+8993C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462198 | |||||||
| chr17:4462200 | T | C | 19 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0003t0001g0126 others(16): Show |
19 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1113+8995T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462200 | |||||||
| chr17:4462202 | C | A | 19 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0003t0001g0126 others(16): Show |
19 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1113+8997C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462202 | |||||||
| chr17:4462202 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0095 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1113+8997C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462202 | |||||||
| chr17:4462204 | T | C | 2 | a0001c0001t0001g0130 a0001c0006t0001g0047 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1113+8999T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462204 | |||||||
| chr17:4462206 | C | A | 2 | a0001c0001t0001g0130 a0001c0006t0001g0047 |
2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1113+9001C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462206 | |||||||
| chr17:4462206 | C | T | 75 | a0001c0001t0001g0028 a0001c0001t0001g0129 a0001c0001t0001g0131 others(72): Show |
75 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.1113+9001C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462206 | |||||||
| chr17:4462208 | T | C | 2 | a0001c0003t0001g0320 a0001c0012t0002g0042 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1113+9003T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462208 | |||||||
| chr17:4462210 | C | A | 2 | a0001c0003t0001g0320 a0001c0012t0002g0042 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1113+9005C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462210 | |||||||
| chr17:4462210 | C | T | 51 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(48): Show |
51 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1113+9005C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462210 | |||||||
| chr17:4462212 | T | C | 1 | a0001c0012t0001g0039 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1113+9007T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462212 | |||||||
| chr17:4462214 | C | A | 1 | a0001c0012t0001g0039 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1113+9009C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462214 | |||||||
| chr17:4462214 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0095 others(80): Show |
84 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1113+9009C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462214 | |||||||
| chr17:4462216 | T | C | 4 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(1): Show |
4 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+9011T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462216 | |||||||
| chr17:4462218 | C | A | 4 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(1): Show |
4 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+9013C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462218 | |||||||
| chr17:4462218 | C | T | 20 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0003t0001g0126 others(17): Show |
20 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1113+9013C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462218 | |||||||
| chr17:4462220 | T | C | 26 | a0001c0001t0001g0166 a0001c0001t0001g0186 a0001c0001t0001g0191 others(23): Show |
26 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1113+9015T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462220 | |||||||
| chr17:4462222 | C | A | 26 | a0001c0001t0001g0166 a0001c0001t0001g0186 a0001c0001t0001g0191 others(23): Show |
26 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1113+9017C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462222 | |||||||
| chr17:4462222 | C | T | 5 | a0001c0001t0001g0130 a0002c0002t0001g0264 a0002c0002t0001g0265 others(2): Show |
5 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+9017C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462222 | |||||||
| chr17:4462224 | T | C | 116 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(113): Show |
116 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1113+9019T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462224 | |||||||
| chr17:4462226 | C | A | 116 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(113): Show |
116 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1113+9021C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462226 | |||||||
| chr17:4462226 | C | T | 28 | a0001c0001t0001g0166 a0001c0001t0001g0186 a0001c0001t0001g0191 others(25): Show |
28 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.1113+9021C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462226 | |||||||
| chr17:4462228 | T | C | 49 | a0001c0001t0001g0028 a0001c0001t0001g0215 a0001c0001t0001g0223 others(46): Show |
49 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.1113+9023T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462228 | |||||||
| chr17:4462230 | C | A | 48 | a0001c0001t0001g0028 a0001c0001t0001g0215 a0001c0001t0001g0223 others(45): Show |
48 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1113+9025C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462230 | |||||||
| chr17:4462230 | C | T | 117 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(114): Show |
117 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1113+9025C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462230 | |||||||
| chr17:4462232 | T | C | 38 | a0001c0001t0001g0030 a0001c0001t0001g0168 a0001c0001t0001g0190 others(35): Show |
38 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1113+9027T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462232 | |||||||
| chr17:4462234 | C | A | 29 | a0001c0001t0001g0030 a0001c0001t0001g0168 a0001c0001t0001g0190 others(26): Show |
29 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1113+9029C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462234 | |||||||
| chr17:4462234 | C | T | 52 | a0001c0001t0001g0028 a0001c0001t0001g0215 a0001c0001t0001g0223 others(49): Show |
52 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.1113+9029C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462234 | |||||||
| chr17:4462236 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0105 others(76): Show |
80 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1113+9031T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462236 | |||||||
| chr17:4462238 | C | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0105 others(68): Show |
72 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1113+9033C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462238 | |||||||
| chr17:4462238 | C | CACCAATC others(329): Show |
1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+9034_1113+903 others(340): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462238 | ||||||
| chr17:4462238 | C | T | 55 | a0001c0001t0001g0030 a0001c0001t0001g0166 a0001c0001t0001g0168 others(52): Show |
55 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1113+9033C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462238 | |||||||
| chr17:4462240 | T | C | 29 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0129 others(26): Show |
29 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.1113+9035T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462240 | |||||||
| chr17:4462242 | C | A | 17 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0003t0001g0122 others(14): Show |
17 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1113+9037C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462242 | |||||||
| chr17:4462242 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0096 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1113+9037C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462242 | |||||||
| chr17:4462244 | T | C | 7 | a0001c0001t0001g0035 a0001c0001t0001g0130 a0001c0001t0001g0147 others(4): Show |
7 | HG01074.hp1 HG02109.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9039T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462244 | |||||||
| chr17:4462246 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1113+9041C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462246 | |||||||
| chr17:4462246 | C | T | 63 | a0001c0001t0001g0028 a0001c0001t0001g0129 a0001c0001t0001g0131 others(60): Show |
63 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1113+9041C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462246 | |||||||
| chr17:4462248 | T | C | 17 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0328 others(14): Show |
17 | HG01109.hp1 HG02280.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.1113+9043T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462248 | |||||||
| chr17:4462250 | C | A | 1 | a0001c0003t0001g0320 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1113+9045C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462250 | |||||||
| chr17:4462250 | C | T | 29 | a0001c0001t0001g0030 a0001c0001t0001g0130 a0001c0001t0001g0168 others(26): Show |
29 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1113+9045C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462250 | |||||||
| chr17:4462252 | T | C | 9 | a0001c0001t0002g0160 a0001c0004t0001g0026 a0001c0006t0001g0047 others(6): Show |
9 | HG01099.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+9047T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462252 | |||||||
| chr17:4462254 | C | A | 2 | a0001c0006t0001g0047 a0001c0023t0003g0014 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1113+9049C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462254 | |||||||
| chr17:4462254 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0105 others(69): Show |
73 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1113+9049C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462254 | |||||||
| chr17:4462256 | T | C | 22 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0317 others(19): Show |
22 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1113+9051T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462256 | |||||||
| chr17:4462258 | C | A | 9 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0328 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+9053C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462258 | |||||||
| chr17:4462258 | C | T | 17 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0003t0001g0122 others(14): Show |
17 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1113+9053C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462258 | |||||||
| chr17:4462260 | T | C | 13 | a0001c0001t0001g0035 a0001c0001t0001g0147 a0001c0001t0002g0160 others(10): Show |
13 | HG01074.hp1 HG01099.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+9055T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462260 | |||||||
| chr17:4462262 | C | A | 7 | a0001c0001t0002g0160 a0001c0004t0001g0026 a0001c0018t0002g0349 others(4): Show |
7 | HG01099.hp1 HG02055.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+9057C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462262 | |||||||
| chr17:4462262 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1113+9057C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462262 | |||||||
| chr17:4462263 | A | T | 1 | a0001c0004t0001g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1113+9058A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462263 | |||||||
| chr17:4462264 | T | C | 17 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0317 others(14): Show |
17 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1113+9059T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462264 | |||||||
| chr17:4462266 | C | A | 12 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0317 others(9): Show |
12 | HG02145.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1113+9061C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462266 | |||||||
| chr17:4462266 | C | T | 1 | a0001c0003t0001g0320 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1113+9061C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462266 | |||||||
| chr17:4462268 | T | C | 9 | a0001c0001t0001g0035 a0001c0001t0001g0147 a0001c0001t0002g0344 others(6): Show |
9 | HG01074.hp1 HG01192.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+9063T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462268 | |||||||
| chr17:4462270 | C | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0147 a0001c0001t0002g0344 others(2): Show |
5 | HG01074.hp1 HG02602.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+9065C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462270 | |||||||
| chr17:4462270 | C | T | 1 | a0001c0006t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1113+9065C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462270 | |||||||
| chr17:4462272 | T | C | 94 | a0001c0001t0001g0154 a0001c0001t0001g0166 a0001c0001t0001g0186 others(91): Show |
94 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1113+9067T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462272 | |||||||
| chr17:4462274 | C | A | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+9069C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462274 | |||||||
| chr17:4462276 | T | C | 88 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(85): Show |
88 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1113+9071T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462276 | |||||||
| chr17:4462278 | C | T | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+9073C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462278 | |||||||
| chr17:4462280 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(82): Show |
86 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1113+9075T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462280 | |||||||
| chr17:4462282 | C | A | 9 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(6): Show |
9 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+9077C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462282 | |||||||
| chr17:4462284 | T | C | 40 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0002g0046 others(37): Show |
40 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1113+9079T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462284 | |||||||
| chr17:4462286 | C | A | 9 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0328 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+9081C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462286 | |||||||
| chr17:4462288 | T | C | 29 | a0001c0001t0001g0095 a0001c0001t0001g0130 a0001c0001t0001g0164 others(26): Show |
29 | HG00621.hp2 HG01099.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1113+9083T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462288 | |||||||
| chr17:4462290 | C | A | 8 | a0001c0001t0002g0160 a0001c0004t0001g0026 a0001c0012t0002g0042 others(5): Show |
8 | HG01099.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+9085C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462290 | |||||||
| chr17:4462292 | T | C | 23 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0242 others(20): Show |
23 | HG01070.hp2 HG01109.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1113+9087T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462292 | |||||||
| chr17:4462294 | C | A | 14 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0317 others(11): Show |
14 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1113+9089C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462294 | |||||||
| chr17:4462296 | T | C | 11 | a0001c0001t0001g0035 a0001c0001t0001g0147 a0001c0001t0002g0344 others(8): Show |
11 | HG01074.hp1 HG01192.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+9091T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462296 | |||||||
| chr17:4462298 | C | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0147 a0001c0001t0002g0344 others(2): Show |
5 | HG01074.hp1 HG02602.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+9093C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462298 | |||||||
| chr17:4462298 | C | T | 1 | a0001c0006t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1113+9093C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462298 | |||||||
| chr17:4462300 | T | C | 88 | a0001c0001t0001g0166 a0001c0001t0001g0186 a0001c0001t0001g0191 others(85): Show |
88 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1113+9095T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462300 | |||||||
| chr17:4462304 | T | C | 92 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(89): Show |
92 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1113+9099T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462304 | |||||||
| chr17:4462308 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(170): Show |
174 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.1113+9103T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462308 | |||||||
| chr17:4462310 | C | A | 12 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(9): Show |
12 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+9105C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462310 | |||||||
| chr17:4462310 | C | T | 1 | a0001c0006t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1113+9105C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462310 | |||||||
| chr17:4462312 | T | C | 118 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(115): Show |
118 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1113+9107T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462312 | |||||||
| chr17:4462314 | C | A | 4 | a0002c0011t0003g0287 a0002c0037t0002g0323 a0003c0005t0001g0140 others(1): Show |
4 | HG01192.hp2 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+9109C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462314 | |||||||
| chr17:4462316 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(181): Show |
185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1113+9111T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462316 | |||||||
| chr17:4462318 | C | A | 85 | a0001c0001t0001g0166 a0001c0001t0001g0186 a0001c0001t0001g0191 others(82): Show |
85 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1113+9113C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462318 | |||||||
| chr17:4462320 | T | C | 121 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(118): Show |
121 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1113+9115T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462320 | |||||||
| chr17:4462322 | C | A | 89 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(86): Show |
89 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1113+9117C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462322 | |||||||
| chr17:4462324 | T | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(98): Show |
102 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1113+9119T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462324 | |||||||
| chr17:4462326 | C | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(75): Show |
79 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1113+9121C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462326 | |||||||
| chr17:4462326 | C | CACCAATC others(328): Show |
1 | a0001c0023t0003g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1113+9122_1113+912 others(339): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462326 | ||||||
| chr17:4462328 | T | C | 33 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0242 others(30): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1113+9123T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462328 | |||||||
| chr17:4462330 | C | A | 28 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0002g0046 others(25): Show |
28 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1113+9125C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462330 | |||||||
| chr17:4462330 | C | CACCAATC others(329): Show |
8 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0328 others(5): Show |
8 | HG01109.hp1 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+9126_1113+912 others(340): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462330 | ||||||
| chr17:4462330 | C | CACCAATC others(485): Show |
1 | a0004c0017t0002g0331 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1113+9126_1113+912 others(496): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462330 | ||||||
| chr17:4462332 | T | C | 23 | a0001c0001t0001g0095 a0001c0001t0001g0130 a0001c0001t0001g0164 others(20): Show |
23 | HG00621.hp2 HG02040.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1113+9127T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462332 | |||||||
| chr17:4462334 | C | A | 22 | a0001c0001t0001g0095 a0001c0001t0001g0130 a0001c0001t0001g0164 others(19): Show |
22 | HG00621.hp2 HG02040.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1113+9129C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462334 | |||||||
| chr17:4462334 | C | CACCAATC others(329): Show |
5 | a0001c0018t0002g0349 a0001c0018t0002g0350 a0004c0017t0002g0029 others(2): Show |
5 | HG01099.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+9130_1113+913 others(340): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462334 | ||||||
| chr17:4462334 | C | CACCAATC others(333): Show |
1 | a0001c0004t0001g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1113+9130_1113+913 others(344): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462334 | ||||||
| chr17:4462334 | C | CACCAATC others(333): Show |
1 | a0001c0052t0002g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1113+9130_1113+913 others(344): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462334 | ||||||
| chr17:4462336 | T | C | 12 | a0001c0001t0001g0242 a0001c0001t0002g0343 a0001c0003t0002g0315 others(9): Show |
12 | HG01070.hp2 HG01109.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+9131T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462336 | |||||||
| chr17:4462338 | C | A | 11 | a0001c0001t0001g0242 a0001c0001t0002g0343 a0001c0003t0002g0315 others(8): Show |
11 | HG01070.hp2 HG01109.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+9133C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462338 | |||||||
| chr17:4462338 | C | CACCAATC others(329): Show |
1 | a0001c0009t0002g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1113+9134_1113+913 others(340): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462338 | ||||||
| chr17:4462338 | C | CACCAATC others(333): Show |
3 | a0001c0006t0001g0049 a0001c0006t0001g0050 a0001c0006t0001g0051 |
3 | HG02486.hp2 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1113+9134_1113+913 others(344): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462338 | ||||||
| chr17:4462338 | C | CACCAATC others(333): Show |
1 | a0001c0006t0001g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1113+9134_1113+913 others(344): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462338 | ||||||
| chr17:4462340 | T | C | 10 | a0001c0001t0001g0147 a0001c0001t0002g0160 a0001c0001t0002g0317 others(7): Show |
10 | HG01074.hp1 HG01192.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1113+9135T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462340 | |||||||
| chr17:4462342 | C | A | 9 | a0001c0001t0001g0147 a0001c0001t0002g0160 a0001c0001t0002g0317 others(6): Show |
9 | HG01074.hp1 HG01192.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+9137C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462342 | |||||||
| chr17:4462342 | C | CACCAATC others(485): Show |
3 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 |
3 | HG02809.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1113+9138_1113+913 others(496): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462342 | ||||||
| chr17:4462342 | C | CACCAATC others(333): Show |
1 | a0001c0006t0002g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1113+9138_1113+913 others(344): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462342 | ||||||
| chr17:4462342 | C | T | 1 | a0001c0001t0002g0343 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1113+9137C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462342 | |||||||
| chr17:4462344 | T | C | 93 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0166 others(90): Show |
93 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1113+9139T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462344 | |||||||
| chr17:4462346 | C | A | 92 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0166 others(89): Show |
92 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1113+9141C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462346 | |||||||
| chr17:4462346 | C | CACCAATC others(329): Show |
1 | a0001c0014t0002g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1113+9142_1113+914 others(340): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462346 | ||||||
| chr17:4462346 | C | CACCAATC others(333): Show |
1 | a0001c0006t0001g0077 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1113+9142_1113+914 others(344): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462346 | ||||||
| chr17:4462346 | C | T | 4 | a0001c0001t0001g0147 a0001c0001t0002g0160 a0001c0001t0002g0317 others(1): Show |
4 | HG01074.hp1 HG02055.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+9141C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462346 | |||||||
| chr17:4462348 | T | C | 87 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(84): Show |
87 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1113+9143T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462348 | |||||||
| chr17:4462350 | C | A | 87 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(84): Show |
87 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1113+9145C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462350 | |||||||
| chr17:4462350 | C | CACCAATC others(329): Show |
1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1113+9146_1113+914 others(340): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462350 | ||||||
| chr17:4462350 | C | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0012t0001g0036 others(5): Show |
8 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+9145C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462350 | |||||||
| chr17:4462352 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(77): Show |
81 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1113+9147T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462352 | |||||||
| chr17:4462353 | C | T | 1 | a0001c0001t0002g0343 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1113+9148C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462353 | |||||||
| chr17:4462354 | C | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(77): Show |
81 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1113+9149C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462354 | |||||||
| chr17:4462354 | C | CACCAATC others(337): Show |
1 | a0001c0012t0001g0039 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1113+9150_1113+915 others(348): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462354 | ||||||
| chr17:4462356 | T | C | 27 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0002g0046 others(24): Show |
27 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113+9151T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462356 | |||||||
| chr17:4462357 | C | T | 4 | a0001c0001t0001g0147 a0001c0001t0002g0160 a0001c0001t0002g0317 others(1): Show |
4 | HG01074.hp1 HG02055.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+9152C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462357 | |||||||
| chr17:4462358 | C | A | 27 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0002g0046 others(24): Show |
27 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113+9153C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462358 | |||||||
| chr17:4462358 | C | T | 1 | a0001c0012t0002g0042 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1113+9153C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462358 | |||||||
| chr17:4462360 | T | C | 23 | a0001c0001t0001g0095 a0001c0001t0001g0130 a0001c0001t0001g0164 others(20): Show |
23 | HG00621.hp2 HG02040.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1113+9155T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462360 | |||||||
| chr17:4462361 | C | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0012t0001g0036 others(5): Show |
8 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+9156C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462361 | |||||||
| chr17:4462362 | C | A | 23 | a0001c0001t0001g0095 a0001c0001t0001g0130 a0001c0001t0001g0164 others(20): Show |
23 | HG00621.hp2 HG02040.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1113+9157C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462362 | |||||||
| chr17:4462362 | C | CACCAGTC others(5): Show |
1 | a0004c0017t0002g0331 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1113+9158_1113+915 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462362 | ||||||
| chr17:4462364 | T | C | 12 | a0001c0001t0001g0147 a0001c0001t0001g0242 a0001c0001t0002g0160 others(9): Show |
12 | HG01070.hp2 HG01074.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+9159T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462364 | |||||||
| chr17:4462366 | C | A | 10 | a0001c0001t0001g0147 a0001c0001t0001g0242 a0001c0001t0002g0160 others(7): Show |
10 | HG01070.hp2 HG01074.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1113+9161C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462366 | |||||||
| chr17:4462366 | C | CACCAATC others(565): Show |
