Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11276 |
| ensemblid | ENSG00000275066.5 |
| hgncid | 557 |
| symbol | SYNRG |
| name | synergin gamma |
| refseq_nuc | NM_007247.6 |
| refseq_prot | NP_009178.3 |
| ensembl_nuc | ENST00000612223.5 |
| ensembl_prot | ENSP00000483453.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 37514807 |
| end | 37609418 |
| strand | - |
| ver | v1.2 |
| region | chr17:37514807-37609418 |
| region5000 | chr17:37509807-37614418 |
| regionname0 | SYNRG_chr17_37514807_37609418 |
| regionname5000 | SYNRG_chr17_37509807_37614418 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1314 | 206 | 62 | 32 | 87 | 6 | 19 | 70 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| a0002 | 0/0 | 1314 | 80 | 11 | 20 | 36 | 4 | 9 | 31 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| a0003 | 0/1 | 1314 | 49 | 7 | 12 | 19 | 4 | 6 | 15 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| a0004 | 0/0 | 1314 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| a0005 | 0/0 | 1314 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| a0006 | 0/0 | 1314 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| a0007 | 0/0 | 1314 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| a0008 | 0/0 | 1314 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| a0009 | 0/0 | 1314 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| a0010 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| a0011 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| a0012 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| a0013 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| a0014 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | MALRP others(1309): Show |
chr17 | 37509807 | 37614418 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3942 | 121 | 36 | 12 | 59 | 2 | 12 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0001c0003 | 0/0 | 3942 | 63 | 5 | 20 | 27 | 4 | 7 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0001c0005 | 0/0 | 3942 | 15 | 15 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0001c0006 | 0/0 | 3942 | 6 | 6 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0001c0016 | 0/0 | 3942 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0002c0002 | 0/0 | 3942 | 78 | 9 | 20 | 36 | 4 | 9 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0002c0011 | 0/0 | 3942 | 2 | 2 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0003c0004 | 0/1 | 3942 | 46 | 7 | 9 | 19 | 4 | 6 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0003c0010 | 0/0 | 3942 | 2 | 0 | 2 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0003c0013 | 0/0 | 3942 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0004c0008 | 0/0 | 3942 | 2 | 1 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0005c0007 | 0/0 | 3942 | 2 | 2 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0006c0009 | 0/0 | 3942 | 2 | 0 | 0 | 0 | 0 | 2 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0007c0017 | 0/0 | 3942 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0008c0021 | 0/0 | 3942 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0009c0012 | 0/0 | 3942 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0010c0014 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0011c0018 | 0/0 | 3942 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0012c0019 | 0/0 | 3942 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0013c0020 | 0/0 | 3942 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 | ||
| a0014c0015 | 0/0 | 3942 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | ATGGC others(3937): Show |
chr17 | 37509807 | 37614418 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8143 | 72 | 9 | 9 | 46 | 0 | 8 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0002 | 0/0 | 8143 | 3 | 0 | 2 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0003 | 0/0 | 8141 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8136): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0004 | 0/0 | 8144 | 3 | 0 | 0 | 3 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0005 | 0/0 | 8143 | 3 | 3 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0008 | 0/0 | 8143 | 5 | 5 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0010 | 0/0 | 8143 | 5 | 5 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0011 | 0/0 | 8143 | 6 | 6 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0012 | 0/0 | 8143 | 5 | 0 | 0 | 5 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0013 | 0/0 | 8144 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0015 | 0/0 | 8142 | 2 | 0 | 0 | 2 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8137): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0017 | 0/0 | 8144 | 3 | 3 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0021 | 0/0 | 8143 | 2 | 0 | 0 | 0 | 0 | 2 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0022 | 0/0 | 8143 | 2 | 0 | 0 | 0 | 2 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0028 | 0/0 | 8143 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0031 | 0/0 | 8142 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8137): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0035 | 0/0 | 8143 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0036 | 0/0 | 8144 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0037 | 0/0 | 8143 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0038 | 0/0 | 8143 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0039 | 0/0 | 8142 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8137): Show |
chr17 | 37509807 | 37614418 |
| a0001c0001t0040 | 0/0 | 8143 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0003t0001 | 0/0 | 8143 | 13 | 0 | 1 | 11 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0003t0002 | 0/0 | 8143 | 3 | 0 | 2 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0003t0003 | 0/0 | 8141 | 32 | 2 | 11 | 11 | 2 | 6 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8136): Show |
chr17 | 37509807 | 37614418 |
| a0001c0003t0006 | 0/0 | 8143 | 3 | 0 | 0 | 3 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0003t0007 | 0/0 | 8142 | 8 | 1 | 6 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8137): Show |
chr17 | 37509807 | 37614418 |
| a0001c0003t0030 | 0/0 | 8144 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0001c0003t0032 | 0/0 | 8142 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8137): Show |
chr17 | 37509807 | 37614418 |
| a0001c0003t0034 | 0/0 | 8144 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0001c0003t0041 | 0/0 | 8143 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0005t0005 | 0/0 | 8143 | 9 | 9 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0005t0008 | 0/0 | 8143 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0005t0009 | 0/0 | 8143 | 4 | 4 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0005t0029 | 0/0 | 8142 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8137): Show |
chr17 | 37509807 | 37614418 |
| a0001c0006t0001 | 0/0 | 8143 | 2 | 2 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0001c0006t0013 | 0/0 | 8144 | 4 | 4 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0001c0016t0006 | 0/0 | 8143 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0002c0002t0001 | 0/0 | 8143 | 3 | 0 | 0 | 2 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0002c0002t0002 | 0/0 | 8143 | 55 | 7 | 18 | 22 | 2 | 6 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0002c0002t0004 | 0/0 | 8144 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0002c0002t0005 | 0/0 | 8143 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0002c0002t0006 | 0/0 | 8143 | 8 | 0 | 0 | 8 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0002c0002t0008 | 0/0 | 8143 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0002c0002t0014 | 0/0 | 8143 | 4 | 0 | 1 | 0 | 2 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0002c0002t0016 | 0/0 | 8142 | 3 | 0 | 1 | 1 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8137): Show |
chr17 | 37509807 | 37614418 |
| a0002c0002t0024 | 0/0 | 8143 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0002c0002t0033 | 0/0 | 8142 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8137): Show |
chr17 | 37509807 | 37614418 |
| a0002c0011t0007 | 0/0 | 8142 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8137): Show |
chr17 | 37509807 | 37614418 |
| a0002c0011t0015 | 0/0 | 8142 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8137): Show |
chr17 | 37509807 | 37614418 |
| a0003c0004t0001 | 0/0 | 8143 | 4 | 0 | 0 | 4 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0003c0004t0002 | 0/0 | 8143 | 9 | 0 | 6 | 2 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0003c0004t0003 | 0/0 | 8141 | 3 | 0 | 0 | 0 | 1 | 2 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8136): Show |
chr17 | 37509807 | 37614418 |
| a0003c0004t0004 | 0/1 | 8144 | 21 | 3 | 3 | 10 | 3 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0003c0004t0007 | 0/0 | 8142 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8137): Show |
chr17 | 37509807 | 37614418 |
| a0003c0004t0009 | 0/0 | 8143 | 2 | 2 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0003c0004t0010 | 0/0 | 8143 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0003c0004t0015 | 0/0 | 8142 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8137): Show |
chr17 | 37509807 | 37614418 |
| a0003c0004t0018 | 0/0 | 8144 | 2 | 0 | 0 | 0 | 0 | 2 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0003c0004t0025 | 0/0 | 8144 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0003c0004t0026 | 0/0 | 8143 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0003c0010t0002 | 0/0 | 8143 | 2 | 0 | 2 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0003c0013t0009 | 0/0 | 8143 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0004c0008t0020 | 0/0 | 8144 | 2 | 1 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0005c0007t0019 | 0/0 | 8142 | 2 | 2 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8137): Show |
chr17 | 37509807 | 37614418 |
| a0006c0009t0003 | 0/0 | 8141 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8136): Show |
chr17 | 37509807 | 37614418 |
| a0006c0009t0004 | 0/0 | 8144 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0007c0017t0002 | 0/0 | 8143 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0008c0021t0002 | 0/0 | 8143 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0009c0012t0004 | 0/0 | 8144 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8139): Show |
chr17 | 37509807 | 37614418 |
| a0010c0014t0023 | 0/0 | 8143 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0011c0018t0003 | 0/0 | 8141 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8136): Show |
chr17 | 37509807 | 37614418 |
| a0012c0019t0002 | 0/0 | 8143 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0013c0020t0027 | 0/0 | 8143 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| a0014c0015t0001 | 0/0 | 8143 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | GTGTT others(8138): Show |
chr17 | 37509807 | 37614418 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0008g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0010g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0010g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0011g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0011g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0011g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0011g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0011g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0012g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0012g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0012g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0012g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0012g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0013g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0015g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0015g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0017g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0017g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0017g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0021g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0021g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0022g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0022g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0028g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0031g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0035g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0036g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0037g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0038g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0039g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0001t0040g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0006g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0007g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0007g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0007g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0007g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0007g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0007g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0030g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0032g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0034g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0003t0041g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0009g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0009g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0009g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0005t0029g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0006t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0006t0013g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0006t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0006t0013g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0006t0013g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0001c0016t0006g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0006g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0014g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0014g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0014g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0014g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0016g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0016g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0016g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0024g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0002t0033g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0011t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0002c0011t0015g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0299 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0004g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0009g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0010g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0015g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0018g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0018g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0025g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0004t0026g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0010t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0010t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0003c0013t0009g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0004c0008t0020g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0004c0008t0020g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0005c0007t0019g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0005c0007t0019g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0006c0009t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0006c0009t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0007c0017t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0008c0021t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0009c0012t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0010c0014t0023g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0011c0018t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0012c0019t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0013c0020t0027g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| a0014c0015t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0003 | g0158 | EUR | GBR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0227 | EUR | GBR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00140 | hp1 | a0003 | c0004 | t0004 | g0297 | EUR | GBR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0149 | EUR | GBR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00323 | hp1 | a0001 | c0003 | t0007 | g0143 | EUR | FIN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00323 | hp2 | a0003 | c0004 | t0004 | g0313 | EUR | FIN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0330 | EAS | CHS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0218 | EAS | CHS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00558 | hp1 | a0003 | c0004 | t0004 | g0300 | EAS | CHS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00609 | hp1 | a0003 | c0004 | t0015 | g0288 | EAS | CHS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00609 | hp2 | a0001 | c0001 | t0035 | g0104 | EAS | CHS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00621 | hp1 | a0003 | c0004 | t0004 | g0285 | EAS | CHS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00621 | hp2 | a0001 | c0003 | t0001 | g0179 | EAS | CHS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00639 | hp1 | a0007 | c0017 | t0002 | g0295 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0223 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00642 | hp1 | a0008 | c0021 | t0002 | g0224 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00642 | hp2 | a0001 | c0003 | t0003 | g0152 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0165 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00733 | hp2 | a0001 | c0003 | t0003 | g0147 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00738 | hp1 | a0003 | c0004 | t0002 | g0124 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00741 | hp1 | a0001 | c0003 | t0007 | g0174 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG00741 | hp2 | a0003 | c0010 | t0002 | g0284 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0200 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0199 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01074 | hp2 | a0001 | c0003 | t0003 | g0001 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0166 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01081 | hp2 | a0003 | c0004 | t0004 | g0294 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01099 | hp1 | a0001 | c0003 | t0003 | g0320 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0332 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01106 | hp1 | a0001 | c0003 | t0007 | g0185 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01106 | hp2 | a0003 | c0010 | t0002 | g0120 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01109 | hp1 | a0003 | c0013 | t0009 | g0305 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01167 | hp1 | a0002 | c0002 | t0016 | g0193 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01167 | hp2 | a0001 | c0003 | t0007 | g0188 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0195 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01175 | hp1 | a0001 | c0003 | t0003 | g0184 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01175 | hp2 | a0003 | c0004 | t0004 | g0310 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01192 | hp1 | a0009 | c0012 | t0004 | g0177 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0327 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0335 | AMR | PUR | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0151 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0333 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01256 | hp1 | a0001 | c0003 | t0003 | g0161 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01256 | hp2 | a0002 | c0002 | t0014 | g0252 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0236 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01257 | hp2 | a0001 | c0003 | t0007 | g0171 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01258 | hp1 | a0001 | c0003 | t0007 | g0170 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01258 | hp2 | a0001 | c0003 | t0003 | g0150 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01261 | hp1 | a0003 | c0004 | t0002 | g0314 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01261 | hp2 | a0001 | c0003 | t0003 | g0007 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0225 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01346 | hp2 | a0001 | c0003 | t0007 | g0172 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01358 | hp1 | a0003 | c0004 | t0002 | g0126 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01358 | hp2 | a0004 | c0008 | t0020 | g0258 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01433 | hp1 | a0003 | c0004 | t0004 | g0302 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0186 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0226 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01515 | hp1 | a0001 | c0001 | t0022 | g0009 | EUR | IBS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0331 | EUR | IBS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01517 | hp1 | a0001 | c0001 | t0022 | g0264 | EUR | IBS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01517 | hp2 | a0001 | c0003 | t0003 | g0140 | EUR | IBS | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0018 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0253 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01891 | hp1 | a0001 | c0003 | t0041 | g0176 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0118 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0245 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01952 | hp1 | a0001 | c0003 | t0003 | g0163 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0239 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0237 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01981 | hp2 | a0001 | c0003 | t0003 | g0146 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0228 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02004 | hp1 | a0003 | c0004 | t0002 | g0122 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02027 | hp1 | a0001 | c0003 | t0003 | g0183 | EAS | KHV | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02040 | hp2 | a0002 | c0002 | t0006 | g0034 | EAS | KHV | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0315 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02055 | hp2 | a0001 | c0005 | t0005 | g0110 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02080 | hp2 | a0002 | c0002 | t0006 | g0244 | EAS | KHV | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | KHV | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02132 | hp2 | a0001 | c0003 | t0006 | g0153 | EAS | KHV | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02145 | hp2 | a0001 | c0006 | t0013 | g0017 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02155 | hp1 | a0003 | c0004 | t0004 | g0267 | EAS | CDX | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02257 | hp1 | a0001 | c0001 | t0017 | g0028 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02257 | hp2 | a0001 | c0003 | t0003 | g0180 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02258 | hp1 | a0003 | c0004 | t0004 | g0306 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0191 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02273 | hp1 | a0003 | c0004 | t0002 | g0125 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0240 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02300 | hp1 | a0001 | c0003 | t0001 | g0135 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0316 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02615 | hp1 | a0002 | c0002 | t0005 | g0203 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02615 | hp2 | a0001 | c0006 | t0013 | g0020 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0048 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0342 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02630 | hp1 | a0003 | c0004 | t0004 | g0301 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02630 | hp2 | a0001 | c0001 | t0028 | g0116 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02647 | hp2 | a0001 | c0005 | t0005 | g0278 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0233 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02698 | hp2 | a0002 | c0002 | t0016 | g0219 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02717 | hp1 | a0001 | c0006 | t0013 | g0030 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02717 | hp2 | a0001 | c0005 | t0005 | g0279 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02735 | hp1 | a0001 | c0001 | t0039 | g0040 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02735 | hp2 | a0003 | c0004 | t0003 | g0283 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02809 | hp1 | a0001 | c0001 | t0040 | g0033 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02809 | hp2 | a0001 | c0006 | t0013 | g0022 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0254 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02886 | hp2 | a0005 | c0007 | t0019 | g0015 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02895 | hp1 | a0001 | c0006 | t0001 | g0031 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02895 | hp2 | a0001 | c0005 | t0009 | g0265 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02896 | hp1 | a0001 | c0006 | t0001 | g0011 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02896 | hp2 | a0010 | c0014 | t0023 | g0263 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02965 | hp1 | a0001 | c0001 | t0011 | g0341 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02965 | hp2 | a0001 | c0005 | t0009 | g0005 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0324 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02976 | hp1 | a0002 | c0011 | t0015 | g0167 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02976 | hp2 | a0001 | c0005 | t0029 | g0276 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0026 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0343 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03098 | hp1 | a0001 | c0003 | t0007 | g0169 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03130 | hp1 | a0001 | c0001 | t0031 | g0021 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03130 | hp2 | a0001 | c0005 | t0005 | g0273 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03139 | hp1 | a0001 | c0001 | t0013 | g0023 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03139 | hp2 | a0001 | c0005 | t0005 | g0109 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03195 | hp1 | a0001 | c0005 | t0005 | g0280 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03195 | hp2 | a0001 | c0001 | t0017 | g0025 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03209 | hp1 | a0001 | c0005 | t0009 | g0281 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03209 | hp2 | a0001 | c0005 | t0008 | g0266 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0012 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03453 | hp2 | a0003 | c0004 | t0004 | g0307 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03486 | hp1 | a0001 | c0005 | t0009 | g0005 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03486 | hp2 | a0001 | c0001 | t0011 | g0117 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03490 | hp1 | a0001 | c0001 | t0021 | g0082 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03490 | hp2 | a0001 | c0003 | t0003 | g0144 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0326 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03491 | hp2 | a0003 | c0004 | t0004 | g0287 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0192 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03492 | hp2 | a0001 | c0003 | t0003 | g0145 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03516 | hp1 | a0004 | c0008 | t0020 | g0257 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03516 | hp2 | a0001 | c0001 | t0010 | g0190 | AFR | ESN | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03540 | hp2 | a0003 | c0004 | t0009 | g0309 | AFR | GWD | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03579 | hp1 | a0001 | c0001 | t0037 | g0057 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03654 | hp1 | a0002 | c0002 | t0014 | g0251 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03654 | hp2 | a0001 | c0003 | t0003 | g0128 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03669 | hp1 | a0001 | c0003 | t0003 | g0155 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03669 | hp2 | a0003 | c0004 | t0018 | g0322 | SAS | PJL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0242 | SAS | BEB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03831 | hp2 | a0003 | c0004 | t0003 | g0123 | SAS | BEB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03834 | hp1 | a0001 | c0003 | t0003 | g0159 | SAS | BEB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03927 | hp1 | a0006 | c0009 | t0003 | g0142 | SAS | BEB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03942 | hp1 | a0003 | c0004 | t0018 | g0321 | SAS | BEB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03942 | hp2 | a0006 | c0009 | t0004 | g0141 | SAS | BEB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0205 | SAS | STU | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG04115 | hp2 | a0001 | c0001 | t0021 | g0039 | SAS | STU | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG04199 | hp2 | a0001 | c0003 | t0003 | g0162 | SAS | STU | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0221 | SAS | STU | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18522 | hp2 | a0001 | c0001 | t0017 | g0019 | AFR | YRI | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18906 | hp1 | a0003 | c0004 | t0009 | g0304 | AFR | YRI | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18906 | hp2 | a0005 | c0007 | t0019 | g0014 | AFR | YRI | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18939 | hp2 | a0003 | c0004 | t0001 | g0338 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18941 | hp2 | a0003 | c0004 | t0004 | g0311 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18943 | hp1 | a0001 | c0016 | t0006 | g0336 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18944 | hp1 | a0003 | c0004 | t0002 | g0293 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18947 | hp1 | a0001 | c0003 | t0003 | g0319 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18947 | hp2 | a0003 | c0004 | t0001 | g0119 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18948 | hp1 | a0002 | c0002 | t0033 | g0006 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18948 | hp2 | a0001 | c0003 | t0032 | g0134 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18949 | hp1 | a0002 | c0002 | t0006 | g0246 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18950 | hp1 | a0001 | c0003 | t0003 | g0260 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18951 | hp1 | a0002 | c0002 | t0016 | g0230 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18952 | hp2 | a0003 | c0004 | t0004 | g0289 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18953 | hp1 | a0001 | c0003 | t0003 | g0181 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18954 | hp1 | a0001 | c0001 | t0015 | g0062 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18956 | hp1 | a0001 | c0003 | t0003 | g0182 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18956 | hp2 | a0001 | c0001 | t0012 | g0076 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0334 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18957 | hp2 | a0001 | c0001 | t0038 | g0072 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18960 | hp1 | a0002 | c0002 | t0006 | g0210 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0164 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18964 | hp2 | a0003 | c0004 | t0004 | g0282 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18967 | hp1 | a0003 | c0004 | t0025 | g0303 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18967 | hp2 | a0001 | c0001 | t0036 | g0081 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18969 | hp1 | a0002 | c0002 | t0006 | g0222 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18972 | hp1 | a0003 | c0004 | t0002 | g0323 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18974 | hp1 | a0002 | c0002 | t0004 | g0235 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18974 | hp2 | a0011 | c0018 | t0003 | g0160 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0132 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18977 | hp1 | a0012 | c0019 | t0002 | g0209 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18978 | hp2 | a0001 | c0003 | t0001 | g0178 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18982 | hp1 | a0002 | c0002 | t0006 | g0247 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18983 | hp1 | a0001 | c0003 | t0034 | g0130 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18985 | hp1 | a0001 | c0003 | t0001 | g0131 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18989 | hp1 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18990 | hp2 | a0001 | c0003 | t0003 | g0156 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0329 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18991 | hp2 | a0001 | c0003 | t0006 | g0325 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18993 | hp1 | a0002 | c0002 | t0024 | g0255 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18993 | hp2 | a0003 | c0004 | t0004 | g0291 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0328 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19000 | hp2 | a0003 | c0004 | t0004 | g0127 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19001 | hp2 | a0001 | c0003 | t0003 | g0157 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19003 | hp1 | a0013 | c0020 | t0027 | g0220 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19003 | hp2 | a0001 | c0001 | t0012 | g0112 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19005 | hp2 | a0002 | c0002 | t0006 | g0198 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19009 | hp2 | a0002 | c0002 | t0006 | g0197 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19011 | hp1 | a0001 | c0001 | t0012 | g0108 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19011 | hp2 | a0001 | c0003 | t0003 | g0001 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19030 | hp1 | a0001 | c0003 | t0030 | g0187 | AFR | LWK | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0189 | AFR | LWK | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19043 | hp1 | a0002 | c0011 | t0007 | g0194 | AFR | LWK | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19043 | hp2 | a0001 | c0005 | t0005 | g0275 | AFR | LWK | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19054 | hp2 | a0003 | c0004 | t0004 | g0290 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19055 | hp1 | a0001 | c0003 | t0003 | g0148 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19055 | hp2 | a0001 | c0001 | t0012 | g0111 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19057 | hp1 | a0003 | c0004 | t0001 | g0337 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19058 | hp1 | a0003 | c0004 | t0026 | g0286 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19062 | hp2 | a0001 | c0003 | t0006 | g0154 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0133 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19074 | hp1 | a0003 | c0004 | t0004 | g0296 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19082 | hp2 | a0001 | c0003 | t0001 | g0317 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19083 | hp1 | a0001 | c0003 | t0001 | g0318 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19083 | hp2 | a0001 | c0003 | t0003 | g0137 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19084 | hp2 | a0003 | c0004 | t0001 | g0339 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19085 | hp2 | a0014 | c0015 | t0001 | g0090 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19087 | hp1 | a0001 | c0001 | t0015 | g0051 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19091 | hp1 | a0001 | c0003 | t0001 | g0129 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19091 | hp2 | a0001 | c0001 | t0012 | g0035 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19240 | hp1 | a0001 | c0005 | t0005 | g0274 | AFR | YRI | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA19240 | hp2 | a0003 | c0004 | t0010 | g0308 | AFR | YRI | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0261 | AFR | ASW | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ASW | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA20752 | hp1 | a0002 | c0002 | t0014 | g0250 | EUR | TSI | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA20752 | hp2 | a0003 | c0004 | t0004 | g0312 | EUR | TSI | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA20805 | hp1 | a0003 | c0004 | t0003 | g0292 | EUR | TSI | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA20805 | hp2 | a0002 | c0002 | t0014 | g0212 | EUR | TSI | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0202 | SAS | GIH | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA20905 | hp2 | a0003 | c0004 | t0002 | g0298 | SAS | GIH | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01123 | hp1 | a0003 | c0004 | t0002 | g0175 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG01123 | hp2 | a0001 | c0003 | t0003 | g0173 | AMR | CLM | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02109 | hp1 | a0001 | c0003 | t0003 | g0139 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0024 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0115 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0340 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG02559 | hp2 | a0002 | c0002 | t0008 | g0196 | AFR | ACB | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0204 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| HG03471 | hp2 | a0001 | c0005 | t0005 | g0277 | AFR | MSL | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0238 | AFR | USA | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| NA20300 | hp2 | a0003 | c0004 | t0007 | g0121 | AFR | USA | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| homoSapiens | chm13v2 | a0003 | c0004 | t0004 | g0299 | REF | REF | SYNRG_chr17_37509807_37614418 | SYNRG | chr17 | 37509807 | 37614418 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:37542214 | T | G | 1 | a0005 | 2 | HG02886.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.2960A>C | p.Asp987Ala | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/22 | 3023/8141 | 2960/3945 | 987/1314 | chr17 | 37542214 | |||
| chr17:37542284 | G | A | 1 | a0004 | 2 | HG01358.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.2890C>T | p.Leu964Phe | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/22 | 2953/8141 | 2890/3945 | 964/1314 | chr17 | 37542284 | |||
| chr17:37553258 | C | A | 1 | a0012 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.2465G>T | p.Ser822Ile | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/22 | 2528/8141 | 2465/3945 | 822/1314 | chr17 | 37553258 | |||
| chr17:37553487 | C | T | 1 | a0007 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.2236G>A | p.Asp746Asn | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/22 | 2299/8141 | 2236/3945 | 746/1314 | chr17 | 37553487 | |||
| chr17:37553565 | T | A | 1 | a0013 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.2158A>T | p.Ser720Cys | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/22 | 2221/8141 | 2158/3945 | 720/1314 | chr17 | 37553565 | |||
| chr17:37553694 | C | T | 1 | a0014 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.2029G>A | p.Gly677Arg | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/22 | 2092/8141 | 2029/3945 | 677/1314 | chr17 | 37553694 | |||
| chr17:37553816 | A | G | 1 | a0010 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1907T>C | p.Val636Ala | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/22 | 1970/8141 | 1907/3945 | 636/1314 | chr17 | 37553816 | |||
| chr17:37568860 | T | C | 1 | a0006 | 2 | HG03927.hp1 HG03942.hp2 |
missense_variant | MODERATE | c.1412A>G | p.Asp471Gly | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/22 | 1475/8141 | 1412/3945 | 471/1314 | chr17 | 37568860 | |||
| chr17:37577479 | T | C | 1 | a0008 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.724A>G | p.Met242Val | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 7/22 | 787/8141 | 724/3945 | 242/1314 | chr17 | 37577479 | |||
| chr17:37577539 | T | C | 2 | a0003 a0007 |
49 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(46): Show |
missense_variant | MODERATE | c.664A>G | p.Thr222Ala | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 7/22 | 727/8141 | 664/3945 | 222/1314 | chr17 | 37577539 | |||
| chr17:37584693 | C | T | 1 | a0009 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.544G>A | p.Asp182Asn | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/22 | 607/8141 | 544/3945 | 182/1314 | chr17 | 37584693 | |||
| chr17:37586518 | G | A | 1 | a0011 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.272C>T | p.Ala91Val | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/22 | 335/8141 | 272/3945 | 91/1314 | chr17 | 37586518 | |||
| chr17:37596344 | G | C | 4 | a0002 a0008 a0012 others(1): Show |
83 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
missense_variant&splice_region_variant | MODERATE | c.119C>G | p.Ala40Gly | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/22 | 182/8141 | 119/3945 | 40/1314 | chr17 | 37596344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:37536021 | T | C | 7 | a0001c0006 a0001c0016 a0002c0002 others(4): Show |
90 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
synonymous_variant | LOW | c.3624A>G | p.Val1208Val | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/22 | 3687/8141 | 3624/3945 | 1208/1314 | chr17 | 37536021 | |||
| chr17:37542123 | C | G | 10 | a0001c0001 a0001c0006 a0003c0004 others(7): Show |
182 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(179): Show |
synonymous_variant | LOW | c.3051G>C | p.Pro1017Pro | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/22 | 3114/8141 | 3051/3945 | 1017/1314 | chr17 | 37542123 | |||
| chr17:37542288 | T | G | 1 | a0001c0005 | 15 | HG02055.hp2 HG02647.hp2 HG02717.hp2 others(12): Show |
synonymous_variant | LOW | c.2886A>C | p.Pro962Pro | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/22 | 2949/8141 | 2886/3945 | 962/1314 | chr17 | 37542288 | |||
| chr17:37584673 | A | C | 1 | a0003c0013 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.564T>G | p.Thr188Thr | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/22 | 627/8141 | 564/3945 | 188/1314 | chr17 | 37584673 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:37514833 | A | G | 66 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(63): Show |
301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*4107T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 4107 | chr17 | 37514833 | ||||||
| chr17:37515384 | T | G | 5 | a0001c0001t0031 a0001c0003t0007 a0001c0003t0041 others(2): Show |
12 | HG00323.hp1 HG00741.hp1 HG01106.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3556A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 3556 | chr17 | 37515384 | ||||||
| chr17:37515385 | G | C | 1 | a0013c0020t0027 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3555C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 3555 | chr17 | 37515385 | ||||||
| chr17:37515408 | C | CAA | 70 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(67): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*3531_*3532insTT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 3531 | chr17 | 37515408 | ||||||
| chr17:37515526 | T | C | 51 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(48): Show |
210 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*3414A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 3414 | chr17 | 37515526 | ||||||
| chr17:37515584 | G | A | 1 | a0001c0001t0038 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3356C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 3356 | chr17 | 37515584 | ||||||
| chr17:37515655 | C | T | 1 | a0001c0001t0037 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3285G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 3285 | chr17 | 37515655 | ||||||
| chr17:37515730 | G | A | 1 | a0001c0001t0022 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3210C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 3210 | chr17 | 37515730 | ||||||
| chr17:37516299 | C | T | 1 | a0001c0001t0011 | 6 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2641G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 2641 | chr17 | 37516299 | ||||||
| chr17:37516404 | C | T | 1 | a0002c0002t0024 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2536G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 2536 | chr17 | 37516404 | ||||||
| chr17:37516642 | A | G | 2 | a0001c0001t0012 a0002c0002t0033 |
6 | NA18948.hp1 NA18956.hp2 NA19003.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2298T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 2298 | chr17 | 37516642 | ||||||
| chr17:37516661 | C | CT | 14 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0017 others(11): Show |
42 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2278dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 2278 | chr17 | 37516661 | ||||||
| chr17:37516661 | CT | C | 13 | a0001c0001t0015 a0001c0001t0031 a0001c0001t0039 others(10): Show |
24 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2278delA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 2278 | chr17 | 37516661 | ||||||
| chr17:37516711 | C | T | 10 | a0001c0001t0004 a0001c0001t0035 a0001c0003t0034 others(7): Show |
32 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2229G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 2229 | chr17 | 37516711 | ||||||
| chr17:37516828 | T | C | 1 | a0001c0005t0029 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2112A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 2112 | chr17 | 37516828 | ||||||
| chr17:37516920 | G | T | 1 | a0003c0004t0025 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2020C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 2020 | chr17 | 37516920 | ||||||
| chr17:37516994 | C | T | 2 | a0001c0001t0010 a0003c0004t0010 |
6 | HG02258.hp2 HG02970.hp2 HG03453.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1946G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1946 | chr17 | 37516994 | ||||||
| chr17:37517041 | C | T | 14 | a0001c0001t0002 a0001c0003t0002 a0001c0005t0009 others(11): Show |
90 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1899G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1899 | chr17 | 37517041 | ||||||
| chr17:37517069 | C | T | 1 | a0001c0003t0041 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1871G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1871 | chr17 | 37517069 | ||||||
| chr17:37517075 | G | A | 3 | a0001c0001t0021 a0001c0001t0022 a0001c0001t0039 |
5 | HG01515.hp1 HG01517.hp1 HG02735.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1865C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1865 | chr17 | 37517075 | ||||||
| chr17:37517082 | T | C | 1 | a0001c0003t0030 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1858A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1858 | chr17 | 37517082 | ||||||
| chr17:37517139 | G | A | 1 | a0010c0014t0023 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1801C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1801 | chr17 | 37517139 | ||||||
| chr17:37517287 | G | A | 1 | a0001c0001t0031 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1653C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1653 | chr17 | 37517287 | ||||||
| chr17:37517372 | T | C | 1 | a0010c0014t0023 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1568A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1568 | chr17 | 37517372 | ||||||
| chr17:37517531 | C | T | 1 | a0002c0002t0014 | 4 | HG01256.hp2 HG03654.hp1 NA20752.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1409G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1409 | chr17 | 37517531 | ||||||
| chr17:37517559 | T | A | 36 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0010 others(33): Show |
159 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*1381A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1381 | chr17 | 37517559 | ||||||
| chr17:37517613 | A | T | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1327T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1327 | chr17 | 37517613 | ||||||
| chr17:37517614 | G | C | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1326C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1326 | chr17 | 37517614 | ||||||
| chr17:37517615 | A | T | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1325T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1325 | chr17 | 37517615 | ||||||
| chr17:37517616 | G | T | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1324C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1324 | chr17 | 37517616 | ||||||
| chr17:37517617 | G | T | 2 | a0001c0003t0032 a0002c0002t0033 |
2 | NA18948.hp1 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1323C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1323 | chr17 | 37517617 | ||||||
| chr17:37517639 | C | A | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1301G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1301 | chr17 | 37517639 | ||||||
| chr17:37517640 | A | G | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1300T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1300 | chr17 | 37517640 | ||||||
| chr17:37517642 | C | G | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1298G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1298 | chr17 | 37517642 | ||||||
| chr17:37517676 | A | C | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1264T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1264 | chr17 | 37517676 | ||||||
| chr17:37517677 | A | T | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1263T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1263 | chr17 | 37517677 | ||||||
| chr17:37517679 | A | G | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1261T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1261 | chr17 | 37517679 | ||||||
| chr17:37517680 | T | C | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1260A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1260 | chr17 | 37517680 | ||||||
| chr17:37517687 | C | T | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1253G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1253 | chr17 | 37517687 | ||||||
| chr17:37517707 | C | G | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1233G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1233 | chr17 | 37517707 | ||||||
| chr17:37517722 | A | G | 1 | a0001c0003t0032 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1218T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1218 | chr17 | 37517722 | ||||||
| chr17:37517905 | C | G | 2 | a0001c0001t0013 a0001c0006t0013 |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1035G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 1035 | chr17 | 37517905 | ||||||
| chr17:37518185 | T | C | 3 | a0001c0005t0009 a0003c0004t0009 a0003c0013t0009 |
7 | HG01109.hp1 HG02895.hp2 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*755A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 755 | chr17 | 37518185 | ||||||
| chr17:37518210 | C | T | 1 | a0010c0014t0023 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*730G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 730 | chr17 | 37518210 | ||||||
| chr17:37518752 | G | A | 1 | a0001c0001t0040 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 188 | chr17 | 37518752 | ||||||
| chr17:37518790 | G | A | 21 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0015 others(18): Show |
117 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*150C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 150 | chr17 | 37518790 | ||||||
| chr17:37518816 | T | C | 4 | a0001c0001t0013 a0001c0001t0017 a0001c0003t0041 others(1): Show |
9 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*124A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 124 | chr17 | 37518816 | ||||||
| chr17:37518860 | C | T | 1 | a0003c0004t0018 | 2 | HG03669.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*80G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 22/22 | 80 | chr17 | 37518860 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:37519521 | G | C | 2 | a0001c0001t0008g0016 a0001c0001t0008g0018 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3814-450C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 21/21 | chr17 | 37519521 | |||||||
| chr17:37519525 | G | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3814-454C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 21/21 | chr17 | 37519525 | |||||||
| chr17:37519574 | A | C | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3814-503T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 21/21 | chr17 | 37519574 | |||||||
| chr17:37519615 | T | C | 1 | a0001c0001t0013g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3814-544A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 21/21 | chr17 | 37519615 | |||||||
| chr17:37519644 | TA | T | 5 | a0001c0005t0005g0109 a0001c0005t0005g0110 a0001c0005t0005g0277 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3813+534delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 21/21 | chr17 | 37519644 | |||||||
| chr17:37519654 | T | A | 1 | a0002c0002t0002g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3813+525A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 21/21 | chr17 | 37519654 | |||||||
| chr17:37519660 | G | A | 35 | a0001c0001t0004g0334 a0001c0003t0006g0153 a0001c0003t0006g0154 others(32): Show |
35 | HG00140.hp1 HG00323.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.3813+519C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 21/21 | chr17 | 37519660 | |||||||
| chr17:37519867 | T | C | 1 | a0003c0010t0002g0284 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3813+312A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 21/21 | chr17 | 37519867 | |||||||
| chr17:37519882 | G | A | 1 | a0003c0004t0004g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3813+297C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 21/21 | chr17 | 37519882 | |||||||
| chr17:37520314 | C | T | 1 | a0002c0002t0014g0212 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3778-100G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 20/21 | chr17 | 37520314 | |||||||
| chr17:37520724 | C | T | 1 | a0003c0004t0004g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3667-76G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37520724 | |||||||
| chr17:37520765 | C | T | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3667-117G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37520765 | |||||||
| chr17:37520846 | C | G | 11 | a0001c0001t0013g0023 a0001c0001t0017g0019 a0001c0001t0017g0025 others(8): Show |
11 | HG01358.hp2 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3667-198G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37520846 | |||||||
| chr17:37521033 | CT | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
290 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.3667-386delA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521033 | |||||||
| chr17:37521034 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3667-386A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521034 | |||||||
| chr17:37521091 | G | A | 6 | a0001c0001t0010g0012 a0001c0001t0010g0189 a0001c0001t0010g0190 others(3): Show |
6 | HG02258.hp2 HG02970.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.3667-443C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521091 | |||||||
| chr17:37521108 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0059 a0001c0001t0001g0074 |
3 | NA18969.hp2 NA19057.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.3667-460G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521108 | |||||||
| chr17:37521179 | C | T | 7 | a0001c0001t0011g0117 a0001c0001t0011g0118 a0001c0001t0011g0340 others(4): Show |
7 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3667-531G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521179 | |||||||
| chr17:37521180 | G | A | 3 | a0002c0002t0002g0199 a0002c0002t0002g0200 a0002c0002t0002g0221 |
3 | HG01070.hp1 HG01074.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.3667-532C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521180 | |||||||
| chr17:37521182 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3667-534G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521182 | |||||||
| chr17:37521183 | A | C | 1 | a0001c0001t0001g0038 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3667-535T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521183 | |||||||
| chr17:37521184 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3667-536G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521184 | |||||||
| chr17:37521273 | A | G | 100 | a0001c0001t0002g0065 a0001c0001t0002g0080 a0001c0001t0010g0012 others(97): Show |
100 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.3667-625T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521273 | |||||||
| chr17:37521276 | C | T | 1 | a0003c0004t0004g0313 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3667-628G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521276 | |||||||
| chr17:37521334 | T | C | 1 | a0003c0004t0004g0307 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3667-686A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521334 | |||||||
| chr17:37521389 | G | A | 6 | a0001c0001t0011g0117 a0001c0001t0011g0118 a0001c0001t0011g0340 others(3): Show |
6 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.3667-741C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521389 | |||||||
| chr17:37521539 | C | G | 34 | a0001c0001t0004g0334 a0003c0004t0002g0122 a0003c0004t0002g0124 others(31): Show |
34 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.3667-891G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521539 | |||||||
| chr17:37521539 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3667-891G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521539 | |||||||
| chr17:37521754 | T | C | 6 | a0001c0001t0010g0012 a0001c0001t0010g0189 a0001c0001t0010g0190 others(3): Show |
6 | HG02258.hp2 HG02970.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.3667-1106A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521754 | |||||||
| chr17:37521775 | C | A | 1 | a0001c0001t0031g0021 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3667-1127G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521775 | |||||||
| chr17:37521845 | G | C | 3 | a0001c0005t0009g0005 a0001c0005t0009g0265 a0001c0005t0009g0281 |
4 | HG02895.hp2 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3667-1197C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521845 | |||||||
| chr17:37521850 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3667-1202C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37521850 | |||||||
| chr17:37522022 | C | T | 4 | a0001c0001t0002g0268 a0001c0001t0008g0024 a0001c0001t0008g0026 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.3667-1374G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522022 | |||||||
| chr17:37522051 | A | G | 38 | a0001c0001t0004g0334 a0001c0003t0006g0153 a0001c0003t0006g0154 others(35): Show |
38 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.3667-1403T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522051 | |||||||
| chr17:37522060 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3667-1412T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522060 | |||||||
| chr17:37522122 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3667-1474A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522122 | |||||||
| chr17:37522134 | T | TACACAC | 6 | a0001c0001t0001g0269 a0001c0001t0021g0039 a0001c0001t0021g0082 others(3): Show |
6 | HG01515.hp1 HG01517.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.3667-1492_3667-148 others(10): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522134 | |||||||
