Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79058 |
| ensemblid | ENSG00000169696.16 |
| hgncid | 13825 |
| symbol | ASPSCR1 |
| name | ASPSCR1 tether for SLC2A4, UBX domain containing |
| refseq_nuc | NM_024083.4 |
| refseq_prot | NP_076988.1 |
| ensembl_nuc | ENST00000306739.9 |
| ensembl_prot | ENSP00000302176.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 81977629 |
| end | 82017406 |
| strand | + |
| ver | v1.2 |
| region | chr17:81977629-82017406 |
| region5000 | chr17:81972629-82022406 |
| regionname0 | ASPSCR1_chr17_81977629_82017406 |
| regionname5000 | ASPSCR1_chr17_81972629_82022406 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 553 | 207 | 47 | 31 | 91 | 8 | 28 | 74 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | MAAPA others(548): Show |
chr17 | 81972629 | 82022406 |
| a0002 | 0/0 | 553 | 132 | 28 | 34 | 50 | 8 | 12 | 31 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | MAAPA others(548): Show |
chr17 | 81972629 | 82022406 |
| a0003 | 0/0 | 553 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | MAAPA others(548): Show |
chr17 | 81972629 | 82022406 |
| a0004 | 0/0 | 553 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | MAAPA others(548): Show |
chr17 | 81972629 | 82022406 |
| a0005 | 0/0 | 342 | 5 | 4 | 0 | 1 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | MAAPA others(337): Show |
chr17 | 81972629 | 82022406 |
| a0006 | 0/0 | 553 | 4 | 0 | 2 | 2 | 0 | 0 | 2 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | MAAPA others(548): Show |
chr17 | 81972629 | 82022406 |
| a0007 | 0/0 | 342 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | MAAPA others(337): Show |
chr17 | 81972629 | 82022406 |
| a0008 | 0/0 | 553 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | MAAPA others(548): Show |
chr17 | 81972629 | 82022406 |
| a0009 | 0/0 | 553 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | MAAPA others(548): Show |
chr17 | 81972629 | 82022406 |
| a0010 | 0/0 | 553 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | MAAPA others(548): Show |
chr17 | 81972629 | 82022406 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1659 | 126 | 12 | 18 | 70 | 5 | 19 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0001c0003 | 0/0 | 1659 | 39 | 13 | 8 | 9 | 1 | 8 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0001c0004 | 0/0 | 1659 | 21 | 6 | 3 | 9 | 2 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0001c0007 | 0/0 | 1659 | 7 | 7 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0001c0008 | 0/0 | 1659 | 6 | 6 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0001c0012 | 0/0 | 1659 | 3 | 1 | 2 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0001c0014 | 0/0 | 1659 | 2 | 0 | 0 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0001c0017 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0001c0022 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0001c0024 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0002c0002 | 0/0 | 1659 | 116 | 26 | 30 | 42 | 6 | 12 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0002c0005 | 0/0 | 1659 | 12 | 2 | 1 | 7 | 2 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0002c0013 | 0/0 | 1659 | 3 | 0 | 3 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0002c0019 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0003c0006 | 0/0 | 1659 | 7 | 7 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0004c0010 | 0/0 | 1659 | 4 | 2 | 2 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0004c0015 | 0/0 | 1659 | 2 | 2 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0005c0009 | 0/0 | 1646 | 4 | 4 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1641): Show |
chr17 | 81972629 | 82022406 | ||
| a0005c0020 | 0/0 | 1646 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1641): Show |
chr17 | 81972629 | 82022406 | ||
| a0006c0011 | 0/0 | 1659 | 4 | 0 | 2 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0007c0016 | 0/0 | 1646 | 2 | 0 | 0 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1641): Show |
chr17 | 81972629 | 82022406 | ||
| a0008c0018 | 0/0 | 1659 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0009c0021 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 | ||
| a0010c0023 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | ATGGC others(1654): Show |
chr17 | 81972629 | 82022406 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1764 | 126 | 12 | 18 | 70 | 5 | 19 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0001c0003t0001 | 0/0 | 1764 | 39 | 13 | 8 | 9 | 1 | 8 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0001c0004t0001 | 0/0 | 1764 | 21 | 6 | 3 | 9 | 2 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0001c0007t0001 | 0/0 | 1764 | 7 | 7 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0001c0008t0002 | 0/0 | 1764 | 6 | 6 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0001c0012t0001 | 0/0 | 1764 | 3 | 1 | 2 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0001c0014t0001 | 0/0 | 1764 | 2 | 0 | 0 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0001c0017t0001 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0001c0022t0001 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0001c0024t0001 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0002c0002t0001 | 0/0 | 1764 | 116 | 26 | 30 | 42 | 6 | 12 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0002c0005t0001 | 0/0 | 1764 | 12 | 2 | 1 | 7 | 2 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0002c0013t0001 | 0/0 | 1764 | 3 | 0 | 3 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0002c0019t0001 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0003c0006t0001 | 0/0 | 1764 | 7 | 7 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0004c0010t0001 | 0/0 | 1764 | 4 | 2 | 2 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0004c0015t0001 | 0/0 | 1764 | 2 | 2 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0005c0009t0001 | 0/0 | 1751 | 4 | 4 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1746): Show |
chr17 | 81972629 | 82022406 |
| a0005c0020t0001 | 0/0 | 1751 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1746): Show |
chr17 | 81972629 | 82022406 |
| a0006c0011t0001 | 0/0 | 1764 | 4 | 0 | 2 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0007c0016t0001 | 0/0 | 1751 | 2 | 0 | 0 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1746): Show |
chr17 | 81972629 | 82022406 |
| a0008c0018t0001 | 0/0 | 1764 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0009c0021t0001 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| a0010c0023t0001 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | GGGTC others(1759): Show |
chr17 | 81972629 | 82022406 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0012 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0007t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0007t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0007t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0007t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0007t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0008t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0008t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0008t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0008t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0012t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0012t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0014t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0014t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0017t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0022t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0001c0024t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0003 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0005t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0005t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0005t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0005t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0005t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0005t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0005t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0005t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0005t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0005t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0013t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0013t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0002c0019t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0003c0006t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0003c0006t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0003c0006t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0003c0006t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0003c0006t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0003c0006t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0004c0010t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0004c0010t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0004c0010t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0004c0010t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0004c0015t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0005c0009t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0005c0009t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0005c0009t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0005c0020t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0006c0011t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0006c0011t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0006c0011t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0007c0016t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0007c0016t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0008c0018t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0009c0021t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| a0010c0023t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00099 | hp2 | a0002 | c0005 | t0001 | g0196 | EUR | GBR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | GBR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00140 | hp2 | a0002 | c0005 | t0001 | g0197 | EUR | GBR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0216 | EUR | FIN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0261 | EUR | FIN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0043 | EUR | FIN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0257 | EUR | FIN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | CHS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | CHS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | CHS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | CHS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00621 | hp2 | a0001 | c0014 | t0001 | g0214 | EAS | CHS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0272 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00642 | hp2 | a0002 | c0013 | t0001 | g0032 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | CHS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00735 | hp1 | a0002 | c0005 | t0001 | g0198 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00741 | hp1 | a0006 | c0011 | t0001 | g0100 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0234 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0160 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01074 | hp2 | a0001 | c0004 | t0001 | g0170 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0298 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01106 | hp1 | a0008 | c0018 | t0001 | g0283 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0025 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01167 | hp1 | a0001 | c0012 | t0001 | g0017 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01167 | hp2 | a0002 | c0013 | t0001 | g0294 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01168 | hp2 | a0004 | c0010 | t0001 | g0158 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01169 | hp1 | a0004 | c0010 | t0001 | g0157 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01169 | hp2 | a0001 | c0012 | t0001 | g0017 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01192 | hp2 | a0002 | c0013 | t0001 | g0032 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0090 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0299 | AMR | PUR | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0204 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0246 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0236 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01346 | hp1 | a0001 | c0004 | t0001 | g0184 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0201 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0095 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01361 | hp1 | a0001 | c0004 | t0001 | g0177 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0208 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0195 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0113 | AMR | CLM | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01516 | hp1 | a0001 | c0004 | t0001 | g0028 | EUR | IBS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0293 | EUR | IBS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01517 | hp1 | a0001 | c0004 | t0001 | g0028 | EUR | IBS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0253 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01884 | hp2 | a0001 | c0008 | t0002 | g0009 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01891 | hp1 | a0001 | c0007 | t0001 | g0008 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0145 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0199 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0284 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01975 | hp1 | a0006 | c0011 | t0001 | g0006 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0247 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0104 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02027 | hp1 | a0002 | c0005 | t0001 | g0267 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0022 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02040 | hp2 | a0002 | c0005 | t0001 | g0258 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02055 | hp1 | a0005 | c0009 | t0001 | g0152 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02056 | hp2 | a0002 | c0005 | t0001 | g0305 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02071 | hp1 | a0002 | c0005 | t0001 | g0282 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | CDX | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0233 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0205 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02280 | hp1 | a0001 | c0008 | t0002 | g0212 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0269 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0175 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0166 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0235 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0150 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02630 | hp2 | a0001 | c0008 | t0002 | g0211 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02647 | hp1 | a0003 | c0006 | t0001 | g0241 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0171 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0232 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02717 | hp1 | a0001 | c0007 | t0001 | g0144 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0287 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02723 | hp1 | a0005 | c0009 | t0001 | g0033 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02723 | hp2 | a0009 | c0021 | t0001 | g0133 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0295 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02809 | hp1 | a0001 | c0008 | t0002 | g0009 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0249 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02895 | hp1 | a0001 | c0007 | t0001 | g0008 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02895 | hp2 | a0003 | c0006 | t0001 | g0238 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0221 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02896 | hp2 | a0005 | c0009 | t0001 | g0033 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02897 | hp1 | a0001 | c0007 | t0001 | g0143 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02897 | hp2 | a0005 | c0009 | t0001 | g0244 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02922 | hp1 | a0001 | c0007 | t0001 | g0135 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02922 | hp2 | a0001 | c0024 | t0001 | g0149 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0291 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0230 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0176 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0227 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0215 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0273 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0228 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03041 | hp2 | a0003 | c0006 | t0001 | g0296 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03098 | hp1 | a0004 | c0010 | t0001 | g0154 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03098 | hp2 | a0001 | c0008 | t0002 | g0213 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03139 | hp1 | a0010 | c0023 | t0001 | g0134 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0167 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0290 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0091 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0245 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03225 | hp2 | a0001 | c0012 | t0001 | g0105 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0162 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03453 | hp1 | a0002 | c0005 | t0001 | g0304 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03453 | hp2 | a0004 | c0015 | t0001 | g0024 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0222 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0174 | AFR | ESN | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0292 | AFR | GWD | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03579 | hp1 | a0003 | c0006 | t0001 | g0031 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0111 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0311 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03669 | hp2 | a0001 | c0004 | t0001 | g0182 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0268 | SAS | STU | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0058 | SAS | STU | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0165 | SAS | BEB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0231 | SAS | BEB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0270 | SAS | BEB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0275 | SAS | BEB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0147 | SAS | STU | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0003 | SAS | BEB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0312 | SAS | STU | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0300 | SAS | STU | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0025 | SAS | STU | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0146 | AFR | YRI | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18522 | hp2 | a0003 | c0006 | t0001 | g0031 | AFR | YRI | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | CHB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18612 | hp2 | a0002 | c0005 | t0001 | g0259 | EAS | CHB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | CHB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18906 | hp1 | a0001 | c0004 | t0001 | g0172 | AFR | YRI | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0289 | AFR | YRI | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18943 | hp2 | a0001 | c0004 | t0001 | g0178 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18948 | hp1 | a0001 | c0004 | t0001 | g0186 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18948 | hp2 | a0001 | c0022 | t0001 | g0117 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18949 | hp2 | a0002 | c0005 | t0001 | g0280 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0026 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18970 | hp2 | a0007 | c0016 | t0001 | g0225 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18971 | hp1 | a0002 | c0005 | t0001 | g0278 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18974 | hp1 | a0002 | c0019 | t0001 | g0306 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18975 | hp1 | a0005 | c0020 | t0001 | g0065 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18975 | hp2 | a0001 | c0004 | t0001 | g0027 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0159 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18983 | hp2 | a0007 | c0016 | t0001 | g0224 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18997 | hp2 | a0001 | c0003 | t0001 | g0092 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18998 | hp1 | a0006 | c0011 | t0001 | g0042 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18998 | hp2 | a0001 | c0014 | t0001 | g0185 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0163 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19005 | hp2 | a0001 | c0003 | t0001 | g0026 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19007 | hp2 | a0001 | c0004 | t0001 | g0183 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19011 | hp1 | a0001 | c0004 | t0001 | g0027 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19030 | hp1 | a0003 | c0006 | t0001 | g0242 | AFR | LWK | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | LWK | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19043 | hp1 | a0001 | c0017 | t0001 | g0169 | AFR | LWK | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19056 | hp2 | a0001 | c0004 | t0001 | g0180 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19064 | hp2 | a0001 | c0004 | t0001 | g0179 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19080 | hp1 | a0006 | c0011 | t0001 | g0006 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19081 | hp1 | a0001 | c0004 | t0001 | g0187 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19088 | hp1 | a0001 | c0004 | t0001 | g0181 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0271 | AFR | YRI | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | YRI | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA20129 | hp1 | a0002 | c0005 | t0001 | g0210 | AFR | ASW | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA20129 | hp2 | a0001 | c0007 | t0001 | g0049 | AFR | ASW | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0003 | EUR | TSI | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | TSI | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0274 | EUR | TSI | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | GIH | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0094 | SAS | GIH | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02559 | hp1 | a0004 | c0010 | t0001 | g0148 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0083 | AFR | ACB | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03471 | hp1 | a0004 | c0015 | t0001 | g0024 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG03471 | hp2 | a0001 | c0008 | t0002 | g0009 | AFR | MSL | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0297 | AFR | USA | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0067 | AFR | USA | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0093 | AFR | USA | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA20300 | hp2 | a0001 | c0007 | t0001 | g0008 | AFR | USA | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA21309 | hp1 | a0003 | c0006 | t0001 | g0239 | AFR | LWK | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0173 | AFR | LWK | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0012 | REF | REF | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0112 | REF | REF | ASPSCR1_chr17_81972629_82022406 | ASPSCR1 | chr17 | 81972629 | 82022406 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81983668 | G | T | 1 | a0006 | 4 | HG00741.hp1 HG01975.hp1 NA18998.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.273G>T | p.Met91Ile | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/16 | 291/1764 | 273/1662 | 91/553 | chr17 | 81983668 | |||
| chr17:81996668 | T | A | 4 | a0002 a0003 a0007 others(1): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
missense_variant | MODERATE | c.755T>A | p.Leu252Gln | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/16 | 773/1764 | 755/1662 | 252/553 | chr17 | 81996668 | |||
| chr17:81996668 | T | G | 1 | a0002 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.755T>G | p.Leu252Arg | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/16 | 773/1764 | 755/1662 | 252/553 | chr17 | 81996668 | |||
| chr17:82009034 | CAGCCCGT others(8): Show |
C | 2 | a0005 a0007 |
7 | HG02055.hp1 HG02723.hp1 HG02896.hp2 others(4): Show |
disruptive_inframe_deletion | MODERATE | c.951_965delCGTGGACC others(7): Show |
p.Val318_Pro322del | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 8/16 | 969/1764 | 951/1662 | 317/553 | INFO_REALIGN_3_PRIME | chr17 | 82009034 | ||
| chr17:82009055 | G | A | 2 | a0003 a0009 |
8 | HG02647.hp1 HG02723.hp2 HG02895.hp2 others(5): Show |
missense_variant | MODERATE | c.952G>A | p.Val318Met | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 8/16 | 970/1764 | 952/1662 | 318/553 | chr17 | 82009055 | |||
| chr17:82016477 | C | T | 1 | a0010 | 1 | HG03139.hp1 | missense_variant&splice_region_variant | MODERATE | c.1355C>T | p.Ala452Val | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 13/16 | 1373/1764 | 1355/1662 | 452/553 | chr17 | 82016477 | |||
| chr17:82016848 | C | T | 1 | a0004 | 6 | HG01168.hp2 HG01169.hp1 HG02559.hp1 others(3): Show |
missense_variant | MODERATE | c.1454C>T | p.Ala485Val | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 14/16 | 1472/1764 | 1454/1662 | 485/553 | chr17 | 82016848 | |||
| chr17:82017057 | C | T | 1 | a0008 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.1592C>T | p.Thr531Met | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 15/16 | 1610/1764 | 1592/1662 | 531/553 | chr17 | 82017057 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81983635 | C | T | 1 | a0002c0013 | 3 | HG00642.hp2 HG01167.hp2 HG01192.hp2 |
synonymous_variant | LOW | c.240C>T | p.Pro80Pro | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/16 | 258/1764 | 240/1662 | 80/553 | chr17 | 81983635 | |||
| chr17:81985599 | A | G | 1 | a0001c0012 | 3 | HG01167.hp1 HG01169.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.366A>G | p.Pro122Pro | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/16 | 384/1764 | 366/1662 | 122/553 | chr17 | 81985599 | |||
| chr17:81994824 | G | A | 4 | a0001c0004 a0001c0014 a0001c0017 others(1): Show |
26 | HG00621.hp2 HG01074.hp2 HG01346.hp1 others(23): Show |
synonymous_variant | LOW | c.378G>A | p.Glu126Glu | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/16 | 396/1764 | 378/1662 | 126/553 | chr17 | 81994824 | |||
| chr17:82010834 | C | T | 3 | a0001c0007 a0001c0017 a0001c0024 |
9 | HG01891.hp1 HG02717.hp1 HG02895.hp1 others(6): Show |
synonymous_variant | LOW | c.1203C>T | p.Tyr401Tyr | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 10/16 | 1221/1764 | 1203/1662 | 401/553 | chr17 | 82010834 | |||
| chr17:82016804 | C | G | 2 | a0001c0017 a0001c0024 |
2 | HG02922.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.1410C>G | p.Val470Val | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 14/16 | 1428/1764 | 1410/1662 | 470/553 | chr17 | 82016804 | |||
| chr17:82016855 | T | C | 18 | a0001c0003 a0001c0004 a0001c0007 others(15): Show |
220 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
synonymous_variant | LOW | c.1461T>C | p.Asp487Asp | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 14/16 | 1479/1764 | 1461/1662 | 487/553 | chr17 | 82016855 | |||
| chr17:82017028 | G | A | 1 | a0001c0022 | 1 | NA18948.hp2 | synonymous_variant | LOW | c.1563G>A | p.Ala521Ala | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 15/16 | 1581/1764 | 1563/1662 | 521/553 | chr17 | 82017028 | |||
| chr17:82017097 | G | A | 1 | a0001c0008 | 6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
synonymous_variant | LOW | c.1632G>A | p.Lys544Lys | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 15/16 | 1650/1764 | 1632/1662 | 544/553 | chr17 | 82017097 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:82017345 | A | G | 1 | a0001c0008t0002 | 6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*23A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 16/16 | 23 | chr17 | 82017345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81977760 | C | G | 186 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(183): Show |
209 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.102+12C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81977760 | |||||||
| chr17:81977929 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
6 | HG01943.hp2 HG01993.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+181G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81977929 | |||||||
| chr17:81978065 | G | A | 186 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(183): Show |
209 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.102+317G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81978065 | |||||||
| chr17:81978066 | G | A | 2 | a0001c0003t0001g0145 a0001c0003t0001g0146 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.102+318G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81978066 | |||||||
| chr17:81978098 | G | T | 1 | a0001c0003t0001g0312 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.102+350G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81978098 | |||||||
| chr17:81978102 | G | A | 27 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(24): Show |
30 | HG01070.hp2 HG01109.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.102+354G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81978102 | |||||||
| chr17:81978339 | G | C | 1 | a0002c0002t0001g0168 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.102+591G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81978339 | |||||||
| chr17:81978525 | C | CA | 30 | a0001c0001t0001g0041 a0001c0001t0001g0153 a0001c0001t0001g0155 others(27): Show |
33 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.103-642dupA | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 81978525 | ||||||
| chr17:81978525 | C | CAA | 24 | a0001c0003t0001g0147 a0001c0004t0001g0027 a0001c0004t0001g0028 others(21): Show |
26 | HG01074.hp2 HG01346.hp1 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.103-643_103-642dup others(2): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 81978525 | ||||||
| chr17:81978638 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG01099.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.103-546A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81978638 | |||||||
| chr17:81978649 | G | C | 1 | a0001c0003t0001g0043 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.103-535G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81978649 | |||||||
| chr17:81978740 | G | A | 8 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0004t0001g0172 others(5): Show |
8 | HG01074.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.103-444G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81978740 | |||||||
| chr17:81978925 | T | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG02155.hp1 NA18952.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-259T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81978925 | |||||||
| chr17:81978989 | G | C | 1 | a0002c0002t0001g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.103-195G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81978989 | |||||||
| chr17:81979110 | T | C | 20 | a0001c0003t0001g0003 a0001c0003t0001g0199 a0002c0002t0001g0003 others(17): Show |
23 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.103-74T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81979110 | |||||||
| chr17:81979134 | C | T | 3 | a0001c0007t0001g0008 a0001c0007t0001g0143 a0001c0007t0001g0144 |
5 | HG01891.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-50C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81979134 | |||||||
| chr17:81979135 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.103-49G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 1/15 | chr17 | 81979135 | |||||||
| chr17:81979262 | G | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02523.hp2 NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.158+23G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81979262 | |||||||
| chr17:81979578 | C | T | 1 | a0001c0003t0001g0022 | 2 | HG02027.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.158+339C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81979578 | |||||||
| chr17:81979665 | G | C | 28 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(25): Show |
31 | HG01070.hp2 HG01109.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.158+426G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81979665 | |||||||
| chr17:81979858 | T | C | 1 | a0001c0001t0001g0012 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.158+619T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81979858 | |||||||
| chr17:81979905 | C | T | 1 | a0001c0001t0001g0012 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.158+666C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81979905 | |||||||
| chr17:81979974 | TG | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
5 | HG00423.hp1 NA18942.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.158+736delG | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81979974 | |||||||
| chr17:81980028 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG01099.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.158+789G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81980028 | |||||||
| chr17:81980260 | G | C | 53 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(50): Show |
60 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.158+1021G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81980260 | |||||||
| chr17:81980308 | G | T | 1 | a0002c0002t0001g0311 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.158+1069G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81980308 | |||||||
| chr17:81980378 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.158+1139C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81980378 | |||||||
| chr17:81980669 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.158+1430C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81980669 | |||||||
| chr17:81980714 | C | G | 3 | a0001c0003t0001g0145 a0001c0003t0001g0146 a0001c0003t0001g0167 |
3 | HG01891.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.158+1475C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81980714 | |||||||
| chr17:81980807 | G | C | 1 | a0001c0004t0001g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.158+1568G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81980807 | |||||||
| chr17:81980936 | C | T | 3 | a0002c0002t0001g0308 a0002c0002t0001g0309 a0002c0002t0001g0310 |
3 | HG02074.hp1 NA18941.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.158+1697C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81980936 | |||||||
| chr17:81980937 | G | A | 4 | a0001c0008t0002g0009 a0001c0008t0002g0211 a0001c0008t0002g0212 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.158+1698G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81980937 | |||||||
| chr17:81981098 | G | A | 3 | a0001c0004t0001g0027 a0001c0004t0001g0178 a0001c0004t0001g0179 |
4 | NA18943.hp2 NA18975.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+1859G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81981098 | |||||||
| chr17:81981224 | G | A | 1 | a0001c0007t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.158+1985G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81981224 | |||||||
| chr17:81981491 | G | A | 1 | a0002c0002t0001g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.159-2063G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81981491 | |||||||
| chr17:81981590 | G | T | 2 | a0002c0002t0001g0307 a0002c0019t0001g0306 |
2 | NA18974.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.159-1964G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81981590 | |||||||
| chr17:81981762 | G | A | 1 | a0001c0003t0001g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.159-1792G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81981762 | |||||||
| chr17:81982054 | C | T | 2 | a0001c0004t0001g0186 a0001c0004t0001g0187 |
2 | NA18948.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.159-1500C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982054 | |||||||
| chr17:81982081 | A | G | 5 | a0001c0007t0001g0008 a0001c0007t0001g0049 a0001c0007t0001g0135 others(2): Show |
7 | HG01891.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.159-1473A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982081 | |||||||
| chr17:81982215 | C | T | 1 | a0002c0005t0001g0305 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.159-1339C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982215 | |||||||
| chr17:81982246 | G | A | 1 | a0002c0002t0001g0215 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.159-1308G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982246 | |||||||
| chr17:81982258 | C | T | 1 | a0010c0023t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.159-1296C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982258 | |||||||
| chr17:81982298 | G | A | 1 | a0002c0002t0001g0193 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.159-1256G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982298 | |||||||
| chr17:81982305 | G | C | 1 | a0001c0003t0001g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.159-1249G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982305 | |||||||
| chr17:81982329 | A | G | 1 | a0002c0005t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.159-1225A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982329 | |||||||
| chr17:81982420 | G | A | 1 | a0004c0015t0001g0024 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.159-1134G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982420 | |||||||
| chr17:81982486 | C | T | 7 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0004t0001g0172 others(4): Show |
7 | HG01074.hp2 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-1068C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982486 | |||||||
| chr17:81982498 | G | A | 25 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(22): Show |
28 | HG01070.hp2 HG01109.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.159-1056G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982498 | |||||||
| chr17:81982526 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.159-1028G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982526 | |||||||
| chr17:81982582 | T | C | 1 | a0001c0017t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.159-972T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982582 | |||||||
| chr17:81982613 | G | C | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.159-941G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982613 | |||||||
| chr17:81982717 | CTTTTCTT others(3): Show |
C | 1 | a0002c0002t0001g0216 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.159-825_159-816del others(10): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr17 | 81982717 | ||||||
