Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3927 |
| ensemblid | ENSG00000002834.19 |
| hgncid | 6513 |
| symbol | LASP1 |
| name | LIM and SH3 protein 1 |
| refseq_nuc | NM_006148.4 |
| refseq_prot | NP_006139.1 |
| ensembl_nuc | ENST00000318008.11 |
| ensembl_prot | ENSP00000325240.6 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 38870058 |
| end | 38921770 |
| strand | + |
| ver | v1.2 |
| region | chr17:38870058-38921770 |
| region5000 | chr17:38865058-38926770 |
| regionname0 | LASP1_chr17_38870058_38921770 |
| regionname5000 | LASP1_chr17_38865058_38926770 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 261 | 394 | 96 | 77 | 155 | 16 | 48 | 112 | LASP1_chr17_38865058_38926770 | LASP1 | MNPNC others(256): Show |
chr17 | 38865058 | 38926770 |
| a0002 | 0/0 | 261 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | MNPNC others(256): Show |
chr17 | 38865058 | 38926770 |
| a0003 | 0/0 | 261 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | MNPNC others(256): Show |
chr17 | 38865058 | 38926770 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 783 | 147 | 59 | 19 | 51 | 4 | 14 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0001c0002 | 1/0 | 783 | 108 | 9 | 25 | 58 | 3 | 12 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0001c0003 | 0/0 | 783 | 58 | 15 | 16 | 14 | 4 | 9 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0001c0004 | 0/0 | 783 | 17 | 0 | 1 | 15 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0001c0005 | 0/1 | 783 | 17 | 0 | 6 | 1 | 1 | 8 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0001c0006 | 0/0 | 783 | 12 | 0 | 0 | 9 | 0 | 3 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0001c0007 | 0/0 | 783 | 12 | 11 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0001c0008 | 0/0 | 783 | 12 | 1 | 7 | 0 | 3 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0001c0009 | 0/0 | 783 | 4 | 0 | 0 | 4 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0001c0010 | 0/0 | 783 | 2 | 0 | 0 | 2 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0001c0011 | 0/0 | 783 | 2 | 0 | 0 | 1 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0001c0012 | 0/0 | 783 | 2 | 0 | 2 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0001c0013 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0002c0015 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 | ||
| a0003c0014 | 0/0 | 783 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | ATGAA others(778): Show |
chr17 | 38865058 | 38926770 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3925 | 59 | 9 | 7 | 34 | 0 | 9 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0002 | 0/0 | 3925 | 28 | 10 | 7 | 5 | 1 | 5 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0003 | 0/0 | 3910 | 13 | 5 | 0 | 8 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3905): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0004 | 0/0 | 3925 | 16 | 10 | 3 | 1 | 2 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0006 | 0/0 | 3925 | 5 | 5 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0007 | 0/0 | 3925 | 4 | 4 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0008 | 0/0 | 3925 | 3 | 2 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0009 | 0/0 | 3925 | 3 | 3 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0010 | 0/0 | 3925 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0011 | 0/0 | 3910 | 2 | 0 | 0 | 2 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3905): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0014 | 0/0 | 3925 | 2 | 2 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0015 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0016 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0021 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0023 | 0/0 | 3925 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0024 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0025 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0027 | 0/0 | 3925 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0028 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0030 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0031 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0001t0032 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0002t0001 | 0/0 | 3925 | 17 | 1 | 10 | 2 | 0 | 4 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0002t0002 | 0/0 | 3925 | 21 | 1 | 4 | 13 | 0 | 3 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0002t0003 | 1/0 | 3910 | 56 | 0 | 9 | 39 | 3 | 4 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3905): Show |
chr17 | 38865058 | 38926770 |
| a0001c0002t0004 | 0/0 | 3925 | 4 | 1 | 2 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0002t0005 | 0/0 | 3925 | 2 | 0 | 0 | 2 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0002t0006 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0002t0010 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0002t0012 | 0/0 | 3910 | 2 | 0 | 0 | 2 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3905): Show |
chr17 | 38865058 | 38926770 |
| a0001c0002t0015 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0002t0017 | 0/0 | 3925 | 2 | 2 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0002t0029 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0003t0001 | 0/0 | 3925 | 33 | 1 | 14 | 10 | 2 | 6 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0003t0002 | 0/0 | 3925 | 7 | 3 | 0 | 1 | 0 | 3 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0003t0003 | 0/0 | 3910 | 2 | 0 | 0 | 2 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3905): Show |
chr17 | 38865058 | 38926770 |
| a0001c0003t0004 | 0/0 | 3925 | 13 | 10 | 1 | 0 | 2 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0003t0005 | 0/0 | 3925 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0003t0006 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0003t0026 | 0/0 | 3925 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0004t0001 | 0/0 | 3925 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0004t0002 | 0/0 | 3925 | 14 | 0 | 0 | 14 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0004t0020 | 0/0 | 3925 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0004t0022 | 0/0 | 3925 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0005t0001 | 0/0 | 3925 | 2 | 0 | 1 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0005t0002 | 0/0 | 3925 | 7 | 0 | 3 | 1 | 1 | 2 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0005t0003 | 0/1 | 3910 | 8 | 0 | 2 | 0 | 0 | 5 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3905): Show |
chr17 | 38865058 | 38926770 |
| a0001c0006t0001 | 0/0 | 3925 | 2 | 0 | 0 | 2 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0006t0002 | 0/0 | 3925 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0006t0003 | 0/0 | 3910 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3905): Show |
chr17 | 38865058 | 38926770 |
| a0001c0006t0005 | 0/0 | 3925 | 6 | 0 | 0 | 5 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0006t0018 | 0/0 | 3925 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0006t0019 | 0/0 | 3910 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3905): Show |
chr17 | 38865058 | 38926770 |
| a0001c0007t0002 | 0/0 | 3925 | 12 | 11 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0008t0002 | 0/0 | 3925 | 12 | 1 | 7 | 0 | 3 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0009t0001 | 0/0 | 3925 | 3 | 0 | 0 | 3 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0009t0002 | 0/0 | 3925 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0010t0013 | 0/0 | 3925 | 2 | 0 | 0 | 2 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0011t0002 | 0/0 | 3925 | 2 | 0 | 0 | 1 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0012t0002 | 0/0 | 3925 | 2 | 0 | 2 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0001c0013t0016 | 0/0 | 3925 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0002c0015t0001 | 0/0 | 3925 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| a0003c0014t0002 | 0/0 | 3925 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | GCCAG others(3920): Show |
chr17 | 38865058 | 38926770 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0002g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0003g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0004g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0006g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0007g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0009g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0011g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0011g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0014g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0014g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0015g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0016g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0021g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0023g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0024g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0025g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0027g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0028g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0030g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0031g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0001t0032g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0002g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0317 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0003g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0010g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0012g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0012g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0015g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0017g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0017g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0002t0029g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0003t0026g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0002g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0020g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0004t0022g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0003g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0003g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0005t0003g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0006t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0006t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0006t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0006t0003g0389 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0006t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0006t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0006t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0006t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0006t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0006t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0006t0018g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0006t0019g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0007t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0007t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0007t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0007t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0007t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0007t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0007t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0007t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0007t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0007t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0007t0002g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0007t0002g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0008t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0008t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0008t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0008t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0008t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0008t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0008t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0008t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0008t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0008t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0008t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0008t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0009t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0009t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0009t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0009t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0010t0013g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0010t0013g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0011t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0011t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0012t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0012t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0001c0013t0016g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0002c0015t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| a0003c0014t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0004 | g0121 | EUR | GBR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0007 | EUR | GBR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0279 | EUR | GBR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00140 | hp2 | a0001 | c0003 | t0004 | g0120 | EUR | GBR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00280 | hp1 | a0001 | c0011 | t0002 | g0298 | EUR | FIN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00280 | hp2 | a0001 | c0008 | t0002 | g0053 | EUR | FIN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0182 | EUR | FIN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00323 | hp2 | a0001 | c0005 | t0002 | g0101 | EUR | FIN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00408 | hp1 | a0001 | c0004 | t0002 | g0171 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0291 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0191 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0227 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00544 | hp2 | a0001 | c0002 | t0003 | g0169 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00558 | hp1 | a0002 | c0015 | t0001 | g0386 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00558 | hp2 | a0001 | c0004 | t0020 | g0042 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00621 | hp1 | a0001 | c0003 | t0005 | g0215 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00639 | hp1 | a0001 | c0005 | t0001 | g0068 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0179 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00642 | hp2 | a0001 | c0008 | t0002 | g0176 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00673 | hp2 | a0001 | c0010 | t0013 | g0163 | EAS | CHS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00733 | hp1 | a0001 | c0002 | t0004 | g0259 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0278 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0356 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00735 | hp2 | a0001 | c0003 | t0004 | g0111 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0363 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00741 | hp1 | a0001 | c0005 | t0002 | g0114 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0305 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01070 | hp1 | a0001 | c0008 | t0002 | g0069 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0098 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01071 | hp1 | a0001 | c0008 | t0002 | g0070 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01071 | hp2 | a0003 | c0014 | t0002 | g0260 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01074 | hp1 | a0001 | c0008 | t0002 | g0052 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0071 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01081 | hp1 | a0001 | c0007 | t0002 | g0141 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01081 | hp2 | a0001 | c0008 | t0002 | g0051 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01099 | hp2 | a0001 | c0012 | t0002 | g0102 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0160 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01109 | hp2 | a0001 | c0001 | t0027 | g0095 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0282 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0381 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0283 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01169 | hp2 | a0001 | c0003 | t0026 | g0119 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0276 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01175 | hp2 | a0001 | c0008 | t0002 | g0137 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01192 | hp1 | a0001 | c0012 | t0002 | g0103 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01192 | hp2 | a0001 | c0002 | t0004 | g0123 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0032 | AMR | PUR | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0159 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0248 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01256 | hp1 | a0001 | c0005 | t0003 | g0097 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0067 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0112 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0357 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0235 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0367 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01358 | hp2 | a0001 | c0005 | t0003 | g0274 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0026 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01433 | hp1 | a0001 | c0005 | t0002 | g0143 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01515 | hp1 | a0001 | c0001 | t0010 | g0100 | EUR | IBS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01515 | hp2 | a0001 | c0008 | t0002 | g0049 | EUR | IBS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01517 | hp1 | a0001 | c0008 | t0002 | g0054 | EUR | IBS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0108 | EUR | IBS | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01928 | hp1 | a0001 | c0004 | t0022 | g0153 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0350 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0369 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0109 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0157 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0154 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0361 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0144 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0362 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0136 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02015 | hp2 | a0001 | c0006 | t0005 | g0089 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02055 | hp1 | a0001 | c0007 | t0002 | g0140 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0379 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02129 | hp1 | a0001 | c0004 | t0002 | g0351 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02129 | hp2 | a0001 | c0006 | t0005 | g0231 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02132 | hp1 | a0001 | c0011 | t0002 | g0129 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02135 | hp1 | a0001 | c0004 | t0002 | g0221 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02135 | hp2 | a0001 | c0010 | t0013 | g0164 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0110 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02148 | hp1 | a0001 | c0008 | t0002 | g0048 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02148 | hp2 | a0001 | c0005 | t0002 | g0116 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02155 | hp1 | a0001 | c0001 | t0023 | g0217 | EAS | CDX | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02155 | hp2 | a0001 | c0006 | t0019 | g0211 | EAS | CDX | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02165 | hp2 | a0001 | c0006 | t0001 | g0210 | EAS | CDX | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02257 | hp2 | a0001 | c0001 | t0014 | g0074 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02258 | hp2 | a0001 | c0003 | t0004 | g0337 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0340 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02280 | hp1 | a0001 | c0007 | t0002 | g0039 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0175 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02451 | hp1 | a0001 | c0003 | t0004 | g0338 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0263 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02523 | hp2 | a0001 | c0004 | t0002 | g0370 | EAS | KHV | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0368 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02602 | hp2 | a0001 | c0006 | t0005 | g0029 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02615 | hp1 | a0001 | c0003 | t0004 | g0047 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02615 | hp2 | a0001 | c0003 | t0004 | g0334 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0382 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0371 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02647 | hp2 | a0001 | c0001 | t0030 | g0020 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02698 | hp1 | a0001 | c0005 | t0003 | g0346 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0188 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02717 | hp2 | a0001 | c0007 | t0002 | g0087 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02723 | hp1 | a0001 | c0003 | t0004 | g0266 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02723 | hp2 | a0001 | c0003 | t0004 | g0077 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02735 | hp1 | a0001 | c0002 | t0004 | g0168 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0288 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0241 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02738 | hp2 | a0001 | c0006 | t0003 | g0389 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02809 | hp1 | a0001 | c0001 | t0031 | g0331 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02809 | hp2 | a0001 | c0008 | t0002 | g0255 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02818 | hp1 | a0001 | c0001 | t0028 | g0178 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02886 | hp2 | a0001 | c0002 | t0010 | g0080 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0325 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02922 | hp1 | a0001 | c0001 | t0014 | g0269 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02922 | hp2 | a0001 | c0002 | t0006 | g0016 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0323 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02965 | hp2 | a0001 | c0003 | t0004 | g0088 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02970 | hp1 | a0001 | c0001 | t0021 | g0184 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0327 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02976 | hp1 | a0001 | c0002 | t0017 | g0086 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02976 | hp2 | a0001 | c0003 | t0002 | g0076 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0107 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0004 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03041 | hp1 | a0001 | c0001 | t0009 | g0099 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03041 | hp2 | a0001 | c0002 | t0029 | g0324 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0383 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03098 | hp2 | a0001 | c0001 | t0015 | g0265 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03130 | hp2 | a0001 | c0003 | t0006 | g0019 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03139 | hp1 | a0001 | c0007 | t0002 | g0378 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0374 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0275 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03195 | hp2 | a0001 | c0002 | t0017 | g0332 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03209 | hp1 | a0001 | c0007 | t0002 | g0268 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0328 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03225 | hp1 | a0001 | c0001 | t0025 | g0012 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03225 | hp2 | a0001 | c0003 | t0004 | g0090 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03486 | hp1 | a0001 | c0013 | t0016 | g0094 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0286 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03492 | hp1 | a0001 | c0003 | t0002 | g0277 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0314 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03516 | hp1 | a0001 | c0007 | t0002 | g0172 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03516 | hp2 | a0001 | c0007 | t0002 | g0185 | AFR | ESN | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03540 | hp1 | a0001 | c0007 | t0002 | g0186 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03540 | hp2 | a0001 | c0001 | t0032 | g0330 | AFR | GWD | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0075 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03579 | hp2 | a0001 | c0007 | t0002 | g0270 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0390 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03669 | hp1 | a0001 | c0006 | t0002 | g0347 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03688 | hp1 | a0001 | c0005 | t0001 | g0147 | SAS | STU | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03688 | hp2 | a0001 | c0005 | t0002 | g0145 | SAS | STU | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0148 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03710 | hp2 | a0001 | c0005 | t0003 | g0273 | SAS | PJL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03831 | hp1 | a0001 | c0005 | t0003 | g0380 | SAS | BEB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03831 | hp2 | a0001 | c0008 | t0002 | g0146 | SAS | BEB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0139 | SAS | BEB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0354 | SAS | BEB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0240 | SAS | BEB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03927 | hp2 | a0001 | c0005 | t0003 | g0385 | SAS | BEB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0293 | SAS | BEB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0247 | SAS | BEB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | STU | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0093 | SAS | BEB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG04184 | hp2 | a0001 | c0005 | t0002 | g0113 | SAS | BEB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG04199 | hp1 | a0001 | c0004 | t0001 | g0359 | SAS | STU | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0387 | SAS | STU | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0365 | SAS | STU | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0170 | SAS | STU | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0349 | SAS | STU | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0034 | SAS | STU | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | YRI | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18522 | hp2 | a0001 | c0003 | t0004 | g0082 | AFR | YRI | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | CHB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18747 | hp1 | a0001 | c0006 | t0005 | g0207 | EAS | CHB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18747 | hp2 | a0001 | c0009 | t0001 | g0024 | EAS | CHB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | YRI | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18940 | hp1 | a0001 | c0003 | t0001 | g0205 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18941 | hp1 | a0001 | c0004 | t0002 | g0218 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18941 | hp2 | a0001 | c0002 | t0003 | g0285 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18942 | hp2 | a0001 | c0004 | t0002 | g0131 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0316 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18946 | hp1 | a0001 | c0002 | t0003 | g0303 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18946 | hp2 | a0001 | c0003 | t0001 | g0250 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18947 | hp1 | a0001 | c0002 | t0003 | g0313 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18947 | hp2 | a0001 | c0002 | t0003 | g0228 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18950 | hp1 | a0001 | c0001 | t0011 | g0043 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0375 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0209 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0358 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0251 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18953 | hp2 | a0001 | c0004 | t0002 | g0128 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18961 | hp1 | a0001 | c0002 | t0003 | g0212 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0307 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18966 | hp1 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18967 | hp1 | a0001 | c0005 | t0002 | g0364 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18967 | hp2 | a0001 | c0002 | t0003 | g0252 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18969 | hp1 | a0001 | c0002 | t0005 | g0194 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0301 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18971 | hp2 | a0001 | c0002 | t0003 | g0133 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18973 | hp2 | a0001 | c0002 | t0003 | g0059 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18974 | hp1 | a0001 | c0002 | t0003 | g0060 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18974 | hp2 | a0001 | c0006 | t0005 | g0165 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18975 | hp2 | a0001 | c0002 | t0003 | g0063 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18981 | hp2 | a0001 | c0004 | t0002 | g0377 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0058 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18984 | hp2 | a0001 | c0002 | t0003 | g0238 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0360 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18988 | hp2 | a0001 | c0009 | t0001 | g0023 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18991 | hp1 | a0001 | c0002 | t0003 | g0061 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18992 | hp2 | a0001 | c0003 | t0001 | g0203 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0343 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18999 | hp1 | a0001 | c0003 | t0003 | g0199 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0056 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19002 | hp1 | a0001 | c0009 | t0002 | g0025 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0134 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19003 | hp1 | a0001 | c0006 | t0018 | g0249 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0292 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0388 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0135 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0272 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19010 | hp2 | a0001 | c0002 | t0012 | g0045 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19011 | hp1 | a0001 | c0006 | t0001 | g0229 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19011 | hp2 | a0001 | c0006 | t0005 | g0096 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0384 | AFR | LWK | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0177 | AFR | LWK | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0329 | AFR | LWK | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0035 | AFR | LWK | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19054 | hp1 | a0001 | c0002 | t0003 | g0208 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19056 | hp1 | a0001 | c0002 | t0012 | g0062 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19056 | hp2 | a0001 | c0004 | t0002 | g0254 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19057 | hp2 | a0001 | c0009 | t0001 | g0022 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0192 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19064 | hp1 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19064 | hp2 | a0001 | c0004 | t0002 | g0355 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19065 | hp1 | a0001 | c0001 | t0011 | g0065 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19065 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0297 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0348 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19074 | hp1 | a0001 | c0002 | t0005 | g0198 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19074 | hp2 | a0001 | c0004 | t0002 | g0376 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19079 | hp1 | a0001 | c0004 | t0002 | g0213 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19080 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19083 | hp2 | a0001 | c0004 | t0002 | g0344 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0345 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19086 | hp2 | a0001 | c0003 | t0003 | g0057 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19088 | hp1 | a0001 | c0004 | t0002 | g0158 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19090 | hp1 | a0001 | c0003 | t0002 | g0200 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0315 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0290 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | YRI | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0271 | AFR | YRI | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0122 | AFR | ASW | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ASW | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA20752 | hp1 | a0001 | c0002 | t0003 | g0310 | EUR | TSI | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0036 | EUR | TSI | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA20805 | hp1 | a0001 | c0002 | t0003 | g0239 | EUR | TSI | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0009 | EUR | TSI | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA20905 | hp1 | a0001 | c0005 | t0003 | g0041 | SAS | GIH | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | GIH | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0294 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0280 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02486 | hp1 | a0001 | c0002 | t0015 | g0339 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02486 | hp2 | a0001 | c0003 | t0004 | g0336 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0014 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG03471 | hp2 | a0001 | c0007 | t0002 | g0046 | AFR | MSL | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | USA | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| HG06807 | hp2 | a0001 | c0001 | t0016 | g0262 | AFR | USA | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA20300 | hp1 | a0001 | c0007 | t0002 | g0373 | AFR | USA | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | USA | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0372 | AFR | LWK | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| NA21309 | hp2 | a0001 | c0001 | t0024 | g0055 | AFR | LWK | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| homoSapiens | chm13v2 | a0001 | c0005 | t0003 | g0222 | REF | REF | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0317 | REF | REF | LASP1_chr17_38865058_38926770 | LASP1 | chr17 | 38865058 | 38926770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38914356 | G | A | 1 | a0003 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.389G>A | p.Arg130His | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/7 | 521/3910 | 389/786 | 130/261 | chr17 | 38914356 | |||
| chr17:38914473 | C | T | 1 | a0002 | 1 | HG00558.hp1 | missense_variant&splice_region_variant | MODERATE | c.506C>T | p.Pro169Leu | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/7 | 638/3910 | 506/786 | 169/261 | chr17 | 38914473 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38878112 | C | T | 1 | a0001c0009 | 4 | NA18747.hp2 NA18988.hp2 NA19002.hp1 others(1): Show |
synonymous_variant | LOW | c.96C>T | p.Cys32Cys | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/7 | 228/3910 | 96/786 | 32/261 | chr17 | 38878112 | |||
| chr17:38898519 | C | T | 6 | a0001c0003 a0001c0005 a0001c0008 others(3): Show |
90 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
splice_region_variant&synonymous_variant | LOW | c.357C>T | p.Asn119Asn | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/7 | 489/3910 | 357/786 | 119/261 | chr17 | 38898519 | |||
| chr17:38914393 | G | A | 2 | a0001c0006 a0001c0010 |
14 | HG00673.hp2 HG02015.hp2 HG02129.hp2 others(11): Show |
synonymous_variant | LOW | c.426G>A | p.Glu142Glu | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/7 | 558/3910 | 426/786 | 142/261 | chr17 | 38914393 | |||
| chr17:38914405 | A | G | 8 | a0001c0001 a0001c0003 a0001c0004 others(5): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
synonymous_variant | LOW | c.438A>G | p.Ser146Ser | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/7 | 570/3910 | 438/786 | 146/261 | chr17 | 38914405 | |||
| chr17:38915071 | G | A | 1 | a0001c0007 | 12 | HG01081.hp1 HG02055.hp1 HG02280.hp1 others(9): Show |
synonymous_variant | LOW | c.537G>A | p.Val179Val | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/7 | 669/3910 | 537/786 | 179/261 | chr17 | 38915071 | |||
| chr17:38918616 | C | T | 1 | a0001c0013 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.624C>T | p.Arg208Arg | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 756/3910 | 624/786 | 208/261 | chr17 | 38918616 | |||
| chr17:38918679 | C | T | 5 | a0001c0004 a0001c0008 a0001c0010 others(2): Show |
35 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(32): Show |
synonymous_variant | LOW | c.687C>T | p.Ile229Ile | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 819/3910 | 687/786 | 229/261 | chr17 | 38918679 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38870091 | G | T | 3 | a0001c0001t0007 a0001c0001t0031 a0001c0001t0032 |
6 | HG02809.hp1 HG02970.hp2 HG03195.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-99G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/7 | 99 | chr17 | 38870091 | ||||||
| chr17:38918888 | G | A | 2 | a0001c0001t0010 a0001c0002t0010 |
2 | HG01515.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*110G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 110 | chr17 | 38918888 | ||||||
| chr17:38919031 | G | GAAGGGCG others(8): Show |
4 | a0001c0002t0005 a0001c0003t0005 a0001c0006t0005 others(1): Show |
10 | HG00621.hp1 HG02015.hp2 HG02129.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*253_*254insAAGGGC others(9): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 254 | chr17 | 38919031 | ||||||
| chr17:38919033 | A | AGGGCGAG others(8): Show |
51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(48): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*257_*258insGCGAGG others(9): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 258 | INFO_REALIGN_3_PRIME | chr17 | 38919033 | |||||