1 | a0001c0001t0002g0322 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1113+9162_1113+916 others(576): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462366 | ||||||
| chr17:4462366 | C | T | 1 | a0001c0001t0002g0343 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1113+9161C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462366 | |||||||
| chr17:4462368 | T | C | 23 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0326 others(20): Show |
23 | HG01099.hp1 HG01109.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1113+9163T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462368 | |||||||
| chr17:4462369 | C | T | 1 | a0001c0012t0002g0042 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1113+9164C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462369 | |||||||
| chr17:4462370 | C | A | 22 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0326 others(19): Show |
22 | HG01099.hp1 HG01109.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1113+9165C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462370 | |||||||
| chr17:4462370 | C | T | 6 | a0001c0001t0001g0147 a0001c0001t0002g0160 a0001c0001t0002g0317 others(3): Show |
6 | HG01074.hp1 HG02055.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+9165C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462370 | |||||||
| chr17:4462372 | T | C | 3 | a0001c0006t0001g0047 a0001c0009t0002g0031 a0001c0049t0002g0003 |
3 | HG01891.hp1 HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1113+9167T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462372 | |||||||
| chr17:4462373 | C | A | 1 | a0001c0010t0001g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1113+9168C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462373 | |||||||
| chr17:4462374 | C | A | 1 | a0001c0009t0002g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1113+9169C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462374 | |||||||
| chr17:4462374 | C | T | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0326 others(18): Show |
21 | HG01099.hp1 HG01109.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.1113+9169C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462374 | |||||||
| chr17:4462375 | A | ACCAG | 3 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 |
3 | HG02809.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1113+9170_1113+917 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462375 | |||||||
| chr17:4462376 | T | C | 5 | a0001c0004t0001g0026 a0001c0012t0002g0042 a0001c0031t0005g0033 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+9171T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462376 | |||||||
| chr17:4462378 | C | A | 3 | a0001c0004t0001g0026 a0001c0012t0002g0042 a0001c0052t0002g0063 |
3 | HG02559.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1113+9173C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462378 | |||||||
| chr17:4462378 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+9173C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462378 | |||||||
| chr17:4462380 | T | C | 10 | a0001c0001t0002g0322 a0001c0001t0002g0343 a0001c0006t0001g0032 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1113+9175T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462380 | |||||||
| chr17:4462381 | C | CCACCAAT others(348): Show |
1 | a0001c0001t0001g0203 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1113+9178_1113+917 others(359): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462381 | ||||||
| chr17:4462382 | C | A | 11 | a0001c0001t0001g0035 a0001c0001t0002g0322 a0001c0001t0002g0344 others(8): Show |
11 | HG01891.hp1 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1113+9177C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462382 | |||||||
| chr17:4462382 | C | CACCAATC others(345): Show |
21 | a0001c0001t0001g0166 a0001c0001t0001g0186 a0001c0001t0001g0191 others(18): Show |
21 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1113+9178_1113+917 others(356): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462382 | ||||||
| chr17:4462382 | C | CACCAATC others(581): Show |
11 | a0001c0001t0001g0111 a0001c0001t0001g0223 a0001c0001t0001g0335 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+9178_1113+917 others(592): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462382 | ||||||
| chr17:4462382 | C | CACCAATC others(589): Show |
2 | a0001c0004t0001g0071 a0001c0004t0001g0075 |
2 | NA18962.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1113+9178_1113+917 others(600): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462382 | ||||||
| chr17:4462382 | C | T | 3 | a0001c0004t0001g0026 a0001c0012t0002g0042 a0001c0052t0002g0063 |
3 | HG02559.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1113+9177C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462382 | |||||||
| chr17:4462384 | T | C | 11 | a0001c0001t0001g0147 a0001c0001t0001g0154 a0001c0001t0002g0160 others(8): Show |
11 | HG01074.hp1 HG01109.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+9179T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462384 | |||||||
| chr17:4462386 | C | A | 6 | a0001c0001t0001g0154 a0002c0002t0001g0264 a0002c0002t0001g0265 others(3): Show |
6 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+9181C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462386 | |||||||
| chr17:4462386 | C | CACCAATC others(341): Show |
3 | a0002c0002t0001g0245 a0002c0002t0001g0280 a0002c0037t0002g0323 |
3 | HG01358.hp1 HG03195.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1113+9182_1113+918 others(352): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462386 | ||||||
| chr17:4462386 | C | CACCAATC others(345): Show |
50 | a0001c0001t0001g0028 a0001c0001t0001g0096 a0001c0001t0001g0097 others(47): Show |
50 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1113+9182_1113+918 others(356): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462386 | ||||||
| chr17:4462386 | C | CACCAATC others(581): Show |
7 | a0001c0001t0001g0168 a0001c0001t0001g0190 a0001c0001t0002g0135 others(4): Show |
7 | HG00323.hp2 HG02129.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9182_1113+918 others(592): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462386 | ||||||
| chr17:4462386 | C | T | 5 | a0001c0006t0001g0032 a0001c0006t0001g0049 a0001c0006t0001g0050 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+9181C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462386 | |||||||
| chr17:4462388 | T | C | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0162 others(15): Show |
18 | HG01192.hp2 HG01358.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1113+9183T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462388 | |||||||
| chr17:4462390 | C | A | 9 | a0001c0001t0002g0162 a0001c0001t0002g0343 a0001c0006t0001g0077 others(6): Show |
9 | HG01192.hp2 HG01358.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113+9185C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462390 | |||||||
| chr17:4462390 | C | CACCAATC others(553): Show |
2 | a0001c0003t0001g0318 a0001c0003t0002g0112 |
2 | HG02055.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1113+9186_1113+918 others(564): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462390 | ||||||
| chr17:4462390 | C | CACCAATC others(555): Show |
1 | a0001c0003t0001g0121 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1113+9186_1113+918 others(566): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462390 | ||||||
| chr17:4462390 | C | CACCAATC others(341): Show |
37 | a0001c0001t0001g0263 a0001c0013t0001g0259 a0001c0013t0001g0359 others(34): Show |
37 | HG00099.hp2 HG00609.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.1113+9186_1113+918 others(352): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462390 | ||||||
| chr17:4462390 | C | CACCAATC others(345): Show |
34 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(31): Show |
35 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1113+9186_1113+918 others(356): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462390 | ||||||
| chr17:4462390 | C | CACCAATC others(557): Show |
3 | a0001c0001t0001g0221 a0001c0003t0001g0170 a0001c0006t0002g0089 |
3 | HG03654.hp2 NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1113+9186_1113+918 others(568): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462390 | ||||||
| chr17:4462390 | C | CACCAATC others(581): Show |
1 | a0001c0001t0001g0246 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1113+9186_1113+918 others(592): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462390 | ||||||
| chr17:4462390 | C | CACCAATC others(349): Show |
1 | a0001c0009t0001g0005 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1113+9186_1113+918 others(360): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462390 | ||||||
| chr17:4462390 | C | CACCAATC others(485): Show |
2 | a0001c0001t0001g0311 a0001c0004t0001g0027 |
2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1113+9186_1113+918 others(496): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462390 | ||||||
| chr17:4462390 | C | T | 8 | a0001c0001t0001g0035 a0001c0001t0001g0154 a0001c0001t0002g0344 others(5): Show |
8 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+9185C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462390 | |||||||
| chr17:4462392 | T | C | 23 | a0001c0001t0001g0147 a0001c0001t0002g0160 a0001c0001t0002g0317 others(20): Show |
23 | HG01074.hp1 HG01081.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1113+9187T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462392 | |||||||
| chr17:4462393 | C | T | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1113+9188C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462393 | |||||||
| chr17:4462394 | C | A | 10 | a0001c0001t0001g0147 a0001c0001t0002g0160 a0001c0001t0002g0317 others(7): Show |
10 | HG01074.hp1 HG01081.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1113+9189C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462394 | |||||||
| chr17:4462394 | C | CACCAATC others(555): Show |
1 | a0001c0009t0001g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1113+9190_1113+919 others(566): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462394 | ||||||
| chr17:4462394 | C | CACCAATC others(341): Show |
18 | a0001c0001t0001g0238 a0001c0001t0001g0271 a0001c0001t0001g0272 others(15): Show |
18 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1113+9190_1113+919 others(352): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462394 | ||||||
| chr17:4462394 | C | CACCAATC others(341): Show |
1 | a0002c0002t0002g0289 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1113+9190_1113+919 others(352): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462394 | ||||||
| chr17:4462394 | C | CACCAATC others(345): Show |
2 | a0001c0001t0001g0198 a0003c0005t0002g0155 |
2 | HG01106.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1113+9190_1113+919 others(356): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462394 | ||||||
| chr17:4462394 | C | CACCAATC others(553): Show |
1 | a0001c0006t0001g0010 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1113+9190_1113+919 others(564): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462394 | ||||||
| chr17:4462394 | C | CACCAATC others(557): Show |
14 | a0001c0003t0001g0122 a0001c0003t0001g0123 a0001c0003t0001g0124 others(11): Show |
14 | HG00642.hp1 HG01106.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1113+9190_1113+919 others(568): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462394 | ||||||
| chr17:4462394 | C | CACCAATC others(565): Show |
1 | a0001c0046t0002g0316 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1113+9190_1113+919 others(576): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462394 | ||||||
| chr17:4462394 | C | CACCAATC others(349): Show |
7 | a0001c0003t0001g0132 a0001c0003t0001g0239 a0001c0003t0001g0309 others(4): Show |
7 | HG00323.hp1 HG00639.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+9190_1113+919 others(360): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462394 | ||||||
| chr17:4462394 | C | CACCCACC others(561): Show |
1 | a0003c0051t0001g0013 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1113+9190_1113+919 others(572): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462394 | ||||||
| chr17:4462394 | C | T | 7 | a0001c0001t0002g0162 a0001c0006t0001g0077 a0001c0006t0002g0048 others(4): Show |
7 | HG01192.hp2 HG01358.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9189C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462394 | |||||||
| chr17:4462396 | T | C | 14 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0129 others(11): Show |
14 | HG00741.hp2 HG01167.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1113+9191T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462396 | |||||||
| chr17:4462398 | C | A | 12 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0129 others(9): Show |
12 | HG00741.hp2 HG01167.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1113+9193C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462398 | |||||||
| chr17:4462398 | C | CACCAATC others(341): Show |
5 | a0001c0001t0001g0030 a0001c0001t0002g0143 a0001c0007t0003g0337 others(2): Show |
5 | HG01069.hp2 HG01943.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+9194_1113+919 others(352): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462398 | ||||||
| chr17:4462398 | C | CACCAATC others(561): Show |
1 | a0001c0038t0003g0291 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1113+9194_1113+919 others(572): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462398 | ||||||
| chr17:4462398 | C | CACCAATC others(345): Show |
23 | a0001c0001t0001g0095 a0001c0001t0001g0130 a0001c0001t0001g0179 others(20): Show |
23 | HG00621.hp2 HG00642.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.1113+9194_1113+919 others(356): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462398 | ||||||
| chr17:4462398 | C | CACCAATC others(553): Show |
2 | a0001c0007t0003g0158 a0001c0007t0003g0319 |
2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1113+9194_1113+919 others(564): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462398 | ||||||
| chr17:4462398 | C | CACCAATC others(557): Show |
13 | a0001c0001t0001g0215 a0001c0003t0002g0315 a0001c0034t0002g0045 others(10): Show |
13 | HG01169.hp2 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+9194_1113+919 others(568): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462398 | ||||||
| chr17:4462398 | C | CACCAATC others(349): Show |
2 | a0001c0009t0001g0058 a0001c0028t0003g0173 |
2 | HG00099.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1113+9194_1113+919 others(360): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462398 | ||||||
| chr17:4462398 | C | CACCAATC others(343): Show |
1 | a0001c0010t0001g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1113+9194_1113+919 others(354): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462398 | ||||||
| chr17:4462398 | C | CACCCACC others(345): Show |
1 | a0005c0015t0003g0159 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1113+9194_1113+919 others(356): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462398 | ||||||
| chr17:4462398 | C | CGCCA | 13 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0328 others(10): Show |
13 | HG01099.hp1 HG01109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1113+9193_1113+919 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462398 | |||||||
| chr17:4462398 | C | T | 12 | a0001c0001t0001g0221 a0001c0003t0001g0121 a0001c0003t0001g0152 others(9): Show |
12 | HG01081.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+9193C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462398 | |||||||
| chr17:4462400 | T | C | 2 | a0001c0004t0001g0026 a0001c0052t0002g0063 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1113+9195T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462400 | |||||||
| chr17:4462401 | C | T | 5 | a0001c0001t0001g0154 a0002c0002t0001g0264 a0002c0002t0001g0265 others(2): Show |
5 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+9196C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462401 | |||||||
| chr17:4462402 | C | CACCAATC others(285): Show |
7 | a0001c0003t0002g0256 a0001c0007t0003g0163 a0001c0010t0001g0084 others(4): Show |
7 | HG00639.hp1 HG01175.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9198_1113+919 others(296): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462402 | ||||||
| chr17:4462402 | C | CACCAATC others(341): Show |
3 | a0001c0001t0002g0046 a0001c0009t0004g0061 a0001c0013t0001g0113 |
3 | HG02258.hp1 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1113+9198_1113+919 others(352): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462402 | ||||||
| chr17:4462402 | C | CACCAATC others(345): Show |
7 | a0001c0001t0001g0164 a0001c0001t0001g0242 a0001c0007t0003g0172 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+9198_1113+919 others(356): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462402 | ||||||
| chr17:4462402 | C | CACCAATC others(557): Show |
3 | a0001c0006t0002g0052 a0001c0044t0002g0236 a0003c0005t0001g0235 |
3 | HG02717.hp2 NA19064.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1113+9198_1113+919 others(568): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462402 | ||||||
| chr17:4462402 | C | T | 21 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0260 others(18): Show |
21 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1113+9197C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462402 | |||||||
| chr17:4462404 | T | C | 11 | a0001c0001t0001g0035 a0001c0001t0002g0343 a0001c0001t0002g0344 others(8): Show |
11 | HG02486.hp2 HG02622.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1113+9199T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462404 | |||||||
| chr17:4462405 | C | T | 3 | a0001c0001t0002g0162 a0002c0011t0003g0287 a0003c0005t0001g0140 |
3 | HG01192.hp2 HG01358.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1113+9200C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462405 | |||||||
| chr17:4462406 | C | A | 5 | a0001c0001t0001g0035 a0001c0001t0002g0343 a0001c0001t0002g0344 others(2): Show |
5 | HG02809.hp2 HG02818.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+9201C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462406 | |||||||
| chr17:4462406 | C | CACCAATC others(341): Show |
2 | a0001c0010t0002g0086 a0001c0010t0002g0090 |
2 | HG00738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1113+9202_1113+920 others(352): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462406 | ||||||
| chr17:4462406 | C | CACCAATC others(557): Show |
1 | a0001c0003t0001g0320 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1113+9202_1113+920 others(568): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462406 | ||||||
| chr17:4462406 | C | T | 16 | a0001c0001t0001g0215 a0001c0003t0002g0315 a0001c0007t0003g0158 others(13): Show |
16 | HG01169.hp2 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1113+9201C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462406 | |||||||
| chr17:4462408 | T | C | 12 | a0001c0001t0001g0147 a0001c0001t0001g0154 a0001c0001t0002g0160 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+9203T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462408 | |||||||
| chr17:4462409 | C | T | 6 | a0001c0003t0001g0152 a0001c0009t0002g0076 a0001c0024t0003g0062 others(3): Show |
6 | HG01081.hp2 HG02735.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+9204C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462409 | |||||||
| chr17:4462410 | C | A | 12 | a0001c0001t0001g0147 a0001c0001t0001g0154 a0001c0001t0002g0160 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+9205C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462410 | |||||||
| chr17:4462410 | C | CGCCA | 5 | a0001c0006t0001g0032 a0001c0006t0001g0049 a0001c0006t0001g0050 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+9205_1113+920 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462410 | |||||||
| chr17:4462410 | C | T | 3 | a0001c0006t0002g0052 a0001c0044t0002g0236 a0003c0005t0001g0235 |
3 | HG02717.hp2 NA19064.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1113+9205C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462410 | |||||||
| chr17:4462412 | T | C | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0221 others(18): Show |
21 | HG01192.hp2 HG01358.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1113+9207T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462412 | |||||||
| chr17:4462413 | C | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0260 others(1): Show |
4 | HG00741.hp2 HG01167.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+9208C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462413 | |||||||
| chr17:4462414 | C | A | 17 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0221 others(14): Show |
17 | HG01192.hp2 HG01358.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1113+9209C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462414 | |||||||
| chr17:4462414 | C | T | 6 | a0001c0001t0001g0154 a0001c0003t0001g0320 a0002c0002t0001g0264 others(3): Show |
6 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+9209C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462414 | |||||||
| chr17:4462416 | T | C | 24 | a0001c0001t0002g0343 a0001c0003t0001g0122 a0001c0003t0001g0123 others(21): Show |
24 | HG00642.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1113+9211T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462416 | |||||||
| chr17:4462418 | C | A | 24 | a0001c0001t0002g0343 a0001c0003t0001g0122 a0001c0003t0001g0123 others(21): Show |
24 | HG00642.hp1 HG01081.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1113+9213C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462418 | |||||||
| chr17:4462418 | C | CACCAATC others(57): Show |
1 | a0001c0023t0003g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1113+9214_1113+921 others(68): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462418 | ||||||
| chr17:4462418 | C | CACCAGTC others(5): Show |
2 | a0001c0004t0001g0071 a0001c0004t0001g0075 |
2 | NA18962.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1113+9214_1113+921 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462418 | ||||||
| chr17:4462418 | C | CGCCA | 4 | a0001c0006t0001g0077 a0001c0006t0002g0048 a0001c0012t0001g0039 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+9213_1113+921 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462418 | |||||||
| chr17:4462418 | C | T | 3 | a0001c0001t0002g0162 a0002c0011t0003g0287 a0003c0005t0001g0140 |
3 | HG01192.hp2 HG01358.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1113+9213C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462418 | |||||||
| chr17:4462420 | T | C | 27 | a0001c0001t0001g0028 a0001c0001t0001g0129 a0001c0001t0001g0131 others(24): Show |
27 | HG00741.hp2 HG01074.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113+9215T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462420 | |||||||
| chr17:4462422 | C | A | 26 | a0001c0001t0001g0028 a0001c0001t0001g0129 a0001c0001t0001g0131 others(23): Show |
26 | HG00741.hp2 HG01074.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.1113+9217C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462422 | |||||||
| chr17:4462422 | C | CACCAATC others(57): Show |
13 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0328 others(10): Show |
13 | HG01099.hp1 HG01109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1113+9218_1113+921 others(68): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462422 | ||||||
| chr17:4462422 | C | T | 7 | a0001c0003t0001g0152 a0001c0009t0002g0076 a0001c0024t0003g0062 others(4): Show |
7 | HG01081.hp2 HG02735.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9217C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462422 | |||||||
| chr17:4462424 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1113+9219T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462424 | |||||||
| chr17:4462426 | C | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1113+9221C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462426 | |||||||
| chr17:4462426 | C | CACCAATC others(57): Show |
1 | a0001c0009t0002g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1113+9222_1113+922 others(68): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462426 | ||||||
| chr17:4462426 | C | CACCAATC others(173): Show |
1 | a0002c0002t0001g0280 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1113+9222_1113+922 others(184): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462426 | ||||||
| chr17:4462426 | C | CACCAGTC others(1): Show |
7 | a0001c0001t0001g0168 a0001c0001t0001g0190 a0001c0001t0001g0246 others(4): Show |
7 | HG00323.hp2 HG02129.hp2 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+9222_1113+922 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462426 | ||||||
| chr17:4462426 | C | T | 8 | a0001c0001t0001g0028 a0001c0001t0001g0129 a0001c0001t0001g0131 others(5): Show |
8 | HG00741.hp2 HG01167.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+9221C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462426 | |||||||
| chr17:4462427 | A | ACCAG | 7 | a0001c0001t0001g0335 a0001c0001t0002g0322 a0001c0001t0002g0324 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+9222_1113+922 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462427 | |||||||
| chr17:4462428 | T | C | 70 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(67): Show |
70 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1113+9223T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462428 | |||||||
| chr17:4462430 | C | A | 66 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(63): Show |
66 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1113+9225C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462430 | |||||||
| chr17:4462430 | C | CACCAGTC others(1): Show |
5 | a0001c0001t0001g0111 a0001c0001t0001g0338 a0001c0001t0002g0330 others(2): Show |
5 | HG02280.hp1 HG02647.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+9226_1113+922 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462430 | ||||||
| chr17:4462430 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(47): Show |
51 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.1113+9225C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462430 | |||||||
| chr17:4462432 | T | C | 66 | a0001c0001t0001g0165 a0001c0001t0001g0196 a0001c0001t0001g0207 others(63): Show |
66 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1113+9227T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462432 | |||||||
| chr17:4462434 | C | A | 68 | a0001c0001t0001g0111 a0001c0001t0001g0165 a0001c0001t0001g0196 others(65): Show |
68 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.1113+9229C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462434 | |||||||
| chr17:4462434 | C | CACCAATC others(137): Show |
1 | a0001c0014t0002g0007 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1113+9230_1113+923 others(148): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462434 | ||||||
| chr17:4462434 | C | CACCAGTC others(5): Show |
1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+9230_1113+923 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462434 | ||||||
| chr17:4462434 | C | T | 61 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(58): Show |
61 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1113+9229C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462434 | |||||||
| chr17:4462436 | T | C | 57 | a0001c0001t0001g0130 a0001c0001t0001g0154 a0001c0001t0001g0198 others(54): Show |
57 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1113+9231T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462436 | |||||||
| chr17:4462436 | TCCATCCA others(201): Show |
T | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1113+9235_1113+944 others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462436 | ||||||
| chr17:4462438 | C | A | 46 | a0001c0001t0001g0130 a0001c0001t0001g0154 a0001c0001t0001g0198 others(43): Show |
46 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1113+9233C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462438 | |||||||
| chr17:4462438 | C | T | 68 | a0001c0001t0001g0165 a0001c0001t0001g0168 a0001c0001t0001g0190 others(65): Show |
68 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1113+9233C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462438 | |||||||
| chr17:4462440 | T | C | 28 | a0001c0001t0001g0095 a0001c0001t0001g0129 a0001c0001t0001g0131 others(25): Show |
28 | HG00621.hp2 HG00639.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1113+9235T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462440 | |||||||
| chr17:4462440 | T | G | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1113+9235T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462440 | |||||||
| chr17:4462442 | C | A | 18 | a0001c0001t0001g0095 a0001c0001t0001g0179 a0001c0001t0001g0187 others(15): Show |
18 | HG00621.hp2 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1113+9237C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462442 | |||||||
| chr17:4462442 | C | CACCAATC others(57): Show |
1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1113+9238_1113+923 others(68): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462442 | ||||||
| chr17:4462442 | C | T | 48 | a0001c0001t0001g0111 a0001c0001t0001g0130 a0001c0001t0001g0198 others(45): Show |
48 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1113+9237C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462442 | |||||||
| chr17:4462444 | T | C | 30 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0164 others(27): Show |