| chr17:37522134 | T | TACACACA others(1): Show |
8 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0011g0117 others(5): Show |
8 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.3667-1494_3667-148 others(12): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522134 | |||||||
| chr17:37522134 | T | TACACACA others(3): Show |
84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
87 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.3667-1496_3667-148 others(14): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522134 | |||||||
| chr17:37522134 | T | TACACACA others(5): Show |
38 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0046 others(35): Show |
38 | HG00323.hp1 HG00438.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.3667-1498_3667-148 others(16): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522134 | |||||||
| chr17:37522134 | T | TACACACA others(7): Show |
36 | a0001c0001t0004g0334 a0001c0001t0005g0115 a0001c0003t0006g0153 others(33): Show |
36 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.3667-1500_3667-148 others(18): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522134 | |||||||
| chr17:37522134 | T | TACACACA others(9): Show |
6 | a0001c0001t0005g0048 a0001c0003t0007g0169 a0001c0003t0030g0187 others(3): Show |
6 | HG00140.hp1 HG02040.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.3667-1502_3667-148 others(20): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522134 | |||||||
| chr17:37522134 | T | TACACACA others(11): Show |
8 | a0001c0005t0009g0005 a0001c0005t0009g0265 a0001c0005t0009g0281 others(5): Show |
9 | HG01081.hp2 HG01256.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.3667-1504_3667-148 others(22): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522134 | |||||||
| chr17:37522134 | T | TACACACA others(13): Show |
15 | a0001c0001t0002g0080 a0001c0001t0010g0012 a0001c0001t0010g0189 others(12): Show |
15 | HG01070.hp2 HG01109.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.3667-1506_3667-148 others(24): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522134 | |||||||
| chr17:37522134 | T | TACACACA others(15): Show |
44 | a0001c0001t0013g0023 a0001c0001t0017g0019 a0001c0001t0017g0028 others(41): Show |
44 | HG00438.hp2 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.3667-1508_3667-148 others(26): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522134 | |||||||
| chr17:37522134 | T | TACACACA others(17): Show |
41 | a0001c0001t0002g0065 a0001c0001t0017g0025 a0001c0005t0005g0275 others(38): Show |
41 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.3667-1487_3667-148 others(28): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522134 | |||||||
| chr17:37522134 | T | TACACACA others(19): Show |
7 | a0002c0002t0002g0165 a0002c0002t0002g0168 a0002c0002t0002g0199 others(4): Show |
7 | HG00733.hp1 HG01070.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.3667-1487_3667-148 others(30): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522134 | |||||||
| chr17:37522134 | T | TACACACA others(27): Show |
1 | a0002c0002t0001g0249 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3667-1487_3667-148 others(38): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522134 | |||||||
| chr17:37522204 | CTG | C | 35 | a0001c0001t0004g0334 a0001c0005t0008g0266 a0003c0004t0002g0122 others(32): Show |
35 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.3667-1558_3667-155 others(6): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522204 | |||||||
| chr17:37522336 | G | T | 1 | a0001c0003t0003g0146 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3667-1688C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522336 | |||||||
| chr17:37522469 | T | C | 3 | a0001c0001t0001g0027 a0001c0006t0001g0011 a0001c0006t0001g0031 |
3 | HG02647.hp1 HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.3667-1821A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522469 | |||||||
| chr17:37522571 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3667-1923T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522571 | |||||||
| chr17:37522637 | CT | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
216 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(213): Show |
intron_variant | MODIFIER | c.3667-1990delA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522637 | |||||||
| chr17:37522637 | CTT | C | 52 | a0001c0001t0001g0052 a0001c0001t0004g0334 a0001c0001t0031g0021 others(49): Show |
53 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.3667-1991_3667-199 others(6): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522637 | |||||||
| chr17:37522701 | C | T | 6 | a0001c0001t0011g0117 a0001c0001t0011g0118 a0001c0001t0011g0340 others(3): Show |
6 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.3667-2053G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522701 | |||||||
| chr17:37522752 | T | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
119 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.3667-2104A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522752 | |||||||
| chr17:37522830 | G | A | 1 | a0003c0010t0002g0120 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3667-2182C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522830 | |||||||
| chr17:37522875 | G | A | 1 | a0001c0001t0004g0334 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3667-2227C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522875 | |||||||
| chr17:37522959 | T | C | 5 | a0002c0002t0002g0225 a0002c0002t0002g0228 a0002c0002t0002g0239 others(2): Show |
5 | HG01255.hp2 HG01346.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.3667-2311A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522959 | |||||||
| chr17:37522989 | T | C | 2 | a0001c0003t0007g0172 a0001c0003t0007g0188 |
2 | HG01167.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.3667-2341A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37522989 | |||||||
| chr17:37523218 | C | T | 1 | a0001c0001t0037g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3667-2570G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37523218 | |||||||
| chr17:37523244 | C | T | 3 | a0002c0002t0002g0010 a0002c0002t0002g0204 a0002c0002t0002g0253 |
3 | HG01884.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3667-2596G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37523244 | |||||||
| chr17:37523483 | G | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
257 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(254): Show |
intron_variant | MODIFIER | c.3667-2835C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37523483 | |||||||
| chr17:37523656 | T | A | 1 | a0002c0002t0002g0335 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3667-3008A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37523656 | |||||||
| chr17:37523683 | G | C | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3667-3035C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37523683 | |||||||
| chr17:37523752 | G | T | 2 | a0001c0003t0007g0172 a0001c0003t0007g0188 |
2 | HG01167.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.3667-3104C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37523752 | |||||||
| chr17:37523800 | A | G | 4 | a0001c0005t0005g0273 a0001c0005t0005g0274 a0001c0005t0005g0278 others(1): Show |
4 | HG02647.hp2 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3667-3152T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37523800 | |||||||
| chr17:37523999 | C | T | 1 | a0007c0017t0002g0295 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3667-3351G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37523999 | |||||||
| chr17:37524069 | G | A | 1 | a0001c0003t0001g0316 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3667-3421C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37524069 | |||||||
| chr17:37524162 | A | T | 10 | a0001c0001t0031g0021 a0001c0003t0007g0143 a0001c0003t0007g0170 others(7): Show |
10 | HG00323.hp1 HG00741.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.3667-3514T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37524162 | |||||||
| chr17:37524352 | A | G | 2 | a0002c0002t0002g0165 a0002c0002t0002g0327 |
2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.3667-3704T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37524352 | |||||||
| chr17:37524480 | G | A | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
294 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.3667-3832C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37524480 | |||||||
| chr17:37524614 | T | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
294 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.3667-3966A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37524614 | |||||||
| chr17:37524628 | T | A | 1 | a0001c0005t0008g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3667-3980A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37524628 | |||||||
| chr17:37524872 | C | T | 88 | a0001c0005t0005g0109 a0001c0005t0005g0110 a0001c0005t0005g0273 others(85): Show |
88 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.3667-4224G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37524872 | |||||||
| chr17:37525147 | T | G | 1 | a0001c0003t0003g0147 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3667-4499A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525147 | |||||||
| chr17:37525166 | T | C | 99 | a0001c0001t0002g0065 a0001c0001t0005g0029 a0001c0001t0017g0019 others(96): Show |
99 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.3667-4518A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525166 | |||||||
| chr17:37525275 | A | T | 1 | a0001c0003t0007g0188 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3667-4627T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525275 | |||||||
| chr17:37525546 | G | A | 9 | a0002c0002t0002g0223 a0002c0002t0002g0225 a0002c0002t0002g0228 others(6): Show |
9 | HG00639.hp2 HG00642.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.3667-4898C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525546 | |||||||
| chr17:37525648 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3667-5000G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525648 | |||||||
| chr17:37525693 | A | C | 2 | a0002c0002t0006g0246 a0003c0004t0004g0267 |
2 | HG02155.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.3667-5045T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525693 | |||||||
| chr17:37525695 | C | T | 1 | a0002c0002t0033g0006 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3667-5047G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525695 | |||||||
| chr17:37525702 | T | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0103 others(1): Show |
5 | HG00738.hp2 HG01496.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.3667-5054A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525702 | |||||||
| chr17:37525716 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0095 |
2 | HG00544.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.3667-5068A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525716 | |||||||
| chr17:37525738 | C | T | 5 | a0001c0001t0013g0023 a0001c0006t0013g0017 a0001c0006t0013g0020 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3667-5090G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525738 | |||||||
| chr17:37525742 | C | T | 5 | a0001c0001t0013g0023 a0001c0006t0013g0017 a0001c0006t0013g0020 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3667-5094G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525742 | |||||||
| chr17:37525749 | C | CCT | 5 | a0001c0001t0013g0023 a0001c0006t0013g0017 a0001c0006t0013g0020 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3667-5102_3667-510 others(6): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525749 | |||||||
| chr17:37525758 | G | A | 5 | a0001c0001t0013g0023 a0001c0006t0013g0017 a0001c0006t0013g0020 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3667-5110C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525758 | |||||||
| chr17:37525759 | C | A | 5 | a0001c0001t0013g0023 a0001c0006t0013g0017 a0001c0006t0013g0020 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3667-5111G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525759 | |||||||
| chr17:37525760 | T | G | 5 | a0001c0001t0013g0023 a0001c0006t0013g0017 a0001c0006t0013g0020 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3667-5112A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525760 | |||||||
| chr17:37525763 | G | A | 5 | a0001c0001t0013g0023 a0001c0006t0013g0017 a0001c0006t0013g0020 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3667-5115C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525763 | |||||||
| chr17:37525766 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02165.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3667-5118C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525766 | |||||||
| chr17:37525768 | C | T | 4 | a0001c0001t0005g0029 a0001c0001t0017g0019 a0001c0001t0017g0025 others(1): Show |
4 | HG02257.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3667-5120G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525768 | |||||||
| chr17:37525770 | A | G | 9 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0059 others(6): Show |
9 | NA18939.hp1 NA18950.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.3667-5122T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525770 | |||||||
| chr17:37525771 | G | T | 8 | a0001c0001t0001g0042 a0001c0003t0002g0149 a0001c0003t0002g0151 others(5): Show |
8 | HG00140.hp2 HG01123.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.3667-5123C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525771 | |||||||
| chr17:37525776 | G | A | 31 | a0001c0001t0004g0334 a0001c0003t0001g0131 a0001c0003t0001g0179 others(28): Show |
31 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.3667-5128C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525776 | |||||||
| chr17:37525794 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3667-5146G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525794 | |||||||
| chr17:37525795 | G | A | 1 | a0001c0003t0003g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3667-5147C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525795 | |||||||
| chr17:37525804 | A | C | 8 | a0001c0001t0008g0315 a0001c0001t0011g0117 a0001c0001t0011g0118 others(5): Show |
8 | HG01358.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3667-5156T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525804 | |||||||
| chr17:37525823 | A | G | 96 | a0001c0001t0002g0065 a0001c0001t0005g0029 a0001c0001t0017g0019 others(93): Show |
96 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.3667-5175T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525823 | |||||||
| chr17:37525826 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
114 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.3667-5178A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525826 | |||||||
| chr17:37525827 | G | A | 1 | a0001c0003t0034g0130 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3667-5179C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525827 | |||||||
| chr17:37525836 | C | T | 6 | a0001c0001t0010g0012 a0001c0001t0010g0189 a0001c0001t0010g0190 others(3): Show |
6 | HG02258.hp2 HG02970.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.3667-5188G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525836 | |||||||
| chr17:37525837 | T | A | 6 | a0001c0001t0010g0012 a0001c0001t0010g0189 a0001c0001t0010g0190 others(3): Show |
6 | HG02258.hp2 HG02970.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.3667-5189A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525837 | |||||||
| chr17:37525849 | C | T | 96 | a0001c0001t0002g0065 a0001c0001t0005g0029 a0001c0001t0017g0019 others(93): Show |
96 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.3667-5201G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525849 | |||||||
| chr17:37525907 | A | T | 1 | a0001c0003t0003g0144 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3667-5259T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525907 | |||||||
| chr17:37525922 | C | T | 1 | a0001c0003t0030g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3667-5274G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525922 | |||||||
| chr17:37525960 | C | T | 1 | a0001c0005t0005g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3667-5312G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525960 | |||||||
| chr17:37525986 | G | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
237 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(234): Show |
intron_variant | MODIFIER | c.3667-5338C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525986 | |||||||
| chr17:37525994 | G | A | 1 | a0001c0005t0008g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3667-5346C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37525994 | |||||||
| chr17:37526001 | C | T | 3 | a0001c0001t0002g0268 a0001c0001t0008g0024 a0001c0001t0008g0026 |
3 | HG01243.hp1 HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3667-5353G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37526001 | |||||||
| chr17:37526086 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3667-5438A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37526086 | |||||||
| chr17:37526106 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3667-5458G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37526106 | |||||||
| chr17:37526214 | C | T | 1 | a0001c0003t0003g0156 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3667-5566G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37526214 | |||||||
| chr17:37526466 | T | C | 1 | a0009c0012t0004g0177 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3667-5818A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37526466 | |||||||
| chr17:37526568 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3667-5920T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37526568 | |||||||
| chr17:37526725 | C | T | 5 | a0001c0001t0013g0023 a0001c0006t0013g0017 a0001c0006t0013g0020 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3667-6077G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37526725 | |||||||
| chr17:37527267 | TTC | T | 4 | a0001c0001t0005g0048 a0001c0001t0005g0115 a0001c0001t0028g0116 others(1): Show |
4 | HG02486.hp1 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3667-6621_3667-662 others(6): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37527267 | |||||||
| chr17:37527289 | C | T | 93 | a0001c0001t0002g0065 a0001c0001t0005g0029 a0001c0005t0005g0109 others(90): Show |
93 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.3667-6641G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37527289 | |||||||
| chr17:37527567 | A | G | 2 | a0001c0003t0003g0183 a0011c0018t0003g0160 |
2 | HG02027.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.3667-6919T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37527567 | |||||||
| chr17:37528527 | C | T | 2 | a0001c0001t0008g0016 a0001c0001t0008g0018 |
2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3666+7452G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37528527 | |||||||
| chr17:37528634 | C | T | 1 | a0001c0001t0028g0116 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3666+7345G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37528634 | |||||||
| chr17:37528696 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3666+7283A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37528696 | |||||||
| chr17:37528877 | C | T | 1 | a0003c0004t0004g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3666+7102G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37528877 | |||||||
| chr17:37528885 | A | G | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3666+7094T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37528885 | |||||||
| chr17:37529214 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3666+6765G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529214 | |||||||
| chr17:37529268 | T | A | 1 | a0002c0002t0001g0233 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3666+6711A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529268 | |||||||
| chr17:37529268 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3666+6711A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529268 | |||||||
| chr17:37529428 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
121 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.3666+6551C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529428 | |||||||
| chr17:37529507 | C | T | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3666+6472G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529507 | |||||||
| chr17:37529538 | C | CA | 78 | a0001c0003t0030g0187 a0001c0006t0013g0017 a0001c0016t0006g0336 others(75): Show |
78 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.3666+6440dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529538 | |||||||
| chr17:37529538 | C | CAA | 6 | a0001c0001t0001g0013 a0001c0001t0008g0315 a0001c0003t0007g0169 others(3): Show |
6 | HG01070.hp1 HG02055.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.3666+6439_3666+644 others(6): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529538 | |||||||
| chr17:37529538 | CA | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.3666+6440delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529538 | |||||||
| chr17:37529538 | CAAAAAAA | C | 37 | a0001c0001t0004g0334 a0003c0004t0002g0122 a0003c0004t0002g0124 others(34): Show |
37 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.3666+6434_3666+644 others(11): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529538 | |||||||
| chr17:37529551 | A | G | 1 | a0002c0002t0002g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3666+6428T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529551 | |||||||
| chr17:37529689 | A | C | 1 | a0002c0002t0002g0261 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3666+6290T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529689 | |||||||
| chr17:37529714 | A | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0070 a0001c0001t0001g0270 |
3 | HG02145.hp1 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3666+6265T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529714 | |||||||
| chr17:37529811 | G | C | 1 | a0001c0005t0008g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3666+6168C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529811 | |||||||
| chr17:37529886 | T | C | 1 | a0003c0004t0004g0307 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3666+6093A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37529886 | |||||||
| chr17:37530195 | T | C | 43 | a0001c0001t0001g0013 a0001c0001t0004g0334 a0003c0004t0002g0122 others(40): Show |
43 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.3666+5784A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37530195 | |||||||
| chr17:37530457 | C | T | 1 | a0002c0011t0015g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3666+5522G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37530457 | |||||||
| chr17:37530862 | T | C | 18 | a0001c0001t0010g0012 a0001c0001t0010g0189 a0001c0001t0010g0190 others(15): Show |
18 | HG00323.hp1 HG00741.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.3666+5117A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37530862 | |||||||
| chr17:37530907 | C | T | 2 | a0001c0003t0007g0169 a0001c0003t0030g0187 |
2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3666+5072G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37530907 | |||||||
| chr17:37530908 | G | A | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3666+5071C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37530908 | |||||||
| chr17:37531181 | C | T | 1 | a0002c0002t0002g0241 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.3666+4798G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37531181 | |||||||
| chr17:37531234 | A | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
115 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.3666+4745T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37531234 | |||||||
| chr17:37531241 | G | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
229 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.3666+4738C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37531241 | |||||||
| chr17:37531282 | C | G | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
288 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.3666+4697G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37531282 | |||||||
| chr17:37531442 | A | G | 109 | a0001c0001t0008g0315 a0001c0001t0011g0117 a0001c0001t0011g0118 others(106): Show |
109 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.3666+4537T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37531442 | |||||||
| chr17:37531530 | C | A | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3666+4449G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37531530 | |||||||
| chr17:37531784 | G | GA | 7 | a0001c0001t0012g0112 a0001c0001t0036g0081 a0001c0006t0001g0011 others(4): Show |
7 | HG02895.hp1 HG02896.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.3666+4194dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37531784 | |||||||
| chr17:37531784 | GA | G | 8 | a0001c0001t0005g0115 a0001c0001t0012g0035 a0001c0003t0041g0176 others(5): Show |
8 | HG01257.hp1 HG01891.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.3666+4194delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37531784 | |||||||
| chr17:37531851 | T | G | 84 | a0001c0016t0006g0336 a0002c0002t0001g0201 a0002c0002t0001g0233 others(81): Show |
84 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.3666+4128A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37531851 | |||||||
| chr17:37531913 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3666+4066C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37531913 | |||||||
| chr17:37531926 | C | G | 86 | a0001c0006t0001g0011 a0001c0006t0001g0031 a0001c0016t0006g0336 others(83): Show |
86 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.3666+4053G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37531926 | |||||||
| chr17:37532297 | T | C | 84 | a0001c0016t0006g0336 a0002c0002t0001g0201 a0002c0002t0001g0233 others(81): Show |
84 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.3666+3682A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37532297 | |||||||
| chr17:37532399 | G | A | 13 | a0001c0003t0007g0143 a0001c0003t0007g0169 a0001c0003t0007g0170 others(10): Show |
13 | HG00323.hp1 HG00741.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.3666+3580C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37532399 | |||||||
| chr17:37532533 | C | T | 86 | a0001c0006t0001g0011 a0001c0006t0001g0031 a0001c0016t0006g0336 others(83): Show |
86 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.3666+3446G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37532533 | |||||||
| chr17:37532534 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3666+3445C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37532534 | |||||||
| chr17:37532537 | G | A | 1 | a0001c0003t0002g0186 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3666+3442C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37532537 | |||||||
| chr17:37532605 | G | A | 1 | a0001c0005t0009g0005 | 2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3666+3374C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37532605 | |||||||
| chr17:37532613 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG00558.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.3666+3366G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37532613 | |||||||
| chr17:37532671 | C | CA | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
138 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.3666+3307dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37532671 | |||||||
| chr17:37532671 | C | CAA | 75 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0075 others(72): Show |
75 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.3666+3306_3666+330 others(6): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37532671 | |||||||
| chr17:37532671 | C | CAAA | 8 | a0002c0002t0002g0205 a0002c0002t0002g0206 a0002c0002t0002g0218 others(5): Show |
8 | HG00544.hp2 HG01106.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.3666+3305_3666+330 others(7): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37532671 | |||||||
| chr17:37532671 | CA | C | 21 | a0001c0001t0008g0315 a0001c0001t0011g0117 a0001c0001t0011g0118 others(18): Show |
21 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.3666+3307delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37532671 | |||||||
| chr17:37532996 | A | G | 5 | a0001c0001t0001g0027 a0001c0001t0005g0029 a0001c0001t0008g0016 others(2): Show |
5 | HG01884.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3666+2983T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37532996 | |||||||
| chr17:37533086 | C | G | 2 | a0001c0006t0001g0011 a0001c0006t0001g0031 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.3666+2893G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533086 | |||||||
| chr17:37533100 | T | C | 1 | a0009c0012t0004g0177 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3666+2879A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533100 | |||||||
| chr17:37533350 | G | A | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3666+2629C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533350 | |||||||
| chr17:37533410 | A | C | 35 | a0001c0001t0004g0334 a0003c0004t0002g0122 a0003c0004t0002g0124 others(32): Show |
35 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.3666+2569T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533410 | |||||||
| chr17:37533447 | T | C | 1 | a0001c0005t0009g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3666+2532A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533447 | |||||||
| chr17:37533459 | TA | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(47): Show |
53 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.3666+2519delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533459 | |||||||