| chr17:38919033 | A | G | 4 | a0001c0002t0005 a0001c0003t0005 a0001c0006t0005 others(1): Show |
10 | HG00621.hp1 HG02015.hp2 HG02129.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*255A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 255 | chr17 | 38919033 | ||||||
| chr17:38919098 | C | T | 1 | a0001c0002t0017 | 2 | HG02976.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*320C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 320 | chr17 | 38919098 | ||||||
| chr17:38919253 | G | A | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(48): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*475G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 475 | chr17 | 38919253 | ||||||
| chr17:38919417 | T | G | 1 | a0001c0001t0027 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*639T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 639 | chr17 | 38919417 | ||||||
| chr17:38919429 | C | T | 1 | a0001c0003t0026 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*651C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 651 | chr17 | 38919429 | ||||||
| chr17:38919450 | A | G | 2 | a0001c0001t0016 a0001c0013t0016 |
2 | HG03486.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*672A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 672 | chr17 | 38919450 | ||||||
| chr17:38919505 | G | A | 18 | a0001c0001t0002 a0001c0001t0021 a0001c0001t0031 others(15): Show |
116 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*727G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 727 | chr17 | 38919505 | ||||||
| chr17:38919570 | C | A | 1 | a0001c0001t0023 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*792C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 792 | chr17 | 38919570 | ||||||
| chr17:38919625 | G | A | 1 | a0001c0004t0020 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*847G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 847 | chr17 | 38919625 | ||||||
| chr17:38919653 | G | C | 3 | a0001c0001t0006 a0001c0002t0006 a0001c0003t0006 |
7 | HG02280.hp2 HG02630.hp2 HG02922.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*875G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 875 | chr17 | 38919653 | ||||||
| chr17:38919681 | T | C | 1 | a0001c0001t0021 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*903T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 903 | chr17 | 38919681 | ||||||
| chr17:38919752 | C | T | 1 | a0001c0004t0022 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*974C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 974 | chr17 | 38919752 | ||||||
| chr17:38919774 | T | G | 1 | a0001c0001t0008 | 3 | HG01243.hp2 HG02451.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*996T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 996 | chr17 | 38919774 | ||||||
| chr17:38920078 | G | A | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0008 others(39): Show |
255 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*1300G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 1300 | chr17 | 38920078 | ||||||
| chr17:38920093 | A | G | 1 | a0001c0002t0012 | 2 | NA19010.hp2 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1315A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 1315 | chr17 | 38920093 | ||||||
| chr17:38920115 | G | A | 1 | a0001c0010t0013 | 2 | HG00673.hp2 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1337G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 1337 | chr17 | 38920115 | ||||||
| chr17:38920181 | C | T | 4 | a0001c0002t0005 a0001c0003t0005 a0001c0006t0005 others(1): Show |
10 | HG00621.hp1 HG02015.hp2 HG02129.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1403C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 1403 | chr17 | 38920181 | ||||||
| chr17:38920409 | A | G | 1 | a0001c0001t0024 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1631A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 1631 | chr17 | 38920409 | ||||||
| chr17:38920418 | T | A | 1 | a0001c0001t0014 | 2 | HG02257.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1640T>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 1640 | chr17 | 38920418 | ||||||
| chr17:38920770 | A | C | 1 | a0001c0001t0011 | 2 | NA18950.hp1 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1992A>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 1992 | chr17 | 38920770 | ||||||
| chr17:38920902 | C | T | 3 | a0001c0001t0006 a0001c0002t0006 a0001c0003t0006 |
7 | HG02280.hp2 HG02630.hp2 HG02922.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2124C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 2124 | chr17 | 38920902 | ||||||
| chr17:38920913 | T | A | 2 | a0001c0001t0027 a0001c0001t0028 |
2 | HG01109.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2135T>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 2135 | chr17 | 38920913 | ||||||
| chr17:38921008 | C | T | 2 | a0001c0001t0015 a0001c0002t0015 |
2 | HG02486.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2230C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 2230 | chr17 | 38921008 | ||||||
| chr17:38921081 | C | T | 1 | a0001c0001t0025 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2303C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 2303 | chr17 | 38921081 | ||||||
| chr17:38921119 | C | T | 1 | a0001c0006t0019 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2341C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 2341 | chr17 | 38921119 | ||||||
| chr17:38921384 | T | C | 1 | a0001c0001t0009 | 3 | HG02145.hp2 HG02965.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2606T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 2606 | chr17 | 38921384 | ||||||
| chr17:38921494 | C | G | 1 | a0001c0001t0030 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2716C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 2716 | chr17 | 38921494 | ||||||
| chr17:38921574 | G | A | 1 | a0001c0001t0025 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2796G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 2796 | chr17 | 38921574 | ||||||
| chr17:38921582 | G | A | 1 | a0001c0006t0018 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2804G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 2804 | chr17 | 38921582 | ||||||
| chr17:38921693 | A | G | 4 | a0001c0002t0005 a0001c0003t0005 a0001c0006t0005 others(1): Show |
10 | HG00621.hp1 HG02015.hp2 HG02129.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2915A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 7/7 | 2915 | chr17 | 38921693 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:38870542 | G | C | 255 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(252): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.69+284G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38870542 | |||||||
| chr17:38870625 | C | T | 2 | a0001c0001t0001g0256 a0001c0008t0002g0255 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.69+367C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38870625 | |||||||
| chr17:38870678 | C | CG | 15 | a0001c0001t0001g0390 a0001c0001t0002g0253 a0001c0001t0003g0246 others(12): Show |
15 | HG00558.hp1 HG01255.hp2 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.69+427dupG | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38870678 | ||||||
| chr17:38870721 | G | A | 1 | a0001c0002t0003g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.69+463G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38870721 | |||||||
| chr17:38871093 | A | G | 5 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(2): Show |
5 | HG00609.hp2 HG02027.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+835A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38871093 | |||||||
| chr17:38871150 | G | T | 61 | a0001c0001t0001g0201 a0001c0001t0001g0216 a0001c0001t0001g0219 others(58): Show |
61 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.69+892G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38871150 | |||||||
| chr17:38871731 | C | T | 61 | a0001c0001t0001g0201 a0001c0001t0001g0216 a0001c0001t0001g0219 others(58): Show |
61 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.69+1473C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38871731 | |||||||
| chr17:38871867 | C | T | 3 | a0001c0001t0002g0384 a0001c0001t0004g0382 a0001c0001t0004g0383 |
3 | HG02622.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.69+1609C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38871867 | |||||||
| chr17:38872148 | G | C | 3 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0009 |
3 | HG00099.hp2 HG01123.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.69+1890G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38872148 | |||||||
| chr17:38872551 | G | C | 1 | a0001c0001t0002g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69+2293G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38872551 | |||||||
| chr17:38872577 | G | A | 11 | a0001c0001t0001g0011 a0001c0001t0002g0013 a0001c0001t0004g0017 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+2319G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38872577 | |||||||
| chr17:38872592 | G | A | 4 | a0001c0009t0001g0022 a0001c0009t0001g0023 a0001c0009t0001g0024 others(1): Show |
4 | NA18747.hp2 NA18988.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+2334G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38872592 | |||||||
| chr17:38872620 | G | A | 1 | a0001c0002t0003g0026 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.69+2362G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38872620 | |||||||
| chr17:38872697 | C | T | 3 | a0001c0001t0001g0189 a0001c0001t0002g0190 a0001c0001t0004g0188 |
3 | HG02717.hp1 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.69+2439C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38872697 | |||||||
| chr17:38872755 | C | T | 1 | a0001c0002t0001g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.69+2497C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38872755 | |||||||
| chr17:38872816 | C | T | 160 | a0001c0001t0001g0092 a0001c0001t0001g0106 a0001c0001t0001g0127 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.69+2558C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38872816 | |||||||
| chr17:38873128 | G | T | 30 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0002g0013 others(27): Show |
30 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(27): Show |
intron_variant | MODIFIER | c.69+2870G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38873128 | |||||||
| chr17:38873424 | T | C | 326 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(323): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.69+3166T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38873424 | |||||||
| chr17:38873485 | A | G | 1 | a0001c0003t0004g0088 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.69+3227A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38873485 | |||||||
| chr17:38873500 | G | C | 1 | a0001c0006t0005g0089 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.69+3242G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38873500 | |||||||
| chr17:38873719 | A | G | 2 | a0001c0001t0002g0253 a0001c0002t0003g0235 |
2 | HG01346.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.69+3461A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38873719 | |||||||
| chr17:38873722 | G | A | 1 | a0001c0003t0004g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.69+3464G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38873722 | |||||||
| chr17:38873760 | C | G | 83 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0078 others(80): Show |
85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.69+3502C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38873760 | |||||||
| chr17:38873942 | A | G | 77 | a0001c0001t0001g0201 a0001c0001t0001g0216 a0001c0001t0001g0219 others(74): Show |
77 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.69+3684A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38873942 | |||||||
| chr17:38873966 | C | G | 21 | a0001c0001t0001g0073 a0001c0001t0001g0326 a0001c0001t0001g0333 others(18): Show |
21 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.69+3708C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38873966 | |||||||
| chr17:38873989 | G | C | 1 | a0001c0002t0001g0340 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.69+3731G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38873989 | |||||||
| chr17:38874005 | GCCTGTTT others(1): Show |
G | 72 | a0001c0001t0001g0011 a0001c0001t0001g0201 a0001c0001t0001g0216 others(69): Show |
72 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.69+3751_69+3758del others(8): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38874005 | ||||||
| chr17:38874132 | C | T | 1 | a0001c0004t0020g0042 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.69+3874C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874132 | |||||||
| chr17:38874154 | C | T | 6 | a0001c0001t0002g0072 a0001c0001t0002g0183 a0001c0002t0003g0003 others(3): Show |
7 | HG00323.hp1 HG00642.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+3896C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874154 | |||||||
| chr17:38874267 | G | A | 1 | a0001c0002t0003g0191 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.70-3819G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874267 | |||||||
| chr17:38874390 | A | G | 341 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(338): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.70-3696A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874390 | |||||||
| chr17:38874413 | G | A | 1 | a0001c0002t0001g0091 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.70-3673G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874413 | |||||||
| chr17:38874417 | G | T | 1 | a0001c0002t0002g0234 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.70-3669G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874417 | |||||||
| chr17:38874435 | AG | A | 4 | a0001c0001t0001g0078 a0001c0003t0002g0075 a0001c0003t0002g0076 others(1): Show |
4 | HG02559.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-3648delG | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38874435 | ||||||
| chr17:38874458 | C | T | 1 | a0001c0001t0015g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.70-3628C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874458 | |||||||
| chr17:38874506 | G | C | 1 | a0001c0002t0003g0343 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.70-3580G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874506 | |||||||
| chr17:38874518 | T | C | 75 | a0001c0001t0001g0050 a0001c0001t0001g0078 a0001c0001t0001g0189 others(72): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.70-3568T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874518 | |||||||
| chr17:38874673 | C | T | 72 | a0001c0001t0001g0011 a0001c0001t0001g0201 a0001c0001t0001g0216 others(69): Show |
72 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.70-3413C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874673 | |||||||
| chr17:38874692 | T | G | 1 | a0001c0001t0001g0092 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.70-3394T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874692 | |||||||
| chr17:38874841 | G | A | 40 | a0001c0001t0001g0349 a0001c0001t0001g0352 a0001c0001t0001g0366 others(37): Show |
40 | HG00408.hp2 HG00609.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.70-3245G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874841 | |||||||
| chr17:38874913 | C | T | 14 | a0001c0001t0001g0326 a0001c0001t0001g0333 a0001c0001t0001g0335 others(11): Show |
14 | HG01884.hp1 HG02055.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-3173C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874913 | |||||||
| chr17:38874999 | A | G | 2 | a0001c0008t0002g0069 a0001c0008t0002g0070 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.70-3087A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38874999 | |||||||
| chr17:38875002 | T | A | 1 | a0001c0001t0004g0267 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.70-3084T>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38875002 | |||||||
| chr17:38875056 | C | CGT | 5 | a0001c0001t0002g0072 a0001c0001t0004g0009 a0001c0001t0006g0175 others(2): Show |
5 | HG00642.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-2998_70-2997dup others(2): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875056 | ||||||
| chr17:38875056 | C | CGTGT | 5 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0322 others(2): Show |
5 | HG00673.hp1 HG01433.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-3000_70-2997dup others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875056 | ||||||
| chr17:38875056 | C | CGTGTGT | 16 | a0001c0001t0001g0326 a0001c0001t0001g0333 a0001c0001t0001g0335 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.70-3002_70-2997dup others(6): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875056 | ||||||
| chr17:38875056 | C | CGTGTGTG others(5): Show |
1 | a0001c0002t0002g0193 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.70-3008_70-2997dup others(12): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875056 | ||||||
| chr17:38875056 | C | CGTGTGTG others(7): Show |
8 | a0001c0001t0001g0011 a0001c0001t0002g0013 a0001c0001t0004g0017 others(5): Show |
8 | HG01891.hp1 HG02080.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-3010_70-2997dup others(14): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875056 | ||||||
| chr17:38875056 | C | CGTGTGTG others(9): Show |
12 | a0001c0001t0001g0242 a0001c0001t0008g0021 a0001c0001t0030g0020 others(9): Show |
12 | HG02630.hp1 HG02647.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.70-3012_70-2997dup others(16): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875056 | ||||||
| chr17:38875056 | C | CGTGTGTG others(11): Show |
37 | a0001c0001t0001g0201 a0001c0001t0001g0216 a0001c0001t0001g0219 others(34): Show |
37 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.70-3014_70-2997dup others(18): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875056 | ||||||
| chr17:38875056 | C | CGTGTGTG others(13): Show |
14 | a0001c0001t0001g0224 a0001c0001t0001g0226 a0001c0001t0002g0253 others(11): Show |
14 | HG00438.hp2 HG00544.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-3016_70-2997dup others(20): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875056 | ||||||
| chr17:38875056 | C | CGTGTGTG others(15): Show |
7 | a0001c0001t0014g0269 a0001c0002t0002g0232 a0001c0002t0002g0233 others(4): Show |
7 | HG00438.hp1 HG02129.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-3018_70-2997dup others(22): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875056 | ||||||
| chr17:38875056 | C | CGTGTGTG others(17): Show |
1 | a0001c0001t0006g0271 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.70-3020_70-2997dup others(24): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875056 | ||||||
| chr17:38875056 | CGT | C | 151 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0092 others(148): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.70-2998_70-2997del others(2): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875056 | ||||||
| chr17:38875059 | G | C | 1 | a0001c0002t0003g0285 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.70-3027G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38875059 | |||||||
| chr17:38875069 | G | GTGTGTGT others(21): Show |
1 | a0001c0001t0008g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.70-2997_70-2996ins others(28): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875069 | ||||||