30 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1113+9239T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462444 | |||||||
| chr17:4462446 | C | A | 20 | a0001c0001t0001g0030 a0001c0001t0001g0164 a0001c0001t0001g0242 others(17): Show |
20 | HG01069.hp2 HG01070.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1113+9241C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462446 | |||||||
| chr17:4462446 | C | CACCAATC others(565): Show |
1 | a0001c0006t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1113+9242_1113+924 others(576): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462446 | ||||||
| chr17:4462446 | C | CACCCACC others(141): Show |
3 | a0001c0001t0001g0147 a0001c0001t0002g0317 a0001c0001t0002g0343 |
3 | HG01074.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1113+9242_1113+924 others(152): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462446 | ||||||
| chr17:4462446 | C | T | 15 | a0001c0001t0001g0095 a0001c0001t0001g0179 a0001c0001t0001g0187 others(12): Show |
15 | HG00621.hp2 HG01123.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113+9241C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462446 | |||||||
| chr17:4462448 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1113+9243T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462448 | |||||||
| chr17:4462450 | C | A | 6 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0003t0002g0139 others(3): Show |
6 | HG00741.hp2 HG01167.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+9245C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462450 | |||||||
| chr17:4462450 | C | CACCCACC others(385): Show |
6 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(3): Show |
6 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+9246_1113+924 others(396): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462450 | ||||||
| chr17:4462450 | C | CACCCACC others(141): Show |
4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0160 others(1): Show |
4 | HG02055.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+9246_1113+924 others(152): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462450 | ||||||
| chr17:4462450 | C | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0164 a0001c0001t0001g0242 others(8): Show |
11 | HG01069.hp2 HG01070.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+9245C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462450 | |||||||
| chr17:4462451 | A | ACCAG | 4 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 others(1): Show |
4 | HG02809.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+9246_1113+924 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462451 | |||||||
| chr17:4462452 | T | C | 79 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(76): Show |
79 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1113+9247T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462452 | |||||||
| chr17:4462454 | C | A | 17 | a0001c0001t0001g0154 a0001c0001t0001g0168 a0001c0001t0001g0190 others(14): Show |
17 | HG00323.hp2 HG00738.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1113+9249C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462454 | |||||||
| chr17:4462454 | C | CACCAGTC others(1): Show |
10 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0328 others(7): Show |
10 | HG01109.hp1 HG02486.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1113+9250_1113+925 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462454 | ||||||
| chr17:4462454 | C | CACCAGTC others(5): Show |
1 | a0001c0009t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1113+9250_1113+925 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462454 | ||||||
| chr17:4462454 | C | CACCCACC others(45): Show |
1 | a0001c0012t0001g0039 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1113+9250_1113+925 others(56): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462454 | ||||||
| chr17:4462454 | C | CGCCA | 43 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(40): Show |
44 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.1113+9249_1113+925 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462454 | |||||||
| chr17:4462454 | C | T | 5 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 others(2): Show |
5 | HG02809.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+9249C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462454 | |||||||
| chr17:4462455 | A | ACCAG | 3 | a0004c0017t0002g0029 a0004c0030t0002g0009 a0004c0048t0002g0006 |
3 | HG01099.hp1 HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1113+9250_1113+925 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462455 | |||||||
| chr17:4462456 | T | C | 81 | a0001c0001t0001g0111 a0001c0001t0001g0165 a0001c0001t0001g0196 others(78): Show |
81 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1113+9251T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462456 | |||||||
| chr17:4462458 | C | A | 39 | a0001c0001t0001g0035 a0001c0001t0001g0111 a0001c0001t0001g0335 others(36): Show |
39 | HG00639.hp1 HG01109.hp1 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.1113+9253C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462458 | |||||||
| chr17:4462458 | C | CACCCACC others(385): Show |
1 | a0001c0012t0002g0042 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1113+9254_1113+925 others(396): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462458 | ||||||
| chr17:4462458 | C | CGCCA | 57 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(54): Show |
57 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1113+9253_1113+925 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462458 | |||||||
| chr17:4462458 | C | T | 7 | a0001c0001t0002g0046 a0001c0010t0002g0086 a0001c0010t0002g0090 others(4): Show |
7 | HG00738.hp2 HG01099.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+9253C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462458 | |||||||
| chr17:4462459 | A | ACCAG | 11 | a0001c0001t0001g0221 a0001c0003t0001g0121 a0001c0003t0001g0122 others(8): Show |
11 | HG00642.hp1 HG01106.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+9254_1113+925 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462459 | |||||||
| chr17:4462460 | T | C | 54 | a0001c0001t0001g0130 a0001c0001t0001g0147 a0001c0001t0001g0198 others(51): Show |
54 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.1113+9255T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462460 | |||||||
| chr17:4462462 | C | A | 17 | a0001c0001t0001g0311 a0001c0003t0001g0152 a0001c0004t0001g0027 others(14): Show |
17 | HG01081.hp2 HG01099.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1113+9257C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462462 | |||||||
| chr17:4462462 | C | CGCCA | 53 | a0001c0001t0001g0165 a0001c0001t0001g0196 a0001c0001t0001g0207 others(50): Show |
53 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1113+9257_1113+925 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462462 | |||||||
| chr17:4462462 | C | T | 12 | a0001c0001t0001g0221 a0001c0003t0001g0121 a0001c0003t0001g0122 others(9): Show |
12 | HG00642.hp1 HG01106.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+9257C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462462 | |||||||
| chr17:4462463 | A | ACCAG | 14 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0001g0125 others(11): Show |
14 | HG01169.hp2 HG01516.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.1113+9258_1113+925 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462463 | |||||||
| chr17:4462464 | T | C | 29 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0095 others(26): Show |
29 | HG00621.hp2 HG00741.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1113+9259T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462464 | |||||||
| chr17:4462466 | C | A | 19 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0154 others(16): Show |
19 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.1113+9261C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462466 | |||||||
| chr17:4462466 | C | CACCAGTC others(1): Show |
3 | a0001c0003t0002g0315 a0001c0006t0002g0052 a0001c0034t0002g0045 |
3 | HG02717.hp1 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1113+9262_1113+926 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462466 | ||||||
| chr17:4462466 | C | CGCCA | 35 | a0001c0001t0001g0130 a0001c0001t0001g0198 a0001c0001t0001g0238 others(32): Show |
35 | HG00099.hp1 HG00280.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1113+9261_1113+926 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462466 | |||||||
| chr17:4462466 | C | T | 28 | a0001c0001t0001g0035 a0001c0001t0002g0326 a0001c0001t0002g0327 others(25): Show |
28 | HG01109.hp1 HG01169.hp2 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.1113+9261C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462466 | |||||||
| chr17:4462467 | A | ACCAG | 12 | a0001c0001t0001g0215 a0001c0007t0003g0158 a0001c0007t0003g0319 others(9): Show |
12 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+9262_1113+926 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462467 | |||||||
| chr17:4462468 | T | C | 24 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(21): Show |
24 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1113+9263T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462468 | |||||||
| chr17:4462470 | C | A | 25 | a0001c0001t0001g0147 a0001c0001t0002g0162 a0001c0001t0002g0317 others(22): Show |
25 | HG01074.hp1 HG01169.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.1113+9265C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462470 | |||||||
| chr17:4462470 | C | CGCCA | 13 | a0001c0001t0001g0095 a0001c0001t0001g0179 a0001c0001t0001g0187 others(10): Show |
13 | HG00621.hp2 HG01123.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+9265_1113+926 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462470 | |||||||
| chr17:4462470 | C | T | 16 | a0001c0001t0001g0215 a0001c0007t0003g0158 a0001c0007t0003g0319 others(13): Show |
16 | HG01099.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1113+9265C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462470 | |||||||
| chr17:4462472 | T | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0160 others(12): Show |
15 | HG01081.hp2 HG02055.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1113+9267T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462472 | |||||||
| chr17:4462474 | C | A | 22 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0215 others(19): Show |
22 | HG01081.hp2 HG01257.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1113+9269C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462474 | |||||||
| chr17:4462474 | C | CACCAATC others(137): Show |
1 | a0001c0001t0001g0028 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1113+9270_1113+927 others(148): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462474 | ||||||
| chr17:4462474 | C | CGCCA | 11 | a0001c0001t0001g0030 a0001c0001t0001g0164 a0001c0001t0001g0242 others(8): Show |
11 | HG01069.hp2 HG01070.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+9269_1113+927 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462474 | |||||||
| chr17:4462474 | C | T | 11 | a0001c0001t0001g0221 a0001c0003t0001g0121 a0001c0003t0001g0122 others(8): Show |
11 | HG00642.hp1 HG01106.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+9269C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462474 | |||||||
| chr17:4462475 | A | ACCAG | 3 | a0001c0003t0001g0320 a0001c0044t0002g0236 a0003c0005t0001g0235 |
3 | HG02922.hp2 NA19064.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1113+9270_1113+927 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462475 | |||||||
| chr17:4462476 | T | C | 16 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0002g0046 others(13): Show |
16 | HG00738.hp2 HG00741.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.1113+9271T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462476 | |||||||
| chr17:4462478 | C | A | 5 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0003t0002g0139 others(2): Show |
5 | HG00741.hp2 HG01167.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+9273C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462478 | |||||||
| chr17:4462478 | C | CACCAATC others(137): Show |
20 | a0001c0001t0001g0001 a0001c0001t0001g0109 a0001c0001t0001g0183 others(17): Show |
21 | HG00280.hp2 HG00438.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.1113+9274_1113+927 others(148): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462478 | ||||||
| chr17:4462478 | C | CACCAATC others(121): Show |
21 | a0001c0001t0001g0166 a0001c0001t0001g0186 a0001c0001t0001g0191 others(18): Show |
21 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1113+9274_1113+927 others(132): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462478 | ||||||
| chr17:4462478 | C | CACCAATC others(133): Show |
1 | a0001c0001t0001g0105 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1113+9274_1113+927 others(144): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462478 | ||||||
| chr17:4462478 | C | CACCAATC others(137): Show |
1 | a0001c0001t0001g0219 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1113+9274_1113+927 others(148): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462478 | ||||||
| chr17:4462478 | C | T | 20 | a0001c0003t0001g0123 a0001c0003t0001g0124 a0001c0003t0001g0125 others(17): Show |
20 | HG01169.hp2 HG01516.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.1113+9273C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462478 | |||||||
| chr17:4462480 | T | C | 22 | a0001c0001t0001g0035 a0001c0001t0002g0326 a0001c0001t0002g0327 others(19): Show |
22 | HG01109.hp1 HG02486.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.1113+9275T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462480 | |||||||
| chr17:4462482 | C | A | 21 | a0001c0001t0001g0035 a0001c0001t0002g0326 a0001c0001t0002g0327 others(18): Show |
21 | HG01109.hp1 HG02486.hp1 HG02809.hp2 others(18): Show |
intron_variant | MODIFIER | c.1113+9277C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462482 | |||||||
| chr17:4462482 | C | CACCAATC others(113): Show |
1 | a0002c0002t0001g0245 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1113+9278_1113+927 others(124): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462482 | ||||||
| chr17:4462482 | C | CACCAATC others(137): Show |
48 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(45): Show |
48 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.1113+9278_1113+927 others(148): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462482 | ||||||
| chr17:4462482 | C | CGCCA | 4 | a0001c0001t0002g0046 a0001c0010t0002g0086 a0001c0010t0002g0090 others(1): Show |
4 | HG00738.hp2 HG02258.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+9277_1113+927 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462482 | |||||||
| chr17:4462482 | C | T | 12 | a0001c0001t0001g0215 a0001c0007t0003g0158 a0001c0007t0003g0319 others(9): Show |
12 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+9277C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462482 | |||||||
| chr17:4462484 | T | C | 41 | a0001c0001t0001g0111 a0001c0001t0001g0168 a0001c0001t0001g0190 others(38): Show |
41 | HG00323.hp2 HG01099.hp1 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1113+9279T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462484 | |||||||
| chr17:4462486 | C | A | 13 | a0001c0001t0001g0332 a0001c0001t0001g0334 a0001c0003t0002g0136 others(10): Show |
13 | HG01099.hp1 HG01123.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1113+9281C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462486 | |||||||
| chr17:4462486 | C | CACCAATC others(109): Show |
7 | a0001c0003t0001g0132 a0001c0003t0001g0239 a0001c0003t0001g0309 others(4): Show |
7 | HG00323.hp1 HG00639.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+9282_1113+928 others(120): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462486 | ||||||
| chr17:4462486 | C | CACCAATC others(113): Show |
40 | a0001c0001t0001g0263 a0001c0003t0001g0351 a0001c0006t0002g0011 others(37): Show |
40 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1113+9282_1113+928 others(124): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462486 | ||||||
| chr17:4462486 | C | CACCAATC others(137): Show |
6 | a0001c0001t0001g0165 a0001c0001t0001g0196 a0001c0001t0001g0207 others(3): Show |
6 | HG00544.hp2 HG00609.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+9282_1113+928 others(148): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462486 | ||||||
| chr17:4462486 | C | CATCACCA others(116): Show |
1 | a0003c0005t0001g0310 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1113+9284_1113+928 others(127): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462486 | ||||||
| chr17:4462488 | T | C | 19 | a0001c0001t0001g0221 a0001c0003t0001g0121 a0001c0003t0001g0122 others(16): Show |
19 | HG00642.hp1 HG01106.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1113+9283T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462488 | |||||||
| chr17:4462490 | C | A | 11 | a0001c0001t0001g0221 a0001c0003t0001g0121 a0001c0003t0001g0122 others(8): Show |
11 | HG00642.hp1 HG01106.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+9285C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462490 | |||||||
| chr17:4462490 | C | CACCAATC others(109): Show |
1 | a0001c0009t0001g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1113+9286_1113+928 others(120): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462490 | ||||||
| chr17:4462490 | C | CACCAATC others(117): Show |
1 | a0001c0028t0003g0173 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1113+9286_1113+928 others(128): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462490 | ||||||
| chr17:4462490 | C | CACCAATC others(113): Show |
25 | a0001c0001t0001g0130 a0001c0001t0001g0238 a0001c0001t0001g0271 others(22): Show |
25 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1113+9286_1113+928 others(124): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462490 | ||||||
| chr17:4462490 | C | CACCAATC others(121): Show |
5 | a0001c0023t0003g0053 a0002c0002t0001g0277 a0002c0002t0001g0300 others(2): Show |
5 | HG01175.hp2 HG01361.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+9286_1113+928 others(132): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462490 | ||||||
| chr17:4462490 | C | CACCAATC others(137): Show |
2 | a0001c0001t0001g0198 a0001c0001t0002g0197 |
2 | NA18612.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1113+9286_1113+928 others(148): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462490 | ||||||
| chr17:4462490 | C | CACCCACC others(233): Show |
4 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(1): Show |
4 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+9286_1113+928 others(244): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462490 | ||||||
| chr17:4462490 | C | CACCCACC others(377): Show |
1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1113+9286_1113+928 others(388): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462490 | ||||||
| chr17:4462490 | C | T | 6 | a0001c0003t0001g0320 a0001c0014t0002g0007 a0001c0036t0003g0144 others(3): Show |
6 | HG02922.hp2 NA18939.hp2 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+9285C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462490 | |||||||
| chr17:4462492 | T | C | 66 | a0001c0001t0001g0111 a0001c0001t0001g0166 a0001c0001t0001g0168 others(63): Show |
66 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.1113+9287T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462492 | |||||||
| chr17:4462494 | C | A | 60 | a0001c0001t0001g0111 a0001c0001t0001g0166 a0001c0001t0001g0168 others(57): Show |
60 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1113+9289C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462494 | |||||||
| chr17:4462494 | C | CACCAATC others(121): Show |
2 | a0002c0002t0002g0304 a0003c0008t0003g0119 |
2 | HG01123.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1113+9290_1113+929 others(132): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462494 | ||||||
| chr17:4462494 | C | CACCAATC others(137): Show |
10 | a0001c0001t0001g0095 a0001c0001t0001g0179 a0001c0001t0001g0187 others(7): Show |
10 | HG00621.hp2 HG02040.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.1113+9290_1113+929 others(148): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462494 | ||||||
| chr17:4462494 | C | CACCAATC others(138): Show |
1 | a0001c0001t0001g0297 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1113+9290_1113+929 others(149): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462494 | ||||||
| chr17:4462494 | C | CACCCACC others(233): Show |
1 | a0002c0011t0003g0287 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1113+9290_1113+929 others(244): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462494 | ||||||
| chr17:4462494 | C | CACCCACC others(457): Show |
1 | a0003c0005t0001g0140 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1113+9290_1113+929 others(468): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462494 | ||||||
| chr17:4462494 | C | CACCCACC others(453): Show |
1 | a0001c0001t0002g0162 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1113+9290_1113+929 others(464): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462494 | ||||||
| chr17:4462494 | C | CACCCACC others(97): Show |
1 | a0001c0009t0001g0005 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1113+9290_1113+929 others(108): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462494 | ||||||
| chr17:4462494 | C | CACCCACC others(101): Show |
7 | a0001c0001t0001g0332 a0001c0001t0001g0334 a0001c0003t0002g0136 others(4): Show |
7 | HG01123.hp2 HG01433.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+9290_1113+929 others(112): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462494 | ||||||
| chr17:4462494 | C | T | 50 | a0001c0001t0001g0263 a0001c0001t0001g0311 a0001c0003t0001g0132 others(47): Show |
50 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1113+9289C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462494 | |||||||
| chr17:4462496 | T | C | 23 | a0001c0001t0001g0147 a0001c0001t0001g0215 a0001c0001t0002g0317 others(20): Show |
23 | HG01074.hp1 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1113+9291T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462496 | |||||||
| chr17:4462498 | C | A | 20 | a0001c0001t0001g0215 a0001c0001t0001g0311 a0001c0004t0001g0027 others(17): Show |
20 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1113+9293C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462498 | |||||||
| chr17:4462498 | C | CACCAATC others(113): Show |
6 | a0001c0001t0001g0030 a0001c0001t0002g0143 a0001c0007t0003g0337 others(3): Show |
6 | HG01069.hp2 HG01257.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+9294_1113+929 others(124): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462498 | ||||||
| chr17:4462498 | C | CACCAATC others(113): Show |
4 | a0001c0001t0001g0164 a0001c0001t0001g0242 a0001c0007t0003g0172 others(1): Show |
4 | HG01070.hp2 NA18962.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+9294_1113+929 others(124): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462498 | ||||||
| chr17:4462498 | C | CACCAATC others(137): Show |
1 | a0001c0010t0001g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1113+9294_1113+929 others(148): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462498 | ||||||
| chr17:4462498 | C | CACCCACC others(461): Show |
1 | a0002c0002t0001g0307 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1113+9294_1113+929 others(472): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462498 | ||||||
| chr17:4462498 | C | CACCCACC others(457): Show |
1 | a0010c0041t0003g0314 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1113+9294_1113+929 others(468): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462498 | ||||||
| chr17:4462498 | C | CACCCACC others(461): Show |
1 | a0002c0002t0001g0230 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1113+9294_1113+929 others(472): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462498 | ||||||
| chr17:4462498 | C | CACCCACC others(461): Show |
3 | a0001c0003t0001g0152 a0001c0009t0002g0076 a0001c0024t0003g0062 |
3 | HG01081.hp2 NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1113+9294_1113+929 others(472): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462498 | ||||||
| chr17:4462498 | C | T | 26 | a0001c0001t0001g0130 a0001c0001t0001g0238 a0001c0001t0001g0271 others(23): Show |
26 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1113+9293C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462498 | |||||||
| chr17:4462500 | T | C | 11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(8): Show |
11 | HG01074.hp1 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1113+9295T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462500 | |||||||
| chr17:4462502 | C | A | 2 | a0002c0002t0001g0280 a0004c0017t0002g0331 |
2 | HG01358.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1113+9297C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462502 | |||||||
| chr17:4462502 | C | CACCAATC others(121): Show |
1 | a0001c0009t0004g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1113+9298_1113+929 others(132): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462502 | ||||||
| chr17:4462502 | C | CACCCACC others(461): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0003t0002g0139 |
3 | HG00741.hp2 HG01167.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1113+9298_1113+929 others(472): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462502 | ||||||
| chr17:4462502 | C | T | 11 | a0001c0001t0001g0332 a0001c0001t0001g0334 a0001c0001t0002g0162 others(8): Show |
11 | HG01123.hp2 HG01358.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+9297C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462502 | |||||||
| chr17:4462503 | A | ACCAG | 6 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0039 others(3): Show |
6 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+9298_1113+929 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462503 | |||||||
| chr17:4462504 | T | C | 29 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(26): Show |
29 | HG00099.hp1 HG00639.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1113+9299T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462504 | |||||||
| chr17:4462506 | C | A | 24 | a0001c0003t0001g0320 a0001c0003t0002g0256 a0001c0006t0001g0047 others(21): Show |
24 | HG00099.hp1 HG00639.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.1113+9301C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462506 | |||||||
| chr17:4462506 | C | CACCAATC others(121): Show |
4 | a0001c0001t0002g0046 a0001c0010t0002g0086 a0001c0010t0002g0090 others(1): Show |
4 | HG00738.hp2 HG02258.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+9302_1113+930 others(132): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462506 | ||||||
| chr17:4462506 | C | T | 21 | a0001c0001t0001g0030 a0001c0001t0001g0147 a0001c0001t0001g0164 others(18): Show |
21 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1113+9301C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462506 | |||||||
| chr17:4462508 | T | C | 82 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(79): Show |
82 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1113+9303T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462508 | |||||||
| chr17:4462508 | T | TCTACCCA others(5): Show |
2 | a0001c0004t0001g0071 a0001c0004t0001g0075 |
2 | NA18962.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1113+9304_1113+930 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462508 | ||||||
| chr17:4462510 | C | A | 80 | a0001c0001t0001g0111 a0001c0001t0001g0168 a0001c0001t0001g0190 others(77): Show |
80 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1113+9305C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462510 | |||||||
| chr17:4462510 | C | T | 12 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0002g0160 others(9): Show |
12 | HG00639.hp1 HG01175.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+9305C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462510 | |||||||
| chr17:4462512 | T | C | 41 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0130 others(38): Show |
41 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1113+9307T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462512 | |||||||
| chr17:4462514 | C | A | 33 | a0001c0001t0001g0130 a0001c0001t0001g0238 a0001c0001t0001g0271 others(30): Show |
33 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1113+9309C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462514 | |||||||
| chr17:4462514 | C | T | 4 | a0001c0006t0001g0047 a0001c0012t0001g0038 a0004c0017t0002g0331 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+9309C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462514 | |||||||
| chr17:4462516 | T | C | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(18): Show |
21 | HG00741.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1113+9311T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462516 | |||||||
| chr17:4462518 | C | A | 16 | a0001c0001t0001g0035 a0001c0001t0001g0129 a0001c0001t0001g0131 others(13): Show |
16 | HG00741.hp2 HG01123.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.1113+9313C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462518 | |||||||
| chr17:4462518 | C | T | 7 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0039 others(4): Show |