| chr17:37533523 | G | C | 1 | a0003c0004t0007g0121 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3666+2456C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533523 | |||||||
| chr17:37533543 | T | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
110 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.3666+2436A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533543 | |||||||
| chr17:37533569 | T | C | 84 | a0001c0016t0006g0336 a0002c0002t0001g0201 a0002c0002t0001g0233 others(81): Show |
84 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.3666+2410A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533569 | |||||||
| chr17:37533588 | C | CT | 8 | a0001c0001t0001g0063 a0001c0001t0008g0315 a0001c0001t0010g0012 others(5): Show |
8 | HG02055.hp1 HG02258.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.3666+2390dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533588 | |||||||
| chr17:37533734 | T | C | 1 | a0001c0005t0005g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3666+2245A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533734 | |||||||
| chr17:37533759 | G | A | 43 | a0001c0001t0004g0334 a0003c0004t0002g0122 a0003c0004t0002g0124 others(40): Show |
43 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.3666+2220C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533759 | |||||||
| chr17:37533926 | C | CT | 23 | a0001c0001t0001g0032 a0001c0001t0001g0064 a0001c0001t0001g0093 others(20): Show |
23 | HG00438.hp1 HG00621.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.3666+2052dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533926 | |||||||
| chr17:37533926 | C | CTT | 64 | a0001c0001t0005g0115 a0001c0016t0006g0336 a0002c0002t0001g0201 others(61): Show |
64 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.3666+2051_3666+205 others(6): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533926 | |||||||
| chr17:37533926 | C | CTTT | 43 | a0001c0001t0004g0334 a0001c0006t0001g0011 a0001c0006t0001g0031 others(40): Show |
43 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.3666+2050_3666+205 others(7): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533926 | |||||||
| chr17:37533926 | C | CTTTT | 19 | a0002c0002t0002g0221 a0003c0004t0002g0122 a0003c0004t0002g0124 others(16): Show |
19 | HG00609.hp1 HG00621.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.3666+2049_3666+205 others(8): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533926 | |||||||
| chr17:37533926 | CT | C | 18 | a0001c0001t0001g0013 a0001c0001t0001g0046 a0001c0001t0001g0047 others(15): Show |
18 | HG02027.hp2 HG02647.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.3666+2052delA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533926 | |||||||
| chr17:37533930 | T | C | 4 | a0001c0001t0010g0012 a0001c0001t0010g0189 a0001c0001t0010g0190 others(1): Show |
4 | HG02258.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3666+2049A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37533930 | |||||||
| chr17:37534028 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3666+1951C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37534028 | |||||||
| chr17:37534048 | C | T | 1 | a0001c0003t0034g0130 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3666+1931G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37534048 | |||||||
| chr17:37534051 | C | T | 26 | a0001c0003t0007g0143 a0001c0003t0007g0169 a0001c0003t0007g0170 others(23): Show |
27 | HG00323.hp1 HG00741.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.3666+1928G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37534051 | |||||||
| chr17:37534101 | A | AT | 7 | a0001c0001t0001g0272 a0001c0001t0010g0012 a0001c0001t0010g0189 others(4): Show |
7 | HG02258.hp2 HG02970.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.3666+1877dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37534101 | |||||||
| chr17:37534251 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3666+1728A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37534251 | |||||||
| chr17:37534709 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
113 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.3666+1270A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37534709 | |||||||
| chr17:37534902 | T | TA | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
143 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.3666+1076dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37534902 | |||||||
| chr17:37535136 | T | C | 5 | a0001c0001t0010g0012 a0001c0001t0010g0189 a0001c0001t0010g0190 others(2): Show |
5 | HG02258.hp2 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3666+843A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37535136 | |||||||
| chr17:37535158 | C | T | 1 | a0001c0003t0003g0146 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3666+821G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37535158 | |||||||
| chr17:37535184 | A | T | 1 | a0002c0011t0015g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3666+795T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37535184 | |||||||
| chr17:37535304 | A | G | 1 | a0002c0011t0015g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3666+675T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37535304 | |||||||
| chr17:37535324 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3666+655A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37535324 | |||||||
| chr17:37535430 | G | A | 1 | a0001c0003t0001g0129 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3666+549C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37535430 | |||||||
| chr17:37535542 | G | A | 2 | a0001c0003t0007g0169 a0001c0003t0030g0187 |
2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3666+437C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37535542 | |||||||
| chr17:37535645 | G | A | 2 | a0001c0001t0005g0115 a0010c0014t0023g0263 |
2 | HG02486.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3666+334C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 19/21 | chr17 | 37535645 | |||||||
| chr17:37536300 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
112 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.3518-173G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 18/21 | chr17 | 37536300 | |||||||
| chr17:37536447 | G | A | 8 | a0001c0001t0008g0315 a0001c0001t0011g0117 a0001c0001t0011g0118 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3518-320C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 18/21 | chr17 | 37536447 | |||||||
| chr17:37536448 | G | T | 1 | a0001c0001t0004g0049 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3518-321C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 18/21 | chr17 | 37536448 | |||||||
| chr17:37536550 | G | T | 1 | a0001c0003t0001g0316 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3518-423C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 18/21 | chr17 | 37536550 | |||||||
| chr17:37537167 | T | C | 1 | a0006c0009t0003g0142 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3518-1040A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 18/21 | chr17 | 37537167 | |||||||
| chr17:37537230 | C | T | 83 | a0001c0016t0006g0336 a0002c0002t0001g0201 a0002c0002t0001g0233 others(80): Show |
83 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.3517+1094G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 18/21 | chr17 | 37537230 | |||||||
| chr17:37537400 | G | T | 1 | a0002c0002t0016g0219 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3517+924C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 18/21 | chr17 | 37537400 | |||||||
| chr17:37537532 | A | C | 2 | a0002c0002t0002g0192 a0002c0002t0002g0326 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3517+792T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 18/21 | chr17 | 37537532 | |||||||
| chr17:37537665 | A | G | 1 | a0002c0011t0015g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3517+659T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 18/21 | chr17 | 37537665 | |||||||
| chr17:37537979 | G | A | 83 | a0001c0016t0006g0336 a0002c0002t0001g0201 a0002c0002t0001g0233 others(80): Show |
83 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.3517+345C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 18/21 | chr17 | 37537979 | |||||||
| chr17:37538015 | G | T | 2 | a0001c0006t0001g0011 a0001c0006t0001g0031 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.3517+309C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 18/21 | chr17 | 37538015 | |||||||
| chr17:37538240 | G | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
155 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.3517+84C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 18/21 | chr17 | 37538240 | |||||||
| chr17:37538502 | C | T | 2 | a0001c0001t0004g0334 a0003c0004t0004g0296 |
2 | NA18957.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.3421-82G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 17/21 | chr17 | 37538502 | |||||||
| chr17:37538544 | A | C | 1 | a0001c0003t0003g0155 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3421-124T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 17/21 | chr17 | 37538544 | |||||||
| chr17:37538554 | C | T | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3421-134G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 17/21 | chr17 | 37538554 | |||||||
| chr17:37538680 | T | C | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
288 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.3421-260A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 17/21 | chr17 | 37538680 | |||||||
| chr17:37538768 | C | T | 4 | a0003c0004t0003g0123 a0003c0004t0004g0287 a0003c0004t0004g0312 others(1): Show |
4 | HG00323.hp2 HG03491.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.3421-348G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 17/21 | chr17 | 37538768 | |||||||
| chr17:37538808 | T | C | 5 | a0001c0001t0010g0012 a0001c0001t0010g0189 a0001c0001t0010g0190 others(2): Show |
5 | HG02258.hp2 HG02970.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3420+384A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 17/21 | chr17 | 37538808 | |||||||
| chr17:37538836 | G | A | 1 | a0002c0002t0014g0250 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3420+356C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 17/21 | chr17 | 37538836 | |||||||
| chr17:37539039 | T | A | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
288 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.3420+153A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 17/21 | chr17 | 37539039 | |||||||
| chr17:37539061 | T | A | 4 | a0001c0006t0013g0017 a0001c0006t0013g0020 a0001c0006t0013g0022 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3420+131A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 17/21 | chr17 | 37539061 | |||||||
| chr17:37539160 | C | T | 1 | a0001c0003t0003g0152 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3420+32G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 17/21 | chr17 | 37539160 | |||||||
| chr17:37539322 | T | C | 2 | a0001c0001t0010g0189 a0001c0001t0010g0324 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3367-77A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 16/21 | chr17 | 37539322 | |||||||
| chr17:37539372 | A | ATGTTTT | 10 | a0001c0001t0011g0117 a0001c0001t0011g0118 a0001c0001t0011g0340 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3367-133_3367-128d others(8): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 16/21 | chr17 | 37539372 | |||||||
| chr17:37539585 | T | G | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
288 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.3367-340A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 16/21 | chr17 | 37539585 | |||||||
| chr17:37539819 | A | G | 1 | a0002c0002t0002g0228 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3366+561T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 16/21 | chr17 | 37539819 | |||||||
| chr17:37539832 | G | A | 265 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(262): Show |
269 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.3366+548C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 16/21 | chr17 | 37539832 | |||||||
| chr17:37539944 | A | G | 5 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3366+436T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 16/21 | chr17 | 37539944 | |||||||
| chr17:37540188 | G | A | 61 | a0001c0016t0006g0336 a0002c0002t0001g0201 a0002c0002t0001g0233 others(58): Show |
61 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.3366+192C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 16/21 | chr17 | 37540188 | |||||||
| chr17:37540359 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3366+21A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 16/21 | chr17 | 37540359 | |||||||
| chr17:37540623 | C | G | 1 | a0001c0001t0021g0082 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3203-80G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37540623 | |||||||
| chr17:37540630 | C | CT | 28 | a0001c0001t0001g0096 a0001c0001t0001g0102 a0001c0001t0001g0259 others(25): Show |
29 | HG01255.hp1 HG02055.hp2 HG02486.hp2 others(26): Show |
intron_variant | MODIFIER | c.3203-88dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37540630 | |||||||
| chr17:37540630 | CT | C | 13 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0008g0026 others(10): Show |
13 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.3203-88delA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37540630 | |||||||
| chr17:37540674 | G | A | 1 | a0002c0002t0002g0008 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3203-131C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37540674 | |||||||
| chr17:37540690 | G | A | 1 | a0003c0004t0007g0121 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3203-147C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37540690 | |||||||
| chr17:37540776 | A | G | 48 | a0001c0001t0001g0113 a0001c0001t0004g0334 a0003c0004t0001g0119 others(45): Show |
48 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.3203-233T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37540776 | |||||||
| chr17:37540815 | AGTAGAT | A | 83 | a0001c0016t0006g0336 a0002c0002t0001g0201 a0002c0002t0001g0233 others(80): Show |
83 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.3203-278_3203-273d others(8): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37540815 | |||||||
| chr17:37540850 | G | C | 1 | a0003c0004t0007g0121 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3203-307C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37540850 | |||||||
| chr17:37541059 | T | C | 3 | a0003c0004t0003g0123 a0003c0004t0004g0287 a0003c0004t0004g0312 |
3 | HG03491.hp2 HG03831.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3203-516A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37541059 | |||||||
| chr17:37541073 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3203-530T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37541073 | |||||||
| chr17:37541214 | G | C | 1 | a0003c0004t0007g0121 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3203-671C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37541214 | |||||||
| chr17:37541272 | T | C | 84 | a0001c0016t0006g0336 a0002c0002t0001g0201 a0002c0002t0001g0233 others(81): Show |
84 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.3202+700A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37541272 | |||||||
| chr17:37541298 | G | A | 2 | a0001c0003t0003g0150 a0001c0003t0003g0161 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3202+674C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37541298 | |||||||
| chr17:37541357 | C | T | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3202+615G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37541357 | |||||||
| chr17:37541467 | G | T | 1 | a0001c0001t0037g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3202+505C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37541467 | |||||||
| chr17:37541516 | T | C | 1 | a0002c0002t0002g0329 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3202+456A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37541516 | |||||||
| chr17:37541602 | T | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3202+370A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37541602 | |||||||
| chr17:37541694 | CT | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(50): Show |
55 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.3202+277delA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 15/21 | chr17 | 37541694 | |||||||
| chr17:37542744 | C | T | 4 | a0001c0001t0005g0115 a0001c0001t0011g0117 a0001c0001t0011g0118 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2609-179G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37542744 | |||||||
| chr17:37542757 | G | C | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2609-192C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37542757 | |||||||
| chr17:37542787 | C | A | 4 | a0002c0002t0002g0165 a0002c0002t0002g0195 a0002c0002t0002g0327 others(1): Show |
4 | HG00733.hp1 HG01168.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.2609-222G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37542787 | |||||||
| chr17:37542787 | C | T | 9 | a0001c0003t0003g0173 a0001c0003t0003g0184 a0001c0003t0007g0143 others(6): Show |
9 | HG00323.hp1 HG00741.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2609-222G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37542787 | |||||||
| chr17:37542996 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2609-431T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37542996 | |||||||
| chr17:37543054 | T | A | 3 | a0001c0001t0011g0117 a0001c0001t0011g0118 a0001c0001t0028g0116 |
3 | HG01891.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2609-489A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37543054 | |||||||
| chr17:37543271 | T | C | 18 | a0001c0016t0006g0336 a0002c0002t0001g0249 a0002c0002t0002g0232 others(15): Show |
18 | HG01257.hp1 HG01981.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.2609-706A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37543271 | |||||||
| chr17:37543281 | C | T | 2 | a0002c0002t0002g0168 a0002c0002t0002g0206 |
2 | NA18984.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2609-716G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37543281 | |||||||
| chr17:37543366 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG02165.hp2 NA18970.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.2609-801G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37543366 | |||||||
| chr17:37543474 | T | C | 3 | a0004c0008t0020g0257 a0004c0008t0020g0258 a0010c0014t0023g0263 |
3 | HG01358.hp2 HG02896.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2609-909A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37543474 | |||||||
| chr17:37543504 | T | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2609-939A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37543504 | |||||||
| chr17:37543656 | A | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(19): Show |
22 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2609-1091T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37543656 | |||||||
| chr17:37543662 | T | C | 5 | a0001c0001t0001g0269 a0001c0001t0021g0039 a0001c0001t0022g0009 others(2): Show |
5 | HG01515.hp1 HG01517.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.2609-1097A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37543662 | |||||||
| chr17:37543926 | A | T | 2 | a0001c0003t0003g0183 a0011c0018t0003g0160 |
2 | HG02027.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.2609-1361T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37543926 | |||||||
| chr17:37544140 | G | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2609-1575C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37544140 | |||||||
| chr17:37544272 | A | T | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2609-1707T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37544272 | |||||||
| chr17:37544296 | G | C | 2 | a0001c0003t0002g0151 a0001c0003t0002g0186 |
2 | HG01255.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2609-1731C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37544296 | |||||||
| chr17:37544309 | T | G | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2609-1744A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37544309 | |||||||
| chr17:37544495 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
95 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.2609-1930T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37544495 | |||||||
| chr17:37544936 | G | A | 3 | a0002c0002t0002g0234 a0002c0002t0002g0241 a0002c0002t0002g0242 |
3 | HG03831.hp1 NA18941.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2609-2371C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37544936 | |||||||
| chr17:37545017 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2609-2452G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37545017 | |||||||
| chr17:37545047 | C | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(19): Show |
22 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2609-2482G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37545047 | |||||||
| chr17:37545127 | G | A | 3 | a0001c0001t0010g0012 a0001c0006t0001g0011 a0001c0006t0001g0031 |
3 | HG02895.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2609-2562C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37545127 | |||||||
| chr17:37545229 | A | T | 12 | a0001c0001t0001g0037 a0001c0001t0008g0315 a0001c0001t0010g0012 others(9): Show |
12 | HG01891.hp2 HG02040.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2609-2664T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37545229 | |||||||
| chr17:37545232 | T | A | 17 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(14): Show |
17 | HG00140.hp2 HG00621.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.2609-2667A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37545232 | |||||||
| chr17:37545315 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2609-2750C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37545315 | |||||||
| chr17:37545405 | G | A | 1 | a0002c0002t0002g0327 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2609-2840C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37545405 | |||||||
| chr17:37545489 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02165.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2609-2924A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37545489 | |||||||
| chr17:37545787 | C | A | 1 | a0001c0003t0003g0162 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2609-3222G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37545787 | |||||||
| chr17:37545858 | C | T | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2609-3293G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37545858 | |||||||
| chr17:37545991 | G | A | 14 | a0001c0005t0005g0109 a0001c0005t0005g0110 a0001c0005t0005g0273 others(11): Show |
15 | HG02055.hp2 HG02647.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.2609-3426C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37545991 | |||||||
| chr17:37546360 | G | A | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2609-3795C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37546360 | |||||||
| chr17:37546387 | G | A | 1 | a0002c0002t0002g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2609-3822C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37546387 | |||||||
| chr17:37546407 | T | C | 26 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(23): Show |
26 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.2609-3842A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37546407 | |||||||
| chr17:37546816 | T | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
198 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.2609-4251A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37546816 | |||||||
| chr17:37547054 | A | G | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609-4489T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37547054 | |||||||
| chr17:37547463 | C | CT | 26 | a0001c0001t0001g0089 a0001c0003t0003g0162 a0001c0003t0030g0187 others(23): Show |
27 | HG00741.hp2 HG01358.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.2609-4899dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37547463 | |||||||
| chr17:37547543 | A | C | 2 | a0001c0001t0010g0189 a0001c0001t0010g0324 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2609-4978T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37547543 | |||||||
| chr17:37547555 | C | T | 1 | a0001c0001t0010g0012 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2609-4990G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37547555 | |||||||
| chr17:37547624 | G | A | 3 | a0002c0002t0002g0223 a0002c0002t0002g0332 a0008c0021t0002g0224 |
3 | HG00639.hp2 HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.2609-5059C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37547624 | |||||||
| chr17:37547698 | G | T | 1 | a0003c0004t0004g0306 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2609-5133C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37547698 | |||||||
| chr17:37547708 | C | T | 1 | a0001c0003t0030g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2609-5143G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37547708 | |||||||
| chr17:37548268 | C | T | 1 | a0002c0002t0002g0202 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2608+4847G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37548268 | |||||||
| chr17:37548552 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2608+4563A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37548552 | |||||||
| chr17:37548779 | T | C | 27 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(24): Show |
27 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.2608+4336A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37548779 | |||||||
| chr17:37548825 | T | TA | 23 | a0001c0001t0001g0032 a0001c0001t0001g0044 a0001c0001t0001g0078 others(20): Show |
23 | HG00438.hp1 HG01070.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2608+4289dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37548825 | |||||||
| chr17:37548825 | TA | T | 6 | a0001c0003t0003g0144 a0003c0004t0025g0303 a0004c0008t0020g0257 others(3): Show |
6 | HG01358.hp2 HG02886.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.2608+4289delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37548825 | |||||||
| chr17:37548842 | A | AC | 13 | a0001c0001t0001g0027 a0001c0001t0005g0029 a0001c0001t0008g0024 others(10): Show |
13 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2608+4272_2608+427 others(5): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37548842 | |||||||
| chr17:37548843 | A | C | 1 | a0003c0004t0002g0314 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2608+4272T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37548843 | |||||||
| chr17:37548848 | C | A | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2608+4267G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37548848 | |||||||
| chr17:37548857 | G | A | 1 | a0002c0002t0002g0225 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2608+4258C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37548857 | |||||||
| chr17:37548933 | G | A | 1 | a0001c0005t0009g0005 | 2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2608+4182C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37548933 | |||||||
| chr17:37548960 | C | A | 1 | a0002c0002t0002g0008 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2608+4155G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37548960 | |||||||
| chr17:37549515 | A | C | 2 | a0001c0005t0008g0266 a0001c0005t0009g0265 |
2 | HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2608+3600T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37549515 | |||||||
| chr17:37549710 | C | T | 1 | a0001c0001t0012g0035 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2608+3405G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37549710 | |||||||
| chr17:37549734 | G | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2608+3381C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37549734 | |||||||
| chr17:37549882 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2608+3233C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37549882 | |||||||
| chr17:37550194 | T | C | 2 | a0001c0005t0008g0266 a0001c0005t0009g0265 |
2 | HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2608+2921A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37550194 | |||||||
| chr17:37550492 | C | T | 1 | a0003c0004t0002g0125 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2608+2623G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37550492 | |||||||
| chr17:37550619 | G | A | 1 | a0001c0001t0004g0083 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2608+2496C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37550619 | |||||||
| chr17:37550633 | T | C | 277 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(274): Show |
281 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(278): Show |
intron_variant | MODIFIER | c.2608+2482A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37550633 | |||||||
| chr17:37550697 | CA | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
188 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.2608+2417delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37550697 | |||||||
| chr17:37550868 | C | A | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2608+2247G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37550868 | |||||||
| chr17:37550869 | G | C | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2608+2246C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37550869 | |||||||
| chr17:37550870 | T | A | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2608+2245A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37550870 | |||||||
| chr17:37550872 | A | T | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2608+2243T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37550872 | |||||||
| chr17:37550886 | C | T | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2608+2229G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37550886 | |||||||