| chr17:38875071 | G | GTGTGTGT others(13): Show |
31 | a0001c0001t0001g0349 a0001c0001t0001g0352 a0001c0001t0001g0366 others(28): Show |
31 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.70-2997_70-2996ins others(20): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875071 | ||||||
| chr17:38875071 | G | GTGTGTGT others(15): Show |
7 | a0001c0001t0001g0390 a0001c0001t0003g0030 a0001c0001t0003g0031 others(4): Show |
7 | HG00733.hp1 HG01884.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-2997_70-2996ins others(22): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875071 | ||||||
| chr17:38875071 | G | GTGTGTGT others(25): Show |
2 | a0001c0001t0027g0095 a0001c0001t0028g0178 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.70-2997_70-2996ins others(32): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875071 | ||||||
| chr17:38875073 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0004g0267 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.70-3002_70-3001ins others(12): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875073 | ||||||
| chr17:38875086 | TGTGA | T | 12 | a0001c0001t0002g0079 a0001c0001t0002g0081 a0001c0001t0002g0083 others(9): Show |
12 | HG02258.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.70-2998_70-2995del others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875086 | ||||||
| chr17:38875088 | TGA | T | 22 | a0001c0001t0001g0050 a0001c0001t0001g0189 a0001c0001t0002g0190 others(19): Show |
22 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-2995_70-2994del others(2): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875088 | ||||||
| chr17:38875090 | A | T | 182 | a0001c0001t0001g0011 a0001c0001t0001g0073 a0001c0001t0001g0078 others(179): Show |
184 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.70-2996A>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38875090 | |||||||
| chr17:38875156 | GAGGCAGG others(17): Show |
G | 1 | a0001c0001t0002g0013 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.70-2918_70-2895del others(24): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38875156 | ||||||
| chr17:38875269 | T | G | 4 | a0001c0009t0001g0022 a0001c0009t0001g0023 a0001c0009t0001g0024 others(1): Show |
4 | NA18747.hp2 NA18988.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-2817T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38875269 | |||||||
| chr17:38875270 | C | T | 4 | a0001c0009t0001g0022 a0001c0009t0001g0023 a0001c0009t0001g0024 others(1): Show |
4 | NA18747.hp2 NA18988.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-2816C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38875270 | |||||||
| chr17:38875350 | G | A | 1 | a0001c0006t0005g0096 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.70-2736G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38875350 | |||||||
| chr17:38875428 | T | C | 3 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0013t0016g0094 |
3 | HG01884.hp2 HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.70-2658T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38875428 | |||||||
| chr17:38875586 | C | T | 1 | a0001c0003t0004g0266 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.70-2500C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38875586 | |||||||
| chr17:38875632 | C | T | 1 | a0001c0002t0002g0368 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.70-2454C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38875632 | |||||||
| chr17:38876048 | A | G | 314 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(311): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.70-2038A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38876048 | |||||||
| chr17:38876176 | C | CT | 54 | a0001c0001t0001g0073 a0001c0001t0001g0092 a0001c0001t0001g0326 others(51): Show |
54 | HG00408.hp2 HG00609.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.70-1890dupT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38876176 | ||||||
| chr17:38876176 | C | CTT | 7 | a0001c0001t0002g0384 a0001c0001t0003g0031 a0001c0002t0002g0258 others(4): Show |
7 | HG02145.hp1 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-1891_70-1890dup others(2): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38876176 | ||||||
| chr17:38876176 | CT | C | 21 | a0001c0001t0001g0078 a0001c0001t0001g0287 a0001c0001t0003g0223 others(18): Show |
21 | HG00323.hp2 HG01070.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.70-1890delT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38876176 | ||||||
| chr17:38876343 | C | CTATT | 11 | a0001c0001t0001g0289 a0001c0001t0002g0079 a0001c0001t0003g0033 others(8): Show |
11 | HG01099.hp2 HG01109.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.70-1713_70-1710dup others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38876343 | ||||||
| chr17:38876343 | CTATT | C | 21 | a0001c0001t0001g0073 a0001c0001t0001g0326 a0001c0001t0001g0333 others(18): Show |
21 | HG00609.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.70-1713_70-1710del others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 38876343 | ||||||
| chr17:38876523 | G | A | 39 | a0001c0001t0001g0349 a0001c0001t0001g0352 a0001c0001t0001g0366 others(36): Show |
39 | HG00408.hp2 HG00609.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.70-1563G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38876523 | |||||||
| chr17:38876552 | C | T | 1 | a0001c0002t0003g0169 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.70-1534C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38876552 | |||||||
| chr17:38876652 | C | CGATTCAA others(5): Show |
1 | a0001c0004t0002g0344 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.70-1434_70-1433ins others(12): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38876652 | |||||||
| chr17:38876654 | G | C | 1 | a0001c0004t0002g0344 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.70-1432G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38876654 | |||||||
| chr17:38876852 | G | A | 4 | a0001c0009t0001g0022 a0001c0009t0001g0023 a0001c0009t0001g0024 others(1): Show |
4 | NA18747.hp2 NA18988.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-1234G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38876852 | |||||||
| chr17:38876969 | C | T | 4 | a0001c0009t0001g0022 a0001c0009t0001g0023 a0001c0009t0001g0024 others(1): Show |
4 | NA18747.hp2 NA18988.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-1117C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38876969 | |||||||
| chr17:38877108 | C | T | 1 | a0001c0002t0004g0168 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.70-978C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38877108 | |||||||
| chr17:38877215 | A | T | 1 | a0001c0004t0002g0344 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.70-871A>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38877215 | |||||||
| chr17:38877256 | C | T | 14 | a0001c0001t0001g0326 a0001c0001t0001g0333 a0001c0001t0001g0335 others(11): Show |
14 | HG01884.hp1 HG02055.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-830C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38877256 | |||||||
| chr17:38877350 | C | T | 1 | a0001c0001t0004g0267 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.70-736C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38877350 | |||||||
| chr17:38877400 | G | A | 1 | a0001c0001t0004g0267 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.70-686G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38877400 | |||||||
| chr17:38877407 | C | T | 72 | a0001c0001t0001g0011 a0001c0001t0001g0201 a0001c0001t0001g0216 others(69): Show |
72 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.70-679C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38877407 | |||||||
| chr17:38877417 | C | T | 72 | a0001c0001t0001g0011 a0001c0001t0001g0201 a0001c0001t0001g0216 others(69): Show |
72 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.70-669C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38877417 | |||||||
| chr17:38877743 | G | T | 256 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(253): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.70-343G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38877743 | |||||||
| chr17:38877744 | C | G | 1 | a0001c0003t0006g0019 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.70-342C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 1/6 | chr17 | 38877744 | |||||||
| chr17:38878228 | C | T | 4 | a0001c0001t0001g0078 a0001c0003t0002g0075 a0001c0003t0002g0076 others(1): Show |
4 | HG02559.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+48C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38878228 | |||||||
| chr17:38878261 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | NA18973.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.164+81C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38878261 | |||||||
| chr17:38878291 | CCCTACTT others(3): Show |
C | 1 | a0001c0002t0012g0045 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.164+113_164+122del others(10): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38878291 | ||||||
| chr17:38878565 | G | C | 290 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(287): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.164+385G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38878565 | |||||||
| chr17:38878631 | C | T | 2 | a0001c0001t0002g0010 a0001c0007t0002g0039 |
2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.164+451C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38878631 | |||||||
| chr17:38878790 | T | C | 7 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0008g0032 others(4): Show |
7 | HG00733.hp1 HG01109.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.164+610T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38878790 | |||||||
| chr17:38878963 | CTCCCA | C | 4 | a0001c0009t0001g0022 a0001c0009t0001g0023 a0001c0009t0001g0024 others(1): Show |
4 | NA18747.hp2 NA18988.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+805_164+809del others(5): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38878963 | ||||||
| chr17:38878964 | T | C | 1 | a0001c0001t0003g0223 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.164+784T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38878964 | |||||||
| chr17:38878965 | C | T | 1 | a0001c0001t0003g0223 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.164+785C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38878965 | |||||||
| chr17:38878968 | A | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0149 a0001c0005t0003g0041 |
3 | HG02683.hp1 NA20905.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.164+788A>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38878968 | |||||||
| chr17:38879059 | G | A | 84 | a0001c0001t0001g0011 a0001c0001t0001g0106 a0001c0001t0001g0201 others(81): Show |
84 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.164+879G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879059 | |||||||
| chr17:38879087 | C | T | 5 | a0001c0001t0001g0092 a0001c0001t0001g0162 a0001c0006t0005g0165 others(2): Show |
5 | HG00673.hp2 HG02056.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.164+907C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879087 | |||||||
| chr17:38879144 | C | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0005t0002g0101 |
3 | HG00323.hp2 HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.164+964C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879144 | |||||||
| chr17:38879161 | C | CT | 23 | a0001c0001t0001g0073 a0001c0001t0001g0326 a0001c0001t0001g0333 others(20): Show |
23 | HG00733.hp1 HG01109.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.164+997dupT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38879161 | ||||||
| chr17:38879161 | C | CTT | 78 | a0001c0001t0001g0011 a0001c0001t0001g0106 a0001c0001t0001g0201 others(75): Show |
78 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.164+996_164+997dup others(2): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38879161 | ||||||
| chr17:38879161 | C | CTTT | 8 | a0001c0001t0001g0244 a0001c0001t0001g0349 a0001c0001t0002g0013 others(5): Show |
8 | HG01891.hp1 HG02027.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.164+995_164+997dup others(3): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38879161 | ||||||
| chr17:38879161 | C | CTTTT | 187 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(184): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.164+994_164+997dup others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38879161 | ||||||
| chr17:38879161 | C | CTTTTT | 15 | a0001c0001t0001g0161 a0001c0001t0001g0173 a0001c0001t0001g0287 others(12): Show |
15 | HG00609.hp1 HG01106.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.164+993_164+997dup others(5): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38879161 | ||||||
| chr17:38879249 | G | A | 1 | a0001c0002t0002g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.164+1069G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879249 | |||||||
| chr17:38879250 | G | C | 1 | a0001c0002t0002g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.164+1070G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879250 | |||||||
| chr17:38879256 | A | G | 1 | a0001c0002t0002g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.164+1076A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879256 | |||||||
| chr17:38879258 | C | T | 1 | a0001c0002t0002g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.164+1078C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879258 | |||||||
| chr17:38879261 | TTCTTGTA others(41): Show |
T | 1 | a0001c0002t0002g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.164+1082_164+1129d others(50): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879261 | |||||||
| chr17:38879310 | C | G | 1 | a0001c0002t0002g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.164+1130C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879310 | |||||||
| chr17:38879311 | A | T | 1 | a0001c0002t0002g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.164+1131A>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879311 | |||||||
| chr17:38879446 | C | T | 1 | a0001c0001t0004g0267 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.164+1266C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879446 | |||||||
| chr17:38879564 | G | GT | 7 | a0001c0002t0002g0258 a0001c0002t0003g0315 a0001c0005t0002g0364 others(4): Show |
7 | NA18747.hp2 NA18940.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.164+1398dupT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38879564 | ||||||
| chr17:38879775 | C | G | 32 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0092 others(29): Show |
32 | HG00323.hp2 HG00544.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.164+1595C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879775 | |||||||
| chr17:38879795 | G | C | 1 | a0001c0002t0015g0339 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.164+1615G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879795 | |||||||
| chr17:38879816 | C | T | 5 | a0001c0001t0006g0271 a0001c0001t0014g0269 a0001c0007t0002g0268 others(2): Show |
5 | HG02922.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+1636C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879816 | |||||||
| chr17:38879923 | G | A | 38 | a0001c0001t0001g0349 a0001c0001t0001g0352 a0001c0001t0001g0366 others(35): Show |
38 | HG00408.hp2 HG00609.hp1 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.164+1743G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879923 | |||||||
| chr17:38879926 | A | G | 297 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(294): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.164+1746A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879926 | |||||||
| chr17:38879927 | A | G | 1 | a0001c0002t0002g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.164+1747A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38879927 | |||||||
| chr17:38880127 | A | G | 1 | a0001c0005t0001g0068 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.164+1947A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38880127 | |||||||
| chr17:38880235 | C | T | 361 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(358): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.164+2055C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38880235 | |||||||
| chr17:38880301 | G | A | 234 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(231): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.164+2121G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38880301 | |||||||
| chr17:38880318 | C | A | 1 | a0001c0006t0018g0249 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.164+2138C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38880318 | |||||||
| chr17:38880395 | G | C | 1 | a0001c0001t0001g0326 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.164+2215G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38880395 | |||||||
| chr17:38880667 | G | A | 2 | a0001c0012t0002g0102 a0001c0012t0002g0103 |
2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.164+2487G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38880667 | |||||||
| chr17:38880742 | G | T | 1 | a0001c0006t0018g0249 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.164+2562G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38880742 | |||||||
| chr17:38880749 | C | T | 43 | a0001c0001t0001g0040 a0001c0001t0001g0149 a0001c0001t0002g0180 others(40): Show |
45 | HG00323.hp1 HG00642.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.164+2569C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38880749 | |||||||
| chr17:38880777 | C | A | 43 | a0001c0001t0001g0040 a0001c0001t0001g0149 a0001c0001t0002g0180 others(40): Show |
45 | HG00323.hp1 HG00642.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.164+2597C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38880777 | |||||||
| chr17:38880931 | C | T | 1 | a0001c0006t0018g0249 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.164+2751C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38880931 | |||||||
| chr17:38880990 | C | G | 4 | a0001c0001t0001g0375 a0001c0004t0002g0370 a0001c0004t0002g0376 others(1): Show |
4 | HG02523.hp2 NA18950.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+2810C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38880990 | |||||||
| chr17:38881079 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.164+2899C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38881079 | |||||||
| chr17:38881465 | G | T | 75 | a0001c0001t0001g0038 a0001c0001t0001g0050 a0001c0001t0001g0078 others(72): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.164+3285G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38881465 | |||||||
| chr17:38881515 | CTCG | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0326 a0001c0001t0001g0333 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.164+3337_164+3339d others(5): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38881515 | ||||||
| chr17:38881518 | G | C | 277 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0050 others(274): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.164+3338G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38881518 | |||||||
| chr17:38881937 | T | C | 71 | a0001c0001t0001g0038 a0001c0001t0001g0050 a0001c0001t0001g0073 others(68): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.164+3757T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38881937 | |||||||
| chr17:38882012 | C | G | 27 | a0001c0001t0001g0050 a0001c0001t0002g0279 a0001c0001t0002g0281 others(24): Show |