7 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+9313C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462518 | |||||||
| chr17:4462519 | A | ACCAG | 69 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0096 others(66): Show |
70 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1113+9314_1113+931 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462519 | |||||||
| chr17:4462520 | T | C | 35 | a0001c0001t0001g0030 a0001c0001t0001g0164 a0001c0001t0001g0221 others(32): Show |
35 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1113+9315T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462520 | |||||||
| chr17:4462522 | C | A | 17 | a0001c0001t0001g0030 a0001c0001t0001g0164 a0001c0001t0001g0242 others(14): Show |
17 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1113+9317C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462522 | |||||||
| chr17:4462522 | C | CACCAGTC others(1): Show |
8 | a0001c0001t0001g0134 a0001c0001t0001g0165 a0001c0001t0001g0196 others(5): Show |
8 | HG00544.hp2 HG00609.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+9318_1113+931 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462522 | ||||||
| chr17:4462522 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0096 others(86): Show |
90 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1113+9317C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462522 | |||||||
| chr17:4462524 | T | C | 54 | a0001c0001t0001g0111 a0001c0001t0001g0147 a0001c0001t0001g0168 others(51): Show |
54 | HG00323.hp2 HG01074.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.1113+9319T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462524 | |||||||
| chr17:4462526 | C | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0096 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1113+9321C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462526 | |||||||
| chr17:4462527 | A | ACCAG | 20 | a0001c0001t0001g0198 a0001c0001t0002g0197 a0001c0001t0002g0326 others(17): Show |
20 | HG01099.hp1 HG01109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1113+9322_1113+932 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462527 | |||||||
| chr17:4462527 | A | G | 2 | a0001c0004t0001g0026 a0001c0052t0002g0063 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1113+9322A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462527 | |||||||
| chr17:4462528 | T | C | 54 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0111 others(51): Show |
54 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1113+9323T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462528 | |||||||
| chr17:4462530 | C | A | 26 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0154 others(23): Show |
26 | HG00642.hp1 HG01106.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1113+9325C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462530 | |||||||
| chr17:4462530 | C | CACCAGTC others(1): Show |
32 | a0001c0001t0001g0095 a0001c0001t0001g0166 a0001c0001t0001g0179 others(29): Show |
32 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1113+9326_1113+932 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462530 | ||||||
| chr17:4462530 | C | T | 25 | a0001c0001t0001g0147 a0001c0001t0001g0198 a0001c0001t0002g0197 others(22): Show |
25 | HG01074.hp1 HG01099.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1113+9325C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462530 | |||||||
| chr17:4462531 | A | G | 1 | a0001c0006t0001g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1113+9326A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462531 | |||||||
| chr17:4462532 | T | C | 59 | a0001c0001t0001g0035 a0001c0001t0001g0111 a0001c0001t0001g0168 others(56): Show |
59 | HG00323.hp2 HG01109.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.1113+9327T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462532 | |||||||
| chr17:4462534 | C | A | 111 | a0001c0001t0001g0035 a0001c0001t0001g0095 a0001c0001t0001g0111 others(108): Show |
111 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.1113+9329C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462534 | |||||||
| chr17:4462534 | C | CACCAATC others(85): Show |
1 | a0001c0046t0002g0316 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1113+9330_1113+933 others(96): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462534 | ||||||
| chr17:4462534 | C | CGCCA | 7 | a0001c0003t0002g0256 a0001c0007t0003g0163 a0001c0010t0001g0084 others(4): Show |
7 | HG00639.hp1 HG01175.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9329_1113+933 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462534 | |||||||
| chr17:4462534 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(79): Show |
83 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1113+9329C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462534 | |||||||
| chr17:4462536 | T | C | 7 | a0001c0003t0001g0320 a0001c0004t0001g0071 a0001c0004t0001g0075 others(4): Show |
7 | HG01192.hp2 HG02922.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9331T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462536 | |||||||
| chr17:4462538 | C | A | 5 | a0001c0006t0001g0051 a0001c0006t0001g0077 a0001c0006t0002g0048 others(2): Show |
5 | HG01192.hp2 HG02257.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+9333C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462538 | |||||||
| chr17:4462538 | C | T | 6 | a0001c0001t0001g0154 a0001c0010t0001g0078 a0002c0002t0001g0264 others(3): Show |
6 | HG01081.hp1 HG01109.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+9333C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462538 | |||||||
| chr17:4462540 | T | C | 3 | a0001c0004t0001g0071 a0001c0004t0001g0075 a0003c0005t0001g0235 |
3 | NA18962.hp1 NA18983.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1113+9335T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462540 | |||||||
| chr17:4462542 | C | A | 2 | a0001c0010t0001g0078 a0003c0005t0001g0235 |
2 | HG01081.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1113+9337C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462542 | |||||||
| chr17:4462542 | C | T | 55 | a0001c0001t0001g0095 a0001c0001t0001g0166 a0001c0001t0001g0179 others(52): Show |
55 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1113+9337C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462542 | |||||||
| chr17:4462544 | T | C | 20 | a0001c0001t0001g0221 a0001c0003t0001g0121 a0001c0003t0001g0122 others(17): Show |
20 | HG00642.hp1 HG01106.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1113+9339T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462544 | |||||||
| chr17:4462545 | C | T | 2 | a0001c0004t0001g0071 a0001c0004t0001g0075 |
2 | NA18962.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1113+9340C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462545 | |||||||
| chr17:4462546 | C | A | 20 | a0001c0001t0001g0221 a0001c0003t0001g0121 a0001c0003t0001g0122 others(17): Show |
20 | HG00642.hp1 HG01106.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1113+9341C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462546 | |||||||
| chr17:4462546 | C | T | 6 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 others(3): Show |
6 | HG02257.hp2 HG02602.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+9341C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462546 | |||||||
| chr17:4462548 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0035 others(102): Show |
106 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1113+9343T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462548 | |||||||
| chr17:4462550 | C | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0096 others(97): Show |
101 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1113+9345C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462550 | |||||||
| chr17:4462550 | C | T | 1 | a0001c0010t0001g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1113+9345C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462550 | |||||||
| chr17:4462552 | T | C | 8 | a0001c0001t0001g0035 a0001c0001t0001g0154 a0001c0001t0002g0344 others(5): Show |
8 | HG01358.hp1 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+9347T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462552 | |||||||
| chr17:4462553 | C | T | 2 | a0001c0001t0001g0311 a0001c0004t0001g0027 |
2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1113+9348C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462553 | |||||||
| chr17:4462554 | C | A | 3 | a0001c0001t0001g0154 a0001c0004t0001g0071 a0001c0004t0001g0075 |
3 | HG02970.hp2 NA18962.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1113+9349C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462554 | |||||||
| chr17:4462554 | C | CACCAATC others(85): Show |
1 | a0003c0005t0001g0235 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1113+9350_1113+935 others(96): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462554 | ||||||
| chr17:4462554 | C | CACCAGTC others(165): Show |
1 | a0001c0001t0001g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1113+9350_1113+935 others(176): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462554 | ||||||
| chr17:4462554 | C | CACCAGTC others(169): Show |
42 | a0001c0001t0001g0263 a0001c0013t0001g0259 a0001c0013t0001g0359 others(39): Show |
42 | HG00099.hp2 HG00609.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1113+9350_1113+935 others(180): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462554 | ||||||
| chr17:4462554 | C | CACCAGTC others(165): Show |
8 | a0001c0003t0001g0132 a0001c0003t0001g0239 a0001c0003t0001g0309 others(5): Show |
8 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+9350_1113+935 others(176): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462554 | ||||||
| chr17:4462554 | C | CATCTACC others(73): Show |
17 | a0001c0001t0001g0221 a0001c0003t0001g0121 a0001c0003t0001g0122 others(14): Show |
17 | HG00642.hp1 HG01106.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1113+9352_1113+935 others(84): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462554 | ||||||
| chr17:4462554 | C | CCACCAGT others(171): Show |
1 | a0003c0005t0001g0310 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1113+9349_1113+935 others(182): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462554 | |||||||
| chr17:4462554 | C | T | 1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1113+9349C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462554 | |||||||
| chr17:4462556 | T | C | 65 | a0001c0001t0001g0035 a0001c0001t0001g0095 a0001c0001t0001g0166 others(62): Show |
65 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1113+9351T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462556 | |||||||
| chr17:4462558 | C | A | 61 | a0001c0001t0001g0035 a0001c0001t0001g0095 a0001c0001t0001g0166 others(58): Show |
61 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1113+9353C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462558 | |||||||
| chr17:4462558 | C | CACCAATC others(349): Show |
7 | a0001c0003t0002g0256 a0001c0007t0003g0163 a0001c0010t0001g0084 others(4): Show |
7 | HG00639.hp1 HG01175.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9354_1113+935 others(360): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462558 | ||||||
| chr17:4462558 | C | CACCAATC others(101): Show |
1 | a0002c0002t0001g0280 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1113+9354_1113+935 others(112): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462558 | ||||||
| chr17:4462558 | C | CACCAATC others(85): Show |
3 | a0001c0003t0001g0320 a0001c0014t0002g0007 a0001c0044t0002g0236 |
3 | HG02922.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1113+9354_1113+935 others(96): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462558 | ||||||
| chr17:4462558 | C | CACCAGTC others(161): Show |
1 | a0003c0008t0003g0128 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1113+9354_1113+935 others(172): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462558 | ||||||
| chr17:4462558 | C | CACCAGTC others(165): Show |
11 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0332 others(8): Show |
11 | HG00741.hp2 HG01123.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1113+9354_1113+935 others(176): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462558 | ||||||
| chr17:4462558 | C | CACCAGTC others(169): Show |
44 | a0001c0001t0001g0030 a0001c0001t0001g0238 a0001c0001t0001g0271 others(41): Show |
44 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1113+9354_1113+935 others(180): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462558 | ||||||
| chr17:4462558 | C | CACCAGTC others(165): Show |
5 | a0001c0003t0001g0152 a0001c0009t0001g0005 a0001c0009t0001g0058 others(2): Show |
5 | HG01081.hp2 NA18943.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+9354_1113+935 others(176): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462558 | ||||||
| chr17:4462558 | C | CACCAGTC others(173): Show |
4 | a0001c0001t0001g0164 a0001c0001t0001g0242 a0001c0007t0003g0172 others(1): Show |
4 | HG01070.hp2 NA18962.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+9354_1113+935 others(184): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462558 | ||||||
| chr17:4462558 | C | CACCCACC others(33): Show |
20 | a0001c0001t0001g0111 a0001c0001t0001g0168 a0001c0001t0001g0190 others(17): Show |
20 | HG00323.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1113+9354_1113+935 others(44): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462558 | ||||||
| chr17:4462558 | C | CACCCATC others(109): Show |
1 | a0001c0006t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1113+9354_1113+935 others(120): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462558 | ||||||
| chr17:4462558 | C | CACCCATC others(381): Show |
1 | a0002c0011t0003g0287 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1113+9354_1113+935 others(392): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462558 | ||||||
| chr17:4462558 | C | CATCTACC others(73): Show |
23 | a0001c0001t0001g0215 a0001c0003t0001g0123 a0001c0003t0001g0124 others(20): Show |
23 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.1113+9356_1113+935 others(84): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462558 | ||||||
| chr17:4462558 | C | T | 2 | a0001c0004t0001g0071 a0001c0004t0001g0075 |
2 | NA18962.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1113+9353C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462558 | |||||||
| chr17:4462560 | T | C | 5 | a0001c0006t0001g0051 a0001c0006t0001g0077 a0001c0006t0002g0048 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+9355T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462560 | |||||||
| chr17:4462562 | C | A | 4 | a0001c0006t0001g0051 a0001c0006t0001g0077 a0001c0006t0002g0048 others(1): Show |
4 | HG01081.hp1 HG02257.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+9357C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462562 | |||||||
| chr17:4462562 | C | CGCCA | 4 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(1): Show |
4 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+9357_1113+935 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462562 | |||||||
| chr17:4462562 | C | T | 1 | a0001c0046t0002g0316 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1113+9357C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462562 | |||||||
| chr17:4462564 | T | C | 2 | a0001c0031t0005g0033 a0004c0017t0002g0331 |
2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1113+9359T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462564 | |||||||
| chr17:4462566 | C | T | 1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1113+9361C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462566 | |||||||
| chr17:4462568 | T | C | 2 | a0001c0031t0005g0033 a0001c0049t0002g0003 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1113+9363T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462568 | |||||||
| chr17:4462569 | C | T | 1 | a0004c0017t0002g0331 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1113+9364C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462569 | |||||||
| chr17:4462570 | C | A | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+9365C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462570 | |||||||
| chr17:4462572 | T | C | 5 | a0001c0001t0001g0147 a0001c0001t0001g0311 a0001c0001t0002g0317 others(2): Show |
5 | HG01074.hp1 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+9367T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462572 | |||||||
| chr17:4462574 | C | A | 4 | a0001c0001t0001g0147 a0001c0001t0001g0311 a0001c0001t0002g0317 others(1): Show |
4 | HG01074.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+9369C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462574 | |||||||
| chr17:4462574 | C | CACCAGTC others(173): Show |
2 | a0001c0012t0001g0038 a0007c0025t0002g0041 |
2 | HG02280.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1113+9370_1113+937 others(184): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462574 | ||||||
| chr17:4462574 | C | T | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1113+9369C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462574 | |||||||
| chr17:4462576 | T | C | 77 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0130 others(74): Show |
77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1113+9371T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462576 | |||||||
| chr17:4462578 | C | A | 76 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0130 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1113+9373C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462578 | |||||||
| chr17:4462578 | C | CACCAGTC others(177): Show |
6 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0039 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+9374_1113+937 others(188): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462578 | ||||||
| chr17:4462578 | C | T | 4 | a0001c0001t0001g0147 a0001c0001t0002g0317 a0001c0012t0001g0038 others(1): Show |
4 | HG01074.hp1 HG02280.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+9373C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462578 | |||||||
| chr17:4462580 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(200): Show |
204 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1113+9375T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462580 | |||||||
| chr17:4462582 | C | A | 125 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0129 others(122): Show |
125 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.1113+9377C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462582 | |||||||
| chr17:4462582 | C | CACCAATC others(93): Show |
1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+9378_1113+937 others(104): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462582 | ||||||
| chr17:4462582 | C | CACCAGTC others(165): Show |
1 | a0001c0001t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1113+9378_1113+937 others(176): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462582 | ||||||
| chr17:4462582 | C | CACCCACC others(37): Show |
3 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 |
3 | HG02809.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1113+9378_1113+937 others(48): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462582 | ||||||
| chr17:4462582 | C | CACCCATC others(117): Show |
8 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0328 others(5): Show |
8 | HG01109.hp1 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+9378_1113+937 others(128): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462582 | ||||||
| chr17:4462582 | C | CACCCATC others(113): Show |
2 | a0001c0018t0002g0349 a0001c0018t0002g0350 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1113+9378_1113+937 others(124): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462582 | ||||||
| chr17:4462582 | C | CACCCATC others(118): Show |
1 | a0001c0009t0002g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1113+9378_1113+937 others(129): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462582 | ||||||
| chr17:4462582 | C | CACCCATC others(101): Show |
4 | a0001c0009t0002g0031 a0004c0017t0002g0029 a0004c0030t0002g0009 others(1): Show |
4 | HG01099.hp1 HG02145.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+9378_1113+937 others(112): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462582 | ||||||
| chr17:4462582 | C | CATCTACC others(69): Show |
2 | a0001c0001t0001g0311 a0001c0004t0001g0027 |
2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1113+9380_1113+938 others(80): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462582 | ||||||
| chr17:4462582 | C | T | 76 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0130 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1113+9377C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462582 | |||||||
| chr17:4462586 | C | CACCAATC others(373): Show |
4 | a0002c0002t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(1): Show |
4 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+9382_1113+938 others(384): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462586 | ||||||
| chr17:4462586 | C | CACCAATC others(125): Show |
1 | a0001c0001t0001g0189 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1113+9382_1113+938 others(136): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462586 | ||||||
| chr17:4462586 | C | CACCAATC others(131): Show |
1 | a0001c0001t0001g0261 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1113+9382_1113+938 others(142): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462586 | ||||||
| chr17:4462586 | C | CACCAATC others(125): Show |
2 | a0001c0001t0002g0357 a0001c0001t0002g0358 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1113+9382_1113+938 others(136): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462586 | ||||||
| chr17:4462586 | C | CACCAATC others(129): Show |
73 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0096 others(70): Show |
74 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1113+9382_1113+938 others(140): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462586 | ||||||
| chr17:4462586 | C | CACCCATC others(137): Show |
1 | a0001c0010t0001g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1113+9382_1113+938 others(148): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462586 | ||||||
| chr17:4462586 | C | CACCCATC others(137): Show |
34 | a0001c0001t0001g0095 a0001c0001t0001g0166 a0001c0001t0001g0179 others(31): Show |
34 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1113+9382_1113+938 others(148): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462586 | ||||||
| chr17:4462586 | C | T | 124 | a0001c0001t0001g0030 a0001c0001t0001g0111 a0001c0001t0001g0129 others(121): Show |
124 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.1113+9381C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462586 | |||||||
| chr17:4462592 | T | C | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1113+9387T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462592 | |||||||
| chr17:4462594 | C | A | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1113+9389C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462594 | |||||||
| chr17:4462596 | T | C | 10 | a0001c0001t0001g0147 a0001c0001t0002g0317 a0001c0012t0001g0036 others(7): Show |
10 | HG01074.hp1 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1113+9391T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462596 | |||||||
| chr17:4462598 | C | T | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1113+9393C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462598 | |||||||
| chr17:4462600 | T | C | 98 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(95): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1113+9395T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462600 | |||||||
| chr17:4462603 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0002g0317 |
2 | HG01074.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1113+9398A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462603 | |||||||
| chr17:4462604 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(247): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.1113+9399T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462604 | |||||||
| chr17:4462606 | C | A | 10 | a0001c0001t0001g0147 a0001c0001t0002g0317 a0001c0012t0001g0036 others(7): Show |
10 | HG01074.hp1 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1113+9401C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462606 | |||||||
| chr17:4462606 | C | CACCAGTC others(197): Show |
8 | a0001c0004t0001g0026 a0001c0006t0001g0032 a0001c0006t0001g0049 others(5): Show |
8 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+9402_1113+940 others(208): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462606 | ||||||
| chr17:4462606 | C | CACCCATC others(137): Show |
1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1113+9402_1113+940 others(148): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462606 | ||||||
| chr17:4462606 | C | CGCCA | 28 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(25): Show |
28 | HG01099.hp1 HG01109.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1113+9401_1113+940 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462606 | |||||||
| chr17:4462607 | A | G | 69 | a0001c0001t0001g0130 a0001c0001t0001g0221 a0001c0001t0001g0263 others(66): Show |
69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1113+9402A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462607 | |||||||
| chr17:4462608 | T | C | 70 | a0001c0001t0001g0130 a0001c0001t0001g0221 a0001c0001t0001g0263 others(67): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1113+9403T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462608 | |||||||
| chr17:4462610 | C | A | 70 | a0001c0001t0001g0130 a0001c0001t0001g0221 a0001c0001t0001g0263 others(67): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1113+9405C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462610 | |||||||
| chr17:4462610 | C | CATCCATC others(493): Show |
1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1113+9432_1113+943 others(504): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462610 | ||||||
| chr17:4462610 | C | CGCCA | 240 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(237): Show |
241 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.1113+9405_1113+940 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462610 | |||||||
| chr17:4462672 | T | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(4): Show |
7 | HG01074.hp1 HG02055.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9467T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462672 | |||||||
| chr17:4462679 | T | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(4): Show |
7 | HG01074.hp1 HG02055.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9474T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462679 | |||||||
| chr17:4462682 | C | A | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1113+9477C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462682 | |||||||
| chr17:4462684 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1113+9479C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462684 | |||||||
| chr17:4462688 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1113+9483C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462688 | |||||||
| chr17:4462716 | T | TCCACCCA others(1): Show |
3 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0004t0001g0027 |
3 | HG02970.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1113+9519_1113+952 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462716 | ||||||
| chr17:4462718 | C | A | 1 | a0001c0010t0001g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1113+9513C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462718 | |||||||
| chr17:4462719 | A | C | 1 | a0001c0010t0001g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1113+9514A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462719 | |||||||
| chr17:4462720 | C | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(5): Show |
8 | HG01074.hp1 HG02055.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+9515C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462720 | |||||||
| chr17:4462724 | C | CCAGTCTA others(377): Show |
7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(4): Show |
7 | HG01074.hp1 HG02055.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9520_1113+952 others(388): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462724 | ||||||
| chr17:4462728 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(4): Show |
7 | HG01074.hp1 HG02055.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9523C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462728 | |||||||
| chr17:4462728 | CCCATCCA others(5): Show |
C | 1 | a0001c0009t0002g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1113+9531_1113+954 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462728 | ||||||
| chr17:4462728 | CCCATCCA others(9): Show |
C | 22 | a0001c0001t0001g0035 a0001c0001t0002g0326 a0001c0001t0002g0327 others(19): Show |
22 | HG01099.hp1 HG01109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1113+9547_1113+956 others(20): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462728 | ||||||
| chr17:4462738 | A | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(4): Show |
7 | HG01074.hp1 HG02055.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9533A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462738 | |||||||
| chr17:4462740 | T | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(4): Show |
7 | HG01074.hp1 HG02055.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9535T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462740 | |||||||