| chr17:37550887 | C | T | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2608+2228G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37550887 | |||||||
| chr17:37550912 | A | G | 5 | a0001c0003t0003g0173 a0001c0003t0003g0184 a0001c0003t0007g0170 others(2): Show |
5 | HG00741.hp1 HG01123.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.2608+2203T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37550912 | |||||||
| chr17:37550971 | C | T | 1 | a0001c0001t0015g0051 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2608+2144G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37550971 | |||||||
| chr17:37551096 | C | T | 1 | a0002c0002t0014g0251 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2608+2019G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37551096 | |||||||
| chr17:37551337 | C | T | 1 | a0001c0001t0038g0072 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2608+1778G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37551337 | |||||||
| chr17:37551588 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2608+1527C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37551588 | |||||||
| chr17:37551691 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2608+1424C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37551691 | |||||||
| chr17:37551796 | A | C | 26 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(23): Show |
26 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.2608+1319T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37551796 | |||||||
| chr17:37551875 | C | CA | 44 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(41): Show |
45 | HG01243.hp1 HG01358.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.2608+1239dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37551875 | |||||||
| chr17:37551875 | CA | C | 6 | a0001c0001t0005g0115 a0001c0001t0011g0117 a0001c0001t0011g0118 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2608+1239delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37551875 | |||||||
| chr17:37552087 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2608+1028A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37552087 | |||||||
| chr17:37552326 | A | G | 50 | a0001c0001t0004g0334 a0003c0004t0001g0119 a0003c0004t0001g0337 others(47): Show |
50 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.2608+789T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37552326 | |||||||
| chr17:37552784 | G | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2608+331C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37552784 | |||||||
| chr17:37552999 | T | C | 1 | a0001c0005t0005g0280 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2608+116A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37552999 | |||||||
| chr17:37553069 | T | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0075 others(4): Show |
7 | HG02129.hp1 NA18952.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.2608+46A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 14/21 | chr17 | 37553069 | |||||||
| chr17:37554439 | G | A | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1664-380C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37554439 | |||||||
| chr17:37554620 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1664-561C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37554620 | |||||||
| chr17:37555068 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1664-1009A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37555068 | |||||||
| chr17:37555221 | G | A | 1 | a0002c0002t0004g0235 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1664-1162C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37555221 | |||||||
| chr17:37555229 | C | T | 3 | a0001c0001t0010g0012 a0001c0006t0001g0011 a0001c0006t0001g0031 |
3 | HG02895.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1664-1170G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37555229 | |||||||
| chr17:37555600 | G | A | 1 | a0002c0011t0007g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1664-1541C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37555600 | |||||||
| chr17:37555622 | C | T | 4 | a0001c0005t0005g0109 a0001c0005t0005g0110 a0001c0005t0005g0277 others(1): Show |
4 | HG02055.hp2 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1664-1563G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37555622 | |||||||
| chr17:37555897 | T | G | 2 | a0001c0005t0008g0266 a0001c0005t0009g0265 |
2 | HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1664-1838A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37555897 | |||||||
| chr17:37555966 | T | A | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1664-1907A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37555966 | |||||||
| chr17:37555967 | A | T | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1664-1908T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37555967 | |||||||
| chr17:37556035 | C | T | 1 | a0002c0002t0002g0253 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1664-1976G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37556035 | |||||||
| chr17:37556178 | G | A | 1 | a0003c0004t0004g0313 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1664-2119C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37556178 | |||||||
| chr17:37556210 | A | G | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1664-2151T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37556210 | |||||||
| chr17:37556221 | G | A | 1 | a0001c0003t0001g0318 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1664-2162C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37556221 | |||||||
| chr17:37556500 | A | T | 1 | a0003c0004t0004g0313 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1664-2441T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37556500 | |||||||
| chr17:37556546 | GA | G | 119 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(116): Show |
120 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.1664-2488delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37556546 | |||||||
| chr17:37556905 | CTTTG | C | 49 | a0001c0001t0004g0334 a0003c0004t0001g0119 a0003c0004t0001g0338 others(46): Show |
49 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1664-2850_1664-284 others(8): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37556905 | |||||||
| chr17:37557013 | A | G | 1 | a0002c0002t0006g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1664-2954T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37557013 | |||||||
| chr17:37557068 | G | A | 2 | a0001c0001t0010g0190 a0001c0001t0010g0191 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1664-3009C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37557068 | |||||||
| chr17:37557124 | G | C | 1 | a0001c0001t0037g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1664-3065C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37557124 | |||||||
| chr17:37557193 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1664-3134G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37557193 | |||||||
| chr17:37557362 | T | C | 1 | a0007c0017t0002g0295 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1664-3303A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37557362 | |||||||
| chr17:37557392 | C | T | 1 | a0003c0004t0004g0312 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1664-3333G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37557392 | |||||||
| chr17:37557626 | C | G | 1 | a0002c0002t0002g0245 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1664-3567G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37557626 | |||||||
| chr17:37558208 | C | T | 2 | a0002c0002t0014g0251 a0002c0002t0014g0252 |
2 | HG01256.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1663+2987G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37558208 | |||||||
| chr17:37558253 | T | C | 1 | a0002c0011t0015g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1663+2942A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37558253 | |||||||
| chr17:37558311 | A | G | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1663+2884T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37558311 | |||||||
| chr17:37558409 | G | A | 15 | a0001c0001t0001g0027 a0001c0001t0005g0029 a0001c0001t0008g0016 others(12): Show |
15 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1663+2786C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37558409 | |||||||
| chr17:37558425 | G | A | 1 | a0001c0003t0003g0183 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1663+2770C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37558425 | |||||||
| chr17:37558472 | C | A | 1 | a0001c0001t0017g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1663+2723G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37558472 | |||||||
| chr17:37558752 | C | T | 277 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(274): Show |
281 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(278): Show |
intron_variant | MODIFIER | c.1663+2443G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37558752 | |||||||
| chr17:37558848 | C | T | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1663+2347G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37558848 | |||||||
| chr17:37559151 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1663+2044G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37559151 | |||||||
| chr17:37559152 | T | C | 12 | a0001c0005t0005g0109 a0001c0005t0005g0110 a0001c0005t0005g0273 others(9): Show |
13 | HG02055.hp2 HG02647.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.1663+2043A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37559152 | |||||||
| chr17:37559173 | G | A | 13 | a0001c0001t0001g0027 a0001c0001t0005g0029 a0001c0001t0008g0024 others(10): Show |
13 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1663+2022C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37559173 | |||||||
| chr17:37559341 | A | G | 2 | a0003c0004t0018g0321 a0003c0004t0018g0322 |
2 | HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1663+1854T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37559341 | |||||||
| chr17:37559342 | C | A | 2 | a0001c0003t0030g0187 a0003c0004t0007g0121 |
2 | NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1663+1853G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37559342 | |||||||
| chr17:37559409 | G | A | 49 | a0001c0001t0004g0334 a0003c0004t0001g0119 a0003c0004t0001g0338 others(46): Show |
49 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1663+1786C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37559409 | |||||||
| chr17:37559455 | C | T | 50 | a0001c0001t0004g0334 a0003c0004t0001g0119 a0003c0004t0001g0337 others(47): Show |
50 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1663+1740G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37559455 | |||||||
| chr17:37559664 | T | TG | 5 | a0001c0003t0003g0148 a0001c0003t0003g0156 a0001c0003t0003g0157 others(2): Show |
5 | NA18947.hp1 NA18950.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1663+1530dupC | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37559664 | |||||||
| chr17:37559796 | A | G | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663+1399T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37559796 | |||||||
| chr17:37559810 | C | A | 1 | a0002c0002t0033g0006 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1663+1385G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37559810 | |||||||
| chr17:37559910 | C | T | 1 | a0003c0004t0002g0124 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1663+1285G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37559910 | |||||||
| chr17:37560052 | C | T | 1 | a0002c0002t0006g0222 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1663+1143G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37560052 | |||||||
| chr17:37560193 | G | A | 1 | a0001c0006t0013g0020 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1663+1002C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37560193 | |||||||
| chr17:37560234 | T | A | 1 | a0001c0001t0005g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1663+961A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37560234 | |||||||
| chr17:37560338 | A | AT | 30 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0272 others(27): Show |
30 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1663+856dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37560338 | |||||||
| chr17:37560470 | G | C | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663+725C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37560470 | |||||||
| chr17:37560669 | A | AT | 22 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(19): Show |
22 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1663+525dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37560669 | |||||||
| chr17:37560715 | T | A | 1 | a0001c0003t0003g0007 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1663+480A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37560715 | |||||||
| chr17:37560737 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
198 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.1663+458T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37560737 | |||||||
| chr17:37560804 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1663+391T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37560804 | |||||||
| chr17:37560916 | T | C | 26 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(23): Show |
26 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1663+279A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 13/21 | chr17 | 37560916 | |||||||
| chr17:37561382 | A | C | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1600+89T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 12/21 | chr17 | 37561382 | |||||||
| chr17:37561400 | T | C | 1 | a0001c0003t0003g0147 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1600+71A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 12/21 | chr17 | 37561400 | |||||||
| chr17:37561622 | T | C | 14 | a0001c0005t0005g0109 a0001c0005t0005g0110 a0001c0005t0005g0273 others(11): Show |
15 | HG02055.hp2 HG02647.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.1482-33A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37561622 | |||||||
| chr17:37561748 | A | T | 2 | a0001c0003t0003g0144 a0001c0003t0003g0145 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1482-159T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37561748 | |||||||
| chr17:37561895 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1482-306C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37561895 | |||||||
| chr17:37561913 | T | TAAAGAAT others(310): Show |
1 | a0003c0004t0004g0285 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1482-325_1482-324i others(319): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37561913 | |||||||
| chr17:37561913 | T | TAAAGAAT others(310): Show |
46 | a0001c0001t0004g0334 a0003c0004t0001g0119 a0003c0004t0001g0337 others(43): Show |
46 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1482-325_1482-324i others(319): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37561913 | |||||||
| chr17:37561913 | T | TAAAGAAT others(311): Show |
2 | a0003c0004t0003g0123 a0003c0004t0004g0127 |
2 | HG03831.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1482-325_1482-324i others(320): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37561913 | |||||||
| chr17:37561913 | T | TAAAGAAT others(331): Show |
3 | a0001c0001t0010g0189 a0001c0001t0010g0191 a0001c0001t0010g0324 |
3 | HG02258.hp2 HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1482-325_1482-324i others(340): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37561913 | |||||||
| chr17:37561913 | T | TAAAGAAT others(332): Show |
1 | a0001c0001t0010g0190 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1482-325_1482-324i others(341): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37561913 | |||||||
| chr17:37561913 | T | TAAAGAAT others(310): Show |
1 | a0003c0004t0004g0307 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1482-325_1482-324i others(319): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37561913 | |||||||
| chr17:37562116 | A | G | 1 | a0002c0002t0002g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1482-527T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37562116 | |||||||
| chr17:37562341 | T | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
95 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1482-752A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37562341 | |||||||
| chr17:37562390 | T | TTTC | 31 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0005g0029 others(28): Show |
31 | HG01884.hp1 HG01981.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1482-804_1482-802d others(5): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37562390 | |||||||
| chr17:37562427 | C | T | 1 | a0001c0005t0005g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1482-838G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37562427 | |||||||
| chr17:37562443 | A | G | 1 | a0002c0002t0002g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1482-854T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37562443 | |||||||
| chr17:37562621 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1482-1032A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37562621 | |||||||
| chr17:37562649 | C | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0088 |
2 | HG00544.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1482-1060G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37562649 | |||||||
| chr17:37562652 | T | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | HG00558.hp2 HG02155.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1482-1063A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37562652 | |||||||
| chr17:37562737 | A | T | 4 | a0001c0001t0005g0115 a0001c0001t0011g0117 a0001c0001t0011g0118 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1482-1148T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37562737 | |||||||
| chr17:37562844 | A | G | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1482-1255T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37562844 | |||||||
| chr17:37562852 | C | A | 1 | a0001c0003t0003g0007 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1482-1263G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37562852 | |||||||
| chr17:37562919 | C | T | 1 | a0003c0004t0004g0306 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1482-1330G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37562919 | |||||||
| chr17:37563043 | T | C | 1 | a0003c0013t0009g0305 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1482-1454A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37563043 | |||||||
| chr17:37563104 | C | T | 1 | a0002c0002t0002g0231 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1482-1515G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37563104 | |||||||
| chr17:37563199 | T | C | 1 | a0002c0002t0002g0228 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1482-1610A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37563199 | |||||||
| chr17:37563227 | C | T | 1 | a0001c0001t0010g0012 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1482-1638G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37563227 | |||||||
| chr17:37563288 | A | C | 4 | a0001c0001t0008g0315 a0001c0003t0007g0169 a0001c0003t0030g0187 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482-1699T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37563288 | |||||||
| chr17:37563338 | C | T | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1482-1749G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37563338 | |||||||
| chr17:37563357 | T | G | 2 | a0001c0005t0008g0266 a0001c0005t0009g0265 |
2 | HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1482-1768A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37563357 | |||||||
| chr17:37563538 | A | T | 1 | a0003c0004t0004g0307 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1482-1949T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37563538 | |||||||
| chr17:37563732 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02027.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1482-2143A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37563732 | |||||||
| chr17:37563860 | T | C | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1482-2271A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37563860 | |||||||
| chr17:37563994 | C | T | 6 | a0001c0003t0002g0149 a0001c0003t0002g0151 a0001c0003t0002g0186 others(3): Show |
6 | HG00140.hp2 HG01255.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1482-2405G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37563994 | |||||||
| chr17:37564304 | T | G | 2 | a0001c0005t0005g0109 a0001c0005t0005g0277 |
2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1482-2715A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564304 | |||||||
| chr17:37564338 | G | A | 1 | a0002c0002t0002g0242 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1482-2749C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564338 | |||||||
| chr17:37564338 | G | C | 2 | a0002c0002t0002g0192 a0002c0002t0002g0326 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1482-2749C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564338 | |||||||
| chr17:37564359 | T | G | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2770A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564359 | |||||||
| chr17:37564360 | A | T | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2771T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564360 | |||||||
| chr17:37564368 | T | A | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2779A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564368 | |||||||
| chr17:37564369 | T | A | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2780A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564369 | |||||||
| chr17:37564374 | G | T | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2785C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564374 | |||||||
| chr17:37564376 | C | A | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2787G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564376 | |||||||
| chr17:37564382 | C | T | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2793G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564382 | |||||||
| chr17:37564388 | A | C | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2799T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564388 | |||||||
| chr17:37564408 | T | G | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2819A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564408 | |||||||
| chr17:37564421 | T | G | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2832A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564421 | |||||||
| chr17:37564440 | T | G | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2851A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564440 | |||||||
| chr17:37564445 | T | G | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2856A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564445 | |||||||
| chr17:37564446 | A | C | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2857T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564446 | |||||||
| chr17:37564463 | T | G | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2874A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564463 | |||||||
| chr17:37564469 | T | G | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2880A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564469 | |||||||
| chr17:37564477 | C | G | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2888G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564477 | |||||||
| chr17:37564491 | T | G | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2902A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564491 | |||||||
| chr17:37564492 | A | G | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2903T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564492 | |||||||
| chr17:37564496 | T | G | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2907A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564496 | |||||||
| chr17:37564500 | T | G | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2911A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564500 | |||||||
| chr17:37564501 | T | C | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2912A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564501 | |||||||
| chr17:37564514 | G | T | 1 | a0011c0018t0003g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1482-2925C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564514 | |||||||
| chr17:37564590 | C | T | 1 | a0001c0003t0006g0325 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1482-3001G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564590 | |||||||
| chr17:37564796 | C | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
94 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1482-3207G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37564796 | |||||||
| chr17:37565213 | G | A | 1 | a0001c0001t0012g0108 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1481+3578C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565213 | |||||||
| chr17:37565262 | TA | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
97 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1481+3528delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565262 | |||||||
| chr17:37565363 | T | C | 6 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0001g0069 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1481+3428A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565363 | |||||||
| chr17:37565461 | G | A | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1481+3330C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565461 | |||||||
| chr17:37565482 | G | A | 1 | a0002c0002t0014g0212 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1481+3309C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565482 | |||||||
| chr17:37565497 | G | C | 1 | a0001c0001t0005g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1481+3294C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565497 | |||||||
| chr17:37565609 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1481+3182A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565609 | |||||||
| chr17:37565617 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1481+3174C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565617 | |||||||
| chr17:37565677 | G | A | 1 | a0001c0001t0011g0340 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1481+3114C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565677 | |||||||
| chr17:37565733 | G | A | 1 | a0001c0001t0010g0012 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1481+3058C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565733 | |||||||
| chr17:37565769 | G | A | 1 | a0001c0003t0030g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1481+3022C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565769 | |||||||
| chr17:37565876 | A | ATCTCCGC others(73): Show |
1 | a0001c0001t0004g0049 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1481+2914_1481+291 others(84): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565876 | |||||||
| chr17:37565876 | A | G | 27 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(24): Show |
27 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1481+2915T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565876 | |||||||
| chr17:37565881 | T | C | 277 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(274): Show |
281 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(278): Show |
intron_variant | MODIFIER | c.1481+2910A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565881 | |||||||
| chr17:37565885 | C | T | 1 | a0001c0001t0012g0035 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1481+2906G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565885 | |||||||
| chr17:37565887 | GCAGCCAC others(42): Show |
G | 1 | a0001c0003t0003g0147 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1481+2855_1481+290 others(53): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565887 | |||||||
| chr17:37565893 | A | ACCCCGTC others(42): Show |
1 | a0003c0004t0002g0298 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1481+2849_1481+289 others(53): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565893 | |||||||
| chr17:37565893 | ACCCCGTC others(42): Show |
A | 19 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(16): Show |
20 | HG02055.hp2 HG02300.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1481+2849_1481+289 others(53): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565893 | |||||||
| chr17:37565961 | TGGGGGGG others(43): Show |
T | 1 | a0001c0005t0005g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1481+2780_1481+282 others(54): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565961 | |||||||
| chr17:37565962 | G | T | 1 | a0001c0006t0013g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1481+2829C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565962 | |||||||
| chr17:37565985 | C | T | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1481+2806G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37565985 | |||||||
| chr17:37566012 | GGGGGGTC others(38): Show |
G | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1481+2734_1481+277 others(49): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37566012 | |||||||
| chr17:37566063 | G | A | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1481+2728C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37566063 | |||||||
| chr17:37566072 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1481+2719G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37566072 | |||||||
| chr17:37566249 | A | G | 3 | a0002c0002t0002g0216 a0002c0002t0002g0217 a0002c0002t0002g0231 |
3 | NA18975.hp1 NA19086.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1481+2542T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37566249 | |||||||