| chr17:81982744 | C | CTCTT | 15 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0177 others(12): Show |
17 | HG00621.hp2 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-793_159-790dup others(4): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr17 | 81982744 | ||||||
| chr17:81982790 | CTCTTT | C | 5 | a0001c0001t0001g0052 a0001c0008t0002g0009 a0001c0008t0002g0211 others(2): Show |
7 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-748_159-744del others(5): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr17 | 81982790 | ||||||
| chr17:81982793 | T | G | 5 | a0002c0002t0001g0034 a0002c0002t0001g0189 a0002c0002t0001g0216 others(2): Show |
5 | HG00280.hp1 HG00323.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.159-761T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982793 | |||||||
| chr17:81982803 | T | C | 1 | a0002c0002t0001g0051 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.159-751T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982803 | |||||||
| chr17:81982985 | T | G | 1 | a0001c0003t0001g0312 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.159-569T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81982985 | |||||||
| chr17:81983024 | A | G | 1 | a0001c0014t0001g0214 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.159-530A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81983024 | |||||||
| chr17:81983173 | G | A | 1 | a0002c0002t0001g0215 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.159-381G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81983173 | |||||||
| chr17:81983205 | C | T | 7 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0004t0001g0172 others(4): Show |
7 | HG01074.hp2 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.159-349C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81983205 | |||||||
| chr17:81983408 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.159-146G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81983408 | |||||||
| chr17:81983412 | C | T | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.159-142C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | chr17 | 81983412 | |||||||
| chr17:81983480 | G | GGGATGGC others(7): Show |
53 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(50): Show |
60 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.159-66_159-53dupGG others(12): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr17 | 81983480 | ||||||
| chr17:81983765 | A | T | 1 | a0002c0002t0001g0168 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.273+97A>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81983765 | |||||||
| chr17:81983851 | G | T | 11 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0003t0001g0025 others(8): Show |
13 | HG01070.hp2 HG01109.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.273+183G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81983851 | |||||||
| chr17:81983860 | A | G | 3 | a0002c0002t0001g0301 a0002c0002t0001g0302 a0002c0002t0001g0303 |
3 | HG00673.hp2 NA18956.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.273+192A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81983860 | |||||||
| chr17:81983888 | C | T | 1 | a0001c0003t0001g0165 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.273+220C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81983888 | |||||||
| chr17:81983927 | G | A | 1 | a0004c0015t0001g0024 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.273+259G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81983927 | |||||||
| chr17:81983979 | C | A | 2 | a0002c0002t0001g0217 a0002c0002t0001g0218 |
2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.273+311C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81983979 | |||||||
| chr17:81984050 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.273+382C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81984050 | |||||||
| chr17:81984193 | G | A | 1 | a0002c0005t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.273+525G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81984193 | |||||||
| chr17:81984339 | A | G | 1 | a0002c0002t0001g0300 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.273+671A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81984339 | |||||||
| chr17:81984483 | A | G | 1 | a0002c0002t0001g0299 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.273+815A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81984483 | |||||||
| chr17:81984490 | T | G | 1 | a0001c0001t0001g0053 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.273+822T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81984490 | |||||||
| chr17:81984513 | C | G | 1 | a0002c0002t0001g0168 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.273+845C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81984513 | |||||||
| chr17:81984626 | C | CT | 15 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0177 others(12): Show |
17 | HG00621.hp2 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.274-880dupT | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 81984626 | ||||||
| chr17:81984676 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.274-831T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81984676 | |||||||
| chr17:81984820 | C | T | 1 | a0009c0021t0001g0133 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.274-687C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81984820 | |||||||
| chr17:81984827 | AC | A | 13 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0178 others(10): Show |
15 | HG00621.hp2 HG01346.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.274-675delC | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 81984827 | ||||||
| chr17:81984831 | C | CACACACC others(4): Show |
1 | a0001c0004t0001g0177 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.274-676_274-675ins others(11): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81984831 | |||||||
| chr17:81984873 | C | T | 15 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0177 others(12): Show |
17 | HG00621.hp2 HG01346.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.274-634C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81984873 | |||||||
| chr17:81984876 | ACACACAC others(4): Show |
A | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.274-623_274-613del others(11): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 81984876 | ||||||
| chr17:81984887 | C | G | 5 | a0001c0024t0001g0149 a0002c0002t0001g0226 a0002c0002t0001g0228 others(2): Show |
5 | HG02055.hp2 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-620C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81984887 | |||||||
| chr17:81984931 | C | A | 1 | a0001c0004t0001g0170 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.274-576C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81984931 | |||||||
| chr17:81984931 | CCACACCC others(3): Show |
C | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.274-558_274-549del others(10): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 81984931 | ||||||
| chr17:81984939 | GCACACAC others(12): Show |
G | 14 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0177 others(11): Show |
16 | HG00621.hp2 HG01346.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.274-559_274-541del others(19): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 81984939 | ||||||
| chr17:81984945 | ACCCGCAC others(45): Show |
A | 1 | a0001c0004t0001g0170 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.274-558_274-507del others(52): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 81984945 | ||||||
| chr17:81984955 | ACCCCACA others(35): Show |
A | 8 | a0001c0004t0001g0171 a0001c0004t0001g0172 a0001c0004t0001g0173 others(5): Show |
9 | HG02451.hp2 HG02647.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-530_274-489del others(42): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 81984955 | ||||||
| chr17:81984994 | AC | A | 13 | a0001c0001t0001g0050 a0001c0001t0001g0080 a0001c0001t0001g0082 others(10): Show |
15 | HG01891.hp1 HG01993.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.274-506delC | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 81984994 | ||||||
| chr17:81985000 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.274-507C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985000 | |||||||
| chr17:81985018 | C | T | 2 | a0004c0010t0001g0157 a0004c0010t0001g0158 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.274-489C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985018 | |||||||
| chr17:81985021 | CCACACCA others(5): Show |
C | 2 | a0002c0002t0001g0219 a0002c0002t0001g0220 |
2 | NA18942.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.274-480_274-469del others(12): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 81985021 | ||||||
| chr17:81985034 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.274-473C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985034 | |||||||
| chr17:81985042 | TC | T | 18 | a0001c0001t0001g0052 a0001c0001t0001g0191 a0001c0004t0001g0027 others(15): Show |
21 | HG00621.hp2 HG01346.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.274-458delC | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 81985042 | ||||||
| chr17:81985048 | C | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG02559.hp2 HG03239.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-459C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985048 | |||||||
| chr17:81985048 | C | T | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.274-459C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985048 | |||||||
| chr17:81985052 | ACACACCC others(3): Show |
A | 15 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0003t0001g0025 others(12): Show |
17 | HG01070.hp2 HG01109.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.274-449_274-440del others(10): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 81985052 | ||||||
| chr17:81985072 | G | C | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.274-435G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985072 | |||||||
| chr17:81985143 | T | C | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG03239.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-364T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985143 | |||||||
| chr17:81985149 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.274-358C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985149 | |||||||
| chr17:81985218 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.274-289C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985218 | |||||||
| chr17:81985229 | C | T | 10 | a0001c0001t0001g0156 a0001c0004t0001g0170 a0001c0004t0001g0171 others(7): Show |
11 | HG01074.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-278C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985229 | |||||||
| chr17:81985264 | G | A | 1 | a0004c0010t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.274-243G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985264 | |||||||
| chr17:81985302 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.274-205G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985302 | |||||||
| chr17:81985323 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.274-184G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985323 | |||||||
| chr17:81985393 | C | A | 35 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(32): Show |
38 | HG01070.hp2 HG01074.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-114C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 3/15 | chr17 | 81985393 | |||||||
| chr17:81985670 | C | G | 1 | a0001c0004t0001g0176 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.374+63C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81985670 | |||||||
| chr17:81985696 | C | G | 1 | a0001c0001t0001g0053 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.374+89C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81985696 | |||||||
| chr17:81985916 | C | T | 1 | a0002c0002t0001g0311 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.374+309C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81985916 | |||||||
| chr17:81985949 | C | A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0221 |
3 | HG02258.hp1 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.374+342C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81985949 | |||||||
| chr17:81985969 | G | T | 14 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0177 others(11): Show |
16 | HG00621.hp2 HG01346.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.374+362G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81985969 | |||||||
| chr17:81985970 | T | C | 14 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0177 others(11): Show |
16 | HG00621.hp2 HG01346.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.374+363T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81985970 | |||||||
| chr17:81986129 | ATGGCTGG others(6): Show |
A | 2 | a0002c0002t0001g0222 a0004c0015t0001g0024 |
3 | HG03453.hp2 HG03471.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.374+546_374+558del others(13): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 81986129 | ||||||
| chr17:81986166 | A | C | 2 | a0002c0002t0001g0297 a0002c0002t0001g0298 |
2 | HG01099.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.374+559A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81986166 | |||||||
| chr17:81986192 | G | A | 2 | a0002c0002t0001g0219 a0002c0002t0001g0220 |
2 | NA18942.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.374+585G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81986192 | |||||||
| chr17:81986355 | C | T | 1 | a0004c0015t0001g0024 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.374+748C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81986355 | |||||||
| chr17:81986356 | G | A | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.374+749G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81986356 | |||||||
| chr17:81986377 | C | T | 32 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(29): Show |
34 | HG01070.hp2 HG01074.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.374+770C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81986377 | |||||||
| chr17:81986389 | G | A | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.374+782G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81986389 | |||||||
| chr17:81986725 | G | GTGGGAAG others(19): Show |
49 | a0001c0001t0001g0063 a0001c0001t0001g0153 a0001c0001t0001g0155 others(46): Show |
54 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.374+1131_374+1156d others(28): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 81986725 | ||||||
| chr17:81986774 | G | C | 1 | a0001c0004t0001g0178 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.374+1167G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81986774 | |||||||
| chr17:81986775 | C | T | 3 | a0001c0004t0001g0028 a0001c0004t0001g0178 a0001c0004t0001g0184 |
4 | HG01346.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.374+1168C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81986775 | |||||||
| chr17:81986778 | G | C | 1 | a0001c0001t0001g0140 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.374+1171G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81986778 | |||||||
| chr17:81986955 | C | T | 1 | a0002c0005t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.374+1348C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81986955 | |||||||
| chr17:81986985 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.374+1378C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81986985 | |||||||
| chr17:81987016 | G | C | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.374+1409G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987016 | |||||||
| chr17:81987083 | AAGAGCAA others(117): Show |
A | 9 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0004t0001g0172 others(6): Show |
10 | HG01074.hp2 HG02451.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.374+1519_374+1642d others(2): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 81987083 | ||||||
| chr17:81987098 | C | A | 2 | a0002c0005t0001g0267 a0002c0005t0001g0282 |
2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.374+1491C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987098 | |||||||
| chr17:81987207 | G | A | 192 | a0001c0001t0001g0050 a0001c0001t0001g0057 a0001c0001t0001g0080 others(189): Show |
216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.374+1600G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987207 | |||||||
| chr17:81987217 | C | T | 25 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(22): Show |
27 | HG01070.hp2 HG01109.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.374+1610C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987217 | |||||||
| chr17:81987226 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.374+1619G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987226 | |||||||
| chr17:81987268 | A | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02523.hp2 NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.374+1661A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987268 | |||||||
| chr17:81987318 | G | A | 1 | a0002c0002t0001g0223 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.374+1711G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987318 | |||||||
| chr17:81987431 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.374+1824A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987431 | |||||||
| chr17:81987454 | C | A | 1 | a0005c0020t0001g0065 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.374+1847C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987454 | |||||||
| chr17:81987456 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.374+1849C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987456 | |||||||
| chr17:81987497 | T | G | 1 | a0001c0017t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.374+1890T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987497 | |||||||
| chr17:81987514 | C | T | 14 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0177 others(11): Show |
16 | HG00621.hp2 HG01346.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.374+1907C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987514 | |||||||
| chr17:81987528 | T | C | 2 | a0007c0016t0001g0224 a0007c0016t0001g0225 |
2 | NA18970.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.374+1921T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987528 | |||||||
| chr17:81987609 | G | A | 1 | a0001c0004t0001g0180 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.374+2002G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987609 | |||||||
| chr17:81987622 | C | T | 14 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0177 others(11): Show |
16 | HG00621.hp2 HG01346.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.374+2015C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987622 | |||||||
| chr17:81987749 | G | A | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.374+2142G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987749 | |||||||
| chr17:81987816 | T | C | 54 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(51): Show |
59 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.374+2209T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81987816 | |||||||
| chr17:81988099 | A | G | 1 | a0002c0002t0001g0168 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.374+2492A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81988099 | |||||||
| chr17:81988148 | C | CA | 34 | a0001c0001t0001g0041 a0001c0001t0001g0153 a0001c0001t0001g0155 others(31): Show |
36 | HG01070.hp2 HG01109.hp2 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.374+2557dupA | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 81988148 | ||||||