| chr17:4462744 | T | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(5): Show |
8 | HG01074.hp1 HG02055.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+9539T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462744 | |||||||
| chr17:4462752 | C | T | 1 | a0003c0016t0001g0083 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1113+9547C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462752 | |||||||
| chr17:4462754 | A | AATCT | 14 | a0001c0001t0002g0046 a0001c0001t0002g0143 a0001c0003t0002g0256 others(11): Show |
14 | HG00323.hp1 HG00639.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1113+9552_1113+955 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462754 | ||||||
| chr17:4462754 | A | C | 1 | a0003c0016t0001g0083 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1113+9549A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462754 | |||||||
| chr17:4462754 | AATCC | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0096 others(127): Show |
131 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1113+9595_1113+959 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462754 | ||||||
| chr17:4462754 | AATCCATC others(1): Show |
A | 15 | a0001c0001t0001g0028 a0001c0001t0001g0129 a0001c0001t0001g0130 others(12): Show |
15 | HG00642.hp1 HG01167.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1113+9591_1113+959 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462754 | ||||||
| chr17:4462754 | AATCCATC others(5): Show |
A | 2 | a0001c0013t0001g0113 a0001c0031t0005g0033 |
2 | HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1113+9587_1113+959 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462754 | ||||||
| chr17:4462758 | C | CATCCACC others(33): Show |
1 | a0003c0016t0001g0083 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1113+9558_1113+955 others(44): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462758 | ||||||
| chr17:4462758 | C | T | 132 | a0001c0001t0001g0030 a0001c0001t0001g0154 a0001c0001t0001g0238 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1113+9553C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462758 | |||||||
| chr17:4462762 | C | T | 16 | a0001c0001t0001g0111 a0001c0001t0001g0215 a0001c0001t0001g0335 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.1113+9557C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462762 | |||||||
| chr17:4462766 | C | T | 1 | a0002c0002t0001g0284 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1113+9561C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462766 | |||||||
| chr17:4462768 | T | C | 30 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(27): Show |
30 | HG01074.hp1 HG01099.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1113+9563T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462768 | |||||||
| chr17:4462770 | C | A | 30 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(27): Show |
30 | HG01074.hp1 HG01099.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1113+9565C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462770 | |||||||
| chr17:4462770 | C | T | 2 | a0001c0013t0001g0113 a0001c0031t0005g0033 |
2 | HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1113+9565C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462770 | |||||||
| chr17:4462774 | C | T | 30 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(27): Show |
30 | HG01074.hp1 HG01099.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1113+9569C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462774 | |||||||
| chr17:4462786 | C | CACCA | 3 | a0001c0006t0001g0032 a0001c0006t0001g0049 a0001c0006t0001g0050 |
3 | HG02486.hp2 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1113+9582_1113+958 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462786 | ||||||
| chr17:4462790 | C | T | 3 | a0001c0006t0001g0032 a0001c0006t0001g0049 a0001c0006t0001g0050 |
3 | HG02486.hp2 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1113+9585C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462790 | |||||||
| chr17:4462800 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1113+9595T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462800 | |||||||
| chr17:4462802 | C | A | 1 | a0001c0001t0002g0135 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1113+9597C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462802 | |||||||
| chr17:4462804 | C | T | 7 | a0001c0001t0001g0260 a0001c0001t0002g0135 a0001c0006t0001g0032 others(4): Show |
7 | HG02486.hp2 HG02622.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+9599C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462804 | |||||||
| chr17:4462806 | A | C | 6 | a0001c0001t0001g0260 a0001c0006t0001g0032 a0001c0006t0001g0049 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+9601A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462806 | |||||||
| chr17:4462806 | A | T | 1 | a0001c0001t0002g0135 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1113+9601A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462806 | |||||||
| chr17:4462808 | T | C | 2 | a0001c0001t0001g0260 a0002c0002t0001g0230 |
2 | HG03654.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1113+9603T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462808 | |||||||
| chr17:4462810 | T | A | 2 | a0001c0001t0001g0260 a0002c0002t0001g0230 |
2 | HG03654.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1113+9605T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462810 | |||||||
| chr17:4462810 | T | C | 5 | a0001c0001t0002g0135 a0001c0006t0001g0032 a0001c0006t0001g0049 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+9605T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462810 | |||||||
| chr17:4462810 | T | TATCC | 8 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0328 others(5): Show |
8 | HG01109.hp1 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+9628_1113+963 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462810 | ||||||
| chr17:4462810 | T | TATCCATC others(1): Show |
12 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0004t0001g0027 others(9): Show |
12 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+9624_1113+963 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462810 | ||||||
| chr17:4462810 | T | TATCCATC others(5): Show |
5 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 others(2): Show |
5 | HG02809.hp2 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+9620_1113+963 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462810 | ||||||
| chr17:4462810 | T | TATCCATC others(9): Show |
7 | a0001c0001t0002g0160 a0001c0009t0002g0031 a0001c0023t0003g0014 others(4): Show |
7 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1113+9616_1113+963 others(20): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462810 | ||||||
| chr17:4462810 | T | TATCCATC others(13): Show |
10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(7): Show |
10 | HG01074.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1113+9612_1113+963 others(24): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462810 | ||||||
| chr17:4462810 | TATCC | T | 65 | a0001c0001t0001g0238 a0001c0001t0001g0263 a0001c0001t0001g0271 others(62): Show |
65 | HG00099.hp2 HG00609.hp2 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.1113+9628_1113+963 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462810 | ||||||
| chr17:4462813 | C | T | 2 | a0001c0006t0001g0047 a0001c0035t0002g0034 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1113+9608C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462813 | |||||||
| chr17:4462814 | C | T | 2 | a0001c0001t0001g0260 a0002c0002t0001g0230 |
2 | HG03654.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1113+9609C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462814 | |||||||
| chr17:4462845 | G | GCACC | 53 | a0001c0001t0001g0111 a0001c0001t0001g0195 a0001c0001t0001g0215 others(50): Show |
53 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.1113+9661_1113+966 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4462845 | ||||||
| chr17:4462935 | T | A | 1 | a0001c0013t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1113+9730T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4462935 | |||||||
| chr17:4463015 | C | A | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+9810C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463015 | |||||||
| chr17:4463043 | T | A | 13 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+9838T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463043 | |||||||
| chr17:4463047 | T | G | 13 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+9842T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463047 | |||||||
| chr17:4463094 | G | A | 1 | a0002c0002t0001g0354 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1113+9889G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463094 | |||||||
| chr17:4463223 | C | A | 9 | a0001c0001t0002g0326 a0001c0001t0002g0327 a0001c0001t0002g0328 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+10018C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463223 | |||||||
| chr17:4463237 | G | T | 2 | a0001c0036t0003g0144 a0001c0044t0002g0236 |
2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1113+10032G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463237 | |||||||
| chr17:4463346 | G | A | 11 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(8): Show |
11 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1113+10141G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463346 | |||||||
| chr17:4463396 | C | CA | 47 | a0001c0001t0001g0030 a0001c0001t0001g0096 a0001c0001t0001g0165 others(44): Show |
47 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1113+10206dupA | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4463396 | ||||||
| chr17:4463396 | C | CAA | 21 | a0001c0001t0001g0147 a0001c0003t0001g0152 a0001c0006t0001g0032 others(18): Show |
21 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1113+10205_1113+10 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4463396 | ||||||
| chr17:4463396 | C | CAAA | 17 | a0001c0001t0001g0020 a0001c0001t0001g0154 a0001c0001t0001g0311 others(14): Show |
17 | HG02257.hp2 HG02559.hp1 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.1113+10204_1113+10 others(9): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4463396 | ||||||
| chr17:4463402 | A | AAAC | 9 | a0001c0001t0002g0327 a0001c0001t0002g0328 a0001c0001t0002g0329 others(6): Show |
9 | HG01109.hp1 HG02486.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1113+10199_1113+10 others(9): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4463402 | ||||||
| chr17:4463407 | A | AAAAC | 6 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 others(3): Show |
6 | HG02809.hp2 HG02818.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+10205_1113+10 others(10): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4463407 | ||||||
| chr17:4463407 | A | AC | 44 | a0001c0001t0001g0111 a0001c0001t0001g0215 a0001c0001t0001g0335 others(41): Show |
44 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.1113+10202_1113+10 others(7): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463407 | |||||||
| chr17:4463407 | A | C | 40 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(37): Show |
40 | HG00741.hp2 HG01109.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1113+10202A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463407 | |||||||
| chr17:4463408 | A | C | 1 | a0003c0005t0001g0310 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1113+10203A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463408 | |||||||
| chr17:4463412 | C | A | 17 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(14): Show |
17 | HG01074.hp1 HG02055.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1113+10207C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463412 | |||||||
| chr17:4463599 | C | T | 7 | a0001c0001t0001g0028 a0001c0003t0001g0145 a0001c0003t0001g0146 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113+10394C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463599 | |||||||
| chr17:4463605 | G | A | 19 | a0001c0001t0001g0030 a0001c0001t0002g0046 a0001c0001t0002g0143 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1113+10400G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463605 | |||||||
| chr17:4463613 | C | T | 1 | a0002c0002t0001g0142 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1113+10408C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463613 | |||||||
| chr17:4463676 | TTGCAGTG others(11): Show |
T | 13 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+10475_1113+10 others(24): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4463676 | ||||||
| chr17:4463693 | C | T | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+10488C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463693 | |||||||
| chr17:4463712 | C | T | 8 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+10507C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463712 | |||||||
| chr17:4463731 | C | T | 1 | a0001c0013t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1113+10526C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463731 | |||||||
| chr17:4463737 | C | T | 2 | a0001c0003t0001g0346 a0001c0034t0002g0045 |
2 | HG02717.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1113+10532C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463737 | |||||||
| chr17:4463738 | G | GA | 20 | a0001c0001t0001g0095 a0001c0001t0001g0133 a0001c0001t0001g0166 others(17): Show |
20 | HG00621.hp1 HG01928.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.1113+10548dupA | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4463738 | ||||||
| chr17:4463738 | GA | G | 8 | a0001c0001t0001g0098 a0001c0001t0001g0198 a0001c0003t0001g0145 others(5): Show |
8 | HG01169.hp2 HG01975.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+10548delA | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4463738 | ||||||
| chr17:4463739 | A | G | 6 | a0001c0001t0001g0242 a0001c0018t0002g0350 a0004c0017t0002g0029 others(3): Show |
6 | HG01099.hp1 HG02818.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+10534A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463739 | |||||||
| chr17:4463823 | T | C | 1 | a0003c0005t0001g0175 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1113+10618T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463823 | |||||||
| chr17:4463952 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0004t0001g0027 |
3 | HG02970.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1113+10747G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4463952 | |||||||
| chr17:4464080 | G | A | 1 | a0001c0044t0002g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1113+10875G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464080 | |||||||
| chr17:4464159 | G | T | 1 | a0001c0006t0002g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1113+10954G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464159 | |||||||
| chr17:4464193 | C | G | 47 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(44): Show |
47 | HG01074.hp1 HG01099.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1113+10988C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464193 | |||||||
| chr17:4464219 | C | A | 1 | a0001c0003t0001g0132 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1113+11014C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464219 | |||||||
| chr17:4464245 | G | A | 1 | a0001c0009t0001g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1113+11040G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464245 | |||||||
| chr17:4464300 | C | T | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(12): Show |
15 | HG01074.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113+11095C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464300 | |||||||
| chr17:4464423 | C | T | 1 | a0002c0002t0001g0278 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1113+11218C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464423 | |||||||
| chr17:4464454 | G | A | 1 | a0002c0002t0001g0286 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1113+11249G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464454 | |||||||
| chr17:4464498 | T | C | 19 | a0001c0001t0001g0030 a0001c0001t0002g0046 a0001c0001t0002g0143 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1113+11293T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464498 | |||||||
| chr17:4464637 | C | T | 2 | a0001c0001t0001g0242 a0001c0013t0001g0178 |
2 | NA18962.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1113+11432C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464637 | |||||||
| chr17:4464671 | CT | C | 3 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 |
3 | HG02809.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1113+11467delT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464671 | |||||||
| chr17:4464742 | G | A | 2 | a0001c0031t0005g0033 a0003c0008t0003g0174 |
2 | HG01169.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1113+11537G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464742 | |||||||
| chr17:4464783 | C | T | 1 | a0002c0002t0001g0157 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1113+11578C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464783 | |||||||
| chr17:4464847 | C | T | 60 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(57): Show |
60 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1113+11642C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464847 | |||||||
| chr17:4464923 | C | T | 1 | a0008c0019t0001g0340 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1113+11718C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464923 | |||||||
| chr17:4464934 | G | A | 33 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(30): Show |
33 | HG01074.hp1 HG01099.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1113+11729G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464934 | |||||||
| chr17:4464998 | T | C | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+11793T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4464998 | |||||||
| chr17:4465156 | A | G | 13 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1113+11951A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465156 | |||||||
| chr17:4465164 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1113+11959G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465164 | |||||||
| chr17:4465165 | G | C | 1 | a0001c0001t0001g0260 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1113+11960G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465165 | |||||||
| chr17:4465172 | C | A | 3 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 |
3 | HG02809.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1113+11967C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465172 | |||||||
| chr17:4465209 | T | C | 2 | a0001c0018t0002g0349 a0001c0018t0002g0350 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1113+12004T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465209 | |||||||
| chr17:4465305 | G | C | 8 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+12100G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465305 | |||||||
| chr17:4465322 | T | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(341): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1113+12117T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465322 | |||||||
| chr17:4465383 | A | AT | 27 | a0001c0001t0001g0164 a0001c0003t0001g0132 a0001c0003t0001g0152 others(24): Show |
27 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113+12189dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4465383 | ||||||
| chr17:4465394 | T | C | 15 | a0001c0001t0002g0327 a0001c0001t0002g0328 a0001c0001t0002g0329 others(12): Show |
15 | HG01099.hp1 HG01109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1113+12189T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465394 | |||||||
| chr17:4465438 | G | A | 1 | a0002c0002t0001g0355 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1113+12233G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465438 | |||||||
| chr17:4465475 | C | G | 5 | a0001c0001t0001g0028 a0001c0003t0001g0346 a0001c0003t0002g0315 others(2): Show |
5 | HG02717.hp1 HG02965.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+12270C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465475 | |||||||
| chr17:4465512 | G | A | 4 | a0001c0001t0001g0111 a0001c0001t0001g0338 a0001c0001t0002g0330 others(1): Show |
4 | HG02280.hp1 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+12307G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465512 | |||||||
| chr17:4465516 | TGAG | T | 3 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 |
3 | HG02809.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1113+12315_1113+12 others(9): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4465516 | ||||||
| chr17:4465548 | C | A | 19 | a0001c0001t0001g0030 a0001c0001t0002g0046 a0001c0001t0002g0143 others(16): Show |
19 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1113+12343C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465548 | |||||||
| chr17:4465557 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1113+12352G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465557 | |||||||
| chr17:4465924 | C | T | 1 | a0003c0005t0001g0116 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1114-12648C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465924 | |||||||
| chr17:4465925 | G | A | 1 | a0001c0049t0002g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1114-12647G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465925 | |||||||
| chr17:4465929 | C | A | 13 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1114-12643C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465929 | |||||||
| chr17:4465986 | C | T | 33 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(30): Show |
33 | HG01074.hp1 HG01099.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1114-12586C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4465986 | |||||||
| chr17:4466024 | C | A | 13 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1114-12548C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4466024 | |||||||
| chr17:4466034 | G | GGGAGCAG others(8): Show |
1 | a0003c0008t0003g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1114-12536_1114-12 others(21): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4466034 | ||||||
| chr17:4466094 | G | A | 2 | a0001c0009t0002g0022 a0001c0009t0002g0023 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1114-12478G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4466094 | |||||||
| chr17:4466236 | T | C | 2 | a0001c0018t0002g0349 a0001c0018t0002g0350 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1114-12336T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4466236 | |||||||
| chr17:4466260 | G | A | 5 | a0003c0008t0003g0099 a0003c0008t0003g0100 a0003c0008t0003g0101 others(2): Show |
5 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1114-12312G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4466260 | |||||||
| chr17:4466397 | G | A | 7 | a0001c0001t0002g0327 a0001c0001t0002g0328 a0001c0001t0002g0329 others(4): Show |
7 | HG01109.hp1 HG02486.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114-12175G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4466397 | |||||||
| chr17:4466497 | G | A | 1 | a0001c0009t0004g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1114-12075G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4466497 | |||||||
| chr17:4466539 | C | CA | 29 | a0001c0001t0001g0166 a0001c0001t0001g0204 a0001c0001t0001g0211 others(26): Show |
29 | HG00609.hp2 HG00621.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.1114-12014dupA | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4466539 | ||||||
| chr17:4466539 | CA | C | 39 | a0001c0001t0001g0130 a0001c0001t0001g0203 a0001c0001t0001g0215 others(36): Show |
39 | HG00741.hp2 HG01109.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.1114-12014delA | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4466539 | ||||||
| chr17:4466539 | CAA | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(116): Show |
120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1114-12015_1114-12 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4466539 | ||||||
| chr17:4466559 | T | A | 6 | a0001c0009t0002g0031 a0001c0018t0002g0350 a0004c0017t0002g0029 others(3): Show |
6 | HG01099.hp1 HG02145.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-12013T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4466559 | |||||||
| chr17:4466603 | A | G | 1 | a0002c0002t0001g0307 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1114-11969A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4466603 | |||||||
| chr17:4466864 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0105 others(107): Show |
111 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1114-11708C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4466864 | |||||||
| chr17:4466946 | A | G | 82 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0030 others(79): Show |
82 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1114-11626A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4466946 | |||||||
| chr17:4467028 | G | A | 13 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1114-11544G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467028 | |||||||
| chr17:4467040 | A | ATGCGGAG others(9): Show |
1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1114-11523_1114-11 others(22): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4467040 | ||||||
| chr17:4467142 | T | C | 1 | a0001c0004t0001g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1114-11430T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467142 | |||||||
| chr17:4467258 | G | A | 13 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1114-11314G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467258 | |||||||
| chr17:4467459 | C | T | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1114-11113C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467459 | |||||||
| chr17:4467460 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0004t0001g0027 |
3 | HG02970.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1114-11112G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467460 | |||||||
| chr17:4467478 | C | T | 11 | a0001c0001t0002g0162 a0001c0003t0002g0136 a0001c0003t0002g0137 others(8): Show |
11 | HG00741.hp2 HG01123.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.1114-11094C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467478 | |||||||
| chr17:4467538 | A | G | 27 | a0001c0001t0001g0030 a0001c0001t0002g0046 a0001c0001t0002g0143 others(24): Show |
27 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1114-11034A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467538 | |||||||
| chr17:4467642 | C | A | 2 | a0001c0001t0001g0360 a0001c0001t0001g0361 |
2 | HG00544.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1114-10930C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467642 | |||||||
| chr17:4467664 | T | A | 11 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 others(8): Show |
11 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1114-10908T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467664 | |||||||
| chr17:4467678 | T | A | 1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1114-10894T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467678 | |||||||
| chr17:4467707 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(152): Show |
156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1114-10865C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467707 | |||||||
| chr17:4467708 | G | A | 18 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0185 others(15): Show |
18 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.1114-10864G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467708 | |||||||
| chr17:4467768 | T | C | 39 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(36): Show |
39 | HG01074.hp1 HG01099.hp1 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.1114-10804T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467768 | |||||||
| chr17:4467775 | T | C | 341 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(338): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.1114-10797T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467775 | |||||||
| chr17:4467812 | C | T | 164 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(161): Show |
164 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1114-10760C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467812 | |||||||
| chr17:4467818 | A | G | 2 | a0001c0036t0003g0144 a0001c0044t0002g0236 |
2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1114-10754A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467818 | |||||||
| chr17:4467826 | C | T | 44 | a0001c0001t0001g0111 a0001c0001t0001g0215 a0001c0001t0001g0335 others(41): Show |
44 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.1114-10746C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467826 | |||||||
| chr17:4467831 | A | C | 1 | a0001c0013t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1114-10741A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467831 | |||||||
| chr17:4467855 | G | A | 1 | a0001c0013t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1114-10717G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467855 | |||||||
| chr17:4467872 | G | T | 1 | a0003c0005t0001g0108 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1114-10700G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467872 | |||||||