| chr17:37566296 | A | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | NA18952.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1481+2495T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37566296 | |||||||
| chr17:37566337 | C | G | 1 | a0001c0001t0002g0268 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1481+2454G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37566337 | |||||||
| chr17:37566382 | A | G | 50 | a0001c0001t0004g0334 a0003c0004t0001g0119 a0003c0004t0001g0337 others(47): Show |
50 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1481+2409T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37566382 | |||||||
| chr17:37566497 | C | T | 1 | a0001c0003t0003g0139 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1481+2294G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37566497 | |||||||
| chr17:37566607 | T | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1481+2184A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37566607 | |||||||
| chr17:37566687 | GA | G | 39 | a0001c0016t0006g0336 a0002c0002t0001g0201 a0002c0002t0001g0249 others(36): Show |
39 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1481+2103delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37566687 | |||||||
| chr17:37566690 | A | G | 1 | a0001c0003t0041g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1481+2101T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37566690 | |||||||
| chr17:37566791 | T | C | 1 | a0001c0005t0005g0280 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1481+2000A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37566791 | |||||||
| chr17:37566935 | A | G | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1481+1856T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37566935 | |||||||
| chr17:37567089 | G | A | 13 | a0001c0001t0001g0027 a0001c0001t0005g0029 a0001c0001t0008g0024 others(10): Show |
13 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1481+1702C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37567089 | |||||||
| chr17:37567312 | T | C | 1 | a0002c0002t0002g0331 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1481+1479A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37567312 | |||||||
| chr17:37567941 | T | C | 1 | a0001c0003t0003g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1481+850A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37567941 | |||||||
| chr17:37568015 | C | A | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1481+776G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37568015 | |||||||
| chr17:37568160 | C | T | 1 | a0001c0003t0003g0184 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1481+631G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37568160 | |||||||
| chr17:37568235 | G | A | 1 | a0013c0020t0027g0220 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1481+556C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37568235 | |||||||
| chr17:37568479 | C | T | 1 | a0013c0020t0027g0220 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1481+312G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37568479 | |||||||
| chr17:37568494 | G | T | 1 | a0007c0017t0002g0295 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1481+297C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37568494 | |||||||
| chr17:37568601 | G | A | 1 | a0001c0001t0039g0040 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1481+190C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37568601 | |||||||
| chr17:37568615 | T | A | 1 | a0003c0004t0002g0298 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1481+176A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37568615 | |||||||
| chr17:37568692 | A | G | 1 | a0003c0004t0004g0307 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1481+99T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 11/21 | chr17 | 37568692 | |||||||
| chr17:37569128 | G | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1348-204C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37569128 | |||||||
| chr17:37569167 | T | C | 5 | a0001c0001t0001g0269 a0001c0001t0021g0039 a0001c0001t0022g0009 others(2): Show |
5 | HG01515.hp1 HG01517.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1348-243A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37569167 | |||||||
| chr17:37569181 | A | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
284 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.1348-257T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37569181 | |||||||
| chr17:37569277 | GCATGTGC others(8): Show |
G | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1348-368_1348-354d others(17): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37569277 | |||||||
| chr17:37569321 | A | G | 2 | a0001c0001t0012g0035 a0001c0001t0012g0076 |
2 | NA18956.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1348-397T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37569321 | |||||||
| chr17:37569364 | T | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
284 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.1348-440A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37569364 | |||||||
| chr17:37569409 | G | GA | 68 | a0001c0001t0001g0045 a0001c0001t0001g0113 a0001c0001t0001g0262 others(65): Show |
68 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1348-486dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37569409 | |||||||
| chr17:37569654 | C | CA | 57 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0113 others(54): Show |
57 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1348-731dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37569654 | |||||||
| chr17:37569695 | C | CA | 23 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0080 others(20): Show |
23 | HG01070.hp2 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1348-772dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37569695 | |||||||
| chr17:37570058 | A | G | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1347+579T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37570058 | |||||||
| chr17:37570073 | C | T | 1 | a0001c0001t0015g0062 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1347+564G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37570073 | |||||||
| chr17:37570143 | CT | C | 6 | a0001c0001t0001g0063 a0001c0001t0001g0272 a0001c0003t0032g0134 others(3): Show |
6 | HG03491.hp1 NA18947.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.1347+493delA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37570143 | |||||||
| chr17:37570143 | CTT | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1347+492_1347+493d others(4): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37570143 | |||||||
| chr17:37570143 | CTTT | C | 41 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0084 others(38): Show |
42 | HG00609.hp1 HG01175.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.1347+491_1347+493d others(5): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37570143 | |||||||
| chr17:37570183 | G | A | 2 | a0005c0007t0019g0014 a0005c0007t0019g0015 |
2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1347+454C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37570183 | |||||||
| chr17:37570241 | T | C | 2 | a0001c0005t0008g0266 a0001c0005t0009g0265 |
2 | HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1347+396A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37570241 | |||||||
| chr17:37570246 | G | A | 1 | a0003c0004t0002g0125 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1347+391C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37570246 | |||||||
| chr17:37570370 | AC | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
94 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1347+266delG | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37570370 | |||||||
| chr17:37570473 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1347+164T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37570473 | |||||||
| chr17:37570582 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0087 |
3 | NA18951.hp2 NA19060.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1347+55C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 10/21 | chr17 | 37570582 | |||||||
| chr17:37570916 | G | A | 1 | a0003c0010t0002g0284 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1099-31C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 9/21 | chr17 | 37570916 | |||||||
| chr17:37570954 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0088 |
2 | HG00544.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1099-69G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 9/21 | chr17 | 37570954 | |||||||
| chr17:37570984 | T | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1099-99A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 9/21 | chr17 | 37570984 | |||||||
| chr17:37571308 | G | A | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-423C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 9/21 | chr17 | 37571308 | |||||||
| chr17:37571482 | T | G | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1098+309A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 9/21 | chr17 | 37571482 | |||||||
| chr17:37571656 | T | G | 1 | a0004c0008t0020g0258 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1098+135A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 9/21 | chr17 | 37571656 | |||||||
| chr17:37572021 | C | T | 1 | a0001c0001t0015g0062 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.902-34G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572021 | |||||||
| chr17:37572101 | C | A | 1 | a0001c0006t0013g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.902-114G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572101 | |||||||
| chr17:37572153 | C | A | 1 | a0001c0003t0032g0134 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.902-166G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572153 | |||||||
| chr17:37572166 | G | A | 1 | a0002c0002t0002g0202 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.902-179C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572166 | |||||||
| chr17:37572218 | G | A | 3 | a0001c0001t0010g0012 a0001c0006t0001g0011 a0001c0006t0001g0031 |
3 | HG02895.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.902-231C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572218 | |||||||
| chr17:37572303 | T | C | 26 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(23): Show |
26 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.902-316A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572303 | |||||||
| chr17:37572352 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.902-365G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572352 | |||||||
| chr17:37572426 | G | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.902-439C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572426 | |||||||
| chr17:37572485 | A | G | 1 | a0003c0004t0004g0294 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.902-498T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572485 | |||||||
| chr17:37572575 | C | T | 1 | a0002c0002t0002g0166 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.902-588G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572575 | |||||||
| chr17:37572678 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.902-691G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572678 | |||||||
| chr17:37572679 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0270 |
2 | HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.902-692T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572679 | |||||||
| chr17:37572796 | G | C | 1 | a0009c0012t0004g0177 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.902-809C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572796 | |||||||
| chr17:37572818 | T | C | 84 | a0001c0001t0004g0334 a0001c0016t0006g0336 a0002c0002t0001g0201 others(81): Show |
84 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.902-831A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37572818 | |||||||
| chr17:37573179 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.902-1192C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37573179 | |||||||
| chr17:37573293 | C | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.902-1306G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37573293 | |||||||
| chr17:37573360 | G | A | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.902-1373C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37573360 | |||||||
| chr17:37573395 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.902-1408G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37573395 | |||||||
| chr17:37573508 | T | A | 1 | a0002c0011t0015g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.902-1521A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37573508 | |||||||
| chr17:37573521 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.902-1534T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37573521 | |||||||
| chr17:37573661 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.902-1674C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37573661 | |||||||
| chr17:37573736 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.902-1749T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37573736 | |||||||
| chr17:37573749 | T | TA | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.902-1763dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37573749 | |||||||
| chr17:37573788 | T | G | 26 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(23): Show |
26 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.902-1801A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37573788 | |||||||
| chr17:37573859 | A | G | 1 | a0001c0003t0001g0138 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.902-1872T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37573859 | |||||||
| chr17:37573871 | T | A | 3 | a0001c0001t0011g0117 a0001c0001t0011g0118 a0001c0001t0028g0116 |
3 | HG01891.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.902-1884A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37573871 | |||||||
| chr17:37573987 | C | T | 1 | a0002c0011t0015g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.902-2000G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37573987 | |||||||
| chr17:37574130 | T | C | 3 | a0001c0001t0011g0117 a0001c0001t0011g0118 a0001c0001t0028g0116 |
3 | HG01891.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.902-2143A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37574130 | |||||||
| chr17:37574142 | C | T | 1 | a0001c0001t0021g0039 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.902-2155G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37574142 | |||||||
| chr17:37574237 | C | T | 3 | a0002c0002t0002g0223 a0002c0002t0002g0332 a0008c0021t0002g0224 |
3 | HG00639.hp2 HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.901+2104G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37574237 | |||||||
| chr17:37574397 | G | C | 19 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(16): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.901+1944C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37574397 | |||||||
| chr17:37574528 | A | G | 19 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(16): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.901+1813T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37574528 | |||||||
| chr17:37574647 | A | G | 1 | a0003c0004t0002g0293 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.901+1694T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37574647 | |||||||
| chr17:37574738 | A | G | 1 | a0001c0001t0004g0334 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.901+1603T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37574738 | |||||||
| chr17:37574893 | A | T | 1 | a0001c0003t0001g0133 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.901+1448T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37574893 | |||||||
| chr17:37574895 | C | T | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.901+1446G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37574895 | |||||||
| chr17:37574916 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.901+1425C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37574916 | |||||||
| chr17:37574977 | T | C | 2 | a0001c0003t0003g0183 a0011c0018t0003g0160 |
2 | HG02027.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.901+1364A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37574977 | |||||||
| chr17:37575203 | A | G | 1 | a0001c0003t0001g0164 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.901+1138T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37575203 | |||||||
| chr17:37575285 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.901+1056T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37575285 | |||||||
| chr17:37575337 | T | A | 1 | a0002c0011t0015g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.901+1004A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37575337 | |||||||
| chr17:37575392 | T | C | 1 | a0001c0003t0003g0146 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.901+949A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37575392 | |||||||
| chr17:37575457 | TA | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
150 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.901+883delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37575457 | |||||||
| chr17:37575460 | A | T | 1 | a0001c0003t0041g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.901+881T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37575460 | |||||||
| chr17:37575475 | A | G | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.901+866T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37575475 | |||||||
| chr17:37575833 | C | T | 2 | a0002c0002t0006g0197 a0002c0002t0006g0198 |
2 | NA19005.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.901+508G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37575833 | |||||||
| chr17:37575840 | C | CA | 16 | a0001c0001t0001g0068 a0001c0001t0011g0340 a0001c0001t0011g0341 others(13): Show |
16 | HG00323.hp2 HG00621.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.901+500dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37575840 | |||||||
| chr17:37575840 | CA | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0027 others(57): Show |
61 | HG00735.hp1 HG01167.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.901+500delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37575840 | |||||||
| chr17:37575861 | G | C | 6 | a0001c0001t0001g0058 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG01081.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.901+480C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37575861 | |||||||
| chr17:37576184 | C | T | 83 | a0001c0016t0006g0336 a0002c0002t0001g0201 a0002c0002t0001g0233 others(80): Show |
83 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.901+157G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 8/21 | chr17 | 37576184 | |||||||
| chr17:37576480 | G | A | 1 | a0002c0011t0015g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.824-62C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 7/21 | chr17 | 37576480 | |||||||
| chr17:37576487 | G | A | 1 | a0003c0004t0002g0125 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.824-69C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 7/21 | chr17 | 37576487 | |||||||
| chr17:37576496 | C | T | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
284 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.824-78G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 7/21 | chr17 | 37576496 | |||||||
| chr17:37577089 | A | G | 26 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(23): Show |
26 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.823+291T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 7/21 | chr17 | 37577089 | |||||||
| chr17:37577257 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.823+123A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 7/21 | chr17 | 37577257 | |||||||
| chr17:37577687 | C | T | 1 | a0001c0001t0037g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.590-74G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37577687 | |||||||
| chr17:37577695 | C | CTT | 17 | a0001c0001t0001g0027 a0001c0001t0005g0029 a0001c0001t0008g0016 others(14): Show |
17 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.590-84_590-83dupAA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37577695 | |||||||
| chr17:37577695 | CT | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0042 others(109): Show |
113 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.590-83delA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37577695 | |||||||
| chr17:37577695 | CTT | C | 7 | a0003c0004t0002g0122 a0003c0004t0002g0124 a0003c0004t0002g0125 others(4): Show |
7 | HG00738.hp1 HG01123.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.590-84_590-83delAA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37577695 | |||||||
| chr17:37577923 | C | T | 1 | a0001c0003t0003g0146 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.590-310G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37577923 | |||||||
| chr17:37577944 | C | T | 1 | a0001c0003t0007g0185 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.590-331G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37577944 | |||||||
| chr17:37578032 | G | A | 3 | a0001c0003t0007g0172 a0001c0003t0007g0185 a0001c0003t0007g0188 |
3 | HG01106.hp1 HG01167.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.590-419C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37578032 | |||||||
| chr17:37578204 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.590-591T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37578204 | |||||||
| chr17:37578287 | C | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.590-674G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37578287 | |||||||
| chr17:37578379 | G | A | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.590-766C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37578379 | |||||||
| chr17:37579044 | A | G | 1 | a0003c0004t0002g0125 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.590-1431T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37579044 | |||||||
| chr17:37579161 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0087 |
3 | NA18951.hp2 NA19060.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.590-1548C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37579161 | |||||||
| chr17:37579263 | A | G | 1 | a0003c0004t0004g0300 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.590-1650T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37579263 | |||||||
| chr17:37579590 | G | T | 4 | a0001c0001t0005g0115 a0001c0001t0011g0117 a0001c0001t0011g0118 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-1977C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37579590 | |||||||
| chr17:37579747 | T | C | 2 | a0002c0002t0002g0192 a0002c0002t0002g0326 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.590-2134A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37579747 | |||||||
| chr17:37579750 | G | T | 2 | a0001c0003t0003g0144 a0001c0003t0003g0145 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.590-2137C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37579750 | |||||||
| chr17:37579773 | T | C | 19 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(16): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.590-2160A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37579773 | |||||||
| chr17:37580196 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG00438.hp1 HG00735.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-2583A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580196 | |||||||
| chr17:37580296 | CT | C | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(270): Show |
277 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.590-2684delA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580296 | |||||||
| chr17:37580387 | T | C | 1 | a0003c0004t0009g0309 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.590-2774A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580387 | |||||||
| chr17:37580478 | C | CGT | 46 | a0001c0003t0001g0178 a0001c0003t0003g0137 a0001c0003t0007g0172 others(43): Show |
46 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.590-2867_590-2866d others(4): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580478 | |||||||
| chr17:37580478 | C | CGTGT | 10 | a0001c0001t0008g0315 a0001c0001t0011g0117 a0001c0001t0011g0118 others(7): Show |
10 | HG00609.hp1 HG01106.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.590-2869_590-2866d others(6): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580478 | |||||||
| chr17:37580478 | C | CGTGTGT | 4 | a0001c0003t0001g0138 a0003c0004t0003g0283 a0003c0004t0003g0292 others(1): Show |
4 | HG01175.hp2 HG02735.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-2871_590-2866d others(8): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580478 | |||||||
| chr17:37580478 | C | CGTGTGTG others(1): Show |
6 | a0001c0001t0001g0042 a0001c0001t0001g0079 a0001c0001t0001g0096 others(3): Show |
6 | HG02145.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.590-2873_590-2866d others(10): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580478 | |||||||
| chr17:37580478 | C | CGTGTGTG others(3): Show |
65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): Show |
68 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.590-2875_590-2866d others(12): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580478 | |||||||
| chr17:37580478 | C | CGTGTGTG others(5): Show |
18 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0056 others(15): Show |
18 | HG01070.hp2 HG01515.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.590-2877_590-2866d others(14): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580478 | |||||||
| chr17:37580478 | C | CGTGTGTG others(7): Show |
6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0113 others(3): Show |
6 | HG02258.hp2 HG03927.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-2879_590-2866d others(16): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580478 | |||||||
| chr17:37580478 | C | CGTGTGTG others(9): Show |
2 | a0001c0001t0001g0106 a0001c0001t0010g0190 |
2 | HG03516.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.590-2881_590-2866d others(18): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580478 | |||||||
| chr17:37580478 | C | CGTGTGTG others(11): Show |
2 | a0001c0001t0010g0189 a0001c0001t0010g0324 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.590-2883_590-2866d others(20): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580478 | |||||||
| chr17:37580478 | C | CGTGTGTG others(15): Show |
1 | a0001c0005t0008g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.590-2887_590-2866d others(24): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580478 | |||||||
| chr17:37580506 | T | TGAGAGAG others(3): Show |
1 | a0002c0002t0006g0247 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.590-2894_590-2893i others(12): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580506 | |||||||
| chr17:37580508 | T | A | 2 | a0002c0002t0002g0225 a0002c0002t0006g0247 |
2 | HG01346.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.590-2895A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580508 | |||||||
| chr17:37580508 | T | TGAGAGAG others(3): Show |
60 | a0001c0001t0004g0334 a0001c0016t0006g0336 a0002c0002t0001g0201 others(57): Show |
60 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.590-2896_590-2895i others(12): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580508 | |||||||
| chr17:37580508 | T | TGAGAGAG others(5): Show |
6 | a0002c0002t0002g0242 a0002c0002t0005g0203 a0002c0002t0006g0210 others(3): Show |
6 | HG02615.hp1 HG03831.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.590-2896_590-2895i others(14): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580508 | |||||||
| chr17:37580508 | T | TGAGAGAG others(7): Show |
4 | a0002c0002t0002g0216 a0002c0002t0002g0231 a0002c0002t0002g0237 others(1): Show |
4 | HG01981.hp1 NA18948.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.590-2896_590-2895i others(16): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580508 | |||||||
| chr17:37580508 | T | TGAGAGAG others(9): Show |
3 | a0002c0002t0002g0166 a0002c0002t0002g0217 a0002c0002t0006g0244 |
3 | HG01081.hp1 HG02080.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.590-2896_590-2895i others(18): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580508 | |||||||
| chr17:37580508 | T | TGAGAGAG others(17): Show |
1 | a0002c0011t0007g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.590-2896_590-2895i others(26): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580508 | |||||||
| chr17:37580508 | T | TGAGAGAG others(21): Show |
1 | a0002c0002t0008g0196 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.590-2896_590-2895i others(30): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580508 | |||||||
| chr17:37580508 | TGTGAGAG others(1): Show |
T | 9 | a0001c0005t0005g0109 a0001c0005t0005g0110 a0001c0005t0005g0273 others(6): Show |
9 | HG02055.hp2 HG02647.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.590-2903_590-2896d others(10): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580508 | |||||||
| chr17:37580510 | T | A | 78 | a0001c0001t0004g0334 a0001c0016t0006g0336 a0002c0002t0001g0201 others(75): Show |
78 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.590-2897A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580510 | |||||||
| chr17:37580510 | T | TGAGAGAG others(3): Show |
1 | a0002c0002t0001g0233 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.590-2907_590-2898d others(12): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580510 | |||||||
| chr17:37580510 | T | TGAGAGAG others(5): Show |
2 | a0002c0002t0002g0226 a0002c0002t0002g0330 |
2 | HG00438.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.590-2909_590-2898d others(14): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580510 | |||||||
| chr17:37580510 | T | TGAGAGAG others(7): Show |
2 | a0002c0002t0002g0165 a0002c0002t0002g0327 |
2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.590-2911_590-2898d others(16): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580510 | |||||||