| chr17:81988148 | CA | C | 8 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(5): Show |
8 | HG01167.hp2 HG02735.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.374+2557delA | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 81988148 | ||||||
| chr17:81988271 | G | A | 1 | a0002c0002t0001g0232 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.374+2664G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81988271 | |||||||
| chr17:81988318 | G | C | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.374+2711G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81988318 | |||||||
| chr17:81988397 | G | A | 2 | a0002c0002t0001g0233 a0002c0002t0001g0234 |
2 | HG00741.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.374+2790G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81988397 | |||||||
| chr17:81988448 | C | T | 14 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0177 others(11): Show |
16 | HG00621.hp2 HG01346.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.374+2841C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81988448 | |||||||
| chr17:81988454 | C | CA | 21 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0001t0001g0066 others(18): Show |
23 | HG00423.hp1 HG00733.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.374+2864dupA | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 81988454 | ||||||
| chr17:81988497 | G | A | 1 | a0002c0002t0001g0299 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.374+2890G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81988497 | |||||||
| chr17:81988562 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.374+2955G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81988562 | |||||||
| chr17:81988644 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0131 |
2 | HG02080.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.374+3037G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81988644 | |||||||
| chr17:81988665 | A | G | 24 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(21): Show |
26 | HG01070.hp2 HG01109.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.374+3058A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81988665 | |||||||
| chr17:81988747 | C | T | 4 | a0001c0008t0002g0009 a0001c0008t0002g0211 a0001c0008t0002g0212 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.374+3140C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81988747 | |||||||
| chr17:81988939 | G | A | 9 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0004t0001g0172 others(6): Show |
10 | HG01074.hp2 HG02451.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.374+3332G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81988939 | |||||||
| chr17:81989157 | G | A | 1 | a0001c0003t0001g0150 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.374+3550G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81989157 | |||||||
| chr17:81989240 | C | G | 1 | a0003c0006t0001g0296 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.374+3633C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81989240 | |||||||
| chr17:81989258 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(13): Show |
22 | HG01943.hp2 HG01993.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.374+3651C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81989258 | |||||||
| chr17:81989292 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.374+3685A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81989292 | |||||||
| chr17:81989362 | G | C | 23 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0170 others(20): Show |
26 | HG00621.hp2 HG01074.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.374+3755G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81989362 | |||||||
| chr17:81989408 | C | T | 1 | a0001c0003t0001g0150 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.374+3801C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81989408 | |||||||
| chr17:81989649 | C | T | 1 | a0004c0015t0001g0024 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.374+4042C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81989649 | |||||||
| chr17:81989706 | T | C | 1 | a0002c0002t0001g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.374+4099T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81989706 | |||||||
| chr17:81989727 | C | T | 1 | a0001c0003t0001g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.374+4120C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81989727 | |||||||
| chr17:81989728 | G | A | 9 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0004t0001g0172 others(6): Show |
10 | HG01074.hp2 HG02451.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.374+4121G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81989728 | |||||||
| chr17:81990200 | A | G | 1 | a0002c0002t0001g0216 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.374+4593A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81990200 | |||||||
| chr17:81990351 | C | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0121 a0001c0001t0001g0122 |
5 | HG00099.hp1 HG00140.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.375-4470C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81990351 | |||||||
| chr17:81990465 | C | CGCCTGCC others(61): Show |
7 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0004t0001g0172 others(4): Show |
7 | HG01074.hp2 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.375-4264_375-4197d others(70): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 81990465 | ||||||
| chr17:81990465 | CGCCTGCC others(61): Show |
C | 3 | a0001c0001t0001g0057 a0007c0016t0001g0224 a0007c0016t0001g0225 |
3 | NA18970.hp2 NA18983.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.375-4264_375-4197d others(70): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 81990465 | ||||||
| chr17:81990580 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
7 | NA18747.hp2 NA18954.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.375-4241G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81990580 | |||||||
| chr17:81990589 | G | A | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.375-4232G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81990589 | |||||||
| chr17:81990678 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.375-4143G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81990678 | |||||||
| chr17:81990926 | C | T | 1 | a0001c0024t0001g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.375-3895C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81990926 | |||||||
| chr17:81990989 | G | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0037 others(4): Show |
9 | HG01943.hp2 HG01993.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.375-3832G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81990989 | |||||||
| chr17:81991102 | A | G | 1 | a0002c0002t0001g0293 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.375-3719A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81991102 | |||||||
| chr17:81991288 | C | T | 1 | a0001c0003t0001g0022 | 2 | HG02027.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.375-3533C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81991288 | |||||||
| chr17:81991336 | G | A | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.375-3485G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81991336 | |||||||
| chr17:81991355 | T | C | 204 | a0001c0001t0001g0050 a0001c0001t0001g0057 a0001c0001t0001g0078 others(201): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.375-3466T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81991355 | |||||||
| chr17:81991703 | G | T | 27 | a0001c0001t0001g0082 a0001c0001t0001g0153 a0001c0001t0001g0155 others(24): Show |
29 | HG01070.hp2 HG01109.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.375-3118G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81991703 | |||||||
| chr17:81991724 | G | A | 1 | a0004c0015t0001g0024 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.375-3097G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81991724 | |||||||
| chr17:81991826 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.375-2995A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81991826 | |||||||
| chr17:81991848 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.375-2973G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81991848 | |||||||
| chr17:81991969 | A | G | 1 | a0002c0002t0001g0292 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.375-2852A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81991969 | |||||||
| chr17:81991976 | C | G | 5 | a0001c0007t0001g0008 a0001c0007t0001g0049 a0001c0007t0001g0135 others(2): Show |
7 | HG01891.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.375-2845C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81991976 | |||||||
| chr17:81991977 | G | A | 1 | a0002c0002t0001g0051 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.375-2844G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81991977 | |||||||
| chr17:81992054 | T | C | 1 | a0009c0021t0001g0133 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.375-2767T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81992054 | |||||||
| chr17:81992098 | A | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0081 |
2 | HG01261.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.375-2723A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81992098 | |||||||
| chr17:81992122 | G | T | 1 | a0004c0015t0001g0024 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.375-2699G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81992122 | |||||||
| chr17:81992184 | C | A | 14 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0177 others(11): Show |
16 | HG00621.hp2 HG01346.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.375-2637C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81992184 | |||||||
| chr17:81992186 | G | A | 1 | a0001c0003t0001g0083 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.375-2635G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81992186 | |||||||
| chr17:81992210 | C | T | 1 | a0002c0002t0001g0311 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.375-2611C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81992210 | |||||||
| chr17:81992289 | G | A | 25 | a0001c0003t0001g0166 a0001c0004t0001g0027 a0001c0004t0001g0028 others(22): Show |
28 | HG00621.hp2 HG01074.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.375-2532G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81992289 | |||||||
| chr17:81992331 | G | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0131 |
2 | HG02080.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.375-2490G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81992331 | |||||||
| chr17:81992387 | C | T | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.375-2434C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81992387 | |||||||
| chr17:81992629 | T | G | 8 | a0002c0002t0001g0221 a0002c0002t0001g0240 a0003c0006t0001g0031 others(5): Show |
9 | HG02647.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.375-2192T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81992629 | |||||||
| chr17:81992685 | C | T | 1 | a0004c0015t0001g0024 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.375-2136C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81992685 | |||||||
| chr17:81992700 | C | T | 1 | a0002c0002t0001g0193 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.375-2121C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81992700 | |||||||
| chr17:81993003 | G | A | 1 | a0001c0017t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.375-1818G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993003 | |||||||
| chr17:81993048 | G | A | 1 | a0001c0008t0002g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.375-1773G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993048 | |||||||
| chr17:81993221 | T | C | 2 | a0002c0013t0001g0032 a0002c0013t0001g0294 |
3 | HG00642.hp2 HG01167.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.375-1600T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993221 | |||||||
| chr17:81993275 | G | A | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.375-1546G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993275 | |||||||
| chr17:81993292 | C | T | 3 | a0001c0003t0001g0151 a0001c0003t0001g0290 a0001c0003t0001g0291 |
3 | HG02965.hp1 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.375-1529C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993292 | |||||||
| chr17:81993338 | C | T | 15 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0003t0001g0025 others(12): Show |
17 | HG01070.hp2 HG01109.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.375-1483C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993338 | |||||||
| chr17:81993359 | G | A | 4 | a0001c0008t0002g0009 a0001c0008t0002g0211 a0001c0008t0002g0212 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.375-1462G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993359 | |||||||
| chr17:81993380 | A | T | 1 | a0002c0002t0001g0232 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.375-1441A>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993380 | |||||||
| chr17:81993404 | G | A | 1 | a0002c0002t0001g0243 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.375-1417G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993404 | |||||||
| chr17:81993404 | G | C | 25 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(22): Show |
28 | HG01070.hp2 HG01109.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.375-1417G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993404 | |||||||
| chr17:81993721 | C | T | 3 | a0001c0003t0001g0026 a0001c0003t0001g0159 a0001c0003t0001g0163 |
4 | NA18951.hp2 NA18977.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.375-1100C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993721 | |||||||
| chr17:81993754 | C | T | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.375-1067C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993754 | |||||||
| chr17:81993908 | G | A | 1 | a0005c0009t0001g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.375-913G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993908 | |||||||
| chr17:81993972 | T | C | 1 | a0003c0006t0001g0296 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.375-849T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993972 | |||||||
| chr17:81993991 | G | A | 1 | a0001c0004t0001g0170 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.375-830G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81993991 | |||||||
| chr17:81994130 | G | A | 1 | a0002c0002t0001g0223 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.375-691G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81994130 | |||||||
| chr17:81994133 | G | T | 1 | a0002c0002t0001g0298 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.375-688G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81994133 | |||||||
| chr17:81994158 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | NA19011.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.375-663A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81994158 | |||||||
| chr17:81994259 | A | C | 10 | a0001c0001t0001g0050 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
12 | HG01261.hp1 HG01891.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.375-562A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81994259 | |||||||
| chr17:81994299 | C | T | 1 | a0002c0002t0001g0209 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.375-522C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81994299 | |||||||
| chr17:81994400 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.375-421G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81994400 | |||||||
| chr17:81994434 | A | C | 7 | a0002c0002t0001g0240 a0003c0006t0001g0031 a0003c0006t0001g0238 others(4): Show |
8 | HG02647.hp1 HG02895.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.375-387A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81994434 | |||||||
| chr17:81994461 | C | T | 1 | a0007c0016t0001g0225 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.375-360C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81994461 | |||||||
| chr17:81994558 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.375-263A>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81994558 | |||||||
| chr17:81994586 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.375-235C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81994586 | |||||||
| chr17:81994599 | G | A | 8 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0004t0001g0172 others(5): Show |
8 | HG01074.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.375-222G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 4/15 | chr17 | 81994599 | |||||||
| chr17:81994908 | C | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
7 | NA18747.hp2 NA18954.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.432+30C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81994908 | |||||||
| chr17:81994954 | G | A | 2 | a0001c0001t0001g0191 a0001c0004t0001g0028 |
3 | HG01516.hp1 HG01517.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.432+76G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81994954 | |||||||
| chr17:81994983 | C | T | 1 | a0002c0002t0001g0188 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.432+105C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81994983 | |||||||
| chr17:81995004 | C | T | 1 | a0002c0002t0001g0288 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.432+126C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995004 | |||||||
| chr17:81995040 | G | A | 4 | a0001c0024t0001g0149 a0002c0005t0001g0196 a0002c0005t0001g0197 others(1): Show |
4 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+162G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995040 | |||||||
| chr17:81995056 | C | T | 1 | a0002c0002t0001g0208 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.432+178C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995056 | |||||||
| chr17:81995068 | C | G | 1 | a0002c0002t0001g0287 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.432+190C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995068 | |||||||
| chr17:81995068 | C | T | 6 | a0001c0003t0001g0151 a0001c0003t0001g0290 a0001c0003t0001g0291 others(3): Show |
6 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.432+190C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995068 | |||||||
| chr17:81995178 | T | G | 2 | a0009c0021t0001g0133 a0010c0023t0001g0134 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.432+300T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995178 | |||||||
| chr17:81995219 | C | G | 4 | a0001c0001t0001g0191 a0001c0003t0001g0151 a0001c0003t0001g0290 others(1): Show |
4 | HG02572.hp1 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+341C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995219 | |||||||
| chr17:81995362 | G | T | 1 | a0002c0002t0001g0293 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.432+484G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995362 | |||||||
| chr17:81995394 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.432+516G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995394 | |||||||
| chr17:81995396 | C | A | 53 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(50): Show |
59 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.432+518C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995396 | |||||||
| chr17:81995418 | C | T | 2 | a0002c0002t0001g0232 a0002c0002t0001g0234 |
2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.432+540C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995418 | |||||||
| chr17:81995453 | G | T | 1 | a0001c0024t0001g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.433-539G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995453 | |||||||