27 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.164+3832C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38882012 | |||||||
| chr17:38882085 | G | A | 1 | a0001c0002t0003g0292 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.164+3905G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38882085 | |||||||
| chr17:38882191 | G | C | 10 | a0001c0001t0001g0011 a0001c0001t0004g0017 a0001c0001t0006g0271 others(7): Show |
10 | HG02109.hp2 HG02630.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.164+4011G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38882191 | |||||||
| chr17:38882276 | G | A | 1 | a0001c0002t0002g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.164+4096G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38882276 | |||||||
| chr17:38882310 | C | T | 1 | a0001c0001t0009g0323 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.164+4130C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38882310 | |||||||
| chr17:38882663 | G | A | 1 | a0001c0001t0024g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.164+4483G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38882663 | |||||||
| chr17:38882798 | A | C | 1 | a0001c0002t0002g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.164+4618A>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38882798 | |||||||
| chr17:38882874 | C | T | 3 | a0001c0005t0002g0145 a0001c0005t0003g0041 a0001c0008t0002g0146 |
3 | HG03688.hp2 HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.164+4694C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38882874 | |||||||
| chr17:38882990 | TGCCCCTT others(7): Show |
T | 4 | a0001c0001t0001g0326 a0001c0001t0001g0333 a0001c0001t0001g0335 others(1): Show |
4 | HG01884.hp1 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+4813_164+4826d others(16): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38882990 | ||||||
| chr17:38883140 | G | A | 4 | a0001c0001t0014g0269 a0001c0007t0002g0268 a0001c0007t0002g0270 others(1): Show |
4 | HG02922.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+4960G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38883140 | |||||||
| chr17:38883236 | C | A | 5 | a0001c0001t0002g0183 a0001c0002t0003g0003 a0001c0002t0003g0071 others(2): Show |
6 | HG00323.hp1 HG00642.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.164+5056C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38883236 | |||||||
| chr17:38883320 | T | C | 61 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0073 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.164+5140T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38883320 | |||||||
| chr17:38883332 | A | G | 1 | a0001c0013t0016g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.164+5152A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38883332 | |||||||
| chr17:38883350 | A | C | 2 | a0001c0001t0001g0078 a0001c0003t0004g0077 |
2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.164+5170A>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38883350 | |||||||
| chr17:38883444 | C | T | 61 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0073 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.164+5264C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38883444 | |||||||
| chr17:38883457 | C | T | 1 | a0001c0002t0012g0045 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.164+5277C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38883457 | |||||||
| chr17:38883459 | T | C | 1 | a0001c0002t0012g0045 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.164+5279T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38883459 | |||||||
| chr17:38883461 | C | T | 1 | a0001c0002t0012g0045 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.164+5281C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38883461 | |||||||
| chr17:38883739 | CT | C | 167 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0050 others(164): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.164+5577delT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38883739 | ||||||
| chr17:38883739 | CTTT | C | 11 | a0001c0001t0001g0011 a0001c0001t0004g0017 a0001c0001t0006g0175 others(8): Show |
11 | HG00621.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.164+5575_164+5577d others(5): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38883739 | ||||||
| chr17:38883739 | CTTTT | C | 79 | a0001c0001t0001g0073 a0001c0001t0001g0092 a0001c0001t0001g0162 others(76): Show |
79 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.164+5574_164+5577d others(6): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38883739 | ||||||
| chr17:38883757 | T | C | 1 | a0001c0001t0001g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.164+5577T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38883757 | |||||||
| chr17:38883842 | CTGAT | C | 10 | a0001c0001t0001g0011 a0001c0001t0004g0017 a0001c0001t0006g0175 others(7): Show |
10 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.164+5666_164+5669d others(6): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38883842 | ||||||
| chr17:38883851 | C | T | 3 | a0001c0001t0003g0372 a0001c0001t0006g0177 a0001c0007t0002g0373 |
3 | NA19030.hp2 NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.164+5671C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38883851 | |||||||
| chr17:38883911 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.164+5731A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38883911 | |||||||
| chr17:38883989 | C | T | 1 | a0001c0003t0004g0047 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.164+5809C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38883989 | |||||||
| chr17:38884022 | G | GT | 17 | a0001c0001t0001g0311 a0001c0001t0003g0031 a0001c0001t0003g0044 others(14): Show |
17 | HG00544.hp2 HG00642.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.164+5854dupT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38884022 | ||||||
| chr17:38884330 | TA | T | 28 | a0001c0001t0001g0050 a0001c0001t0001g0073 a0001c0001t0002g0190 others(25): Show |
28 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.165-6088delA | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38884330 | ||||||
| chr17:38884333 | C | T | 74 | a0001c0001t0001g0092 a0001c0001t0001g0162 a0001c0001t0001g0189 others(71): Show |
74 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.165-6087C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38884333 | |||||||
| chr17:38884372 | CT | C | 14 | a0001c0001t0001g0264 a0001c0001t0001g0320 a0001c0001t0003g0033 others(11): Show |
14 | HG00323.hp2 HG00673.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.165-6030delT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38884372 | ||||||
| chr17:38884372 | CTT | C | 58 | a0001c0001t0001g0092 a0001c0001t0001g0162 a0001c0001t0001g0201 others(55): Show |
58 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.165-6031_165-6030d others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38884372 | ||||||
| chr17:38884456 | T | C | 208 | a0001c0001t0001g0050 a0001c0001t0001g0073 a0001c0001t0001g0078 others(205): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.165-5964T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38884456 | |||||||
| chr17:38884504 | C | T | 21 | a0001c0001t0002g0010 a0001c0001t0002g0072 a0001c0001t0002g0374 others(18): Show |
21 | HG00642.hp2 HG01081.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.165-5916C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38884504 | |||||||
| chr17:38884506 | G | T | 4 | a0001c0001t0001g0326 a0001c0001t0001g0333 a0001c0001t0001g0335 others(1): Show |
4 | HG01884.hp1 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.165-5914G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38884506 | |||||||
| chr17:38884519 | C | T | 1 | a0001c0003t0001g0379 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.165-5901C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38884519 | |||||||
| chr17:38884610 | A | G | 243 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0050 others(240): Show |
245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.165-5810A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38884610 | |||||||
| chr17:38884669 | G | A | 3 | a0001c0002t0029g0324 a0001c0003t0004g0266 a0001c0007t0002g0046 |
3 | HG02723.hp1 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.165-5751G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38884669 | |||||||
| chr17:38884687 | C | CT | 22 | a0001c0001t0001g0237 a0001c0001t0001g0308 a0001c0001t0001g0309 others(19): Show |
22 | HG00609.hp1 HG00738.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.165-5712dupT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38884687 | ||||||
| chr17:38884687 | C | CTT | 38 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0073 others(35): Show |
38 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.165-5713_165-5712d others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38884687 | ||||||
| chr17:38884687 | C | CTTTT | 10 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0004g0188 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.165-5715_165-5712d others(6): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38884687 | ||||||
| chr17:38884687 | CT | C | 6 | a0001c0001t0004g0282 a0001c0001t0004g0283 a0001c0001t0009g0099 others(3): Show |
6 | HG01168.hp1 HG01169.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.165-5712delT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38884687 | ||||||
| chr17:38884687 | CTTTTTTT others(3): Show |
C | 2 | a0001c0002t0029g0324 a0001c0007t0002g0046 |
2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.165-5721_165-5712d others(12): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38884687 | ||||||
| chr17:38884794 | G | A | 5 | a0001c0001t0027g0095 a0001c0001t0028g0178 a0001c0002t0004g0259 others(2): Show |
5 | HG00733.hp1 HG01109.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-5626G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38884794 | |||||||
| chr17:38885096 | G | A | 136 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0073 others(133): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.165-5324G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38885096 | |||||||
| chr17:38885134 | T | G | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0003c0014t0002g0260 |
3 | HG01071.hp2 HG01243.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.165-5286T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38885134 | |||||||
| chr17:38885140 | C | T | 2 | a0001c0001t0004g0104 a0001c0001t0004g0105 |
2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.165-5280C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38885140 | |||||||
| chr17:38885144 | A | G | 23 | a0001c0001t0001g0040 a0001c0001t0001g0149 a0001c0001t0002g0180 others(20): Show |
25 | HG00323.hp1 HG00642.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.165-5276A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38885144 | |||||||
| chr17:38885255 | C | T | 1 | a0001c0003t0001g0157 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.165-5165C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38885255 | |||||||
| chr17:38885276 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.165-5144G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38885276 | |||||||
| chr17:38885322 | G | C | 5 | a0001c0001t0027g0095 a0001c0001t0028g0178 a0001c0002t0004g0259 others(2): Show |
5 | HG00733.hp1 HG01109.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-5098G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38885322 | |||||||
| chr17:38885619 | A | C | 3 | a0001c0009t0001g0022 a0001c0009t0001g0023 a0001c0009t0002g0025 |
3 | NA18988.hp2 NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.165-4801A>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38885619 | |||||||
| chr17:38885643 | A | AC | 281 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0040 others(278): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.165-4775dupC | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38885643 | ||||||
| chr17:38885695 | G | T | 3 | a0001c0009t0001g0022 a0001c0009t0001g0023 a0001c0009t0002g0025 |
3 | NA18988.hp2 NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.165-4725G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38885695 | |||||||
| chr17:38885697 | G | A | 1 | a0001c0001t0002g0190 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.165-4723G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38885697 | |||||||
| chr17:38885753 | G | A | 124 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0073 others(121): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.165-4667G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38885753 | |||||||
| chr17:38886004 | C | T | 9 | a0001c0001t0004g0017 a0001c0001t0006g0175 a0001c0001t0008g0021 others(6): Show |
9 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.165-4416C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38886004 | |||||||
| chr17:38886129 | A | ACT | 9 | a0001c0001t0004g0188 a0001c0001t0004g0325 a0001c0001t0004g0382 others(6): Show |
9 | HG02622.hp2 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.165-4272_165-4271d others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38886129 | ||||||
| chr17:38886129 | ACT | A | 3 | a0001c0009t0001g0022 a0001c0009t0001g0023 a0001c0009t0002g0025 |
3 | NA18988.hp2 NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.165-4272_165-4271d others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38886129 | ||||||
| chr17:38886140 | C | T | 1 | a0001c0003t0002g0035 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.165-4280C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38886140 | |||||||
| chr17:38886218 | A | G | 8 | a0001c0008t0002g0048 a0001c0008t0002g0049 a0001c0008t0002g0051 others(5): Show |
8 | HG00280.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.165-4202A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38886218 | |||||||
| chr17:38886242 | T | TAGTGAGC others(18): Show |
2 | a0001c0001t0001g0326 a0001c0001t0001g0333 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.165-4174_165-4150d others(27): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38886242 | ||||||
| chr17:38886301 | G | A | 1 | a0001c0002t0015g0339 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.165-4119G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38886301 | |||||||
| chr17:38886517 | C | T | 3 | a0001c0009t0001g0022 a0001c0009t0001g0023 a0001c0009t0002g0025 |
3 | NA18988.hp2 NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.165-3903C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38886517 | |||||||
| chr17:38886559 | G | A | 4 | a0001c0001t0024g0055 a0001c0002t0017g0086 a0001c0002t0017g0332 others(1): Show |
4 | HG02615.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.165-3861G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38886559 | |||||||
| chr17:38886705 | G | A | 1 | a0001c0003t0004g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165-3715G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38886705 | |||||||
| chr17:38886777 | A | G | 4 | a0001c0003t0001g0294 a0001c0003t0001g0361 a0001c0003t0001g0363 others(1): Show |
4 | HG00738.hp1 HG01123.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.165-3643A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38886777 | |||||||
| chr17:38886781 | A | G | 11 | a0001c0001t0004g0188 a0001c0001t0004g0325 a0001c0001t0004g0382 others(8): Show |
11 | HG02622.hp2 HG02717.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.165-3639A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38886781 | |||||||
| chr17:38886932 | G | A | 16 | a0001c0001t0001g0326 a0001c0001t0001g0333 a0001c0001t0001g0335 others(13): Show |
16 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.165-3488G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38886932 | |||||||
| chr17:38887032 | C | G | 1 | a0001c0003t0004g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165-3388C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887032 | |||||||
| chr17:38887086 | C | T | 3 | a0001c0001t0009g0099 a0001c0001t0009g0110 a0001c0001t0009g0323 |
3 | HG02145.hp2 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.165-3334C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887086 | |||||||
| chr17:38887155 | C | T | 1 | a0001c0001t0030g0020 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.165-3265C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887155 | |||||||
| chr17:38887199 | C | T | 9 | a0001c0001t0002g0010 a0001c0001t0003g0030 a0001c0001t0003g0031 others(6): Show |
9 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.165-3221C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887199 | |||||||
| chr17:38887203 | G | A | 2 | a0001c0001t0001g0201 a0001c0004t0002g0221 |
2 | HG02135.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.165-3217G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887203 | |||||||
| chr17:38887221 | C | T | 1 | a0001c0004t0002g0351 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.165-3199C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887221 | |||||||
| chr17:38887417 | C | T | 8 | a0001c0002t0002g0233 a0001c0002t0002g0234 a0001c0002t0003g0212 others(5): Show |
8 | NA18947.hp2 NA18953.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.165-3003C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887417 | |||||||
| chr17:38887418 | A | G | 284 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0050 others(281): Show |
288 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.165-3002A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887418 | |||||||
| chr17:38887426 | G | C | 21 | a0001c0001t0002g0010 a0001c0001t0003g0030 a0001c0001t0003g0031 others(18): Show |
21 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.165-2994G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887426 | |||||||
| chr17:38887646 | C | T | 4 | a0001c0001t0001g0189 a0001c0001t0002g0190 a0001c0001t0004g0267 others(1): Show |
4 | HG02723.hp1 HG02896.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-2774C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887646 | |||||||
| chr17:38887776 | T | C | 284 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0050 others(281): Show |
288 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.165-2644T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887776 | |||||||
| chr17:38887870 | T | C | 1 | a0001c0001t0001g0326 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.165-2550T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887870 | |||||||
| chr17:38887871 | G | A | 1 | a0001c0001t0001g0326 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.165-2549G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887871 | |||||||
| chr17:38887914 | T | A | 1 | a0001c0003t0006g0019 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.165-2506T>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887914 | |||||||
| chr17:38887947 | G | T | 1 | a0001c0003t0006g0019 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.165-2473G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887947 | |||||||
| chr17:38887963 | C | A | 1 | a0001c0002t0003g0310 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.165-2457C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38887963 | |||||||
| chr17:38888021 | G | T | 1 | a0001c0003t0004g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165-2399G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38888021 | |||||||
| chr17:38888069 | C | T | 5 | a0001c0001t0001g0306 a0001c0002t0003g0056 a0001c0002t0003g0292 others(2): Show |