| chr17:4467918 | G | A | 1 | a0002c0011t0003g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1114-10654G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467918 | |||||||
| chr17:4467922 | C | T | 4 | a0001c0024t0003g0062 a0001c0028t0003g0173 a0001c0045t0003g0150 others(1): Show |
4 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-10650C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467922 | |||||||
| chr17:4467959 | C | T | 26 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(23): Show |
26 | HG01074.hp1 HG01099.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.1114-10613C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467959 | |||||||
| chr17:4467962 | C | T | 1 | a0003c0016t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1114-10610C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4467962 | |||||||
| chr17:4468031 | A | AGGGGACT others(7): Show |
2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | NA18973.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1114-10531_1114-10 others(20): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468031 | ||||||
| chr17:4468054 | A | G | 3 | a0001c0006t0001g0010 a0001c0007t0003g0158 a0001c0007t0003g0319 |
3 | HG01884.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1114-10518A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468054 | |||||||
| chr17:4468078 | G | T | 1 | a0001c0044t0002g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1114-10494G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468078 | |||||||
| chr17:4468134 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1114-10438G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468134 | |||||||
| chr17:4468218 | A | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0004t0001g0027 |
3 | HG02970.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1114-10354A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468218 | |||||||
| chr17:4468255 | T | C | 8 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114-10317T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468255 | |||||||
| chr17:4468303 | A | T | 1 | a0001c0007t0003g0325 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1114-10269A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468303 | |||||||
| chr17:4468304 | A | T | 1 | a0001c0003t0002g0315 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1114-10268A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468304 | |||||||
| chr17:4468335 | A | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(330): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1114-10237A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468335 | |||||||
| chr17:4468352 | A | C | 48 | a0001c0001t0001g0111 a0001c0001t0001g0215 a0001c0001t0001g0335 others(45): Show |
48 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.1114-10220A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468352 | |||||||
| chr17:4468370 | A | G | 16 | a0001c0023t0003g0053 a0001c0038t0003g0291 a0003c0005t0001g0108 others(13): Show |
16 | HG00280.hp1 HG01106.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.1114-10202A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468370 | |||||||
| chr17:4468460 | A | T | 1 | a0005c0015t0003g0159 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1114-10112A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468460 | |||||||
| chr17:4468508 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 |
3 | HG02809.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1114-10064G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468508 | |||||||
| chr17:4468581 | C | T | 1 | a0002c0002t0001g0094 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1114-9991C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468581 | |||||||
| chr17:4468584 | C | T | 48 | a0001c0001t0001g0111 a0001c0001t0001g0215 a0001c0001t0001g0335 others(45): Show |
48 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.1114-9988C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468584 | |||||||
| chr17:4468589 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0004t0001g0027 |
3 | HG02970.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1114-9983G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468589 | |||||||
| chr17:4468605 | G | A | 1 | a0003c0016t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1114-9967G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468605 | |||||||
| chr17:4468611 | G | T | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1114-9961G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468611 | |||||||
| chr17:4468714 | C | CTCTCTTT others(8): Show |
1 | a0001c0001t0002g0162 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1114-9855_1114-985 others(19): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468714 | ||||||
| chr17:4468721 | T | TCTTTCTT others(10): Show |
1 | a0002c0002t0001g0293 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1114-9851_1114-985 others(21): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468721 | |||||||
| chr17:4468721 | T | TTCTTTCT others(3): Show |
1 | a0001c0013t0001g0259 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1114-9850_1114-984 others(14): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468721 | T | TTCTTTCT others(11): Show |
1 | a0001c0001t0001g0311 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1114-9850_1114-984 others(22): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468721 | T | TTTCTTCT others(7): Show |
1 | a0002c0002t0001g0273 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1114-9849_1114-984 others(18): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468721 | T | TTTCTTCT others(15): Show |
1 | a0001c0001t0001g0262 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1114-9849_1114-984 others(26): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468721 | T | TTTCTTTC others(28): Show |
1 | a0003c0008t0003g0103 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1114-9849_1114-984 others(39): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468721 | T | TTTTC | 32 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(29): Show |
32 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.1114-9813_1114-981 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468721 | T | TTTTCTTT others(1): Show |
47 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0129 others(44): Show |
48 | HG00642.hp1 HG01069.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1114-9817_1114-981 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468721 | T | TTTTCTTT others(5): Show |
59 | a0001c0001t0001g0028 a0001c0001t0001g0195 a0001c0001t0001g0199 others(56): Show |
59 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.1114-9821_1114-981 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468721 | T | TTTTCTTT others(9): Show |
64 | a0001c0001t0001g0095 a0001c0001t0001g0186 a0001c0001t0001g0189 others(61): Show |
64 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1114-9825_1114-981 others(20): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468721 | T | TTTTCTTT others(13): Show |
55 | a0001c0001t0001g0105 a0001c0001t0001g0109 a0001c0001t0001g0133 others(52): Show |
55 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.1114-9829_1114-981 others(24): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468721 | T | TTTTCTTT others(17): Show |
31 | a0001c0001t0001g0134 a0001c0001t0001g0185 a0001c0001t0001g0204 others(28): Show |
31 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1114-9833_1114-981 others(28): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468721 | T | TTTTCTTT others(21): Show |
13 | a0001c0001t0001g0194 a0001c0001t0001g0216 a0001c0001t0001g0261 others(10): Show |
13 | HG00323.hp1 HG01361.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1114-9837_1114-981 others(32): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468721 | T | TTTTCTTT others(25): Show |
4 | a0001c0001t0001g0229 a0002c0002t0001g0274 a0002c0002t0001g0303 others(1): Show |
4 | HG00621.hp1 HG01255.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-9841_1114-981 others(36): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468721 | TTTTCTTT others(9): Show |
T | 1 | a0001c0001t0002g0336 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1114-9825_1114-981 others(20): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468721 | ||||||
| chr17:4468738 | T | TTTCTTTC others(4): Show |
1 | a0003c0008t0003g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1114-9831_1114-982 others(15): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468738 | ||||||
| chr17:4468741 | CTTTCTTT others(23): Show |
C | 3 | a0001c0001t0001g0035 a0001c0001t0002g0344 a0001c0003t0002g0127 |
3 | HG02809.hp2 HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1114-9817_1114-978 others(34): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468741 | ||||||
| chr17:4468758 | T | TTTCTTTC others(4): Show |
1 | a0001c0001t0001g0263 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1114-9810_1114-980 others(15): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468758 | ||||||
| chr17:4468758 | T | TTTCTTTC others(8): Show |
1 | a0003c0005t0001g0107 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1114-9810_1114-980 others(19): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468758 | ||||||
| chr17:4468758 | T | TTTCTTTC others(20): Show |
1 | a0001c0001t0001g0352 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1114-9810_1114-980 others(31): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468758 | ||||||
| chr17:4468763 | C | T | 23 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(20): Show |
23 | HG00642.hp2 HG01074.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.1114-9809C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468763 | |||||||
| chr17:4468763 | CTCTTTCT others(3): Show |
C | 3 | a0004c0017t0002g0029 a0004c0030t0002g0009 a0004c0048t0002g0006 |
3 | HG01099.hp1 HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1114-9799_1114-979 others(14): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468763 | ||||||
| chr17:4468766 | T | TTTCTTTC others(10): Show |
1 | a0003c0005t0001g0156 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1114-9800_1114-979 others(21): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468766 | ||||||
| chr17:4468767 | T | C | 2 | a0001c0044t0002g0236 a0008c0019t0001g0340 |
2 | HG02738.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1114-9805T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468767 | |||||||
| chr17:4468769 | CTT | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0009t0002g0031 |
3 | HG02145.hp2 HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1114-9799_1114-979 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468769 | ||||||
| chr17:4468771 | T | TTC | 10 | a0001c0001t0002g0317 a0001c0001t0002g0342 a0001c0001t0002g0343 others(7): Show |
10 | HG02257.hp2 HG02486.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.1114-9800_1114-979 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468771 | ||||||
| chr17:4468771 | T | TTCTTTCT others(3): Show |
1 | a0001c0006t0001g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1114-9800_1114-979 others(14): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468771 | ||||||
| chr17:4468771 | T | TTCTTTCT others(7): Show |
1 | a0001c0004t0001g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1114-9800_1114-979 others(18): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468771 | ||||||
| chr17:4468771 | T | TTCTTTCT others(11): Show |
1 | a0001c0052t0002g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1114-9800_1114-979 others(22): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468771 | ||||||
| chr17:4468773 | T | C | 24 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0035 others(21): Show |
24 | HG01074.hp1 HG02055.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.1114-9799T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468773 | |||||||
| chr17:4468775 | C | T | 2 | a0001c0044t0002g0236 a0008c0019t0001g0340 |
2 | HG02738.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1114-9797C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468775 | |||||||
| chr17:4468785 | C | T | 2 | a0001c0044t0002g0236 a0008c0019t0001g0340 |
2 | HG02738.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1114-9787C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468785 | |||||||
| chr17:4468789 | CTCTT | C | 3 | a0001c0001t0001g0030 a0001c0001t0002g0046 a0001c0007t0003g0337 |
3 | HG02258.hp1 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1114-9777_1114-977 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4468789 | ||||||
| chr17:4468793 | T | C | 2 | a0001c0044t0002g0236 a0008c0019t0001g0340 |
2 | HG02738.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1114-9779T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468793 | |||||||
| chr17:4468797 | T | C | 1 | a0001c0044t0002g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1114-9775T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468797 | |||||||
| chr17:4468810 | C | T | 1 | a0001c0004t0001g0056 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1114-9762C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468810 | |||||||
| chr17:4468811 | G | A | 8 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114-9761G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468811 | |||||||
| chr17:4468831 | G | A | 17 | a0001c0006t0002g0011 a0001c0006t0002g0012 a0001c0023t0003g0053 others(14): Show |
17 | HG00280.hp1 HG01106.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1114-9741G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468831 | |||||||
| chr17:4468855 | C | T | 1 | a0001c0001t0002g0151 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1114-9717C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468855 | |||||||
| chr17:4468997 | A | T | 1 | a0001c0035t0002g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1114-9575A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4468997 | |||||||
| chr17:4469026 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | NA18973.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1114-9546G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469026 | |||||||
| chr17:4469186 | G | A | 8 | a0001c0012t0001g0036 a0001c0012t0001g0037 a0001c0012t0001g0038 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114-9386G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469186 | |||||||
| chr17:4469205 | C | G | 4 | a0002c0002t0001g0253 a0002c0011t0003g0254 a0002c0011t0003g0255 others(1): Show |
4 | HG00099.hp2 HG01256.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-9367C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469205 | |||||||
| chr17:4469275 | C | T | 165 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(162): Show |
165 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.1114-9297C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469275 | |||||||
| chr17:4469284 | A | G | 346 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(343): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1114-9288A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469284 | |||||||
| chr17:4469329 | C | T | 1 | a0001c0006t0002g0052 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1114-9243C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469329 | |||||||
| chr17:4469339 | G | A | 11 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(8): Show |
11 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.1114-9233G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469339 | |||||||
| chr17:4469408 | C | G | 1 | a0003c0008t0003g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1114-9164C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469408 | |||||||
| chr17:4469421 | T | C | 341 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(338): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.1114-9151T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469421 | |||||||
| chr17:4469586 | G | A | 1 | a0001c0009t0004g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1114-8986G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469586 | |||||||
| chr17:4469590 | G | T | 11 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(8): Show |
11 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.1114-8982G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469590 | |||||||
| chr17:4469620 | C | CA | 128 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0028 others(125): Show |
129 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1114-8932dupA | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4469620 | ||||||
| chr17:4469620 | C | CAA | 32 | a0001c0001t0001g0184 a0001c0001t0001g0227 a0001c0001t0001g0334 others(29): Show |
32 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1114-8933_1114-893 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4469620 | ||||||
| chr17:4469620 | CA | C | 6 | a0001c0001t0002g0343 a0001c0036t0003g0144 a0002c0002t0001g0266 others(3): Show |
6 | HG01169.hp1 HG01169.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114-8932delA | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4469620 | ||||||
| chr17:4469640 | A | G | 3 | a0001c0001t0001g0209 a0001c0004t0001g0067 a0001c0004t0001g0069 |
3 | HG00558.hp1 HG02015.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1114-8932A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469640 | |||||||
| chr17:4469803 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0035 others(126): Show |
130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1114-8769G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469803 | |||||||
| chr17:4469883 | C | T | 45 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(42): Show |
45 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1114-8689C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469883 | |||||||
| chr17:4469891 | A | C | 3 | a0001c0012t0001g0038 a0001c0012t0001g0039 a0001c0012t0002g0042 |
3 | HG02258.hp2 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1114-8681A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469891 | |||||||
| chr17:4469937 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1114-8635C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4469937 | |||||||
| chr17:4470031 | G | A | 2 | a0003c0005t0001g0234 a0003c0005t0001g0235 |
2 | NA19011.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1114-8541G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4470031 | |||||||
| chr17:4470195 | G | A | 1 | a0002c0040t0001g0313 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1114-8377G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4470195 | |||||||
| chr17:4470377 | G | A | 1 | a0001c0009t0001g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1114-8195G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4470377 | |||||||
| chr17:4470454 | A | T | 1 | a0002c0002t0001g0355 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1114-8118A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4470454 | |||||||
| chr17:4470627 | C | T | 3 | a0001c0003t0001g0126 a0001c0009t0004g0061 a0005c0015t0003g0104 |
3 | HG00642.hp1 HG01106.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1114-7945C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4470627 | |||||||
| chr17:4470767 | C | T | 339 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(336): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1114-7805C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4470767 | |||||||
| chr17:4470784 | T | C | 15 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1114-7788T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4470784 | |||||||
| chr17:4470826 | G | A | 1 | a0002c0037t0002g0323 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1114-7746G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4470826 | |||||||
| chr17:4470834 | A | G | 1 | a0001c0003t0001g0346 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1114-7738A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4470834 | |||||||
| chr17:4470844 | T | G | 4 | a0001c0006t0001g0010 a0001c0007t0003g0158 a0001c0007t0003g0319 others(1): Show |
4 | HG01884.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-7728T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4470844 | |||||||
| chr17:4470886 | A | G | 4 | a0001c0001t0001g0111 a0001c0001t0001g0338 a0001c0001t0002g0330 others(1): Show |
4 | HG02280.hp1 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-7686A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4470886 | |||||||
| chr17:4470980 | G | A | 339 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(336): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1114-7592G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4470980 | |||||||
| chr17:4471073 | C | A | 1 | a0001c0006t0001g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1114-7499C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471073 | |||||||
| chr17:4471081 | C | T | 2 | a0001c0012t0001g0036 a0001c0012t0001g0037 |
2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1114-7491C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471081 | |||||||
| chr17:4471175 | C | T | 4 | a0001c0010t0001g0078 a0001c0010t0001g0080 a0003c0005t0001g0140 others(1): Show |
4 | HG01069.hp2 HG01081.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-7397C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471175 | |||||||
| chr17:4471176 | G | A | 1 | a0001c0013t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1114-7396G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471176 | |||||||
| chr17:4471274 | C | T | 343 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(340): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1114-7298C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471274 | |||||||
| chr17:4471289 | A | C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0109 others(33): Show |
37 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1114-7283A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471289 | |||||||
| chr17:4471318 | T | G | 11 | a0001c0003t0002g0315 a0001c0012t0001g0038 a0001c0012t0001g0039 others(8): Show |
11 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1114-7254T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471318 | |||||||
| chr17:4471443 | T | G | 33 | a0001c0001t0001g0111 a0001c0001t0001g0335 a0001c0001t0001g0338 others(30): Show |
33 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1114-7129T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471443 | |||||||
| chr17:4471612 | T | C | 13 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1114-6960T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471612 | |||||||
| chr17:4471614 | C | G | 3 | a0001c0006t0001g0010 a0001c0007t0003g0158 a0001c0007t0003g0319 |
3 | HG01884.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1114-6958C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471614 | |||||||
| chr17:4471694 | C | T | 12 | a0001c0001t0001g0111 a0001c0001t0001g0335 a0001c0001t0001g0338 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1114-6878C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471694 | |||||||
| chr17:4471762 | G | A | 1 | a0003c0005t0001g0156 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1114-6810G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471762 | |||||||
| chr17:4471801 | G | C | 13 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1114-6771G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471801 | |||||||
| chr17:4471807 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0035 others(71): Show |
75 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1114-6765A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471807 | |||||||
| chr17:4471860 | A | ATT | 13 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(10): Show |
13 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.1114-6707_1114-670 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4471860 | ||||||
| chr17:4471867 | G | GT | 157 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0096 others(154): Show |
158 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1114-6696dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4471867 | ||||||
| chr17:4471867 | G | T | 14 | a0001c0003t0001g0132 a0001c0003t0001g0152 a0001c0003t0001g0239 others(11): Show |
14 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1114-6705G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471867 | |||||||
| chr17:4471898 | G | A | 1 | a0001c0009t0002g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1114-6674G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471898 | |||||||
| chr17:4471933 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1114-6639T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471933 | |||||||
| chr17:4471984 | G | A | 3 | a0001c0006t0001g0010 a0001c0007t0003g0158 a0001c0007t0003g0319 |
3 | HG01884.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1114-6588G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4471984 | |||||||
| chr17:4472004 | G | A | 6 | a0001c0010t0001g0078 a0001c0010t0001g0080 a0002c0002t0001g0157 others(3): Show |
6 | HG00642.hp2 HG01069.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-6568G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472004 | |||||||
| chr17:4472015 | C | T | 1 | a0001c0046t0002g0316 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1114-6557C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472015 | |||||||
| chr17:4472047 | T | C | 343 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(340): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1114-6525T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472047 | |||||||
| chr17:4472065 | A | G | 343 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(340): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1114-6507A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472065 | |||||||
| chr17:4472138 | C | T | 1 | a0001c0009t0002g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1114-6434C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472138 | |||||||
| chr17:4472212 | C | T | 343 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(340): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1114-6360C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472212 | |||||||
| chr17:4472594 | T | C | 4 | a0001c0006t0001g0010 a0001c0007t0003g0158 a0001c0007t0003g0319 others(1): Show |
4 | HG01884.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-5978T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472594 | |||||||
| chr17:4472765 | C | T | 1 | a0001c0044t0002g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1114-5807C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472765 | |||||||
| chr17:4472774 | C | CATTTTTT others(8): Show |
1 | a0001c0009t0002g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1114-5798_1114-579 others(19): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472774 | |||||||
| chr17:4472774 | CT | C | 12 | a0001c0001t0002g0317 a0001c0003t0001g0346 a0001c0006t0001g0051 others(9): Show |
12 | HG00099.hp2 HG01358.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1114-5765delT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4472774 | ||||||
| chr17:4472774 | CTT | C | 33 | a0001c0001t0001g0095 a0001c0001t0001g0205 a0001c0001t0001g0215 others(30): Show |
33 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1114-5766_1114-576 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4472774 | ||||||
| chr17:4472774 | CTTT | C | 72 | a0001c0001t0001g0154 a0001c0001t0001g0179 a0001c0001t0001g0187 others(69): Show |
72 | HG00280.hp2 HG01069.hp2 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.1114-5767_1114-576 others(7): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4472774 | ||||||
| chr17:4472774 | CTTTT | C | 8 | a0001c0001t0001g0297 a0001c0001t0002g0357 a0001c0004t0001g0027 others(5): Show |
8 | HG01069.hp1 HG01099.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1114-5768_1114-576 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4472774 | ||||||
| chr17:4472774 | CTTTTT | C | 7 | a0001c0001t0001g0189 a0001c0001t0001g0306 a0001c0001t0002g0330 others(4): Show |
7 | HG02280.hp1 HG02698.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1114-5769_1114-576 others(9): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4472774 | ||||||
| chr17:4472774 | CTTTTTT | C | 33 | a0001c0001t0001g0111 a0001c0001t0001g0133 a0001c0001t0001g0195 others(30): Show |
33 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1114-5770_1114-576 others(10): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4472774 | ||||||
| chr17:4472774 | CTTTTTTT | C | 78 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(75): Show |
78 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1114-5771_1114-576 others(11): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4472774 | ||||||
| chr17:4472774 | CTTTTTTT others(1): Show |
C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0035 others(59): Show |
63 | HG00438.hp2 HG00642.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.1114-5772_1114-576 others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4472774 | ||||||
| chr17:4472774 | CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0168 a0001c0001t0001g0360 a0001c0001t0001g0361 others(3): Show |
6 | HG00323.hp2 HG00544.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-5773_1114-576 others(13): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4472774 | ||||||
| chr17:4472774 | CTTTTTTT others(3): Show |
C | 2 | a0001c0012t0001g0038 a0001c0012t0002g0042 |