| chr17:81995516 | G | A | 1 | a0001c0003t0001g0312 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.433-476G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995516 | |||||||
| chr17:81995569 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.433-423C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995569 | |||||||
| chr17:81995629 | C | T | 3 | a0004c0010t0001g0154 a0004c0010t0001g0157 a0004c0010t0001g0158 |
3 | HG01168.hp2 HG01169.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.433-363C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995629 | |||||||
| chr17:81995747 | C | T | 53 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(50): Show |
59 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.433-245C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995747 | |||||||
| chr17:81995783 | G | T | 1 | a0002c0002t0001g0286 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.433-209G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995783 | |||||||
| chr17:81995880 | G | A | 1 | a0002c0002t0001g0245 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.433-112G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995880 | |||||||
| chr17:81995895 | G | A | 4 | a0001c0008t0002g0009 a0001c0008t0002g0211 a0001c0008t0002g0212 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-97G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995895 | |||||||
| chr17:81995930 | G | A | 1 | a0002c0002t0001g0246 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.433-62G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995930 | |||||||
| chr17:81995960 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.433-32A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 5/15 | chr17 | 81995960 | |||||||
| chr17:81996213 | G | T | 1 | a0004c0015t0001g0024 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.506+148G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 6/15 | chr17 | 81996213 | |||||||
| chr17:81996335 | C | CGGGAGAG others(14): Show |
1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.507-70_507-69insGG others(19): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr17 | 81996335 | ||||||
| chr17:81996415 | C | T | 1 | a0002c0002t0001g0297 | 1 | HG06807.hp1 | splice_region_variant&intron_variant | LOW | c.507-5C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 6/15 | chr17 | 81996415 | |||||||
| chr17:81996985 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.933+139C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81996985 | |||||||
| chr17:81997083 | T | TGCTCCGG others(37): Show |
1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.933+258_933+301dup others(44): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 81997083 | ||||||
| chr17:81997083 | T | TGCTCCGG others(59): Show |
52 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(49): Show |
58 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.933+301_933+302ins others(66): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 81997083 | ||||||
| chr17:81997083 | T | TGCTCCGG others(59): Show |
1 | a0001c0003t0001g0165 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.933+285_933+286ins others(66): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 81997083 | ||||||
| chr17:81997083 | TGCTCCGG others(15): Show |
T | 1 | a0001c0001t0001g0019 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.933+258_933+279del others(22): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 81997083 | ||||||
| chr17:81997105 | C | CGCTCCGG others(15): Show |
133 | a0001c0003t0001g0003 a0001c0003t0001g0199 a0001c0008t0002g0009 others(130): Show |
150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.933+280_933+301dup others(22): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 81997105 | ||||||
| chr17:81997183 | G | A | 1 | a0001c0003t0001g0199 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.933+337G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81997183 | |||||||
| chr17:81997218 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.933+372C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81997218 | |||||||
| chr17:81997230 | G | C | 2 | a0002c0002t0001g0029 a0002c0002t0001g0221 |
3 | HG02258.hp1 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.933+384G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81997230 | |||||||
| chr17:81997295 | C | T | 1 | a0008c0018t0001g0283 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.933+449C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81997295 | |||||||
| chr17:81997418 | A | G | 1 | a0001c0022t0001g0117 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.933+572A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81997418 | |||||||
| chr17:81997484 | T | TG | 11 | a0001c0001t0001g0156 a0001c0003t0001g0166 a0001c0004t0001g0027 others(8): Show |
12 | HG00621.hp2 HG01168.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.933+641dupG | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 81997484 | ||||||
| chr17:81997487 | G | GT | 40 | a0001c0001t0001g0047 a0001c0001t0001g0055 a0001c0001t0001g0069 others(37): Show |
40 | HG00544.hp2 HG00673.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.933+660dupT | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 81997487 | ||||||
| chr17:81997488 | T | G | 43 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0161 others(40): Show |
48 | HG01070.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.933+642T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81997488 | |||||||
| chr17:81997568 | G | A | 53 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(50): Show |
59 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.933+722G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81997568 | |||||||
| chr17:81997662 | T | TAGTATTT others(84): Show |
1 | a0001c0001t0001g0019 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.933+816_933+817ins others(91): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81997662 | |||||||
| chr17:81997670 | T | C | 1 | a0002c0002t0001g0247 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.933+824T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81997670 | |||||||
| chr17:81997827 | A | C | 7 | a0001c0004t0001g0171 a0001c0004t0001g0172 a0001c0004t0001g0173 others(4): Show |
7 | HG02451.hp2 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.933+981A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81997827 | |||||||
| chr17:81997828 | C | CT | 4 | a0001c0008t0002g0009 a0001c0008t0002g0211 a0001c0008t0002g0212 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.933+997dupT | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 81997828 | ||||||
| chr17:81997828 | CT | C | 7 | a0001c0001t0001g0085 a0001c0001t0001g0129 a0001c0007t0001g0143 others(4): Show |
7 | HG01069.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.933+997delT | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 81997828 | ||||||
| chr17:81997829 | T | C | 1 | a0001c0004t0001g0170 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.933+983T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81997829 | |||||||
| chr17:81997888 | G | A | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.933+1042G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81997888 | |||||||
| chr17:81997929 | C | T | 1 | a0001c0003t0001g0165 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.933+1083C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81997929 | |||||||
| chr17:81998001 | A | C | 1 | a0002c0002t0001g0275 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.933+1155A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81998001 | |||||||
| chr17:81998090 | G | C | 1 | a0002c0002t0001g0215 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.933+1244G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81998090 | |||||||
| chr17:81998145 | A | C | 1 | a0001c0003t0001g0162 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.933+1299A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81998145 | |||||||
| chr17:81998159 | C | T | 2 | a0001c0004t0001g0178 a0001c0004t0001g0179 |
2 | NA18943.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.933+1313C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81998159 | |||||||
| chr17:81998278 | T | C | 2 | a0004c0010t0001g0157 a0004c0010t0001g0158 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.933+1432T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81998278 | |||||||
| chr17:81998685 | G | C | 1 | a0002c0002t0001g0248 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.933+1839G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81998685 | |||||||
| chr17:81998937 | C | T | 2 | a0002c0002t0001g0273 a0002c0002t0001g0274 |
2 | HG03017.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.933+2091C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81998937 | |||||||
| chr17:81998950 | G | A | 20 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0191 others(17): Show |
22 | HG01070.hp2 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.933+2104G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81998950 | |||||||
| chr17:81998961 | A | G | 2 | a0002c0002t0001g0232 a0002c0002t0001g0272 |
2 | HG00642.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.933+2115A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81998961 | |||||||
| chr17:81999086 | C | T | 1 | a0002c0005t0001g0197 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.933+2240C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81999086 | |||||||
| chr17:81999237 | A | C | 1 | a0002c0002t0001g0271 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.933+2391A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81999237 | |||||||
| chr17:81999347 | T | C | 3 | a0001c0004t0001g0027 a0001c0004t0001g0178 a0001c0004t0001g0179 |
4 | NA18943.hp2 NA18975.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+2501T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81999347 | |||||||
| chr17:81999602 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | NA18954.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.933+2756G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81999602 | |||||||
| chr17:81999626 | C | CA | 14 | a0001c0001t0001g0086 a0001c0001t0001g0131 a0001c0001t0001g0142 others(11): Show |
14 | HG02523.hp2 HG02615.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.933+2798dupA | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 81999626 | ||||||
| chr17:81999693 | G | T | 3 | a0002c0002t0001g0222 a0002c0002t0001g0231 a0002c0002t0001g0270 |
3 | HG03491.hp2 HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.933+2847G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81999693 | |||||||
| chr17:81999711 | C | T | 1 | a0001c0003t0001g0043 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.933+2865C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81999711 | |||||||
| chr17:81999842 | G | A | 2 | a0002c0002t0001g0217 a0002c0002t0001g0218 |
2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.933+2996G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81999842 | |||||||
| chr17:81999857 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.933+3011G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 81999857 | |||||||
| chr17:82000026 | C | T | 1 | a0001c0024t0001g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.933+3180C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82000026 | |||||||
| chr17:82000106 | G | A | 1 | a0002c0002t0001g0311 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.933+3260G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82000106 | |||||||
| chr17:82000266 | G | C | 130 | a0001c0003t0001g0003 a0001c0003t0001g0014 a0001c0003t0001g0199 others(127): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.933+3420G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82000266 | |||||||
| chr17:82000289 | G | A | 1 | a0002c0002t0001g0273 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.933+3443G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82000289 | |||||||
| chr17:82000319 | T | G | 1 | a0001c0001t0001g0071 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.933+3473T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82000319 | |||||||
| chr17:82000320 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.933+3474G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82000320 | |||||||
| chr17:82000468 | C | T | 21 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0170 others(18): Show |
23 | HG00621.hp2 HG01074.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.933+3622C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82000468 | |||||||
| chr17:82000482 | G | A | 1 | a0002c0002t0001g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.933+3636G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82000482 | |||||||
| chr17:82000656 | G | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(309): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.933+3810G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82000656 | |||||||
| chr17:82000691 | C | T | 20 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0191 others(17): Show |
22 | HG01070.hp2 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.933+3845C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82000691 | |||||||
| chr17:82000981 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0131 |
2 | HG02080.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.933+4135C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82000981 | |||||||
| chr17:82001036 | C | T | 1 | a0001c0003t0001g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.933+4190C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001036 | |||||||
| chr17:82001079 | TCTGTGG | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0014t0001g0185 |
3 | HG02155.hp1 NA18952.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.933+4237_933+4242d others(8): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 82001079 | ||||||
| chr17:82001152 | C | A | 1 | a0002c0002t0001g0250 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.933+4306C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001152 | |||||||
| chr17:82001176 | G | A | 20 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0191 others(17): Show |
22 | HG01070.hp2 HG01109.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.933+4330G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001176 | |||||||
| chr17:82001235 | G | C | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.933+4389G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001235 | |||||||
| chr17:82001283 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.933+4437C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001283 | |||||||
| chr17:82001301 | G | A | 21 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0170 others(18): Show |
23 | HG00621.hp2 HG01074.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.933+4455G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001301 | |||||||
| chr17:82001329 | G | A | 2 | a0005c0009t0001g0033 a0005c0009t0001g0244 |
3 | HG02723.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.933+4483G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001329 | |||||||
| chr17:82001331 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.933+4485G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001331 | |||||||
| chr17:82001570 | T | C | 8 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(5): Show |
9 | HG01168.hp2 HG01169.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.933+4724T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001570 | |||||||
| chr17:82001783 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(203): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.933+4937C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001783 | |||||||
| chr17:82001793 | C | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(175): Show |
205 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.933+4947C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001793 | |||||||
| chr17:82001827 | C | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(236): Show |
274 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.933+4981C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001827 | |||||||
| chr17:82001891 | A | C | 1 | a0001c0024t0001g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.933+5045A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001891 | |||||||
| chr17:82001897 | C | G | 8 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(5): Show |
9 | HG01168.hp2 HG01169.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.933+5051C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001897 | |||||||
| chr17:82001903 | C | A | 12 | a0001c0003t0001g0003 a0001c0003t0001g0199 a0002c0002t0001g0003 others(9): Show |
15 | HG00735.hp2 HG01358.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.933+5057C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001903 | |||||||
| chr17:82001947 | G | A | 8 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0004t0001g0172 others(5): Show |
8 | HG01074.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.933+5101G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001947 | |||||||
| chr17:82001990 | TTTTTTCT others(5): Show |
T | 1 | a0002c0002t0001g0275 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.933+5145_933+5156d others(14): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82001990 | |||||||
| chr17:82002003 | C | CT | 7 | a0001c0001t0001g0071 a0001c0001t0001g0132 a0001c0003t0001g0147 others(4): Show |
7 | HG01168.hp2 HG03486.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.933+5179dupT | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 82002003 | ||||||
| chr17:82002003 | CT | C | 137 | a0001c0001t0001g0059 a0001c0001t0001g0088 a0001c0001t0001g0109 others(134): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.933+5179delT | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 82002003 | ||||||
| chr17:82002003 | CTT | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(50): Show |
62 | HG00558.hp1 HG00639.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.933+5178_933+5179d others(4): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 82002003 | ||||||
| chr17:82002003 | CTTT | C | 5 | a0001c0007t0001g0008 a0001c0007t0001g0049 a0001c0007t0001g0135 others(2): Show |
7 | HG01891.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.933+5177_933+5179d others(5): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 82002003 | ||||||
| chr17:82002004 | T | C | 1 | a0002c0002t0001g0275 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.933+5158T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002004 | |||||||
| chr17:82002074 | T | C | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.933+5228T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002074 | |||||||
| chr17:82002142 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0115 |
2 | HG00733.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.933+5296C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002142 | |||||||
| chr17:82002328 | G | A | 1 | a0001c0003t0001g0312 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.933+5482G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002328 | |||||||
| chr17:82002504 | A | G | 2 | a0002c0002t0001g0206 a0002c0002t0001g0207 |
2 | HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.933+5658A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002504 | |||||||
| chr17:82002507 | G | A | 1 | a0001c0003t0001g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.933+5661G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002507 | |||||||
| chr17:82002554 | C | CTATTTT | 4 | a0001c0001t0001g0015 a0001c0001t0001g0066 a0001c0001t0001g0089 others(1): Show |