5 | NA18944.hp1 NA18962.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-2351C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38888069 | |||||||
| chr17:38888124 | C | T | 8 | a0001c0001t0002g0010 a0001c0001t0003g0030 a0001c0001t0003g0031 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.165-2296C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38888124 | |||||||
| chr17:38888179 | G | A | 3 | a0001c0001t0009g0099 a0001c0001t0009g0110 a0001c0001t0009g0323 |
3 | HG02145.hp2 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.165-2241G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38888179 | |||||||
| chr17:38888284 | C | CT | 8 | a0001c0001t0001g0242 a0001c0001t0002g0010 a0001c0001t0003g0030 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.165-2122dupT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38888284 | ||||||
| chr17:38888479 | T | C | 4 | a0001c0001t0001g0326 a0001c0001t0001g0333 a0001c0001t0001g0335 others(1): Show |
4 | HG01884.hp1 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.165-1941T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38888479 | |||||||
| chr17:38888506 | G | A | 1 | a0002c0015t0001g0386 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.165-1914G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38888506 | |||||||
| chr17:38888845 | G | A | 3 | a0001c0001t0001g0189 a0001c0001t0004g0267 a0001c0003t0004g0266 |
3 | HG02723.hp1 HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.165-1575G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38888845 | |||||||
| chr17:38888880 | TG | T | 201 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0078 others(198): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.165-1536delG | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 38888880 | ||||||
| chr17:38888924 | A | G | 2 | a0001c0002t0002g0160 a0001c0002t0003g0144 |
2 | HG01106.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.165-1496A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38888924 | |||||||
| chr17:38889121 | T | G | 1 | a0001c0002t0003g0235 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.165-1299T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38889121 | |||||||
| chr17:38889233 | C | A | 2 | a0001c0009t0001g0022 a0001c0009t0002g0025 |
2 | NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.165-1187C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38889233 | |||||||
| chr17:38889233 | C | T | 1 | a0001c0001t0002g0190 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.165-1187C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38889233 | |||||||
| chr17:38889516 | C | T | 1 | a0001c0003t0004g0047 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.165-904C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38889516 | |||||||
| chr17:38889519 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0016g0262 a0001c0001t0024g0055 others(3): Show |
6 | HG02055.hp1 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.165-901C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38889519 | |||||||
| chr17:38889647 | T | C | 244 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0073 others(241): Show |
248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.165-773T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38889647 | |||||||
| chr17:38889755 | G | C | 3 | a0001c0009t0001g0022 a0001c0009t0001g0023 a0001c0009t0002g0025 |
3 | NA18988.hp2 NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.165-665G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38889755 | |||||||
| chr17:38889841 | A | T | 1 | a0001c0003t0001g0109 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.165-579A>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38889841 | |||||||
| chr17:38889877 | T | C | 2 | a0001c0001t0002g0124 a0001c0001t0002g0142 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.165-543T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38889877 | |||||||
| chr17:38890209 | C | T | 1 | a0001c0002t0003g0305 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.165-211C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38890209 | |||||||
| chr17:38890228 | G | A | 6 | a0001c0001t0014g0269 a0001c0001t0030g0020 a0001c0002t0029g0324 others(3): Show |
6 | HG02647.hp2 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.165-192G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 2/6 | chr17 | 38890228 | |||||||
| chr17:38890519 | G | A | 1 | a0001c0001t0030g0020 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.249+15G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38890519 | |||||||
| chr17:38890903 | G | T | 42 | a0001c0001t0001g0073 a0001c0001t0001g0078 a0001c0001t0001g0261 others(39): Show |
42 | HG00642.hp2 HG01071.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.249+399G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38890903 | |||||||
| chr17:38891032 | A | G | 277 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0050 others(274): Show |
281 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.249+528A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38891032 | |||||||
| chr17:38891085 | T | G | 1 | a0001c0003t0001g0250 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.249+581T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38891085 | |||||||
| chr17:38891242 | C | G | 2 | a0001c0002t0015g0339 a0001c0003t0004g0077 |
2 | HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.249+738C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38891242 | |||||||
| chr17:38891283 | C | T | 1 | a0001c0002t0015g0339 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.249+779C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38891283 | |||||||
| chr17:38891405 | A | G | 267 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0050 others(264): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.249+901A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38891405 | |||||||
| chr17:38891468 | A | G | 93 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0127 others(90): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.249+964A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38891468 | |||||||
| chr17:38891484 | A | G | 1 | a0001c0001t0007g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.249+980A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38891484 | |||||||
| chr17:38891545 | A | G | 123 | a0001c0001t0001g0078 a0001c0001t0001g0092 a0001c0001t0001g0162 others(120): Show |
124 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.249+1041A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38891545 | |||||||
| chr17:38891606 | A | G | 45 | a0001c0001t0001g0073 a0001c0001t0001g0078 a0001c0001t0001g0261 others(42): Show |
45 | HG00642.hp2 HG01071.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.249+1102A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38891606 | |||||||
| chr17:38891628 | G | A | 1 | a0001c0002t0001g0354 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.249+1124G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38891628 | |||||||
| chr17:38891793 | T | G | 1 | a0001c0003t0003g0057 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.249+1289T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38891793 | |||||||
| chr17:38891860 | C | G | 1 | a0001c0002t0002g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.249+1356C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38891860 | |||||||
| chr17:38891929 | T | TA | 7 | a0001c0001t0001g0243 a0001c0001t0001g0375 a0001c0002t0003g0297 others(4): Show |
7 | HG02523.hp2 HG02922.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.249+1436dupA | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38891929 | ||||||
| chr17:38891994 | C | T | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
4 | HG02027.hp1 NA18975.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+1490C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38891994 | |||||||
| chr17:38892000 | T | G | 250 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0073 others(247): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.249+1496T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892000 | |||||||
| chr17:38892065 | G | C | 17 | a0001c0001t0001g0189 a0001c0001t0002g0010 a0001c0001t0002g0190 others(14): Show |
17 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(14): Show |
intron_variant | MODIFIER | c.249+1561G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892065 | |||||||
| chr17:38892172 | A | G | 382 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(379): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.249+1668A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892172 | |||||||
| chr17:38892176 | G | A | 4 | a0001c0001t0006g0271 a0001c0001t0016g0262 a0001c0003t0004g0266 others(1): Show |
4 | HG02055.hp1 HG02723.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+1672G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892176 | |||||||
| chr17:38892190 | C | A | 2 | a0001c0001t0001g0306 a0001c0002t0003g0307 |
2 | NA18962.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.249+1686C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892190 | |||||||
| chr17:38892191 | G | A | 1 | a0001c0002t0001g0278 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.249+1687G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892191 | |||||||
| chr17:38892484 | C | T | 5 | a0001c0001t0002g0010 a0001c0001t0014g0269 a0001c0007t0002g0268 others(2): Show |
5 | HG02922.hp1 HG03139.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+1980C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892484 | |||||||
| chr17:38892496 | G | A | 11 | a0001c0001t0004g0188 a0001c0001t0004g0325 a0001c0001t0004g0382 others(8): Show |
11 | HG02257.hp2 HG02280.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+1992G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892496 | |||||||
| chr17:38892513 | G | A | 86 | a0001c0001t0001g0092 a0001c0001t0001g0138 a0001c0001t0001g0162 others(83): Show |
88 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.249+2009G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892513 | |||||||
| chr17:38892551 | G | GAC | 28 | a0001c0001t0001g0073 a0001c0001t0001g0106 a0001c0001t0002g0085 others(25): Show |
28 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.249+2086_249+2087d others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892551 | G | GACAC | 28 | a0001c0001t0001g0216 a0001c0001t0001g0220 a0001c0001t0001g0242 others(25): Show |
30 | HG00621.hp2 HG00735.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.249+2084_249+2087d others(6): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892551 | G | GACACAC | 25 | a0001c0001t0001g0189 a0001c0001t0001g0261 a0001c0001t0001g0311 others(22): Show |
25 | HG00408.hp2 HG00609.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.249+2082_249+2087d others(8): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892551 | G | GACACACA others(1): Show |
9 | a0001c0001t0001g0078 a0001c0001t0001g0151 a0001c0001t0001g0244 others(6): Show |
9 | HG02027.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+2080_249+2087d others(10): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892551 | G | GACACACA others(3): Show |
6 | a0001c0001t0001g0011 a0001c0001t0001g0150 a0001c0001t0001g0243 others(3): Show |
6 | HG02155.hp1 HG02809.hp1 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+2078_249+2087d others(12): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892551 | G | GACACACA others(5): Show |
3 | a0001c0001t0001g0127 a0001c0001t0001g0375 a0001c0004t0002g0377 |
3 | NA18612.hp1 NA18950.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.249+2076_249+2087d others(14): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892551 | G | GACACACA others(7): Show |
1 | a0001c0001t0002g0374 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.249+2074_249+2087d others(16): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892551 | GAC | G | 144 | a0001c0001t0001g0050 a0001c0001t0001g0092 a0001c0001t0001g0138 others(141): Show |
146 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.249+2086_249+2087d others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892551 | GACAC | G | 15 | a0001c0001t0001g0304 a0001c0001t0001g0308 a0001c0001t0001g0309 others(12): Show |
15 | HG02109.hp2 HG02451.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.249+2084_249+2087d others(6): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892551 | GACACAC | G | 4 | a0001c0001t0028g0178 a0001c0003t0004g0090 a0001c0003t0004g0121 others(1): Show |
4 | HG00099.hp1 HG02818.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+2082_249+2087d others(8): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892551 | GACACACA others(1): Show |
G | 3 | a0001c0001t0027g0095 a0001c0007t0002g0141 a0001c0007t0002g0186 |
3 | HG01081.hp1 HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.249+2080_249+2087d others(10): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892551 | GACACACA others(7): Show |
G | 3 | a0001c0001t0002g0027 a0001c0002t0001g0028 a0001c0004t0001g0359 |
3 | HG03669.hp2 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.249+2074_249+2087d others(16): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892551 | GACACACA others(9): Show |
G | 4 | a0001c0001t0001g0201 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG00738.hp2 HG01934.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+2072_249+2087d others(18): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892551 | GACACACA others(13): Show |
G | 2 | a0001c0001t0001g0287 a0001c0002t0002g0160 |
2 | HG01106.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.249+2068_249+2087d others(22): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892551 | ||||||
| chr17:38892588 | A | ACC | 8 | a0001c0001t0001g0256 a0001c0001t0004g0280 a0001c0001t0004g0282 others(5): Show |
8 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+2085_249+2086i others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892588 | ||||||
| chr17:38892588 | A | C | 5 | a0001c0003t0001g0363 a0001c0003t0002g0139 a0001c0003t0003g0057 others(2): Show |
5 | HG00099.hp1 HG00738.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+2084A>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892588 | |||||||
| chr17:38892590 | A | C | 1 | a0001c0002t0001g0093 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.249+2086A>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892590 | |||||||
| chr17:38892590 | AC | A | 10 | a0001c0001t0001g0341 a0001c0001t0002g0253 a0001c0001t0002g0300 others(7): Show |
10 | HG00544.hp2 HG02293.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+2089delC | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892590 | ||||||
| chr17:38892591 | C | CA | 3 | a0001c0001t0001g0299 a0001c0002t0001g0247 a0001c0002t0015g0339 |
3 | HG02486.hp1 HG03942.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.249+2087_249+2088i others(3): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892591 | |||||||
| chr17:38892591 | C | CACACACA others(4): Show |
1 | a0001c0001t0003g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.249+2087_249+2088i others(13): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892591 | |||||||
| chr17:38892592 | C | A | 1 | a0001c0001t0001g0320 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.249+2088C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892592 | |||||||
| chr17:38892692 | G | A | 1 | a0001c0002t0001g0360 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.249+2188G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892692 | |||||||
| chr17:38892807 | G | A | 3 | a0001c0006t0003g0389 a0001c0006t0005g0029 a0001c0009t0001g0023 |
3 | HG02602.hp2 HG02738.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.249+2303G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892807 | |||||||
| chr17:38892863 | A | G | 196 | a0001c0001t0001g0073 a0001c0001t0001g0092 a0001c0001t0001g0138 others(193): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.249+2359A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892863 | |||||||
| chr17:38892884 | G | C | 2 | a0001c0001t0001g0256 a0001c0008t0002g0255 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+2380G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892884 | |||||||
| chr17:38892891 | TGG | T | 9 | a0001c0001t0004g0188 a0001c0001t0004g0325 a0001c0001t0004g0382 others(6): Show |
9 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+2389_249+2390d others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892891 | ||||||
| chr17:38892926 | C | T | 299 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(296): Show |
304 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.249+2422C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892926 | |||||||
| chr17:38892950 | C | T | 2 | a0001c0002t0003g0252 a0001c0002t0003g0290 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.249+2446C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892950 | |||||||
| chr17:38892975 | G | A | 9 | a0001c0001t0004g0188 a0001c0001t0004g0325 a0001c0001t0004g0382 others(6): Show |
9 | HG02622.hp2 HG02717.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+2471G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892975 | |||||||
| chr17:38892997 | ATG | A | 81 | a0001c0001t0001g0264 a0001c0001t0002g0010 a0001c0001t0002g0190 others(78): Show |
82 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.249+2510_249+2511d others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38892997 | ||||||
| chr17:38892998 | T | C | 9 | a0001c0001t0006g0018 a0001c0001t0006g0175 a0001c0001t0006g0371 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+2494T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38892998 | |||||||
| chr17:38893167 | G | C | 2 | a0001c0001t0016g0262 a0001c0007t0002g0140 |
2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.249+2663G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38893167 | |||||||
| chr17:38893236 | G | A | 2 | a0001c0002t0017g0086 a0001c0002t0017g0332 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.249+2732G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38893236 | |||||||
| chr17:38893324 | G | A | 1 | a0001c0011t0002g0298 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.249+2820G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38893324 | |||||||
| chr17:38893363 | C | G | 2 | a0001c0001t0001g0341 a0001c0001t0003g0342 |
2 | HG02074.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.249+2859C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38893363 | |||||||
| chr17:38893444 | G | A | 1 | a0001c0001t0001g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.249+2940G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38893444 | |||||||
| chr17:38893657 | G | A | 1 | a0001c0003t0001g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.249+3153G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38893657 | |||||||
| chr17:38893658 | A | G | 1 | a0001c0003t0001g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.249+3154A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38893658 | |||||||
| chr17:38893790 | C | T | 6 | a0001c0006t0003g0389 a0001c0006t0005g0029 a0001c0006t0005g0165 others(3): Show |
6 | HG00673.hp2 HG02135.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+3286C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38893790 | |||||||
| chr17:38893830 | A | C | 176 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0073 others(173): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.249+3326A>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38893830 | |||||||