2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1114-5774_1114-576 others(14): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4472774 | ||||||
| chr17:4472774 | CTTTTTTT others(5): Show |
C | 1 | a0001c0009t0002g0076 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1114-5776_1114-576 others(16): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4472774 | ||||||
| chr17:4472774 | CTTTTTTT others(6): Show |
C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1114-5777_1114-576 others(17): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4472774 | ||||||
| chr17:4472774 | CTTTTTTT others(7): Show |
C | 1 | a0001c0045t0003g0150 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1114-5778_1114-576 others(18): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4472774 | ||||||
| chr17:4472787 | T | A | 1 | a0001c0009t0002g0076 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1114-5785T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472787 | |||||||
| chr17:4472788 | T | A | 14 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(11): Show |
14 | HG00099.hp1 HG00323.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1114-5784T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472788 | |||||||
| chr17:4472789 | T | A | 1 | a0001c0045t0003g0150 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1114-5783T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472789 | |||||||
| chr17:4472856 | A | G | 85 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(82): Show |
85 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1114-5716A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472856 | |||||||
| chr17:4472898 | C | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0311 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1114-5674C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472898 | |||||||
| chr17:4472900 | C | T | 13 | a0001c0001t0002g0326 a0001c0003t0002g0315 a0001c0012t0001g0038 others(10): Show |
13 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1114-5672C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4472900 | |||||||
| chr17:4473014 | C | G | 1 | a0002c0002t0001g0279 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1114-5558C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4473014 | |||||||
| chr17:4473054 | G | A | 11 | a0001c0003t0002g0315 a0001c0012t0001g0038 a0001c0012t0001g0039 others(8): Show |
11 | HG02258.hp2 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1114-5518G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4473054 | |||||||
| chr17:4473145 | A | G | 2 | a0001c0003t0001g0125 a0001c0009t0001g0008 |
2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1114-5427A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4473145 | |||||||
| chr17:4473339 | G | C | 2 | a0001c0001t0002g0326 a0001c0014t0002g0007 |
2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1114-5233G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4473339 | |||||||
| chr17:4473364 | A | T | 1 | a0001c0004t0001g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1114-5208A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4473364 | |||||||
| chr17:4473368 | A | G | 162 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0095 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1114-5204A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4473368 | |||||||
| chr17:4473393 | C | CT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0165 others(58): Show |
62 | HG01109.hp1 HG01109.hp2 HG01169.hp1 others(59): Show |
intron_variant | MODIFIER | c.1114-5160dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4473393 | ||||||
| chr17:4473393 | C | CTT | 75 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(72): Show |
75 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1114-5161_1114-516 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4473393 | ||||||
| chr17:4473393 | CT | C | 13 | a0001c0001t0001g0222 a0001c0001t0002g0162 a0001c0003t0001g0320 others(10): Show |
13 | HG00673.hp2 HG01069.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.1114-5160delT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4473393 | ||||||
| chr17:4473412 | T | A | 4 | a0001c0001t0001g0332 a0001c0001t0001g0334 a0001c0006t0002g0011 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-5160T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4473412 | |||||||
| chr17:4473458 | C | T | 2 | a0001c0001t0001g0332 a0001c0001t0001g0334 |
2 | HG02257.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1114-5114C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4473458 | |||||||
| chr17:4473459 | G | A | 1 | a0001c0006t0001g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1114-5113G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4473459 | |||||||
| chr17:4473537 | G | A | 161 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0095 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1114-5035G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4473537 | |||||||
| chr17:4473539 | C | T | 161 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0095 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1114-5033C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4473539 | |||||||
| chr17:4473567 | T | C | 1 | a0003c0005t0001g0156 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1114-5005T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4473567 | |||||||
| chr17:4473800 | G | A | 164 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0095 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1114-4772G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4473800 | |||||||
| chr17:4473961 | TCTTGGAT others(26): Show |
T | 2 | a0001c0001t0002g0326 a0001c0014t0002g0007 |
2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1114-4608_1114-457 others(37): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4473961 | ||||||
| chr17:4474052 | G | A | 2 | a0002c0002t0001g0269 a0002c0002t0001g0270 |
2 | HG02027.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1114-4520G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474052 | |||||||
| chr17:4474298 | T | C | 260 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0095 others(257): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1114-4274T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474298 | |||||||
| chr17:4474396 | G | T | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1114-4176G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474396 | |||||||
| chr17:4474472 | C | T | 25 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(22): Show |
25 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1114-4100C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474472 | |||||||
| chr17:4474497 | C | G | 2 | a0001c0003t0002g0137 a0001c0003t0002g0138 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1114-4075C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474497 | |||||||
| chr17:4474618 | C | T | 33 | a0001c0001t0001g0035 a0001c0001t0001g0129 a0001c0001t0001g0130 others(30): Show |
33 | HG00741.hp2 HG01123.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1114-3954C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474618 | |||||||
| chr17:4474619 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0210 |
2 | HG02040.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1114-3953G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474619 | |||||||
| chr17:4474652 | C | T | 154 | a0001c0001t0001g0028 a0001c0001t0001g0095 a0001c0001t0001g0111 others(151): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1114-3920C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474652 | |||||||
| chr17:4474684 | G | A | 175 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(172): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1114-3888G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474684 | |||||||
| chr17:4474787 | T | A | 194 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1114-3785T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474787 | |||||||
| chr17:4474810 | G | C | 56 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(53): Show |
56 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1114-3762G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474810 | |||||||
| chr17:4474858 | CAT | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0035 others(225): Show |
229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.1114-3713_1114-371 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474858 | |||||||
| chr17:4474987 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1114-3585T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474987 | |||||||
| chr17:4474988 | C | T | 1 | a0001c0009t0002g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1114-3584C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4474988 | |||||||
| chr17:4475036 | G | T | 343 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(340): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1114-3536G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475036 | |||||||
| chr17:4475041 | G | A | 3 | a0001c0047t0002g0321 a0007c0025t0002g0040 a0007c0025t0002g0041 |
3 | HG02572.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1114-3531G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475041 | |||||||
| chr17:4475044 | C | T | 3 | a0001c0001t0002g0326 a0001c0009t0002g0031 a0001c0014t0002g0007 |
3 | HG02145.hp2 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1114-3528C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475044 | |||||||
| chr17:4475070 | T | C | 1 | a0001c0004t0001g0054 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1114-3502T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475070 | |||||||
| chr17:4475437 | G | A | 1 | a0001c0004t0001g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1114-3135G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475437 | |||||||
| chr17:4475509 | C | T | 19 | a0001c0001t0002g0160 a0001c0001t0002g0326 a0001c0001t0002g0342 others(16): Show |
19 | HG01099.hp1 HG01109.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1114-3063C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475509 | |||||||
| chr17:4475628 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(98): Show |
102 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1114-2944G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475628 | |||||||
| chr17:4475641 | T | A | 2 | a0001c0001t0001g0242 a0001c0013t0001g0178 |
2 | NA18962.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1114-2931T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475641 | |||||||
| chr17:4475649 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.1114-2923A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475649 | |||||||
| chr17:4475660 | T | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.1114-2912T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475660 | |||||||
| chr17:4475772 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0105 others(63): Show |
67 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.1114-2800G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475772 | |||||||
| chr17:4475889 | G | A | 87 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(84): Show |
87 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1114-2683G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475889 | |||||||
| chr17:4475931 | T | G | 88 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(85): Show |
88 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1114-2641T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475931 | |||||||
| chr17:4475985 | A | G | 1 | a0002c0002t0001g0245 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1114-2587A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4475985 | |||||||
| chr17:4476001 | G | A | 1 | a0003c0005t0001g0156 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1114-2571G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476001 | |||||||
| chr17:4476118 | G | C | 1 | a0003c0020t0001g0115 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1114-2454G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476118 | |||||||
| chr17:4476131 | C | A | 1 | a0001c0009t0002g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1114-2441C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476131 | |||||||
| chr17:4476148 | C | T | 25 | a0001c0001t0001g0166 a0001c0001t0001g0186 a0001c0001t0001g0191 others(22): Show |
25 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1114-2424C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476148 | |||||||
| chr17:4476243 | C | T | 1 | a0003c0008t0003g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1114-2329C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476243 | |||||||
| chr17:4476283 | G | A | 55 | a0001c0001t0001g0095 a0001c0001t0001g0111 a0001c0001t0001g0179 others(52): Show |
55 | HG00280.hp1 HG00438.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1114-2289G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476283 | |||||||
| chr17:4476290 | G | A | 3 | a0002c0022t0001g0059 a0002c0033t0003g0091 a0009c0050t0001g0060 |
3 | HG01074.hp2 HG02109.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1114-2282G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476290 | |||||||
| chr17:4476373 | C | A | 1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1114-2199C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476373 | |||||||
| chr17:4476394 | G | A | 1 | a0001c0004t0001g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1114-2178G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476394 | |||||||
| chr17:4476464 | G | A | 3 | a0001c0047t0002g0321 a0007c0025t0002g0040 a0007c0025t0002g0041 |
3 | HG02572.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1114-2108G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476464 | |||||||
| chr17:4476552 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0105 others(88): Show |
92 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.1114-2020G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476552 | |||||||
| chr17:4476610 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1114-1962G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476610 | |||||||
| chr17:4476658 | C | T | 89 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(86): Show |
89 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1114-1914C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476658 | |||||||
| chr17:4476745 | C | T | 3 | a0001c0004t0001g0026 a0001c0006t0001g0049 a0001c0006t0001g0050 |
3 | HG02486.hp2 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1114-1827C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476745 | |||||||
| chr17:4476801 | G | C | 1 | a0001c0006t0002g0052 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1114-1771G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476801 | |||||||
| chr17:4476802 | G | A | 1 | a0001c0006t0002g0052 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1114-1770G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476802 | |||||||
| chr17:4476889 | C | G | 1 | a0001c0001t0001g0361 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1114-1683C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476889 | |||||||
| chr17:4476903 | T | A | 79 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(76): Show |
79 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1114-1669T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476903 | |||||||
| chr17:4476929 | G | A | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1114-1643G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476929 | |||||||
| chr17:4476952 | G | A | 1 | a0001c0010t0001g0044 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1114-1620G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476952 | |||||||
| chr17:4476976 | C | T | 2 | a0001c0001t0001g0332 a0001c0001t0001g0334 |
2 | HG02257.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1114-1596C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476976 | |||||||
| chr17:4476998 | C | T | 1 | a0006c0026t0001g0240 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1114-1574C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4476998 | |||||||
| chr17:4477013 | C | T | 68 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0271 others(65): Show |
68 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1114-1559C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477013 | |||||||
| chr17:4477025 | C | T | 58 | a0001c0001t0001g0028 a0001c0001t0001g0095 a0001c0001t0001g0111 others(55): Show |
58 | HG00280.hp1 HG00438.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1114-1547C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477025 | |||||||
| chr17:4477180 | G | C | 1 | a0002c0002t0001g0302 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1114-1392G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477180 | |||||||
| chr17:4477191 | C | T | 1 | a0001c0013t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1114-1381C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477191 | |||||||
| chr17:4477258 | A | C | 3 | a0001c0006t0001g0032 a0001c0006t0002g0052 a0001c0046t0002g0316 |
3 | HG02717.hp2 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1114-1314A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477258 | |||||||
| chr17:4477488 | C | CT | 71 | a0001c0001t0001g0205 a0001c0001t0001g0260 a0001c0001t0001g0263 others(68): Show |
71 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1114-1077dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4477488 | ||||||
| chr17:4477498 | CTCTT | C | 19 | a0001c0001t0002g0160 a0001c0001t0002g0326 a0001c0001t0002g0342 others(16): Show |
19 | HG01099.hp1 HG01109.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1114-1069_1114-106 others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4477498 | ||||||
| chr17:4477588 | G | T | 1 | a0002c0037t0002g0323 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1114-984G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477588 | |||||||
| chr17:4477713 | C | T | 2 | a0001c0003t0001g0126 a0005c0015t0003g0104 |
2 | HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1114-859C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477713 | |||||||
| chr17:4477729 | C | T | 1 | a0003c0005t0001g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1114-843C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477729 | |||||||
| chr17:4477743 | G | A | 9 | a0001c0001t0001g0098 a0001c0001t0001g0164 a0001c0001t0001g0165 others(6): Show |
9 | HG01975.hp2 HG02027.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-829G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477743 | |||||||
| chr17:4477782 | T | A | 5 | a0001c0003t0001g0126 a0001c0006t0001g0010 a0001c0007t0003g0158 others(2): Show |
5 | HG00642.hp1 HG01106.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1114-790T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477782 | |||||||
| chr17:4477795 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0338 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1114-777G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477795 | |||||||
| chr17:4477805 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1114-767C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477805 | |||||||
| chr17:4477805 | C | T | 2 | a0001c0001t0002g0330 a0001c0042t0002g0339 |
2 | HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1114-767C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477805 | |||||||
| chr17:4477879 | C | T | 1 | a0001c0006t0002g0052 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1114-693C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477879 | |||||||
| chr17:4477880 | G | T | 14 | a0001c0001t0001g0335 a0001c0001t0002g0322 a0001c0001t0002g0324 others(11): Show |
14 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1114-692G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477880 | |||||||
| chr17:4477941 | C | T | 3 | a0001c0047t0002g0321 a0007c0025t0002g0040 a0007c0025t0002g0041 |
3 | HG02572.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1114-631C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477941 | |||||||
| chr17:4477952 | G | GT | 6 | a0001c0001t0001g0184 a0001c0006t0002g0011 a0001c0006t0002g0012 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114-611dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4477952 | ||||||
| chr17:4477970 | C | CT | 38 | a0001c0001t0001g0111 a0001c0001t0001g0338 a0001c0001t0002g0160 others(35): Show |
38 | HG00280.hp1 HG01099.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1114-583dupT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4477970 | ||||||
| chr17:4477970 | C | CTT | 72 | a0001c0001t0001g0205 a0001c0001t0001g0260 a0001c0001t0001g0263 others(69): Show |
72 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.1114-584_1114-583d others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4477970 | ||||||
| chr17:4477970 | C | CTTT | 6 | a0001c0004t0001g0027 a0001c0023t0003g0014 a0001c0036t0003g0144 others(3): Show |
6 | HG01346.hp1 HG02027.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-585_1114-583d others(5): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4477970 | ||||||
| chr17:4477970 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0002g0193 a0001c0003t0002g0112 a0001c0006t0002g0011 others(1): Show |
4 | HG02895.hp2 HG02896.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-592_1114-583d others(12): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4477970 | ||||||
| chr17:4477970 | C | CTTTTTTT others(4): Show |
46 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0105 others(43): Show |
47 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.1114-593_1114-583d others(13): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4477970 | ||||||
| chr17:4477970 | C | CTTTTTTT others(5): Show |
14 | a0001c0001t0001g0218 a0001c0001t0002g0162 a0001c0003t0001g0124 others(11): Show |
14 | HG01358.hp2 HG01433.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1114-594_1114-583d others(14): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4477970 | ||||||
| chr17:4477970 | C | CTTTTTTT others(6): Show |
4 | a0001c0003t0001g0122 a0001c0003t0001g0123 a0001c0003t0001g0318 others(1): Show |
4 | HG01433.hp2 HG02055.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-595_1114-583d others(15): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4477970 | ||||||
| chr17:4477970 | CT | C | 9 | a0001c0001t0001g0020 a0001c0001t0001g0179 a0001c0001t0002g0327 others(6): Show |
9 | HG02280.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-583delT | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4477970 | ||||||
| chr17:4477970 | CTTTTTT | C | 78 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(75): Show |
78 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1114-588_1114-583d others(8): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 4477970 | ||||||
| chr17:4477996 | G | A | 1 | a0002c0002t0001g0307 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1114-576G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4477996 | |||||||
| chr17:4478033 | G | A | 15 | a0001c0001t0001g0335 a0001c0001t0002g0322 a0001c0001t0002g0324 others(12): Show |
15 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1114-539G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4478033 | |||||||
| chr17:4478091 | C | T | 3 | a0001c0047t0002g0321 a0007c0025t0002g0040 a0007c0025t0002g0041 |
3 | HG02572.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1114-481C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4478091 | |||||||
| chr17:4478108 | A | C | 9 | a0001c0001t0001g0335 a0001c0001t0002g0322 a0001c0001t0002g0324 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-464A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4478108 | |||||||
| chr17:4478134 | G | C | 1 | a0001c0001t0001g0275 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1114-438G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4478134 | |||||||
| chr17:4478396 | G | A | 4 | a0001c0001t0001g0154 a0001c0001t0001g0311 a0001c0013t0001g0113 others(1): Show |
4 | HG02970.hp2 NA19240.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-176G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4478396 | |||||||
| chr17:4478453 | G | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0105 others(67): Show |
71 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.1114-119G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4478453 | |||||||
| chr17:4478489 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1114-83C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 8/11 | chr17 | 4478489 | |||||||
| chr17:4478890 | C | T | 2 | a0001c0003t0001g0126 a0005c0015t0003g0104 |
2 | HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1179+253C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4478890 | |||||||
| chr17:4478965 | A | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0105 others(67): Show |
71 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.1179+328A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4478965 | |||||||
| chr17:4479024 | C | T | 2 | a0001c0004t0001g0027 a0001c0036t0003g0144 |
2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1179+387C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4479024 | |||||||
| chr17:4479093 | C | G | 19 | a0001c0001t0002g0160 a0001c0001t0002g0326 a0001c0001t0002g0342 others(16): Show |
19 | HG01099.hp1 HG01109.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1179+456C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4479093 | |||||||
| chr17:4479136 | T | TTC | 83 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(80): Show |
83 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1179+500_1179+501d others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 4479136 | ||||||
| chr17:4479149 | C | T | 1 | a0001c0006t0002g0052 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1179+512C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4479149 | |||||||
| chr17:4479166 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0002g0151 |
3 | NA18977.hp2 NA18982.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1179+529C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4479166 | |||||||
| chr17:4479187 | C | T | 1 | a0001c0023t0003g0014 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1179+550C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4479187 | |||||||
| chr17:4479188 | G | T | 1 | a0002c0002t0001g0288 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1179+551G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4479188 | |||||||
| chr17:4479190 | T | C | 327 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0035 others(324): Show |
328 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.1179+553T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4479190 | |||||||
| chr17:4479198 | C | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0311 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1179+561C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4479198 | |||||||
| chr17:4479434 | T | C | 74 | a0001c0001t0001g0154 a0001c0001t0001g0260 a0001c0001t0001g0263 others(71): Show |
74 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.1179+797T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4479434 | |||||||
| chr17:4479569 | G | C | 68 | a0001c0001t0001g0028 a0001c0001t0001g0095 a0001c0001t0001g0111 others(65): Show |
68 | HG00280.hp1 HG00438.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1179+932G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4479569 | |||||||
| chr17:4479601 | T | C | 82 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(79): Show |
82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.1179+964T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4479601 | |||||||
| chr17:4479699 | G | A | 11 | a0001c0001t0001g0335 a0001c0001t0002g0322 a0001c0001t0002g0324 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1179+1062G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4479699 | |||||||
| chr17:4479939 | G | A | 82 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(79): Show |
82 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.1179+1302G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4479939 | |||||||
| chr17:4480026 | T | A | 1 | a0002c0011t0003g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1179+1389T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480026 | |||||||
| chr17:4480069 | T | C | 86 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(83): Show |
86 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1179+1432T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480069 | |||||||
| chr17:4480098 | G | GC | 22 | a0001c0001t0002g0160 a0001c0001t0002g0326 a0001c0001t0002g0342 others(19): Show |
22 | HG01099.hp1 HG01109.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1179+1465dupC | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 4480098 | ||||||
| chr17:4480107 | C | T | 1 | a0003c0005t0001g0310 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1179+1470C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480107 | |||||||
| chr17:4480228 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1179+1591C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480228 | |||||||
| chr17:4480229 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1179+1592T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480229 | |||||||
| chr17:4480266 | C | T | 3 | a0001c0047t0002g0321 a0007c0025t0002g0040 a0007c0025t0002g0041 |
3 | HG02572.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1179+1629C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480266 | |||||||