5 | HG02273.hp2 HG02572.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.933+5728_933+5733d others(8): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 82002554 | ||||||
| chr17:82002757 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5911C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002757 | |||||||
| chr17:82002759 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5913T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002759 | |||||||
| chr17:82002761 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5915T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002761 | |||||||
| chr17:82002762 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5916T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002762 | |||||||
| chr17:82002763 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5917T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002763 | |||||||
| chr17:82002764 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5918G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002764 | |||||||
| chr17:82002765 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5919T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002765 | |||||||
| chr17:82002769 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5923G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002769 | |||||||
| chr17:82002770 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5924C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002770 | |||||||
| chr17:82002771 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5925T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002771 | |||||||
| chr17:82002774 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5928T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002774 | |||||||
| chr17:82002781 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5935T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002781 | |||||||
| chr17:82002782 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5936T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002782 | |||||||
| chr17:82002784 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5938C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002784 | |||||||
| chr17:82002786 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5940G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002786 | |||||||
| chr17:82002788 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5942C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002788 | |||||||
| chr17:82002790 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5944T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002790 | |||||||
| chr17:82002791 | C | G | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5945C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002791 | |||||||
| chr17:82002793 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5947G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002793 | |||||||
| chr17:82002795 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5949T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002795 | |||||||
| chr17:82002798 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5952T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002798 | |||||||
| chr17:82002800 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5954T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002800 | |||||||
| chr17:82002803 | CTGCTTTG others(8): Show |
C | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5958_933+5972d others(17): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002803 | |||||||
| chr17:82002835 | G | A | 4 | a0001c0008t0002g0009 a0001c0008t0002g0211 a0001c0008t0002g0212 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.933+5989G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002835 | |||||||
| chr17:82002839 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5993T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002839 | |||||||
| chr17:82002840 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5994G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002840 | |||||||
| chr17:82002843 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+5997C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002843 | |||||||
| chr17:82002847 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6001C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002847 | |||||||
| chr17:82002848 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6002G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002848 | |||||||
| chr17:82002851 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6005C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002851 | |||||||
| chr17:82002852 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6006C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002852 | |||||||
| chr17:82002855 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6009G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002855 | |||||||
| chr17:82002856 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6010C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002856 | |||||||
| chr17:82002857 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6011C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002857 | |||||||
| chr17:82002858 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6012T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002858 | |||||||
| chr17:82002859 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6013G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002859 | |||||||
| chr17:82002860 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6014T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002860 | |||||||
| chr17:82002861 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6015T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002861 | |||||||
| chr17:82002863 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6017T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002863 | |||||||
| chr17:82002866 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6020T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002866 | |||||||
| chr17:82002866 | T | C | 1 | a0002c0002t0001g0277 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.933+6020T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002866 | |||||||
| chr17:82002867 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6021C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002867 | |||||||
| chr17:82002869 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6023T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002869 | |||||||
| chr17:82002870 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6024T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002870 | |||||||
| chr17:82002872 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6026T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002872 | |||||||
| chr17:82002877 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6031T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002877 | |||||||
| chr17:82002880 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6034C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002880 | |||||||
| chr17:82002880 | CT | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0106 a0001c0001t0001g0153 others(8): Show |
12 | HG01168.hp2 HG01169.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.933+6045delT | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 82002880 | ||||||
| chr17:82002881 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6035T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002881 | |||||||
| chr17:82002882 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6036T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002882 | |||||||
| chr17:82002883 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6037T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002883 | |||||||
| chr17:82002884 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6038T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002884 | |||||||
| chr17:82002885 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6039T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002885 | |||||||
| chr17:82002886 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6040T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002886 | |||||||
| chr17:82002887 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6041T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002887 | |||||||
| chr17:82002888 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6042T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002888 | |||||||
| chr17:82002889 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6043T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002889 | |||||||
| chr17:82002890 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.933+6044T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002890 | |||||||
| chr17:82002978 | G | A | 1 | a0002c0002t0001g0254 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.934-6059G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82002978 | |||||||
| chr17:82003425 | G | A | 2 | a0002c0002t0001g0226 a0002c0002t0001g0229 |
2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.934-5612G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82003425 | |||||||
| chr17:82003566 | G | A | 13 | a0001c0004t0001g0027 a0001c0004t0001g0028 a0001c0004t0001g0177 others(10): Show |
15 | HG00621.hp2 HG01346.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.934-5471G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82003566 | |||||||
| chr17:82003574 | C | G | 7 | a0001c0004t0001g0170 a0001c0004t0001g0171 a0001c0004t0001g0172 others(4): Show |
7 | HG01074.hp2 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.934-5463C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82003574 | |||||||
| chr17:82003585 | G | T | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.934-5452G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82003585 | |||||||
| chr17:82003600 | A | G | 1 | a0002c0002t0001g0253 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.934-5437A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82003600 | |||||||
| chr17:82003702 | C | T | 1 | a0002c0002t0001g0268 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.934-5335C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82003702 | |||||||
| chr17:82003744 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG02258.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.934-5293G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82003744 | |||||||
| chr17:82003884 | C | T | 3 | a0001c0001t0001g0012 a0002c0005t0001g0267 a0002c0005t0001g0282 |
3 | HG02027.hp1 HG02071.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.934-5153C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82003884 | |||||||
| chr17:82003904 | A | G | 1 | a0009c0021t0001g0133 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.934-5133A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82003904 | |||||||
| chr17:82004092 | A | C | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.934-4945A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82004092 | |||||||
| chr17:82004093 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.934-4944C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82004093 | |||||||
| chr17:82004134 | A | G | 10 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(7): Show |
11 | HG01168.hp2 HG01169.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.934-4903A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82004134 | |||||||
| chr17:82004141 | C | T | 3 | a0001c0008t0002g0009 a0001c0008t0002g0212 a0001c0008t0002g0213 |
5 | HG01884.hp2 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.934-4896C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82004141 | |||||||
| chr17:82004182 | C | T | 1 | a0001c0003t0001g0150 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.934-4855C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82004182 | |||||||
| chr17:82004253 | C | T | 1 | a0001c0003t0001g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.934-4784C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82004253 | |||||||
| chr17:82004255 | C | T | 26 | a0001c0003t0001g0291 a0001c0004t0001g0027 a0001c0004t0001g0028 others(23): Show |
29 | HG00621.hp2 HG01074.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.934-4782C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82004255 | |||||||
| chr17:82004281 | C | T | 4 | a0001c0008t0002g0009 a0001c0008t0002g0211 a0001c0008t0002g0212 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.934-4756C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82004281 | |||||||
| chr17:82004417 | T | C | 14 | a0002c0002t0001g0188 a0002c0002t0001g0202 a0002c0002t0001g0219 others(11): Show |
14 | HG00408.hp1 HG00673.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.934-4620T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82004417 | |||||||
| chr17:82004792 | A | C | 2 | a0002c0002t0001g0307 a0002c0019t0001g0306 |
2 | NA18974.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.934-4245A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82004792 | |||||||
| chr17:82004842 | T | C | 195 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0153 others(192): Show |
219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.934-4195T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82004842 | |||||||
| chr17:82004886 | C | T | 1 | a0001c0004t0001g0171 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.934-4151C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82004886 | |||||||
| chr17:82005002 | C | T | 1 | a0002c0002t0001g0256 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.934-4035C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005002 | |||||||
| chr17:82005076 | G | A | 1 | a0002c0002t0001g0246 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.934-3961G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005076 | |||||||
| chr17:82005136 | C | T | 43 | a0001c0003t0001g0014 a0002c0002t0001g0004 a0002c0002t0001g0010 others(40): Show |
51 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.934-3901C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005136 | |||||||
| chr17:82005247 | G | A | 9 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
10 | HG01168.hp2 HG01169.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.934-3790G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005247 | |||||||
| chr17:82005248 | C | T | 24 | a0001c0003t0001g0014 a0002c0002t0001g0010 a0002c0002t0001g0188 others(21): Show |
27 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.934-3789C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005248 | |||||||
| chr17:82005249 | C | CG | 7 | a0001c0001t0001g0047 a0001c0001t0001g0078 a0001c0001t0001g0124 others(4): Show |
7 | HG00544.hp1 HG00733.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.934-3784dupG | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 82005249 | ||||||
| chr17:82005249 | C | G | 1 | a0002c0005t0001g0280 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.934-3788C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005249 | |||||||
| chr17:82005269 | G | A | 6 | a0001c0001t0001g0088 a0002c0002t0001g0190 a0002c0002t0001g0245 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.934-3768G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005269 | |||||||
| chr17:82005289 | G | T | 2 | a0001c0003t0001g0151 a0001c0003t0001g0290 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.934-3748G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005289 | |||||||
| chr17:82005321 | C | T | 34 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0191 others(31): Show |
37 | HG01070.hp2 HG01074.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.934-3716C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005321 | |||||||
| chr17:82005355 | G | A | 1 | a0001c0003t0001g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.934-3682G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005355 | |||||||
| chr17:82005367 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.934-3670C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005367 | |||||||
| chr17:82005391 | G | A | 1 | a0004c0010t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.934-3646G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005391 | |||||||
| chr17:82005429 | A | G | 1 | a0010c0023t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.934-3608A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005429 | |||||||
| chr17:82005549 | C | G | 4 | a0002c0002t0001g0236 a0002c0002t0001g0261 a0002c0002t0001g0286 others(1): Show |
4 | HG00280.hp2 HG01261.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.934-3488C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005549 | |||||||
| chr17:82005551 | A | G | 4 | a0001c0008t0002g0009 a0001c0008t0002g0211 a0001c0008t0002g0212 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.934-3486A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005551 | |||||||
| chr17:82005676 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.934-3361G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005676 | |||||||
| chr17:82005769 | C | T | 1 | a0002c0002t0001g0261 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.934-3268C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82005769 | |||||||
| chr17:82006068 | CGTGTCCT others(33): Show |
C | 4 | a0001c0008t0002g0009 a0001c0008t0002g0211 a0001c0008t0002g0212 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.934-2957_934-2918d others(42): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 82006068 | ||||||
| chr17:82006103 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(9): Show |
18 | HG01943.hp2 HG01993.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.934-2934G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82006103 | |||||||
| chr17:82006123 | A | G | 52 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(49): Show |
58 | HG01070.hp2 HG01074.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.934-2914A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82006123 | |||||||
| chr17:82006128 | T | C | 1 | a0002c0002t0001g0253 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.934-2909T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82006128 | |||||||
| chr17:82006211 | G | GGT | 10 | a0001c0001t0001g0048 a0001c0001t0001g0153 a0001c0001t0001g0155 others(7): Show |
11 | HG01168.hp2 HG01169.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.934-2807_934-2806d others(4): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 82006211 | ||||||
| chr17:82006211 | G | GGTGT | 4 | a0002c0002t0001g0226 a0002c0002t0001g0228 a0002c0002t0001g0229 others(1): Show |
4 | HG02055.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-2809_934-2806d others(6): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 82006211 | ||||||
| chr17:82006211 | GGT | G | 121 | a0001c0003t0001g0003 a0001c0003t0001g0014 a0001c0003t0001g0067 others(118): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.934-2807_934-2806d others(4): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 82006211 | ||||||
| chr17:82006264 | T | C | 3 | a0001c0003t0001g0026 a0001c0003t0001g0159 a0001c0003t0001g0163 |
4 | NA18951.hp2 NA18977.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-2773T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82006264 | |||||||
| chr17:82006300 | G | GGT | 5 | a0002c0002t0001g0190 a0002c0002t0001g0245 a0002c0002t0001g0251 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.934-2726_934-2725d others(4): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 82006300 | ||||||
| chr17:82006302 | T | G | 1 | a0001c0003t0001g0159 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.934-2735T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82006302 | |||||||