| chr17:38894097 | C | T | 1 | a0001c0003t0004g0088 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.249+3593C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894097 | |||||||
| chr17:38894114 | C | A | 10 | a0001c0001t0004g0188 a0001c0001t0004g0325 a0001c0001t0004g0382 others(7): Show |
10 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+3610C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894114 | |||||||
| chr17:38894135 | G | A | 1 | a0001c0001t0028g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.249+3631G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894135 | |||||||
| chr17:38894151 | C | T | 6 | a0001c0006t0003g0389 a0001c0006t0005g0029 a0001c0006t0005g0165 others(3): Show |
6 | HG00673.hp2 HG02135.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+3647C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894151 | |||||||
| chr17:38894189 | C | T | 1 | a0001c0002t0002g0388 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.249+3685C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894189 | |||||||
| chr17:38894267 | G | A | 1 | a0001c0001t0015g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.249+3763G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894267 | |||||||
| chr17:38894278 | C | T | 1 | a0001c0001t0025g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.249+3774C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894278 | |||||||
| chr17:38894322 | A | G | 181 | a0001c0001t0001g0011 a0001c0001t0001g0073 a0001c0001t0001g0078 others(178): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.249+3818A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894322 | |||||||
| chr17:38894346 | A | G | 63 | a0001c0001t0001g0161 a0001c0001t0001g0306 a0001c0001t0001g0311 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.249+3842A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894346 | |||||||
| chr17:38894489 | G | A | 5 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0001t0016g0262 others(2): Show |
5 | HG01081.hp1 HG02055.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-3923G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894489 | |||||||
| chr17:38894513 | C | T | 1 | a0001c0001t0002g0279 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.250-3899C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894513 | |||||||
| chr17:38894604 | C | T | 1 | a0001c0002t0003g0239 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.250-3808C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894604 | |||||||
| chr17:38894626 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.250-3786A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894626 | |||||||
| chr17:38894740 | A | T | 155 | a0001c0001t0001g0161 a0001c0001t0001g0264 a0001c0001t0001g0306 others(152): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.250-3672A>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894740 | |||||||
| chr17:38894863 | G | A | 11 | a0001c0003t0002g0035 a0001c0003t0002g0075 a0001c0003t0002g0076 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-3549G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38894863 | |||||||
| chr17:38895070 | A | G | 7 | a0001c0001t0001g0256 a0001c0001t0004g0267 a0001c0001t0014g0269 others(4): Show |
7 | HG02486.hp1 HG02622.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.250-3342A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38895070 | |||||||
| chr17:38895178 | A | AT | 11 | a0001c0001t0001g0011 a0001c0001t0002g0190 a0001c0001t0006g0271 others(8): Show |
11 | HG00673.hp2 HG02135.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-3220dupT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38895178 | ||||||
| chr17:38895178 | AT | A | 19 | a0001c0001t0001g0256 a0001c0001t0001g0308 a0001c0001t0004g0267 others(16): Show |
19 | HG02258.hp2 HG02451.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.250-3220delT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38895178 | ||||||
| chr17:38895244 | G | C | 1 | a0001c0002t0003g0251 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.250-3168G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38895244 | |||||||
| chr17:38895471 | G | A | 75 | a0001c0001t0001g0264 a0001c0003t0001g0002 a0001c0003t0001g0004 others(72): Show |
77 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.250-2941G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38895471 | |||||||
| chr17:38895475 | G | A | 2 | a0001c0002t0003g0003 a0001c0002t0003g0071 |
3 | HG00642.hp1 HG01074.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.250-2937G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38895475 | |||||||
| chr17:38895485 | T | A | 3 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0007t0002g0141 |
3 | HG01081.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.250-2927T>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38895485 | |||||||
| chr17:38895518 | G | C | 181 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0001g0161 others(178): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.250-2894G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38895518 | |||||||
| chr17:38895706 | C | T | 1 | a0001c0009t0001g0024 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.250-2706C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38895706 | |||||||
| chr17:38895878 | T | C | 194 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0001g0161 others(191): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.250-2534T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38895878 | |||||||
| chr17:38896088 | A | AGGGGCAA others(11): Show |
143 | a0001c0001t0001g0161 a0001c0001t0001g0256 a0001c0001t0001g0264 others(140): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.250-2323_250-2306d others(20): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38896088 | ||||||
| chr17:38896088 | A | AGGGGCAA others(11): Show |
1 | a0001c0003t0004g0088 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.250-2312_250-2311i others(20): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 38896088 | ||||||
| chr17:38896099 | C | T | 27 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0001g0189 others(24): Show |
27 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.250-2313C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38896099 | |||||||
| chr17:38896548 | C | A | 61 | a0001c0001t0001g0092 a0001c0001t0001g0138 a0001c0001t0001g0162 others(58): Show |
63 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.250-1864C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38896548 | |||||||
| chr17:38896912 | C | T | 136 | a0001c0001t0001g0161 a0001c0001t0001g0256 a0001c0001t0001g0306 others(133): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.250-1500C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38896912 | |||||||
| chr17:38896978 | C | T | 3 | a0001c0001t0003g0044 a0001c0001t0011g0043 a0001c0001t0011g0065 |
3 | NA18950.hp1 NA18981.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.250-1434C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38896978 | |||||||
| chr17:38897297 | C | T | 6 | a0001c0001t0002g0013 a0001c0001t0002g0079 a0001c0001t0002g0081 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.250-1115C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38897297 | |||||||
| chr17:38897349 | G | C | 1 | a0001c0007t0002g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.250-1063G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38897349 | |||||||
| chr17:38897713 | A | G | 6 | a0001c0001t0003g0044 a0001c0001t0003g0064 a0001c0001t0003g0066 others(3): Show |
6 | NA18612.hp2 NA18950.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.250-699A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38897713 | |||||||
| chr17:38897739 | G | A | 94 | a0001c0001t0001g0256 a0001c0001t0004g0267 a0001c0001t0014g0269 others(91): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.250-673G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38897739 | |||||||
| chr17:38897755 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.250-657C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38897755 | |||||||
| chr17:38897881 | A | G | 6 | a0001c0001t0001g0256 a0001c0001t0004g0267 a0001c0001t0014g0269 others(3): Show |
6 | HG02622.hp1 HG02922.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.250-531A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38897881 | |||||||
| chr17:38898000 | A | G | 106 | a0001c0001t0001g0256 a0001c0001t0002g0190 a0001c0001t0004g0267 others(103): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.250-412A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38898000 | |||||||
| chr17:38898205 | T | C | 192 | a0001c0001t0001g0011 a0001c0001t0001g0073 a0001c0001t0001g0078 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.250-207T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38898205 | |||||||
| chr17:38898209 | C | G | 2 | a0001c0001t0030g0020 a0001c0002t0015g0339 |
2 | HG02486.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.250-203C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38898209 | |||||||
| chr17:38898320 | T | A | 3 | a0001c0001t0009g0099 a0001c0001t0009g0110 a0001c0001t0009g0323 |
3 | HG02145.hp2 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.250-92T>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 3/6 | chr17 | 38898320 | |||||||
| chr17:38898532 | C | T | 5 | a0001c0001t0006g0175 a0001c0001t0008g0021 a0001c0001t0008g0263 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.357+13C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38898532 | |||||||
| chr17:38898631 | A | G | 116 | a0001c0001t0001g0219 a0001c0001t0001g0256 a0001c0001t0002g0190 others(113): Show |
118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.357+112A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38898631 | |||||||
| chr17:38898669 | G | A | 2 | a0001c0001t0003g0223 a0001c0009t0001g0022 |
2 | NA18991.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.357+150G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38898669 | |||||||
| chr17:38898707 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.357+188C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38898707 | |||||||
| chr17:38898713 | C | T | 8 | a0001c0003t0001g0286 a0001c0003t0001g0314 a0001c0003t0004g0120 others(5): Show |
8 | HG00140.hp2 HG00323.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.357+194C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38898713 | |||||||
| chr17:38898788 | CTGT | C | 7 | a0001c0001t0001g0161 a0001c0001t0002g0118 a0001c0002t0001g0156 others(4): Show |
7 | HG00408.hp1 HG00544.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+274_357+276del others(3): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38898788 | ||||||
| chr17:38898820 | C | T | 1 | a0001c0003t0001g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.357+301C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38898820 | |||||||
| chr17:38898821 | G | A | 1 | a0001c0003t0001g0034 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.357+302G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38898821 | |||||||
| chr17:38898824 | G | A | 68 | a0001c0001t0001g0078 a0001c0001t0001g0138 a0001c0001t0001g0161 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.357+305G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38898824 | |||||||
| chr17:38898827 | G | A | 2 | a0001c0001t0001g0311 a0001c0001t0002g0072 |
2 | HG01981.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.357+308G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38898827 | |||||||
| chr17:38899051 | G | A | 17 | a0001c0001t0001g0256 a0001c0001t0002g0085 a0001c0001t0002g0384 others(14): Show |
17 | HG01109.hp2 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.357+532G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899051 | |||||||
| chr17:38899172 | C | T | 2 | a0001c0007t0002g0268 a0001c0007t0002g0270 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.357+653C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899172 | |||||||
| chr17:38899320 | G | A | 1 | a0001c0001t0008g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.357+801G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899320 | |||||||
| chr17:38899425 | G | A | 18 | a0001c0001t0001g0256 a0001c0001t0002g0085 a0001c0001t0002g0384 others(15): Show |
18 | HG01109.hp2 HG01884.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+906G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899425 | |||||||
| chr17:38899482 | C | A | 1 | a0001c0003t0004g0047 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.357+963C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899482 | |||||||
| chr17:38899482 | C | G | 2 | a0001c0002t0001g0187 a0001c0002t0002g0122 |
2 | NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.357+963C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899482 | |||||||
| chr17:38899518 | G | A | 1 | a0001c0001t0004g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.357+999G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899518 | |||||||
| chr17:38899562 | A | G | 220 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0078 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.357+1043A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899562 | |||||||
| chr17:38899564 | A | T | 14 | a0001c0002t0001g0360 a0001c0002t0002g0193 a0001c0002t0002g0195 others(11): Show |
14 | HG00438.hp1 NA18940.hp2 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.357+1045A>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899564 | |||||||
| chr17:38899719 | G | A | 6 | a0001c0006t0003g0389 a0001c0006t0005g0029 a0001c0006t0005g0165 others(3): Show |
6 | HG00673.hp2 HG02135.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+1200G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899719 | |||||||
| chr17:38899747 | C | CT | 142 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0078 others(139): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.357+1243dupT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38899747 | ||||||
| chr17:38899747 | C | CTTTTTTT others(3): Show |
53 | a0001c0001t0001g0138 a0001c0001t0001g0161 a0001c0001t0001g0306 others(50): Show |
53 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.357+1234_357+1243d others(12): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38899747 | ||||||
| chr17:38899747 | C | CTTTTTTT others(4): Show |
6 | a0001c0001t0002g0072 a0001c0001t0003g0126 a0001c0001t0007g0327 others(3): Show |
6 | HG02135.hp1 HG02257.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+1233_357+1243d others(13): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38899747 | ||||||
| chr17:38899747 | C | CTTTTTTT others(6): Show |
5 | a0001c0001t0002g0190 a0001c0001t0009g0099 a0001c0001t0009g0323 others(2): Show |
5 | HG00673.hp2 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.357+1231_357+1243d others(15): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38899747 | ||||||
| chr17:38899747 | C | CTTTTTTT others(7): Show |
6 | a0001c0001t0009g0110 a0001c0006t0003g0389 a0001c0006t0005g0029 others(3): Show |
6 | HG02135.hp2 HG02145.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+1230_357+1243d others(16): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38899747 | ||||||
| chr17:38899767 | C | CT | 18 | a0001c0001t0001g0256 a0001c0001t0002g0085 a0001c0001t0002g0384 others(15): Show |
18 | HG01109.hp2 HG01884.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+1248_357+1249i others(3): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899767 | |||||||
| chr17:38899878 | C | T | 10 | a0001c0001t0004g0188 a0001c0001t0004g0325 a0001c0001t0004g0382 others(7): Show |
10 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.357+1359C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899878 | |||||||
| chr17:38899891 | G | A | 2 | a0001c0002t0003g0239 a0001c0002t0015g0339 |
2 | HG02486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.357+1372G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899891 | |||||||
| chr17:38899976 | C | T | 2 | a0001c0004t0002g0128 a0003c0014t0002g0260 |
2 | HG01071.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.357+1457C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38899976 | |||||||
| chr17:38900049 | A | G | 11 | a0001c0001t0002g0190 a0001c0001t0009g0099 a0001c0001t0009g0110 others(8): Show |
11 | HG00673.hp2 HG02135.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.357+1530A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900049 | |||||||
| chr17:38900144 | C | T | 2 | a0001c0002t0002g0160 a0001c0002t0003g0144 |
2 | HG01106.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.357+1625C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900144 | |||||||
| chr17:38900149 | G | C | 1 | a0001c0001t0002g0130 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.357+1630G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900149 | |||||||
| chr17:38900180 | T | C | 199 | a0001c0001t0001g0040 a0001c0001t0001g0138 a0001c0001t0001g0149 others(196): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.357+1661T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900180 | |||||||
| chr17:38900197 | C | CA | 108 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0078 others(105): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.357+1703dupA | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38900197 | ||||||
| chr17:38900197 | C | CAA | 31 | a0001c0001t0001g0149 a0001c0002t0001g0360 a0001c0002t0002g0195 others(28): Show |
31 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.357+1702_357+1703d others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38900197 | ||||||
| chr17:38900197 | CA | C | 34 | a0001c0001t0001g0256 a0001c0001t0001g0311 a0001c0001t0001g0375 others(31): Show |
34 | HG00140.hp1 HG01109.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.357+1703delA | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38900197 | ||||||
| chr17:38900197 | CAA | C | 40 | a0001c0001t0001g0138 a0001c0001t0001g0161 a0001c0001t0001g0306 others(37): Show |
40 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.357+1702_357+1703d others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38900197 | ||||||
| chr17:38900197 | CAAAAAAA others(4): Show |
C | 1 | a0001c0009t0002g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.357+1693_357+1703d others(13): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38900197 | ||||||
| chr17:38900225 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0016g0262 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.357+1706C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900225 | |||||||
| chr17:38900303 | C | T | 18 | a0001c0001t0001g0256 a0001c0001t0002g0085 a0001c0001t0002g0384 others(15): Show |
18 | HG01109.hp2 HG01884.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+1784C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900303 | |||||||
| chr17:38900337 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.357+1818A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900337 | |||||||
| chr17:38900375 | G | GTTTCCAA others(3): Show |
1 | a0001c0002t0003g0285 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.357+1857_357+1866d others(12): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38900375 | ||||||
| chr17:38900380 | C | CAAAAAAA others(1): Show |
66 | a0001c0001t0001g0138 a0001c0001t0001g0161 a0001c0001t0001g0306 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.357+1865_357+1872d others(10): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38900380 | ||||||
| chr17:38900380 | C | CAAAAAAA others(2): Show |
18 | a0001c0001t0001g0256 a0001c0001t0002g0085 a0001c0001t0002g0384 others(15): Show |
18 | HG02280.hp1 HG02622.hp1 HG02895.hp2 others(15): Show |