| chr17:4480294 | C | T | 12 | a0001c0001t0001g0335 a0001c0001t0002g0322 a0001c0001t0002g0324 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1179+1657C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480294 | |||||||
| chr17:4480351 | G | A | 1 | a0003c0016t0001g0083 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1179+1714G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480351 | |||||||
| chr17:4480495 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0105 others(68): Show |
72 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.1179+1858C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480495 | |||||||
| chr17:4480521 | C | T | 1 | a0001c0003t0001g0345 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1179+1884C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480521 | |||||||
| chr17:4480560 | T | G | 4 | a0002c0002t0001g0276 a0002c0002t0001g0277 a0002c0002t0001g0290 others(1): Show |
4 | HG01346.hp1 HG01496.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+1923T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480560 | |||||||
| chr17:4480587 | C | T | 1 | a0001c0006t0002g0052 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1179+1950C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480587 | |||||||
| chr17:4480630 | T | C | 9 | a0001c0001t0001g0335 a0001c0001t0002g0322 a0001c0001t0002g0324 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1179+1993T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480630 | |||||||
| chr17:4480669 | G | A | 71 | a0001c0001t0001g0219 a0001c0001t0001g0260 a0001c0001t0001g0263 others(68): Show |
71 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1179+2032G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480669 | |||||||
| chr17:4480733 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0096 others(182): Show |
186 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.1179+2096A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480733 | |||||||
| chr17:4480826 | GCAC | G | 246 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(243): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1179+2195_1179+219 others(7): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 4480826 | ||||||
| chr17:4480832 | CCAT | C | 25 | a0001c0001t0001g0095 a0001c0001t0001g0179 a0001c0001t0001g0187 others(22): Show |
25 | HG00438.hp1 HG00621.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1179+2197_1179+219 others(7): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 4480832 | ||||||
| chr17:4480834 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1179+2197A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480834 | |||||||
| chr17:4480884 | C | T | 16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(13): Show |
16 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1179+2247C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480884 | |||||||
| chr17:4480961 | T | C | 3 | a0001c0047t0002g0321 a0007c0025t0002g0040 a0007c0025t0002g0041 |
3 | HG02572.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1179+2324T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4480961 | |||||||
| chr17:4481003 | G | C | 346 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(343): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1179+2366G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481003 | |||||||
| chr17:4481172 | C | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0213 |
2 | NA18986.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1179+2535C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481172 | |||||||
| chr17:4481218 | C | T | 5 | a0001c0003t0001g0126 a0001c0006t0001g0010 a0001c0007t0003g0158 others(2): Show |
5 | HG00642.hp1 HG01106.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+2581C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481218 | |||||||
| chr17:4481262 | A | G | 3 | a0001c0001t0002g0326 a0001c0014t0002g0007 a0001c0023t0003g0014 |
3 | HG03130.hp1 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1179+2625A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481262 | |||||||
| chr17:4481342 | T | G | 1 | a0001c0001t0001g0275 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1179+2705T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481342 | |||||||
| chr17:4481392 | C | G | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1179+2755C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481392 | |||||||
| chr17:4481483 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0096 others(177): Show |
181 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.1179+2846G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481483 | |||||||
| chr17:4481492 | G | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0096 others(260): Show |
264 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.1179+2855G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481492 | |||||||
| chr17:4481528 | C | T | 8 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0003t0001g0132 others(5): Show |
8 | HG03130.hp2 HG03927.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.1179+2891C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481528 | |||||||
| chr17:4481529 | G | A | 1 | a0001c0003t0002g0148 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1179+2892G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481529 | |||||||
| chr17:4481559 | G | C | 49 | a0001c0001t0001g0028 a0001c0001t0001g0095 a0001c0001t0001g0111 others(46): Show |
49 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.1179+2922G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481559 | |||||||
| chr17:4481804 | C | T | 245 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0095 others(242): Show |
245 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.1179+3167C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481804 | |||||||
| chr17:4481827 | C | T | 7 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG01167.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179+3190C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481827 | |||||||
| chr17:4481873 | GCT | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(203): Show |
207 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.1179+3249_1179+325 others(6): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 4481873 | ||||||
| chr17:4481883 | TC | T | 13 | a0001c0001t0002g0160 a0001c0001t0002g0317 a0001c0001t0002g0326 others(10): Show |
13 | HG01109.hp1 HG02055.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1179+3247delC | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481883 | |||||||
| chr17:4481883 | TCTC | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0199 others(1): Show |
4 | HG03491.hp2 NA18955.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+3247_1179+324 others(7): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481883 | |||||||
| chr17:4481884 | C | T | 1 | a0001c0036t0003g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1179+3247C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481884 | |||||||
| chr17:4481886 | C | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(271): Show |
275 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.1179+3249C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481886 | |||||||
| chr17:4481923 | A | T | 1 | a0001c0009t0002g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1179+3286A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481923 | |||||||
| chr17:4481928 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1179+3291C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481928 | |||||||
| chr17:4481951 | C | T | 1 | a0005c0015t0003g0153 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1179+3314C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481951 | |||||||
| chr17:4481965 | T | C | 11 | a0001c0003t0001g0126 a0001c0004t0001g0027 a0001c0006t0001g0010 others(8): Show |
11 | HG00642.hp1 HG01106.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1179+3328T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481965 | |||||||
| chr17:4481968 | G | A | 7 | a0001c0003t0001g0126 a0001c0006t0001g0010 a0001c0007t0003g0158 others(4): Show |
7 | HG00642.hp1 HG01106.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1179+3331G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4481968 | |||||||
| chr17:4482034 | A | G | 1 | a0002c0002t0001g0274 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1179+3397A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482034 | |||||||
| chr17:4482034 | A | T | 2 | a0001c0004t0001g0027 a0001c0012t0001g0038 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1179+3397A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482034 | |||||||
| chr17:4482035 | T | C | 5 | a0001c0001t0002g0160 a0001c0004t0001g0027 a0001c0006t0002g0052 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+3398T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482035 | |||||||
| chr17:4482035 | T | G | 1 | a0001c0007t0003g0161 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1179+3398T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482035 | |||||||
| chr17:4482036 | G | A | 2 | a0001c0001t0002g0160 a0001c0006t0002g0052 |
2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1179+3399G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482036 | |||||||
| chr17:4482036 | G | C | 2 | a0001c0004t0001g0027 a0001c0012t0001g0038 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1179+3399G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482036 | |||||||
| chr17:4482037 | C | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(36): Show |
40 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1179+3400C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482037 | |||||||
| chr17:4482037 | C | T | 3 | a0001c0004t0001g0027 a0001c0012t0001g0038 a0002c0002t0001g0274 |
3 | HG01255.hp1 HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1179+3400C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482037 | |||||||
| chr17:4482043 | C | T | 1 | a0010c0041t0003g0314 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1179+3406C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482043 | |||||||
| chr17:4482045 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1179+3408C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482045 | |||||||
| chr17:4482049 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18982.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1179+3412C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482049 | |||||||
| chr17:4482050 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18982.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1179+3413A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482050 | |||||||
| chr17:4482077 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1179+3440C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482077 | |||||||
| chr17:4482078 | G | A | 155 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0095 others(152): Show |
155 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1179+3441G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482078 | |||||||
| chr17:4482100 | A | C | 15 | a0001c0001t0001g0185 a0001c0001t0001g0190 a0001c0001t0002g0046 others(12): Show |
15 | HG00423.hp2 HG01175.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1179+3463A>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482100 | |||||||
| chr17:4482108 | G | A | 2 | a0001c0004t0001g0054 a0001c0004t0001g0092 |
2 | HG02165.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1179+3471G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482108 | |||||||
| chr17:4482114 | T | C | 1 | a0002c0002t0001g0292 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1179+3477T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482114 | |||||||
| chr17:4482133 | C | G | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0003t0002g0315 others(1): Show |
4 | HG02258.hp2 HG03540.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+3496C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482133 | |||||||
| chr17:4482137 | T | C | 1 | a0001c0003t0002g0315 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1179+3500T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482137 | |||||||
| chr17:4482165 | T | C | 115 | a0001c0001t0001g0035 a0001c0001t0001g0105 a0001c0001t0001g0166 others(112): Show |
115 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1179+3528T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482165 | |||||||
| chr17:4482188 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1179+3551G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482188 | |||||||
| chr17:4482208 | C | T | 112 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(109): Show |
112 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1179+3571C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482208 | |||||||
| chr17:4482321 | G | A | 153 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(150): Show |
153 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1179+3684G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482321 | |||||||
| chr17:4482379 | T | C | 2 | a0001c0042t0002g0339 a0001c0046t0002g0316 |
2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1179+3742T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482379 | |||||||
| chr17:4482471 | C | T | 2 | a0002c0002t0001g0265 a0002c0002t0001g0266 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1180-3757C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482471 | |||||||
| chr17:4482562 | C | T | 1 | a0001c0013t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1180-3666C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482562 | |||||||
| chr17:4482627 | A | G | 5 | a0001c0006t0002g0048 a0001c0006t0002g0052 a0001c0009t0002g0031 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-3601A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482627 | |||||||
| chr17:4482657 | G | A | 3 | a0001c0012t0001g0038 a0001c0018t0002g0349 a0001c0018t0002g0350 |
3 | HG02280.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1180-3571G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482657 | |||||||
| chr17:4482698 | G | A | 1 | a0001c0034t0002g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1180-3530G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482698 | |||||||
| chr17:4482796 | G | A | 1 | a0001c0006t0001g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1180-3432G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482796 | |||||||
| chr17:4482908 | C | T | 3 | a0001c0018t0002g0349 a0001c0018t0002g0350 a0001c0034t0002g0045 |
3 | HG02717.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1180-3320C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482908 | |||||||
| chr17:4482919 | G | T | 4 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0165 others(1): Show |
4 | HG02273.hp1 NA18983.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180-3309G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4482919 | |||||||
| chr17:4483030 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1180-3198C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4483030 | |||||||
| chr17:4483073 | C | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(305): Show |
309 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(306): Show |
intron_variant | MODIFIER | c.1180-3155C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4483073 | |||||||
| chr17:4483154 | C | A | 4 | a0001c0003t0001g0345 a0001c0010t0001g0044 a0001c0013t0001g0113 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180-3074C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4483154 | |||||||
| chr17:4483154 | C | T | 2 | a0001c0006t0002g0048 a0001c0006t0002g0052 |
2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1180-3074C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4483154 | |||||||
| chr17:4483205 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0096 a0001c0001t0001g0097 others(49): Show |
53 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1180-3023G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4483205 | |||||||
| chr17:4483244 | C | G | 4 | a0001c0003t0001g0345 a0001c0010t0001g0044 a0001c0013t0001g0113 others(1): Show |
4 | HG02723.hp1 HG02922.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180-2984C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4483244 | |||||||
| chr17:4483259 | C | T | 1 | a0001c0003t0001g0309 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1180-2969C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4483259 | |||||||
| chr17:4483374 | C | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(217): Show |
221 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(218): Show |
intron_variant | MODIFIER | c.1180-2854C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4483374 | |||||||
| chr17:4483634 | C | T | 2 | a0001c0003t0001g0345 a0001c0010t0001g0044 |
2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1180-2594C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4483634 | |||||||
| chr17:4483732 | T | C | 1 | a0001c0007t0003g0247 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1180-2496T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4483732 | |||||||
| chr17:4483792 | A | T | 1 | a0001c0001t0001g0198 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1180-2436A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4483792 | |||||||
| chr17:4483820 | C | T | 2 | a0001c0010t0001g0078 a0001c0010t0001g0080 |
2 | HG01069.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1180-2408C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4483820 | |||||||
| chr17:4483923 | G | A | 2 | a0003c0005t0002g0155 a0003c0016t0002g0082 |
2 | HG01106.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1180-2305G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4483923 | |||||||
| chr17:4484018 | A | T | 1 | a0002c0032t0001g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1180-2210A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4484018 | |||||||
| chr17:4484040 | T | A | 43 | a0001c0001t0001g0189 a0001c0001t0002g0046 a0001c0001t0002g0151 others(40): Show |
43 | HG00438.hp2 HG00738.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1180-2188T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4484040 | |||||||
| chr17:4484123 | A | G | 2 | a0001c0006t0002g0048 a0001c0006t0002g0052 |
2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1180-2105A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4484123 | |||||||
| chr17:4484247 | C | T | 1 | a0001c0007t0003g0247 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1180-1981C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4484247 | |||||||
| chr17:4484393 | T | C | 1 | a0001c0013t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1180-1835T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4484393 | |||||||
| chr17:4484470 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1180-1758G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4484470 | |||||||
| chr17:4484559 | G | A | 3 | a0001c0006t0001g0032 a0001c0007t0003g0325 a0001c0023t0003g0014 |
3 | HG03139.hp1 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1180-1669G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4484559 | |||||||
| chr17:4484579 | C | T | 3 | a0001c0006t0001g0032 a0001c0007t0003g0325 a0001c0023t0003g0014 |
3 | HG03139.hp1 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1180-1649C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4484579 | |||||||
| chr17:4484918 | T | G | 35 | a0001c0001t0001g0334 a0001c0001t0002g0135 a0001c0001t0002g0143 others(32): Show |
35 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1180-1310T>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4484918 | |||||||
| chr17:4484939 | A | T | 1 | a0001c0007t0003g0247 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1180-1289A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4484939 | |||||||
| chr17:4484966 | C | A | 35 | a0001c0001t0001g0334 a0001c0001t0002g0135 a0001c0001t0002g0143 others(32): Show |
35 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1180-1262C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4484966 | |||||||
| chr17:4484968 | C | A | 35 | a0001c0001t0001g0334 a0001c0001t0002g0135 a0001c0001t0002g0143 others(32): Show |
35 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1180-1260C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4484968 | |||||||
| chr17:4484987 | C | A | 1 | a0001c0004t0001g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1180-1241C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4484987 | |||||||
| chr17:4485015 | C | A | 1 | a0001c0001t0001g0243 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1180-1213C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485015 | |||||||
| chr17:4485039 | A | T | 41 | a0001c0001t0001g0189 a0001c0001t0002g0046 a0001c0001t0002g0151 others(38): Show |
41 | HG00438.hp2 HG00738.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1180-1189A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485039 | |||||||
| chr17:4485172 | C | T | 1 | a0001c0007t0003g0247 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1180-1056C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485172 | |||||||
| chr17:4485315 | A | G | 47 | a0001c0001t0001g0189 a0001c0001t0002g0046 a0001c0001t0002g0151 others(44): Show |
47 | HG00438.hp2 HG00738.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.1180-913A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485315 | |||||||
| chr17:4485382 | G | A | 1 | a0001c0009t0001g0004 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1180-846G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485382 | |||||||
| chr17:4485393 | T | A | 3 | a0001c0013t0001g0178 a0003c0005t0001g0114 a0003c0051t0001g0013 |
3 | HG00597.hp2 HG02155.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1180-835T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485393 | |||||||
| chr17:4485405 | T | A | 1 | a0001c0006t0001g0047 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1180-823T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485405 | |||||||
| chr17:4485406 | T | A | 8 | a0001c0009t0002g0031 a0001c0018t0002g0349 a0001c0018t0002g0350 others(5): Show |
8 | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1180-822T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485406 | |||||||
| chr17:4485407 | T | A | 8 | a0001c0003t0001g0345 a0001c0004t0001g0027 a0001c0007t0003g0325 others(5): Show |
8 | HG02723.hp1 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180-821T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485407 | |||||||
| chr17:4485408 | T | A | 1 | a0001c0001t0001g0237 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1180-820T>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485408 | |||||||
| chr17:4485580 | A | G | 1 | a0001c0007t0003g0163 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1180-648A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485580 | |||||||
| chr17:4485627 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1180-601C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485627 | |||||||
| chr17:4485666 | G | C | 1 | a0001c0001t0001g0242 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1180-562G>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485666 | |||||||
| chr17:4485738 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1180-490C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485738 | |||||||
| chr17:4485761 | C | T | 1 | a0001c0006t0001g0010 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1180-467C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485761 | |||||||
| chr17:4485815 | C | T | 1 | a0001c0006t0001g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1180-413C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485815 | |||||||
| chr17:4485882 | G | A | 1 | a0001c0013t0001g0178 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1180-346G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485882 | |||||||
| chr17:4485972 | A | G | 27 | a0001c0001t0001g0189 a0001c0001t0002g0046 a0001c0001t0002g0151 others(24): Show |
27 | HG00438.hp2 HG00738.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1180-256A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 9/11 | chr17 | 4485972 | |||||||
| chr17:4486753 | GAGGCCAA others(4): Show |
G | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1450+176_1450+186d others(13): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 4486753 | ||||||
| chr17:4486820 | G | A | 2 | a0001c0001t0001g0030 a0001c0006t0001g0047 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1450+237G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4486820 | |||||||
| chr17:4486848 | C | A | 1 | a0001c0014t0002g0018 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1450+265C>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4486848 | |||||||
| chr17:4486912 | A | G | 4 | a0001c0001t0001g0111 a0001c0001t0001g0338 a0001c0006t0002g0048 others(1): Show |
4 | HG02257.hp2 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1450+329A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4486912 | |||||||
| chr17:4486931 | G | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0095 others(178): Show |
182 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1450+348G>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4486931 | |||||||
| chr17:4486996 | G | A | 2 | a0003c0008t0003g0099 a0003c0008t0003g0103 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1450+413G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4486996 | |||||||
| chr17:4487000 | T | C | 2 | a0003c0008t0003g0099 a0003c0008t0003g0103 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1450+417T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4487000 | |||||||
| chr17:4487034 | C | T | 3 | a0001c0001t0002g0317 a0001c0006t0002g0048 a0001c0006t0002g0052 |
3 | HG02257.hp2 HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1450+451C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4487034 | |||||||
| chr17:4487167 | C | CA | 50 | a0001c0001t0001g0030 a0001c0001t0001g0096 a0001c0001t0001g0097 others(47): Show |
50 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.1450+608dupA | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 4487167 | ||||||
| chr17:4487167 | C | CAA | 7 | a0001c0003t0001g0318 a0001c0007t0003g0158 a0001c0007t0003g0296 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1450+607_1450+608d others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 4487167 | ||||||
| chr17:4487167 | CA | C | 66 | a0001c0001t0001g0179 a0001c0001t0001g0189 a0001c0001t0001g0243 others(63): Show |
66 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1450+608delA | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 4487167 | ||||||
| chr17:4487167 | CAA | C | 24 | a0001c0001t0002g0317 a0001c0001t0002g0322 a0001c0001t0002g0324 others(21): Show |
24 | HG01256.hp2 HG01891.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.1450+607_1450+608d others(4): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 4487167 | ||||||
| chr17:4487167 | CAAAAAAA | C | 6 | a0001c0001t0002g0162 a0001c0003t0002g0136 a0001c0003t0002g0137 others(3): Show |
6 | HG00741.hp2 HG01358.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1450+602_1450+608d others(9): Show |
SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr17 | 4487167 | ||||||
| chr17:4487220 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1451-586C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4487220 | |||||||
| chr17:4487231 | A | T | 1 | a0001c0031t0005g0033 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1451-575A>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4487231 | |||||||
| chr17:4487234 | C | T | 29 | a0001c0007t0003g0158 a0001c0007t0003g0161 a0001c0007t0003g0163 others(26): Show |
29 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1451-572C>T | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4487234 | |||||||
| chr17:4487262 | C | G | 1 | a0001c0001t0002g0143 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1451-544C>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4487262 | |||||||
| chr17:4487287 | T | C | 123 | a0001c0001t0001g0189 a0001c0001t0002g0046 a0001c0001t0002g0135 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1451-519T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4487287 | |||||||
| chr17:4487352 | A | G | 1 | a0001c0024t0003g0057 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1451-454A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4487352 | |||||||
| chr17:4487395 | A | G | 106 | a0001c0001t0002g0135 a0001c0001t0002g0143 a0001c0001t0002g0160 others(103): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1451-411A>G | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4487395 | |||||||
| chr17:4487613 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0338 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1451-193G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4487613 | |||||||
| chr17:4487661 | G | A | 2 | a0001c0003t0002g0112 a0004c0017t0002g0331 |
2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1451-145G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4487661 | |||||||
| chr17:4487732 | G | A | 1 | a0005c0015t0003g0159 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1451-74G>A | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4487732 | |||||||
| chr17:4487733 | T | C | 15 | a0001c0001t0002g0160 a0001c0001t0002g0342 a0001c0001t0002g0343 others(12): Show |
15 | HG01099.hp1 HG02055.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1451-73T>C | SPNS3 | ENSG00000182557.8 | transcript | ENST00000355530.7 | protein_coding | 11/11 | chr17 | 4487733 |