| chr17:82006472 | C | T | 2 | a0001c0001t0001g0102 a0001c0022t0001g0117 |
2 | NA18947.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.934-2565C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82006472 | |||||||
| chr17:82006598 | C | A | 37 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0191 others(34): Show |
42 | HG01070.hp2 HG01074.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.934-2439C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82006598 | |||||||
| chr17:82006730 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.934-2307G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82006730 | |||||||
| chr17:82006747 | T | C | 14 | a0001c0003t0001g0291 a0001c0004t0001g0170 a0001c0004t0001g0171 others(11): Show |
16 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.934-2290T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82006747 | |||||||
| chr17:82006930 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.934-2107T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82006930 | |||||||
| chr17:82007083 | A | G | 1 | a0002c0002t0001g0237 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.934-1954A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82007083 | |||||||
| chr17:82007084 | C | T | 2 | a0001c0001t0001g0118 a0001c0003t0001g0151 |
2 | HG02074.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.934-1953C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82007084 | |||||||
| chr17:82007187 | T | C | 2 | a0002c0002t0001g0245 a0002c0002t0001g0299 |
2 | HG01243.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.934-1850T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82007187 | |||||||
| chr17:82007316 | G | A | 1 | a0004c0010t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.934-1721G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82007316 | |||||||
| chr17:82007367 | T | C | 3 | a0001c0008t0002g0009 a0001c0008t0002g0211 a0001c0008t0002g0213 |
5 | HG01884.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.934-1670T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82007367 | |||||||
| chr17:82007509 | C | T | 1 | a0001c0003t0001g0312 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.934-1528C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82007509 | |||||||
| chr17:82007634 | G | C | 1 | a0001c0004t0001g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.934-1403G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82007634 | |||||||
| chr17:82007774 | G | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0066 a0001c0001t0001g0089 others(1): Show |
5 | HG02273.hp2 HG03490.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.934-1263G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82007774 | |||||||
| chr17:82007821 | C | A | 1 | a0002c0002t0001g0254 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.934-1216C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82007821 | |||||||
| chr17:82007951 | C | T | 2 | a0002c0002t0001g0190 a0002c0002t0001g0251 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.934-1086C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82007951 | |||||||
| chr17:82008085 | G | A | 2 | a0001c0003t0001g0151 a0001c0003t0001g0290 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.934-952G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008085 | |||||||
| chr17:82008254 | G | A | 1 | a0002c0002t0001g0195 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.934-783G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008254 | |||||||
| chr17:82008306 | A | C | 1 | a0002c0002t0001g0223 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.934-731A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008306 | |||||||
| chr17:82008368 | C | T | 3 | a0005c0009t0001g0033 a0005c0009t0001g0152 a0005c0009t0001g0244 |
4 | HG02055.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-669C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008368 | |||||||
| chr17:82008456 | A | G | 10 | a0001c0003t0001g0291 a0001c0004t0001g0170 a0001c0004t0001g0171 others(7): Show |
11 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.934-581A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008456 | |||||||
| chr17:82008496 | G | A | 1 | a0002c0002t0001g0276 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.934-541G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008496 | |||||||
| chr17:82008506 | A | G | 1 | a0001c0024t0001g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.934-531A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008506 | |||||||
| chr17:82008527 | A | G | 25 | a0001c0003t0001g0291 a0001c0004t0001g0027 a0001c0004t0001g0028 others(22): Show |
29 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.934-510A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008527 | |||||||
| chr17:82008582 | C | A | 3 | a0005c0009t0001g0033 a0005c0009t0001g0152 a0005c0009t0001g0244 |
4 | HG02055.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-455C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008582 | |||||||
| chr17:82008611 | T | G | 205 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0057 others(202): Show |
234 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.934-426T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008611 | |||||||
| chr17:82008711 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.934-326C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008711 | |||||||
| chr17:82008760 | C | G | 8 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(5): Show |
9 | HG01168.hp2 HG01169.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.934-277C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008760 | |||||||
| chr17:82008884 | G | A | 1 | a0010c0023t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.934-153G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008884 | |||||||
| chr17:82008904 | G | T | 1 | a0001c0004t0001g0181 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.934-133G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008904 | |||||||
| chr17:82008960 | G | A | 1 | a0002c0002t0001g0310 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.934-77G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008960 | |||||||
| chr17:82008980 | G | A | 1 | a0001c0003t0001g0163 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.934-57G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008980 | |||||||
| chr17:82008991 | G | A | 22 | a0001c0003t0001g0291 a0001c0004t0001g0027 a0001c0004t0001g0028 others(19): Show |
25 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.934-46G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82008991 | |||||||
| chr17:82009024 | C | T | 1 | a0001c0017t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.934-13C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 7/15 | chr17 | 82009024 | |||||||
| chr17:82009290 | G | A | 24 | a0001c0003t0001g0291 a0001c0004t0001g0027 a0001c0004t0001g0028 others(21): Show |
28 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.1088+99G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 8/15 | chr17 | 82009290 | |||||||
| chr17:82009398 | C | T | 1 | a0002c0002t0001g0246 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1089-88C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 8/15 | chr17 | 82009398 | |||||||
| chr17:82009585 | G | GGGGGCGA others(50): Show |
177 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(174): Show |
201 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1170+42_1170+43ins others(57): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr17 | 82009585 | ||||||
| chr17:82009595 | G | GAGGCACA others(48): Show |
10 | a0001c0003t0001g0291 a0001c0004t0001g0170 a0001c0004t0001g0171 others(7): Show |
11 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+42_1170+43ins others(55): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr17 | 82009595 | ||||||
| chr17:82009610 | G | C | 3 | a0005c0009t0001g0033 a0005c0009t0001g0152 a0005c0009t0001g0244 |
4 | HG02055.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+43G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009610 | |||||||
| chr17:82009620 | CG | C | 3 | a0005c0009t0001g0033 a0005c0009t0001g0152 a0005c0009t0001g0244 |
4 | HG02055.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+54delG | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009620 | |||||||
| chr17:82009621 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1170+54G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009621 | |||||||
| chr17:82009630 | G | A | 3 | a0005c0009t0001g0033 a0005c0009t0001g0152 a0005c0009t0001g0244 |
4 | HG02055.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+63G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009630 | |||||||
| chr17:82009631 | T | C | 3 | a0005c0009t0001g0033 a0005c0009t0001g0152 a0005c0009t0001g0244 |
4 | HG02055.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+64T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009631 | |||||||
| chr17:82009635 | C | T | 5 | a0001c0004t0001g0174 a0001c0004t0001g0175 a0005c0009t0001g0033 others(2): Show |
6 | HG02055.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170+68C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009635 | |||||||
| chr17:82009636 | G | A | 1 | a0002c0002t0001g0311 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1170+69G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009636 | |||||||
| chr17:82009639 | A | ACGT | 4 | a0002c0002t0001g0311 a0005c0009t0001g0033 a0005c0009t0001g0152 others(1): Show |
5 | HG02055.hp1 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1170+72_1170+73ins others(3): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009639 | |||||||
| chr17:82009640 | T | A | 3 | a0005c0009t0001g0033 a0005c0009t0001g0152 a0005c0009t0001g0244 |
4 | HG02055.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+73T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009640 | |||||||
| chr17:82009640 | T | G | 1 | a0002c0002t0001g0311 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1170+73T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009640 | |||||||
| chr17:82009675 | T | C | 3 | a0005c0009t0001g0033 a0005c0009t0001g0152 a0005c0009t0001g0244 |
4 | HG02055.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+108T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009675 | |||||||
| chr17:82009748 | T | C | 3 | a0005c0009t0001g0033 a0005c0009t0001g0152 a0005c0009t0001g0244 |
4 | HG02055.hp1 HG02723.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+181T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009748 | |||||||
| chr17:82009913 | AC | A | 8 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(5): Show |
9 | HG01168.hp2 HG01169.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1170+348delC | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr17 | 82009913 | ||||||
| chr17:82009915 | CT | C | 8 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0055 others(5): Show |
9 | HG00323.hp1 HG02055.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170+361delT | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr17 | 82009915 | ||||||
| chr17:82009984 | A | G | 1 | a0003c0006t0001g0241 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1170+417A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009984 | |||||||
| chr17:82009995 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1170+428C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82009995 | |||||||
| chr17:82010028 | G | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0085 a0001c0001t0001g0096 others(1): Show |
6 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+461G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010028 | |||||||
| chr17:82010087 | G | GT | 8 | a0001c0001t0001g0114 a0001c0024t0001g0149 a0002c0002t0001g0219 others(5): Show |
9 | HG00323.hp2 HG01168.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170+534dupT | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr17 | 82010087 | ||||||
| chr17:82010087 | G | GTT | 151 | a0001c0001t0001g0101 a0001c0003t0001g0003 a0001c0003t0001g0014 others(148): Show |
172 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1170+533_1170+534d others(4): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr17 | 82010087 | ||||||
| chr17:82010087 | G | GTTT | 9 | a0002c0002t0001g0051 a0002c0002t0001g0076 a0002c0002t0001g0077 others(6): Show |
9 | HG01358.hp1 HG01433.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1170+532_1170+534d others(5): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr17 | 82010087 | ||||||
| chr17:82010102 | A | T | 2 | a0002c0002t0001g0273 a0002c0002t0001g0274 |
2 | HG03017.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1170+535A>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010102 | |||||||
| chr17:82010152 | C | T | 2 | a0002c0002t0001g0297 a0002c0002t0001g0298 |
2 | HG01099.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1170+585C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010152 | |||||||
| chr17:82010169 | G | A | 4 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
5 | HG02258.hp2 HG02970.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+602G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010169 | |||||||
| chr17:82010187 | T | G | 10 | a0001c0003t0001g0291 a0001c0004t0001g0170 a0001c0004t0001g0171 others(7): Show |
11 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1171-615T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010187 | |||||||
| chr17:82010257 | T | C | 4 | a0001c0001t0001g0089 a0001c0001t0001g0123 a0002c0002t0001g0217 others(1): Show |
4 | HG00738.hp1 HG01106.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1171-545T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010257 | |||||||
| chr17:82010325 | C | T | 1 | a0002c0002t0001g0252 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1171-477C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010325 | |||||||
| chr17:82010326 | G | C | 1 | a0002c0002t0001g0201 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1171-476G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010326 | |||||||
| chr17:82010340 | T | C | 3 | a0002c0002t0001g0190 a0002c0002t0001g0251 a0002c0002t0001g0289 |
3 | HG02622.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1171-462T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010340 | |||||||
| chr17:82010341 | G | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0040 others(12): Show |
17 | HG01943.hp2 HG01993.hp1 HG02273.hp1 others(14): Show |
intron_variant | MODIFIER | c.1171-461G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010341 | |||||||
| chr17:82010344 | A | G | 3 | a0002c0002t0001g0190 a0002c0002t0001g0251 a0002c0002t0001g0289 |
3 | HG02622.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1171-458A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010344 | |||||||
| chr17:82010345 | C | T | 3 | a0002c0002t0001g0190 a0002c0002t0001g0251 a0002c0002t0001g0289 |
3 | HG02622.hp1 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1171-457C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010345 | |||||||
| chr17:82010346 | G | A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0080 a0001c0001t0001g0082 others(2): Show |
5 | HG02572.hp2 HG02615.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1171-456G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010346 | |||||||
| chr17:82010353 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0040 |
4 | HG01943.hp2 HG01993.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1171-449C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010353 | |||||||
| chr17:82010357 | A | G | 29 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0040 others(26): Show |
37 | HG00544.hp1 HG00639.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.1171-445A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010357 | |||||||
| chr17:82010361 | C | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0040 |
4 | HG01943.hp2 HG01993.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1171-441C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010361 | |||||||
| chr17:82010361 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1171-441C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010361 | |||||||
| chr17:82010374 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1171-428A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010374 | |||||||
| chr17:82010399 | C | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | NA18952.hp1 NA18981.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1171-403C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010399 | |||||||
| chr17:82010400 | A | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | NA18952.hp1 NA18981.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1171-402A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010400 | |||||||
| chr17:82010484 | A | C | 2 | a0002c0002t0001g0217 a0002c0002t0001g0218 |
2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1171-318A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010484 | |||||||
| chr17:82010485 | T | C | 2 | a0002c0002t0001g0217 a0002c0002t0001g0218 |
2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1171-317T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010485 | |||||||
| chr17:82010515 | T | C | 187 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(184): Show |
213 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.1171-287T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010515 | |||||||
| chr17:82010528 | C | CA | 28 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0046 others(25): Show |
29 | HG00408.hp2 HG00741.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.1171-250dupA | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr17 | 82010528 | ||||||
| chr17:82010528 | C | CAA | 6 | a0001c0001t0001g0069 a0001c0001t0001g0097 a0001c0001t0001g0153 others(3): Show |
6 | HG02258.hp2 HG02970.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1171-251_1171-250d others(4): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr17 | 82010528 | ||||||
| chr17:82010535 | A | G | 1 | a0002c0002t0001g0299 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1171-267A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010535 | |||||||
| chr17:82010547 | A | AC | 51 | a0001c0003t0001g0025 a0001c0003t0001g0026 a0001c0003t0001g0058 others(48): Show |
56 | HG00621.hp1 HG01070.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.1171-255_1171-254i others(3): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010547 | |||||||
| chr17:82010547 | A | C | 128 | a0001c0003t0001g0003 a0001c0003t0001g0014 a0001c0003t0001g0022 others(125): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1171-255A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010547 | |||||||
| chr17:82010647 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0040 |
2 | HG02273.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1171-155G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010647 | |||||||
| chr17:82010742 | C | T | 1 | a0001c0017t0001g0169 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1171-60C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 9/15 | chr17 | 82010742 | |||||||
| chr17:82010982 | C | G | 1 | a0001c0001t0001g0012 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1237+114C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 10/15 | chr17 | 82010982 | |||||||
| chr17:82011038 | G | A | 1 | a0002c0002t0001g0231 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1237+170G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 10/15 | chr17 | 82011038 | |||||||
| chr17:82011077 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1237+209C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 10/15 | chr17 | 82011077 | |||||||