| chr17:37580510 | T | TGTGTGTG others(3): Show |
14 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0005g0029 others(11): Show |
14 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.590-2898_590-2897i others(12): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580510 | |||||||
| chr17:37580510 | T | TGTGTGTG others(5): Show |
4 | a0001c0001t0008g0018 a0001c0001t0017g0019 a0001c0006t0013g0020 others(1): Show |
4 | HG01884.hp1 HG02615.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-2898_590-2897i others(14): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580510 | |||||||
| chr17:37580510 | T | TGTGTGTG others(5): Show |
3 | a0001c0001t0011g0340 a0001c0001t0011g0342 a0001c0001t0011g0343 |
3 | HG02486.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.590-2898_590-2897i others(14): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580510 | |||||||
| chr17:37580510 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0011g0341 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.590-2898_590-2897i others(16): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580510 | |||||||
| chr17:37580510 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0010g0012 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.590-2898_590-2897i others(18): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580510 | |||||||
| chr17:37580510 | T | TGTGTGTG others(11): Show |
2 | a0001c0006t0001g0011 a0001c0006t0001g0031 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.590-2898_590-2897i others(20): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580510 | |||||||
| chr17:37580510 | T | TGTGTGTG others(17): Show |
1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.590-2898_590-2897i others(26): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580510 | |||||||
| chr17:37580512 | A | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
141 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.590-2899T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580512 | |||||||
| chr17:37580514 | A | T | 4 | a0001c0001t0008g0315 a0001c0001t0028g0116 a0001c0005t0008g0266 others(1): Show |
4 | HG02055.hp1 HG02630.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-2901T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580514 | |||||||
| chr17:37580516 | A | T | 2 | a0001c0005t0008g0266 a0001c0005t0009g0265 |
2 | HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.590-2903T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580516 | |||||||
| chr17:37580553 | C | T | 1 | a0003c0004t0004g0306 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.590-2940G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580553 | |||||||
| chr17:37580596 | G | A | 1 | a0001c0001t0040g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.590-2983C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580596 | |||||||
| chr17:37580621 | A | G | 20 | a0002c0002t0002g0168 a0002c0002t0002g0206 a0002c0002t0002g0207 others(17): Show |
20 | HG00438.hp2 NA18951.hp1 NA18953.hp2 others(17): Show |
intron_variant | MODIFIER | c.590-3008T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580621 | |||||||
| chr17:37580650 | T | G | 1 | a0003c0004t0004g0301 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.590-3037A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580650 | |||||||
| chr17:37580825 | G | A | 1 | a0002c0002t0002g0245 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.590-3212C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580825 | |||||||
| chr17:37580898 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.590-3285T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37580898 | |||||||
| chr17:37581256 | C | G | 1 | a0002c0002t0002g0327 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.589+3392G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37581256 | |||||||
| chr17:37581274 | C | CTAT | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): Show |
93 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.589+3371_589+3373d others(5): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37581274 | |||||||
| chr17:37581293 | T | G | 3 | a0001c0001t0010g0012 a0001c0006t0001g0011 a0001c0006t0001g0031 |
3 | HG02895.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.589+3355A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37581293 | |||||||
| chr17:37581397 | C | G | 4 | a0001c0001t0005g0115 a0001c0001t0011g0117 a0001c0001t0011g0118 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+3251G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37581397 | |||||||
| chr17:37581428 | T | C | 2 | a0002c0002t0014g0251 a0002c0002t0014g0252 |
2 | HG01256.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.589+3220A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37581428 | |||||||
| chr17:37581625 | C | T | 3 | a0002c0002t0002g0223 a0002c0002t0002g0332 a0008c0021t0002g0224 |
3 | HG00639.hp2 HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.589+3023G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37581625 | |||||||
| chr17:37581765 | C | CT | 9 | a0001c0003t0001g0178 a0001c0003t0034g0130 a0001c0005t0009g0265 others(6): Show |
9 | HG01175.hp2 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.589+2882dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37581765 | |||||||
| chr17:37582015 | G | A | 1 | a0001c0001t0011g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.589+2633C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37582015 | |||||||
| chr17:37582510 | A | G | 19 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(16): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.589+2138T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37582510 | |||||||
| chr17:37582586 | C | A | 1 | a0002c0002t0004g0235 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.589+2062G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37582586 | |||||||
| chr17:37582661 | G | A | 1 | a0002c0002t0006g0222 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.589+1987C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37582661 | |||||||
| chr17:37582751 | C | T | 1 | a0001c0005t0009g0265 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.589+1897G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37582751 | |||||||
| chr17:37582793 | C | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.589+1855G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37582793 | |||||||
| chr17:37582836 | T | C | 1 | a0001c0005t0005g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.589+1812A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37582836 | |||||||
| chr17:37582848 | C | A | 1 | a0006c0009t0003g0142 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.589+1800G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37582848 | |||||||
| chr17:37583112 | T | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
182 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.589+1536A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37583112 | |||||||
| chr17:37583117 | A | C | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.589+1531T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37583117 | |||||||
| chr17:37583323 | A | C | 3 | a0001c0001t0011g0117 a0001c0001t0011g0118 a0001c0001t0028g0116 |
3 | HG01891.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.589+1325T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37583323 | |||||||
| chr17:37583678 | T | G | 2 | a0002c0002t0002g0204 a0002c0002t0002g0253 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.589+970A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37583678 | |||||||
| chr17:37583938 | C | A | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.589+710G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37583938 | |||||||
| chr17:37583939 | A | C | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.589+709T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37583939 | |||||||
| chr17:37583941 | C | T | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.589+707G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37583941 | |||||||
| chr17:37584126 | C | T | 2 | a0002c0002t0008g0196 a0002c0011t0007g0194 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.589+522G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37584126 | |||||||
| chr17:37584170 | A | G | 26 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(23): Show |
26 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.589+478T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37584170 | |||||||
| chr17:37584254 | G | T | 1 | a0001c0001t0001g0262 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.589+394C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37584254 | |||||||
| chr17:37584257 | A | T | 1 | a0003c0004t0001g0119 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.589+391T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37584257 | |||||||
| chr17:37584279 | A | G | 54 | a0001c0001t0004g0334 a0001c0001t0010g0189 a0001c0001t0010g0190 others(51): Show |
54 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.589+369T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37584279 | |||||||
| chr17:37584413 | T | C | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.589+235A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37584413 | |||||||
| chr17:37584431 | A | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.589+217T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37584431 | |||||||
| chr17:37584577 | C | T | 1 | a0001c0001t0010g0324 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.589+71G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37584577 | |||||||
| chr17:37584621 | G | C | 1 | a0001c0003t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.589+27C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 6/21 | chr17 | 37584621 | |||||||
| chr17:37585008 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.478-249C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 5/21 | chr17 | 37585008 | |||||||
| chr17:37585247 | C | T | 1 | a0001c0003t0030g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.477+78G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 5/21 | chr17 | 37585247 | |||||||
| chr17:37585253 | C | G | 1 | a0003c0004t0004g0127 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.477+72G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 5/21 | chr17 | 37585253 | |||||||
| chr17:37585466 | C | T | 1 | a0001c0003t0001g0316 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.372-36G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37585466 | |||||||
| chr17:37585551 | C | T | 14 | a0001c0005t0005g0109 a0001c0005t0005g0110 a0001c0005t0005g0273 others(11): Show |
15 | HG02055.hp2 HG02647.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.372-121G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37585551 | |||||||
| chr17:37585591 | T | C | 1 | a0003c0004t0004g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.372-161A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37585591 | |||||||
| chr17:37585698 | C | T | 1 | a0003c0004t0004g0291 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.372-268G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37585698 | |||||||
| chr17:37585715 | G | A | 1 | a0001c0003t0003g0159 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.372-285C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37585715 | |||||||
| chr17:37585831 | G | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0087 |
3 | NA18951.hp2 NA19060.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.372-401C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37585831 | |||||||
| chr17:37586083 | T | A | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.371+336A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586083 | |||||||
| chr17:37586085 | G | C | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.371+334C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586085 | |||||||
| chr17:37586086 | G | T | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.371+333C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586086 | |||||||
| chr17:37586087 | G | A | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.371+332C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586087 | |||||||
| chr17:37586089 | C | A | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.371+330G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586089 | |||||||
| chr17:37586090 | C | T | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.371+329G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586090 | |||||||
| chr17:37586092 | A | G | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.371+327T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586092 | |||||||
| chr17:37586093 | G | C | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.371+326C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586093 | |||||||
| chr17:37586099 | C | T | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.371+320G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586099 | |||||||
| chr17:37586164 | TTG | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0087 |
3 | NA18951.hp2 NA19060.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.371+253_371+254del others(2): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586164 | |||||||
| chr17:37586168 | A | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0087 |
3 | NA18951.hp2 NA19060.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.371+251T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586168 | |||||||
| chr17:37586369 | T | C | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.371+50A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586369 | |||||||
| chr17:37586386 | C | A | 19 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(16): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.371+33G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586386 | |||||||
| chr17:37586402 | T | C | 1 | a0001c0003t0001g0317 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.371+17A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 4/21 | chr17 | 37586402 | |||||||
| chr17:37586687 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0075 others(4): Show |
7 | HG02129.hp1 NA18952.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-138C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37586687 | |||||||
| chr17:37586706 | T | A | 60 | a0001c0001t0005g0115 a0001c0001t0008g0315 a0001c0001t0010g0189 others(57): Show |
60 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.241-157A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37586706 | |||||||
| chr17:37586714 | T | C | 1 | a0003c0004t0025g0303 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.241-165A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37586714 | |||||||
| chr17:37586818 | C | G | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
292 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(289): Show |
intron_variant | MODIFIER | c.241-269G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37586818 | |||||||
| chr17:37587049 | T | C | 2 | a0001c0005t0008g0266 a0001c0005t0009g0265 |
2 | HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.241-500A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37587049 | |||||||
| chr17:37587118 | T | G | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
183 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.241-569A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37587118 | |||||||
| chr17:37587447 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.241-898T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37587447 | |||||||
| chr17:37587512 | T | C | 1 | a0002c0002t0001g0233 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.241-963A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37587512 | |||||||
| chr17:37587546 | T | G | 1 | a0001c0001t0010g0012 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.241-997A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37587546 | |||||||
| chr17:37587963 | A | G | 1 | a0002c0002t0002g0242 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.241-1414T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37587963 | |||||||
| chr17:37587969 | T | C | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.241-1420A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37587969 | |||||||
| chr17:37588186 | G | A | 4 | a0001c0001t0005g0115 a0001c0001t0011g0117 a0001c0001t0011g0118 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-1637C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37588186 | |||||||
| chr17:37588258 | C | CT | 18 | a0001c0001t0010g0012 a0001c0001t0011g0340 a0001c0001t0011g0341 others(15): Show |
18 | HG00323.hp1 HG00741.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.241-1710dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37588258 | |||||||
| chr17:37588258 | CT | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
153 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.241-1710delA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37588258 | |||||||
| chr17:37588278 | T | C | 5 | a0001c0005t0005g0109 a0001c0005t0005g0110 a0001c0005t0005g0277 others(2): Show |
5 | HG02055.hp2 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.241-1729A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37588278 | |||||||
| chr17:37588634 | A | T | 3 | a0003c0004t0004g0127 a0003c0004t0004g0267 a0003c0004t0015g0288 |
3 | HG00609.hp1 HG02155.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.241-2085T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37588634 | |||||||
| chr17:37588741 | C | CT | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
172 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.241-2193dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37588741 | |||||||
| chr17:37588755 | T | TA | 3 | a0001c0001t0001g0269 a0001c0001t0021g0039 a0001c0001t0039g0040 |
3 | HG02735.hp1 HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.241-2207dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37588755 | |||||||
| chr17:37589165 | A | C | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.241-2616T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589165 | |||||||
| chr17:37589167 | A | C | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.241-2618T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589167 | |||||||
| chr17:37589282 | T | C | 1 | a0001c0003t0003g0183 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.241-2733A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589282 | |||||||
| chr17:37589433 | T | A | 1 | a0002c0011t0015g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.241-2884A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589433 | |||||||
| chr17:37589443 | C | G | 1 | a0003c0004t0002g0124 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.241-2894G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589443 | |||||||
| chr17:37589476 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.241-2927G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589476 | |||||||
| chr17:37589479 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.241-2930C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589479 | |||||||
| chr17:37589609 | C | T | 2 | a0002c0002t0002g0234 a0002c0002t0002g0241 |
2 | NA18941.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.241-3060G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589609 | |||||||
| chr17:37589673 | C | T | 1 | a0001c0003t0003g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.241-3124G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589673 | |||||||
| chr17:37589703 | C | T | 2 | a0006c0009t0003g0142 a0006c0009t0004g0141 |
2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.241-3154G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589703 | |||||||
| chr17:37589704 | G | A | 1 | a0003c0004t0004g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.241-3155C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589704 | |||||||
| chr17:37589718 | C | T | 1 | a0002c0011t0007g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.241-3169G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589718 | |||||||
| chr17:37589754 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.241-3205T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589754 | |||||||
| chr17:37589851 | C | A | 1 | a0001c0001t0004g0049 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.241-3302G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589851 | |||||||
| chr17:37589897 | G | A | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.241-3348C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589897 | |||||||
| chr17:37589900 | T | C | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.241-3351A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589900 | |||||||
| chr17:37589956 | A | G | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.241-3407T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37589956 | |||||||
| chr17:37590026 | C | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
94 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.241-3477G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590026 | |||||||
| chr17:37590082 | A | G | 1 | a0002c0002t0001g0233 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.241-3533T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590082 | |||||||
| chr17:37590154 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.241-3605G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590154 | |||||||
| chr17:37590167 | C | CA | 16 | a0001c0005t0008g0266 a0001c0005t0009g0265 a0002c0002t0002g0223 others(13): Show |
16 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.241-3619dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590167 | |||||||
| chr17:37590177 | A | T | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.241-3628T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590177 | |||||||
| chr17:37590177 | AAAAAG | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(17): Show |
20 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.241-3633_241-3629d others(7): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590177 | |||||||
| chr17:37590206 | CT | C | 26 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(23): Show |
26 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.241-3658delA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590206 | |||||||
| chr17:37590337 | A | G | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.241-3788T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590337 | |||||||
| chr17:37590362 | A | G | 2 | a0001c0003t0007g0170 a0001c0003t0007g0171 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.241-3813T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590362 | |||||||
| chr17:37590556 | A | G | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.241-4007T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590556 | |||||||
| chr17:37590719 | G | A | 2 | a0001c0005t0005g0278 a0001c0005t0005g0279 |
2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.241-4170C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590719 | |||||||
| chr17:37590734 | G | A | 1 | a0001c0003t0001g0135 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.241-4185C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590734 | |||||||
| chr17:37590741 | T | G | 1 | a0001c0001t0001g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.241-4192A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590741 | |||||||
| chr17:37590754 | C | T | 83 | a0001c0001t0004g0334 a0002c0002t0001g0201 a0002c0002t0001g0233 others(80): Show |
83 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.241-4205G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590754 | |||||||
| chr17:37590925 | G | A | 1 | a0001c0003t0002g0186 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.241-4376C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590925 | |||||||
| chr17:37590951 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.241-4402A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37590951 | |||||||
| chr17:37591213 | C | A | 1 | a0001c0003t0001g0136 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.241-4664G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37591213 | |||||||
| chr17:37591213 | C | T | 26 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(23): Show |
26 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.241-4664G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37591213 | |||||||
| chr17:37591398 | A | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
95 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.240+4825T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37591398 | |||||||
| chr17:37591680 | T | C | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+4543A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37591680 | |||||||
| chr17:37591994 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.240+4229C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37591994 | |||||||
| chr17:37592340 | C | T | 50 | a0002c0002t0016g0219 a0003c0004t0001g0119 a0003c0004t0001g0337 others(47): Show |
50 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.240+3883G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37592340 | |||||||
| chr17:37592342 | G | A | 1 | a0001c0005t0008g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.240+3881C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37592342 | |||||||
| chr17:37592876 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
95 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.240+3347T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37592876 | |||||||
| chr17:37593043 | A | G | 1 | a0001c0001t0021g0082 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.240+3180T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37593043 | |||||||
| chr17:37593102 | T | C | 4 | a0001c0001t0005g0115 a0001c0001t0011g0117 a0001c0001t0011g0118 others(1): Show |
4 | HG01891.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.240+3121A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37593102 | |||||||
| chr17:37593106 | A | G | 1 | a0001c0003t0001g0164 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.240+3117T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37593106 | |||||||
| chr17:37593138 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.240+3085G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37593138 | |||||||
| chr17:37593330 | T | C | 1 | a0001c0005t0005g0280 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.240+2893A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37593330 | |||||||
| chr17:37593525 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
122 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.240+2698T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37593525 | |||||||
| chr17:37593701 | A | G | 50 | a0001c0001t0004g0334 a0003c0004t0001g0119 a0003c0004t0001g0337 others(47): Show |
50 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.240+2522T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37593701 | |||||||
| chr17:37593874 | C | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
198 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.240+2349G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37593874 | |||||||
| chr17:37593878 | C | CA | 6 | a0001c0003t0001g0136 a0001c0003t0007g0174 a0001c0005t0005g0110 others(3): Show |
6 | HG00741.hp1 HG02055.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+2344dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37593878 | |||||||
| chr17:37593878 | CA | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
96 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.240+2344delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37593878 | |||||||
| chr17:37594008 | G | C | 1 | a0003c0004t0004g0310 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.240+2215C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594008 | |||||||
| chr17:37594154 | T | TATTATTT others(23): Show |
1 | a0001c0003t0003g0162 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.240+2039_240+2068d others(32): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594154 | |||||||
| chr17:37594154 | TATTATTT others(23): Show |
T | 157 | a0001c0001t0004g0334 a0001c0001t0005g0115 a0001c0001t0008g0315 others(154): Show |
158 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.240+2039_240+2068d others(32): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594154 | |||||||
| chr17:37594154 | TATTATTT others(53): Show |
T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
122 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.240+2009_240+2068d others(62): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594154 | |||||||
| chr17:37594231 | T | C | 12 | a0002c0002t0002g0168 a0002c0002t0002g0206 a0002c0002t0002g0207 others(9): Show |
12 | NA18951.hp1 NA18953.hp2 NA18970.hp1 others(9): Show |
intron_variant | MODIFIER | c.240+1992A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594231 | |||||||
| chr17:37594272 | A | T | 1 | a0001c0003t0034g0130 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.240+1951T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594272 | |||||||
| chr17:37594275 | T | A | 1 | a0001c0003t0034g0130 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.240+1948A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594275 | |||||||
| chr17:37594277 | A | T | 1 | a0001c0003t0034g0130 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.240+1946T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594277 | |||||||
| chr17:37594290 | T | G | 1 | a0001c0001t0001g0038 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.240+1933A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594290 | |||||||
| chr17:37594366 | GTTA | G | 60 | a0001c0001t0005g0115 a0001c0001t0008g0315 a0001c0001t0010g0189 others(57): Show |
60 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.240+1854_240+1856d others(5): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594366 | |||||||
| chr17:37594462 | C | CT | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
94 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.240+1760dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594462 | |||||||