| chr17:82011234 | C | T | 1 | a0001c0024t0001g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1238-309C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 10/15 | chr17 | 82011234 | |||||||
| chr17:82011291 | G | A | 1 | a0004c0010t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1238-252G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 10/15 | chr17 | 82011291 | |||||||
| chr17:82011367 | G | C | 5 | a0001c0007t0001g0008 a0001c0007t0001g0049 a0001c0007t0001g0135 others(2): Show |
7 | HG01891.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1238-176G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 10/15 | chr17 | 82011367 | |||||||
| chr17:82011375 | C | T | 1 | a0003c0006t0001g0242 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1238-168C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 10/15 | chr17 | 82011375 | |||||||
| chr17:82011393 | G | T | 1 | a0005c0009t0001g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1238-150G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 10/15 | chr17 | 82011393 | |||||||
| chr17:82011441 | G | A | 1 | a0002c0002t0001g0229 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1238-102G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 10/15 | chr17 | 82011441 | |||||||
| chr17:82011469 | T | C | 1 | a0001c0001t0001g0019 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1238-74T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 10/15 | chr17 | 82011469 | |||||||
| chr17:82011617 | C | T | 1 | a0005c0009t0001g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1300+12C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 11/15 | chr17 | 82011617 | |||||||
| chr17:82011657 | T | C | 1 | a0001c0003t0001g0022 | 2 | HG02027.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1300+52T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 11/15 | chr17 | 82011657 | |||||||
| chr17:82011691 | C | T | 1 | a0002c0002t0001g0289 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1300+86C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 11/15 | chr17 | 82011691 | |||||||
| chr17:82011737 | G | T | 15 | a0001c0003t0001g0022 a0001c0003t0001g0095 a0001c0003t0001g0113 others(12): Show |
20 | HG00639.hp1 HG01069.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1300+132G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 11/15 | chr17 | 82011737 | |||||||
| chr17:82011804 | G | T | 1 | a0004c0010t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1300+199G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 11/15 | chr17 | 82011804 | |||||||
| chr17:82012046 | C | G | 1 | a0002c0002t0001g0263 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1301-185C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 11/15 | chr17 | 82012046 | |||||||
| chr17:82012415 | G | A | 5 | a0004c0010t0001g0148 a0004c0010t0001g0154 a0004c0010t0001g0157 others(2): Show |
6 | HG01168.hp2 HG01169.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+132G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82012415 | |||||||
| chr17:82012496 | G | C | 1 | a0005c0009t0001g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1353+213G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82012496 | |||||||
| chr17:82012552 | G | A | 2 | a0002c0002t0001g0264 a0002c0002t0001g0277 |
2 | NA19062.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1353+269G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82012552 | |||||||
| chr17:82012599 | C | A | 1 | a0001c0003t0001g0290 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1353+316C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82012599 | |||||||
| chr17:82012604 | G | A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0221 |
3 | HG02258.hp1 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1353+321G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82012604 | |||||||
| chr17:82012643 | G | A | 1 | a0002c0005t0001g0259 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1353+360G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82012643 | |||||||
| chr17:82013063 | C | T | 1 | a0005c0009t0001g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1353+780C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82013063 | |||||||
| chr17:82013084 | C | T | 1 | a0002c0005t0001g0198 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1353+801C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82013084 | |||||||
| chr17:82013169 | G | A | 1 | a0001c0003t0001g0043 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1353+886G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82013169 | |||||||
| chr17:82013189 | C | T | 100 | a0001c0003t0001g0003 a0001c0003t0001g0043 a0001c0003t0001g0067 others(97): Show |
111 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1353+906C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82013189 | |||||||
| chr17:82013414 | C | T | 2 | a0001c0001t0001g0064 a0002c0005t0001g0210 |
2 | HG02698.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1353+1131C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82013414 | |||||||
| chr17:82013416 | T | C | 2 | a0001c0017t0001g0169 a0001c0024t0001g0149 |
2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1353+1133T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82013416 | |||||||
| chr17:82013458 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(26): Show |
36 | HG00558.hp1 HG01943.hp2 HG01993.hp1 others(33): Show |
intron_variant | MODIFIER | c.1353+1175C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82013458 | |||||||
| chr17:82013479 | G | GTGCC | 6 | a0001c0001t0001g0121 a0001c0003t0001g0291 a0001c0004t0001g0172 others(3): Show |
7 | HG00140.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1353+1213_1353+121 others(8): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr17 | 82013479 | ||||||
| chr17:82013479 | GTGCC | G | 4 | a0004c0010t0001g0154 a0004c0010t0001g0157 a0004c0010t0001g0158 others(1): Show |
5 | HG01168.hp2 HG01169.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353+1213_1353+121 others(8): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr17 | 82013479 | ||||||
| chr17:82013567 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG02258.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1353+1284G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82013567 | |||||||
| chr17:82013645 | C | G | 1 | a0001c0024t0001g0149 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1353+1362C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82013645 | |||||||
| chr17:82013648 | G | A | 1 | a0005c0009t0001g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1353+1365G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82013648 | |||||||
| chr17:82013946 | A | G | 9 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
10 | HG01168.hp2 HG01169.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1353+1663A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82013946 | |||||||
| chr17:82014103 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1353+1820A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82014103 | |||||||
| chr17:82014444 | G | A | 10 | a0001c0003t0001g0291 a0001c0004t0001g0170 a0001c0004t0001g0171 others(7): Show |
11 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1354-2032G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82014444 | |||||||
| chr17:82014461 | C | T | 1 | a0002c0002t0001g0261 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1354-2015C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82014461 | |||||||
| chr17:82014514 | C | T | 1 | a0002c0002t0001g0292 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1354-1962C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82014514 | |||||||
| chr17:82014515 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1354-1961G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82014515 | |||||||
| chr17:82014524 | G | A | 1 | a0004c0010t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1354-1952G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82014524 | |||||||
| chr17:82014548 | T | C | 164 | a0001c0003t0001g0003 a0001c0003t0001g0014 a0001c0003t0001g0022 others(161): Show |
186 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1354-1928T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82014548 | |||||||
| chr17:82014694 | C | T | 2 | a0001c0017t0001g0169 a0001c0024t0001g0149 |
2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1354-1782C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82014694 | |||||||
| chr17:82014703 | G | T | 10 | a0001c0003t0001g0291 a0001c0004t0001g0170 a0001c0004t0001g0171 others(7): Show |
11 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1354-1773G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82014703 | |||||||
| chr17:82014704 | C | T | 1 | a0001c0003t0001g0092 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1354-1772C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82014704 | |||||||
| chr17:82014713 | G | A | 5 | a0001c0007t0001g0008 a0001c0007t0001g0049 a0001c0007t0001g0135 others(2): Show |
7 | HG01891.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1354-1763G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82014713 | |||||||
| chr17:82014872 | C | T | 5 | a0004c0010t0001g0148 a0004c0010t0001g0154 a0004c0010t0001g0157 others(2): Show |
6 | HG01168.hp2 HG01169.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-1604C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82014872 | |||||||
| chr17:82014999 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1354-1477C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82014999 | |||||||
| chr17:82015006 | C | T | 2 | a0002c0002t0001g0232 a0002c0002t0001g0272 |
2 | HG00642.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1354-1470C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82015006 | |||||||
| chr17:82015025 | C | T | 141 | a0001c0003t0001g0003 a0001c0003t0001g0014 a0001c0003t0001g0022 others(138): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1354-1451C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82015025 | |||||||
| chr17:82015073 | A | T | 2 | a0002c0002t0001g0217 a0002c0002t0001g0218 |
2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1354-1403A>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82015073 | |||||||
| chr17:82015308 | C | T | 1 | a0005c0009t0001g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1354-1168C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82015308 | |||||||
| chr17:82015309 | G | A | 1 | a0002c0002t0001g0266 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1354-1167G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82015309 | |||||||
| chr17:82015447 | C | T | 5 | a0001c0003t0001g0067 a0001c0003t0001g0083 a0001c0003t0001g0090 others(2): Show |
5 | HG01243.hp1 HG02559.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1354-1029C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82015447 | |||||||
| chr17:82015562 | C | T | 4 | a0001c0008t0002g0009 a0001c0008t0002g0211 a0001c0008t0002g0212 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1354-914C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82015562 | |||||||
| chr17:82015779 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1354-697C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82015779 | |||||||
| chr17:82015935 | G | A | 3 | a0001c0003t0001g0312 a0002c0002t0001g0231 a0002c0002t0001g0270 |
3 | HG03831.hp2 HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1354-541G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82015935 | |||||||
| chr17:82016039 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0098 a0001c0014t0001g0214 |
4 | HG00408.hp2 HG00621.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354-437C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016039 | |||||||
| chr17:82016071 | G | C | 10 | a0001c0003t0001g0291 a0001c0004t0001g0170 a0001c0004t0001g0171 others(7): Show |
11 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1354-405G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016071 | |||||||
| chr17:82016091 | C | CTGGGGCT others(24): Show |
1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-385_1354-384i others(33): Show |
ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016091 | |||||||
| chr17:82016097 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG02258.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1354-379G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016097 | |||||||
| chr17:82016099 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-377C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016099 | |||||||
| chr17:82016100 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-376A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016100 | |||||||
| chr17:82016103 | T | A | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-373T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016103 | |||||||
| chr17:82016109 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-367C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016109 | |||||||
| chr17:82016134 | G | C | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-342G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016134 | |||||||
| chr17:82016147 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-329A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016147 | |||||||
| chr17:82016148 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-328C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016148 | |||||||
| chr17:82016148 | C | T | 5 | a0001c0007t0001g0008 a0001c0007t0001g0049 a0001c0007t0001g0135 others(2): Show |
7 | HG01891.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1354-328C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016148 | |||||||
| chr17:82016149 | G | C | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-327G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016149 | |||||||
| chr17:82016154 | G | C | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-322G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016154 | |||||||
| chr17:82016155 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-321C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016155 | |||||||
| chr17:82016156 | C | G | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-320C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016156 | |||||||
| chr17:82016159 | A | T | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-317A>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016159 | |||||||
| chr17:82016162 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-314T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016162 | |||||||
| chr17:82016167 | C | G | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-309C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016167 | |||||||
| chr17:82016196 | G | T | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-280G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016196 | |||||||
| chr17:82016197 | T | G | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-279T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016197 | |||||||
| chr17:82016198 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-278G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016198 | |||||||
| chr17:82016205 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-271C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016205 | |||||||
| chr17:82016207 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-269T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016207 | |||||||
| chr17:82016208 | G | C | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-268G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016208 | |||||||
| chr17:82016209 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-267G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016209 | |||||||
| chr17:82016217 | A | C | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-259A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016217 | |||||||
| chr17:82016221 | T | G | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-255T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016221 | |||||||
| chr17:82016227 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-249C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016227 | |||||||
| chr17:82016228 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-248C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016228 | |||||||
| chr17:82016230 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-246C>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016230 | |||||||
| chr17:82016245 | T | G | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-231T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016245 | |||||||
| chr17:82016246 | T | A | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-230T>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016246 | |||||||
| chr17:82016253 | T | G | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-223T>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016253 | |||||||
| chr17:82016254 | G | T | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-222G>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016254 | |||||||
| chr17:82016279 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-197T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016279 | |||||||
| chr17:82016282 | C | G | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-194C>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016282 | |||||||
| chr17:82016285 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-191G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016285 | |||||||
| chr17:82016286 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-190A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016286 | |||||||
| chr17:82016294 | G | C | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-182G>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016294 | |||||||
| chr17:82016327 | A | C | 1 | a0001c0001t0001g0055 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1354-149A>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016327 | |||||||
| chr17:82016403 | G | A | 1 | a0002c0002t0001g0035 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1354-73G>A | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016403 | |||||||
| chr17:82016414 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1354-62C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016414 | |||||||
| chr17:82016471 | T | C | 1 | a0001c0003t0001g0090 | 1 | HG01243.hp1 | splice_region_variant&intron_variant | LOW | c.1354-5T>C | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 12/15 | chr17 | 82016471 | |||||||
| chr17:82016655 | C | T | 1 | a0010c0023t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1405+128C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 13/15 | chr17 | 82016655 | |||||||
| chr17:82016738 | C | T | 2 | a0001c0003t0001g0151 a0001c0003t0001g0290 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1406-62C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 13/15 | chr17 | 82016738 | |||||||
| chr17:82016794 | C | T | 5 | a0001c0007t0001g0008 a0001c0007t0001g0049 a0001c0007t0001g0135 others(2): Show |
7 | HG01891.hp1 HG02717.hp1 HG02895.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1406-6C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 13/15 | chr17 | 82016794 | |||||||
| chr17:82016939 | A | G | 2 | a0002c0002t0001g0206 a0002c0002t0001g0207 |
2 | HG02486.hp2 NA19030.hp2 |
splice_acceptor_variant&intron_variant | HIGH | c.1476-2A>G | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 14/15 | chr17 | 82016939 | |||||||
| chr17:82017272 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1649-37C>T | ASPSCR1 | ENSG00000169696.16 | transcript | ENST00000306739.9 | protein_coding | 15/15 | chr17 | 82017272 |