| chr17:37594462 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.240+1761G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594462 | |||||||
| chr17:37594522 | G | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.240+1701C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594522 | |||||||
| chr17:37594609 | G | A | 1 | a0001c0001t0036g0081 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.240+1614C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594609 | |||||||
| chr17:37594809 | T | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.240+1414A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594809 | |||||||
| chr17:37594875 | A | C | 5 | a0001c0001t0001g0269 a0001c0001t0021g0039 a0001c0001t0022g0009 others(2): Show |
5 | HG01515.hp1 HG01517.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+1348T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594875 | |||||||
| chr17:37594919 | G | A | 1 | a0002c0002t0006g0246 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.240+1304C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37594919 | |||||||
| chr17:37595305 | C | T | 1 | a0001c0005t0005g0273 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.240+918G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37595305 | |||||||
| chr17:37595308 | G | A | 2 | a0001c0001t0022g0009 a0001c0001t0022g0264 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.240+915C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37595308 | |||||||
| chr17:37595603 | A | G | 1 | a0002c0002t0016g0193 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.240+620T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37595603 | |||||||
| chr17:37595756 | C | CT | 19 | a0001c0001t0012g0111 a0001c0003t0003g0184 a0001c0005t0005g0109 others(16): Show |
20 | HG01175.hp1 HG01192.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.240+466dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37595756 | |||||||
| chr17:37595794 | G | C | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.240+429C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37595794 | |||||||
| chr17:37595971 | T | C | 88 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(85): Show |
88 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.240+252A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37595971 | |||||||
| chr17:37596107 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.240+116G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37596107 | |||||||
| chr17:37596120 | C | T | 1 | a0003c0004t0026g0286 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.240+103G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37596120 | |||||||
| chr17:37596172 | A | T | 1 | a0001c0001t0004g0049 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.240+51T>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37596172 | |||||||
| chr17:37596216 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0005g0048 |
3 | HG02622.hp1 HG02970.hp1 HG03579.hp2 |
splice_region_variant&intron_variant | LOW | c.240+7G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 3/21 | chr17 | 37596216 | |||||||
| chr17:37596571 | C | T | 3 | a0001c0001t0010g0012 a0001c0006t0001g0011 a0001c0006t0001g0031 |
3 | HG02895.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.119-227G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37596571 | |||||||
| chr17:37596654 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0004g0083 |
2 | NA19058.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.119-310A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37596654 | |||||||
| chr17:37596731 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.119-387C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37596731 | |||||||
| chr17:37596845 | C | A | 2 | a0001c0003t0003g0163 a0001c0003t0003g0320 |
2 | HG01099.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.119-501G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37596845 | |||||||
| chr17:37597001 | C | G | 1 | a0001c0001t0012g0035 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.119-657G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37597001 | |||||||
| chr17:37597263 | C | G | 1 | a0002c0002t0006g0247 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.119-919G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37597263 | |||||||
| chr17:37597291 | T | A | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.119-947A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37597291 | |||||||
| chr17:37597385 | G | A | 1 | a0001c0005t0008g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.119-1041C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37597385 | |||||||
| chr17:37597426 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | NA18952.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.119-1082T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37597426 | |||||||
| chr17:37597428 | A | C | 1 | a0001c0001t0011g0340 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.119-1084T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37597428 | |||||||
| chr17:37597537 | T | C | 1 | a0002c0002t0002g0218 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.119-1193A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37597537 | |||||||
| chr17:37597863 | A | G | 3 | a0001c0001t0010g0012 a0001c0006t0001g0011 a0001c0006t0001g0031 |
3 | HG02895.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.119-1519T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37597863 | |||||||
| chr17:37598301 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | NA18952.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.119-1957T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37598301 | |||||||
| chr17:37598384 | G | A | 14 | a0001c0005t0005g0109 a0001c0005t0005g0110 a0001c0005t0005g0273 others(11): Show |
15 | HG02055.hp2 HG02647.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.118+1979C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37598384 | |||||||
| chr17:37598445 | C | T | 3 | a0001c0001t0002g0268 a0005c0007t0019g0014 a0005c0007t0019g0015 |
3 | HG01243.hp1 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.118+1918G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37598445 | |||||||
| chr17:37598500 | G | A | 1 | a0001c0003t0003g0137 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.118+1863C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37598500 | |||||||
| chr17:37598629 | G | A | 83 | a0002c0002t0001g0201 a0002c0002t0001g0233 a0002c0002t0001g0249 others(80): Show |
83 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.118+1734C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37598629 | |||||||
| chr17:37598660 | A | G | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.118+1703T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37598660 | |||||||
| chr17:37598709 | G | GT | 50 | a0001c0001t0004g0334 a0003c0004t0001g0119 a0003c0004t0001g0337 others(47): Show |
50 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.118+1653dupA | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37598709 | |||||||
| chr17:37599007 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.118+1356G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37599007 | |||||||
| chr17:37599204 | C | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
198 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.118+1159G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37599204 | |||||||
| chr17:37599294 | T | C | 1 | a0001c0003t0001g0164 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.118+1069A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37599294 | |||||||
| chr17:37599297 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.118+1066G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37599297 | |||||||
| chr17:37599311 | T | A | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.118+1052A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37599311 | |||||||
| chr17:37599336 | T | C | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+1027A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37599336 | |||||||
| chr17:37599502 | C | T | 26 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(23): Show |
26 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.118+861G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37599502 | |||||||
| chr17:37599664 | T | A | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+699A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37599664 | |||||||
| chr17:37599670 | A | G | 2 | a0006c0009t0003g0142 a0006c0009t0004g0141 |
2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.118+693T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37599670 | |||||||
| chr17:37599699 | A | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(274): Show |
281 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(278): Show |
intron_variant | MODIFIER | c.118+664T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37599699 | |||||||
| chr17:37599742 | C | A | 1 | a0001c0001t0001g0269 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.118+621G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37599742 | |||||||
| chr17:37599767 | A | G | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.118+596T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37599767 | |||||||
| chr17:37599934 | A | C | 1 | a0001c0003t0034g0130 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.118+429T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37599934 | |||||||
| chr17:37600100 | C | T | 5 | a0001c0001t0008g0315 a0001c0001t0010g0189 a0001c0001t0010g0190 others(2): Show |
5 | HG02055.hp1 HG02258.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+263G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37600100 | |||||||
| chr17:37600147 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.118+216C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37600147 | |||||||
| chr17:37600334 | A | G | 1 | a0001c0005t0005g0109 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.118+29T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 2/21 | chr17 | 37600334 | |||||||
| chr17:37600569 | C | T | 3 | a0001c0001t0011g0117 a0001c0001t0011g0118 a0001c0001t0028g0116 |
3 | HG01891.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.78-166G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37600569 | |||||||
| chr17:37600591 | C | A | 1 | a0001c0003t0001g0138 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.78-188G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37600591 | |||||||
| chr17:37600651 | G | C | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.78-248C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37600651 | |||||||
| chr17:37600840 | T | C | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.78-437A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37600840 | |||||||
| chr17:37600849 | G | GAAGAAAA others(2862): Show |
1 | a0001c0001t0001g0087 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.78-447_78-446insTT others(2867): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37600849 | |||||||
| chr17:37601245 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.78-842A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37601245 | |||||||
| chr17:37601352 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.78-949T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37601352 | |||||||
| chr17:37601359 | G | A | 49 | a0003c0004t0001g0119 a0003c0004t0001g0337 a0003c0004t0001g0338 others(46): Show |
49 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.78-956C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37601359 | |||||||
| chr17:37601611 | T | C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0091 others(11): Show |
15 | HG00558.hp2 HG02027.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.78-1208A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37601611 | |||||||
| chr17:37601871 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
94 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.78-1468C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37601871 | |||||||
| chr17:37601994 | C | T | 42 | a0003c0004t0001g0119 a0003c0004t0001g0337 a0003c0004t0001g0338 others(39): Show |
42 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.78-1591G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37601994 | |||||||
| chr17:37602061 | C | T | 1 | a0009c0012t0004g0177 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.78-1658G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37602061 | |||||||
| chr17:37602200 | T | G | 1 | a0002c0002t0006g0246 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.78-1797A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37602200 | |||||||
| chr17:37602273 | G | T | 2 | a0002c0002t0002g0192 a0002c0002t0002g0326 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.78-1870C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37602273 | |||||||
| chr17:37602298 | T | C | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-1895A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37602298 | |||||||
| chr17:37602360 | C | A | 1 | a0002c0002t0006g0246 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.78-1957G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37602360 | |||||||
| chr17:37602381 | A | G | 2 | a0001c0003t0001g0129 a0001c0003t0001g0317 |
2 | NA19082.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.78-1978T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37602381 | |||||||
| chr17:37602495 | A | G | 1 | a0001c0001t0003g0041 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.78-2092T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37602495 | |||||||
| chr17:37602499 | C | T | 3 | a0001c0001t0010g0012 a0001c0006t0001g0011 a0001c0006t0001g0031 |
3 | HG02895.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.78-2096G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37602499 | |||||||
| chr17:37602724 | C | T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(16): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.78-2321G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37602724 | |||||||
| chr17:37602904 | A | G | 3 | a0001c0001t0001g0269 a0001c0001t0021g0039 a0001c0001t0039g0040 |
3 | HG02735.hp1 HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.78-2501T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37602904 | |||||||
| chr17:37603098 | T | C | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-2695A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37603098 | |||||||
| chr17:37603154 | G | T | 1 | a0003c0004t0002g0122 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.78-2751C>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37603154 | |||||||
| chr17:37603253 | C | T | 1 | a0001c0003t0030g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.78-2850G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37603253 | |||||||
| chr17:37603312 | T | C | 26 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(23): Show |
26 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.78-2909A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37603312 | |||||||
| chr17:37603354 | T | C | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-2951A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37603354 | |||||||
| chr17:37603593 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG02165.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.78-3190A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37603593 | |||||||
| chr17:37603802 | G | C | 340 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(337): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.78-3399C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37603802 | |||||||
| chr17:37603990 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 |
3 | HG02165.hp2 NA18970.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.78-3587G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37603990 | |||||||
| chr17:37604006 | C | T | 1 | a0001c0001t0012g0035 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.78-3603G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37604006 | |||||||
| chr17:37604110 | C | T | 1 | a0003c0004t0004g0285 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.78-3707G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37604110 | |||||||
| chr17:37604165 | G | A | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.78-3762C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37604165 | |||||||
| chr17:37604182 | T | C | 2 | a0001c0001t0001g0100 a0002c0002t0002g0208 |
2 | HG03834.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.78-3779A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37604182 | |||||||
| chr17:37604196 | C | T | 13 | a0001c0003t0001g0129 a0001c0003t0001g0131 a0001c0003t0001g0132 others(10): Show |
13 | HG00621.hp2 HG02300.hp1 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.78-3793G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37604196 | |||||||
| chr17:37604219 | G | A | 2 | a0002c0002t0006g0210 a0012c0019t0002g0209 |
2 | NA18960.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.78-3816C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37604219 | |||||||
| chr17:37604240 | TA | T | 265 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(262): Show |
268 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.78-3838delT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37604240 | |||||||
| chr17:37604274 | C | T | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-3871G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37604274 | |||||||
| chr17:37604275 | G | A | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.78-3872C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37604275 | |||||||
| chr17:37604613 | G | C | 1 | a0001c0005t0009g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.78-4210C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37604613 | |||||||
| chr17:37604617 | T | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
181 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.78-4214A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37604617 | |||||||
| chr17:37604773 | C | G | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.78-4370G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37604773 | |||||||
| chr17:37604804 | G | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(19): Show |
22 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.78-4401C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37604804 | |||||||
| chr17:37605450 | G | A | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.77+3829C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37605450 | |||||||
| chr17:37605459 | A | C | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.77+3820T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37605459 | |||||||
| chr17:37605506 | A | G | 1 | a0002c0002t0002g0232 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.77+3773T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37605506 | |||||||
| chr17:37606009 | C | A | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.77+3270G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37606009 | |||||||
| chr17:37606039 | G | A | 1 | a0001c0003t0041g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.77+3240C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37606039 | |||||||
| chr17:37606118 | T | G | 1 | a0001c0001t0001g0107 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.77+3161A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37606118 | |||||||
| chr17:37606135 | T | G | 1 | a0003c0004t0007g0121 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.77+3144A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37606135 | |||||||
| chr17:37606160 | C | G | 1 | a0001c0001t0040g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.77+3119G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37606160 | |||||||
| chr17:37606208 | C | G | 1 | a0003c0010t0002g0284 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.77+3071G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37606208 | |||||||
| chr17:37606444 | G | A | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
292 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(289): Show |
intron_variant | MODIFIER | c.77+2835C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37606444 | |||||||
| chr17:37606931 | T | A | 1 | a0001c0001t0012g0108 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.77+2348A>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37606931 | |||||||
| chr17:37606931 | T | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): Show |
93 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.77+2348A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37606931 | |||||||
| chr17:37607034 | C | T | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+2245G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607034 | |||||||
| chr17:37607256 | T | G | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+2023A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607256 | |||||||
| chr17:37607325 | C | G | 1 | a0002c0002t0002g0240 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.77+1954G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607325 | |||||||
| chr17:37607424 | T | C | 4 | a0002c0002t0002g0216 a0002c0002t0002g0217 a0002c0002t0002g0231 others(1): Show |
4 | HG00438.hp2 NA18975.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+1855A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607424 | |||||||
| chr17:37607625 | C | T | 1 | a0009c0012t0004g0177 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.77+1654G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607625 | |||||||
| chr17:37607713 | C | T | 1 | a0003c0004t0003g0283 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.77+1566G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607713 | |||||||
| chr17:37607800 | C | G | 1 | a0002c0002t0002g0218 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.77+1479G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607800 | |||||||
| chr17:37607934 | C | A | 19 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(16): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.77+1345G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607934 | |||||||
| chr17:37607955 | C | CA | 10 | a0001c0003t0001g0178 a0001c0003t0001g0179 a0001c0003t0003g0180 others(7): Show |
10 | HG00621.hp2 HG01106.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.77+1323dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607955 | |||||||
| chr17:37607955 | C | CAA | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG01167.hp2 HG01433.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+1322_77+1323dup others(2): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607955 | |||||||
| chr17:37607955 | C | CAAAAA | 33 | a0002c0002t0001g0201 a0002c0002t0002g0010 a0002c0002t0002g0192 others(30): Show |
33 | HG00438.hp2 HG01070.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.77+1319_77+1323dup others(5): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607955 | |||||||
| chr17:37607955 | C | CAAAAAA | 18 | a0002c0002t0002g0218 a0002c0002t0002g0221 a0002c0002t0002g0223 others(15): Show |
18 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.77+1318_77+1323dup others(6): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607955 | |||||||
| chr17:37607955 | C | CAAAAAAA | 10 | a0001c0001t0004g0334 a0002c0002t0001g0233 a0002c0002t0002g0232 others(7): Show |
10 | HG01257.hp1 HG01952.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.77+1317_77+1323dup others(7): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607955 | |||||||
| chr17:37607955 | C | CAAAAAAA others(1): Show |
7 | a0002c0002t0002g0240 a0002c0002t0002g0241 a0002c0002t0002g0242 others(4): Show |
7 | HG01934.hp1 HG02080.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+1316_77+1323dup others(8): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607955 | |||||||
| chr17:37607955 | C | CAAAAAAA others(2): Show |
9 | a0002c0002t0001g0249 a0002c0002t0002g0248 a0002c0002t0002g0253 others(6): Show |
9 | HG01243.hp2 HG01256.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.77+1315_77+1323dup others(9): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607955 | |||||||
| chr17:37607955 | C | CAAAAAAA others(3): Show |
3 | a0001c0016t0006g0336 a0002c0002t0002g0008 a0002c0002t0024g0255 |
3 | HG02280.hp2 NA18943.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.77+1314_77+1323dup others(10): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607955 | |||||||
| chr17:37607955 | CAA | C | 13 | a0001c0005t0005g0109 a0001c0005t0005g0110 a0001c0005t0005g0273 others(10): Show |
14 | HG02055.hp2 HG02647.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.77+1322_77+1323del others(2): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607955 | |||||||
| chr17:37607965 | A | AACAAACA others(3): Show |
1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.77+1313_77+1314ins others(10): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607965 | |||||||
| chr17:37607969 | A | C | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.77+1310T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607969 | |||||||
| chr17:37607971 | A | AAC | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
91 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.77+1307_77+1308ins others(2): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607971 | |||||||
| chr17:37607973 | A | C | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.77+1306T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607973 | |||||||
| chr17:37607977 | A | AAAAC | 11 | a0001c0001t0008g0315 a0003c0004t0002g0122 a0003c0004t0002g0124 others(8): Show |
11 | HG00323.hp2 HG00738.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.77+1298_77+1301dup others(4): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607977 | |||||||
| chr17:37607977 | A | AAAC | 34 | a0003c0004t0001g0119 a0003c0004t0001g0337 a0003c0004t0001g0338 others(31): Show |
34 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.77+1301_77+1302ins others(3): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607977 | |||||||
| chr17:37607977 | A | AAC | 6 | a0001c0001t0011g0117 a0001c0001t0011g0118 a0001c0001t0028g0116 others(3): Show |
6 | HG01358.hp2 HG01891.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+1301_77+1302ins others(2): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607977 | |||||||
| chr17:37607977 | A | AC | 6 | a0001c0001t0005g0115 a0001c0001t0011g0340 a0001c0001t0011g0341 others(3): Show |
6 | HG02486.hp1 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+1301_77+1302ins others(1): Show |
SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607977 | |||||||
| chr17:37607977 | A | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
132 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.77+1302T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607977 | |||||||
| chr17:37607981 | C | A | 1 | a0002c0002t0002g0256 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.77+1298G>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37607981 | |||||||
| chr17:37608184 | TG | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0002g0268 others(19): Show |
22 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.77+1094delC | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37608184 | |||||||
| chr17:37608282 | T | G | 2 | a0004c0008t0020g0257 a0004c0008t0020g0258 |
2 | HG01358.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.77+997A>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37608282 | |||||||
| chr17:37608297 | T | TA | 7 | a0001c0001t0001g0259 a0001c0003t0003g0260 a0002c0002t0002g0261 others(4): Show |
7 | HG02896.hp2 NA18939.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+981dupT | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37608297 | |||||||
| chr17:37608401 | A | G | 1 | a0002c0002t0002g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.77+878T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37608401 | |||||||
| chr17:37608704 | A | C | 1 | a0003c0004t0004g0267 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.77+575T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37608704 | |||||||
| chr17:37608796 | A | G | 2 | a0001c0005t0008g0266 a0001c0005t0009g0265 |
2 | HG02895.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.77+483T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37608796 | |||||||
| chr17:37608799 | G | C | 1 | a0001c0001t0001g0262 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.77+480C>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37608799 | |||||||
| chr17:37608814 | A | C | 5 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+465T>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37608814 | |||||||
| chr17:37608826 | C | G | 2 | a0001c0001t0022g0009 a0001c0001t0022g0264 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.77+453G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37608826 | |||||||
| chr17:37608837 | G | A | 1 | a0010c0014t0023g0263 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.77+442C>T | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37608837 | |||||||
| chr17:37608986 | G | GC | 76 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(73): Show |
77 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.77+292dupG | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37608986 | |||||||
| chr17:37609061 | T | C | 4 | a0001c0001t0011g0340 a0001c0001t0011g0341 a0001c0001t0011g0342 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+218A>G | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37609061 | |||||||
| chr17:37609082 | A | G | 1 | a0002c0002t0002g0008 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.77+197T>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37609082 | |||||||
| chr17:37609104 | C | T | 1 | a0001c0003t0003g0007 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.77+175G>A | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37609104 | |||||||
| chr17:37609176 | C | G | 1 | a0002c0002t0033g0006 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.77+103G>C | SYNRG | ENSG00000275066.5 | transcript | ENST00000612223.5 | protein_coding | 1/21 | chr17 | 37609176 |