intron_variant | MODIFIER | c.357+1864_357+1872d others(11): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38900380 | ||||||
| chr17:38900380 | C | CAAAAAAA others(3): Show |
13 | a0001c0001t0004g0104 a0001c0001t0027g0095 a0001c0002t0002g0233 others(10): Show |
13 | HG00323.hp2 HG00673.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.357+1863_357+1872d others(12): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38900380 | ||||||
| chr17:38900380 | C | CAAAAAAA others(4): Show |
92 | a0001c0001t0001g0040 a0001c0001t0001g0149 a0001c0002t0002g0193 others(89): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.357+1862_357+1872d others(13): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38900380 | ||||||
| chr17:38900380 | C | CAAAAAAA others(5): Show |
7 | a0001c0002t0001g0360 a0001c0003t0001g0015 a0001c0003t0001g0214 others(4): Show |
7 | HG00741.hp1 HG01358.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+1872_357+1873i others(14): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38900380 | ||||||
| chr17:38900380 | C | CAAAAAAA others(6): Show |
2 | a0001c0003t0001g0115 a0001c0008t0002g0176 |
2 | HG00642.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.357+1872_357+1873i others(15): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38900380 | ||||||
| chr17:38900403 | G | A | 3 | a0001c0001t0009g0099 a0001c0001t0009g0110 a0001c0001t0009g0323 |
3 | HG02145.hp2 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.357+1884G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900403 | |||||||
| chr17:38900563 | C | T | 3 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0007t0002g0141 |
3 | HG01081.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.357+2044C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900563 | |||||||
| chr17:38900597 | C | T | 1 | a0001c0001t0028g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.357+2078C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900597 | |||||||
| chr17:38900627 | C | T | 1 | a0001c0001t0002g0312 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.357+2108C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900627 | |||||||
| chr17:38900776 | C | T | 1 | a0001c0002t0001g0369 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.357+2257C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900776 | |||||||
| chr17:38900877 | C | T | 17 | a0001c0001t0001g0256 a0001c0001t0002g0085 a0001c0001t0002g0384 others(14): Show |
17 | HG01109.hp2 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.357+2358C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900877 | |||||||
| chr17:38900923 | G | T | 1 | a0001c0001t0031g0331 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.357+2404G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900923 | |||||||
| chr17:38900957 | C | T | 1 | a0001c0005t0003g0041 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.357+2438C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900957 | |||||||
| chr17:38900973 | G | A | 1 | a0001c0003t0001g0241 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.357+2454G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900973 | |||||||
| chr17:38900982 | A | G | 130 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0078 others(127): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.357+2463A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38900982 | |||||||
| chr17:38901132 | T | G | 1 | a0001c0003t0004g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.357+2613T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38901132 | |||||||
| chr17:38901155 | T | C | 3 | a0001c0008t0002g0052 a0001c0008t0002g0069 a0001c0008t0002g0070 |
3 | HG01070.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.357+2636T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38901155 | |||||||
| chr17:38901185 | T | C | 1 | a0001c0004t0002g0377 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.357+2666T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38901185 | |||||||
| chr17:38901264 | G | A | 129 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0078 others(126): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.357+2745G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38901264 | |||||||
| chr17:38901403 | G | A | 2 | a0001c0001t0001g0341 a0001c0007t0002g0270 |
2 | HG02523.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.357+2884G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38901403 | |||||||
| chr17:38901539 | TAGGGTTG others(18): Show |
T | 1 | a0001c0002t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.357+3021_357+3045d others(27): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38901539 | |||||||
| chr17:38901632 | A | G | 17 | a0001c0001t0001g0256 a0001c0001t0002g0085 a0001c0001t0002g0384 others(14): Show |
17 | HG01109.hp2 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.357+3113A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38901632 | |||||||
| chr17:38901723 | G | T | 1 | a0001c0002t0001g0369 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.357+3204G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38901723 | |||||||
| chr17:38901787 | A | G | 6 | a0001c0002t0002g0206 a0001c0004t0002g0351 a0001c0006t0001g0210 others(3): Show |
6 | HG02129.hp1 HG02129.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+3268A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38901787 | |||||||
| chr17:38901851 | C | T | 1 | a0001c0004t0001g0359 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.357+3332C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38901851 | |||||||
| chr17:38901866 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.357+3347C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38901866 | |||||||
| chr17:38901897 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0002g0190 a0001c0001t0006g0271 others(1): Show |
4 | HG03041.hp2 NA18906.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+3378C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38901897 | |||||||
| chr17:38901951 | T | A | 1 | a0001c0001t0001g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.357+3432T>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38901951 | |||||||
| chr17:38902057 | G | T | 2 | a0001c0002t0003g0313 a0001c0002t0003g0315 |
2 | NA18947.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.357+3538G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38902057 | |||||||
| chr17:38902084 | C | G | 115 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0092 others(112): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.357+3565C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38902084 | |||||||
| chr17:38902092 | C | T | 1 | a0001c0002t0003g0063 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.357+3573C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38902092 | |||||||
| chr17:38902261 | A | G | 1 | a0001c0004t0020g0042 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.357+3742A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38902261 | |||||||
| chr17:38902372 | C | CT | 10 | a0001c0001t0001g0155 a0001c0001t0001g0219 a0001c0001t0001g0226 others(7): Show |
10 | HG00544.hp1 HG01261.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.357+3876dupT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38902372 | ||||||
| chr17:38902372 | CT | C | 120 | a0001c0001t0001g0040 a0001c0001t0001g0092 a0001c0001t0001g0149 others(117): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.357+3876delT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38902372 | ||||||
| chr17:38902372 | CTT | C | 33 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0001g0189 others(30): Show |
33 | HG00408.hp1 HG01070.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.357+3875_357+3876d others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38902372 | ||||||
| chr17:38902372 | CTTT | C | 61 | a0001c0001t0001g0138 a0001c0001t0001g0161 a0001c0001t0001g0306 others(58): Show |
61 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.357+3874_357+3876d others(5): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38902372 | ||||||
| chr17:38902387 | T | C | 1 | a0001c0003t0001g0202 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.357+3868T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38902387 | |||||||
| chr17:38902436 | G | T | 1 | a0001c0001t0014g0269 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.357+3917G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38902436 | |||||||
| chr17:38902440 | T | C | 200 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0078 others(197): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.357+3921T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38902440 | |||||||
| chr17:38902477 | GACT | G | 29 | a0001c0001t0001g0078 a0001c0001t0001g0189 a0001c0001t0001g0261 others(26): Show |
29 | HG00673.hp2 HG01884.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.357+3964_357+3966d others(5): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38902477 | ||||||
| chr17:38902594 | T | G | 1 | a0001c0002t0003g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.357+4075T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38902594 | |||||||
| chr17:38902752 | G | A | 3 | a0001c0003t0004g0047 a0001c0003t0004g0077 a0001c0003t0004g0090 |
3 | HG02615.hp1 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.357+4233G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38902752 | |||||||
| chr17:38902903 | A | G | 50 | a0001c0001t0001g0138 a0001c0001t0001g0161 a0001c0001t0001g0306 others(47): Show |
50 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.357+4384A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38902903 | |||||||
| chr17:38902992 | T | G | 29 | a0001c0001t0001g0078 a0001c0001t0001g0189 a0001c0001t0001g0261 others(26): Show |
29 | HG00673.hp2 HG01884.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.357+4473T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38902992 | |||||||
| chr17:38903222 | C | T | 1 | a0001c0001t0001g0304 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.357+4703C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38903222 | |||||||
| chr17:38903244 | C | T | 29 | a0001c0001t0001g0078 a0001c0001t0001g0189 a0001c0001t0001g0261 others(26): Show |
29 | HG00673.hp2 HG01884.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.357+4725C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38903244 | |||||||
| chr17:38903338 | C | G | 1 | a0001c0001t0002g0284 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.357+4819C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38903338 | |||||||
| chr17:38903491 | C | T | 62 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0127 others(59): Show |
62 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.357+4972C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38903491 | |||||||
| chr17:38903657 | T | A | 1 | a0001c0002t0003g0285 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.357+5138T>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38903657 | |||||||
| chr17:38903658 | G | T | 1 | a0001c0002t0003g0285 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.357+5139G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38903658 | |||||||
| chr17:38903730 | T | C | 30 | a0001c0001t0001g0078 a0001c0001t0001g0189 a0001c0001t0001g0261 others(27): Show |
30 | HG00673.hp2 HG01884.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.357+5211T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38903730 | |||||||
| chr17:38903844 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.357+5325C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38903844 | |||||||
| chr17:38903881 | T | C | 217 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0078 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.357+5362T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38903881 | |||||||
| chr17:38903906 | C | G | 5 | a0001c0001t0006g0175 a0001c0001t0008g0021 a0001c0001t0008g0263 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.357+5387C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38903906 | |||||||
| chr17:38903923 | G | C | 17 | a0001c0001t0001g0073 a0001c0001t0002g0013 a0001c0001t0002g0079 others(14): Show |
17 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.357+5404G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38903923 | |||||||
| chr17:38903948 | T | C | 1 | a0001c0002t0003g0239 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.357+5429T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38903948 | |||||||
| chr17:38904348 | T | G | 112 | a0001c0001t0001g0040 a0001c0001t0001g0092 a0001c0001t0001g0149 others(109): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.357+5829T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38904348 | |||||||
| chr17:38904364 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0016g0262 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.357+5845G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38904364 | |||||||
| chr17:38904383 | T | C | 89 | a0001c0001t0001g0078 a0001c0001t0001g0138 a0001c0001t0001g0161 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.357+5864T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38904383 | |||||||
| chr17:38904409 | A | G | 5 | a0001c0001t0006g0175 a0001c0001t0008g0021 a0001c0001t0008g0263 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.357+5890A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38904409 | |||||||
| chr17:38904430 | T | G | 1 | a0001c0001t0015g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.357+5911T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38904430 | |||||||
| chr17:38904517 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0006g0271 |
2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.357+5998C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38904517 | |||||||
| chr17:38904584 | C | T | 111 | a0001c0001t0001g0040 a0001c0001t0001g0092 a0001c0001t0001g0149 others(108): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.357+6065C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38904584 | |||||||
| chr17:38904588 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0014g0074 |
2 | HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.357+6069G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38904588 | |||||||
| chr17:38904598 | T | TA | 85 | a0001c0001t0001g0078 a0001c0001t0001g0138 a0001c0001t0001g0161 others(82): Show |
85 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.357+6092dupA | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38904598 | ||||||
| chr17:38904785 | C | T | 222 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0078 others(219): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.357+6266C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38904785 | |||||||
| chr17:38904807 | T | C | 1 | a0001c0002t0001g0247 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.357+6288T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38904807 | |||||||
| chr17:38904930 | A | G | 1 | a0001c0003t0001g0204 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.357+6411A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38904930 | |||||||
| chr17:38905073 | G | C | 1 | a0001c0001t0003g0174 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.357+6554G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38905073 | |||||||
| chr17:38905249 | C | T | 11 | a0001c0003t0002g0035 a0001c0003t0002g0075 a0001c0003t0002g0076 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.357+6730C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38905249 | |||||||
| chr17:38905250 | G | A | 7 | a0001c0003t0001g0036 a0001c0006t0003g0389 a0001c0006t0005g0029 others(4): Show |
7 | HG00673.hp2 HG02135.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.357+6731G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38905250 | |||||||
| chr17:38905344 | C | A | 6 | a0001c0006t0003g0389 a0001c0006t0005g0029 a0001c0006t0005g0165 others(3): Show |
6 | HG00673.hp2 HG02135.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+6825C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38905344 | |||||||
| chr17:38905388 | T | C | 224 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0078 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.357+6869T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38905388 | |||||||
| chr17:38905389 | G | A | 67 | a0001c0001t0001g0138 a0001c0001t0001g0161 a0001c0001t0001g0306 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.357+6870G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38905389 | |||||||
| chr17:38905530 | C | CA | 6 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0001t0004g0383 others(3): Show |
6 | HG01081.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+7031dupA | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38905530 | ||||||
| chr17:38905530 | C | CAAA | 57 | a0001c0001t0001g0078 a0001c0001t0001g0138 a0001c0001t0001g0161 others(54): Show |
57 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.357+7029_357+7031d others(5): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38905530 | ||||||
| chr17:38905530 | C | CAAAA | 25 | a0001c0001t0001g0189 a0001c0001t0001g0261 a0001c0001t0001g0326 others(22): Show |
25 | HG00673.hp2 HG01433.hp2 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.357+7028_357+7031d others(6): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38905530 | ||||||
| chr17:38905530 | CA | C | 104 | a0001c0001t0001g0040 a0001c0001t0001g0092 a0001c0001t0001g0149 others(101): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.357+7031delA | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38905530 | ||||||
| chr17:38905530 | CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0001g0011 a0001c0001t0006g0175 a0001c0001t0006g0271 others(4): Show |
7 | HG02280.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+7023_357+7031d others(11): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38905530 | ||||||
| chr17:38905594 | A | G | 1 | a0001c0001t0007g0327 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.357+7075A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38905594 | |||||||
| chr17:38905626 | A | G | 6 | a0001c0006t0003g0389 a0001c0006t0005g0029 a0001c0006t0005g0165 others(3): Show |
6 | HG00673.hp2 HG02135.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+7107A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38905626 | |||||||
| chr17:38905693 | T | C | 1 | a0001c0003t0004g0111 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.357+7174T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38905693 | |||||||
| chr17:38905906 | G | A | 1 | a0001c0001t0015g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.357+7387G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38905906 | |||||||
| chr17:38905941 | T | A | 3 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0007t0002g0141 |
3 | HG01081.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.357+7422T>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38905941 | |||||||
| chr17:38905952 | C | T | 1 | a0001c0005t0002g0114 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.357+7433C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38905952 | |||||||
| chr17:38905953 | G | A | 1 | a0001c0003t0001g0205 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.357+7434G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38905953 | |||||||
| chr17:38906016 | C | T | 27 | a0001c0001t0001g0078 a0001c0001t0001g0189 a0001c0001t0001g0261 others(24): Show |
27 | HG00673.hp2 HG01884.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.357+7497C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38906016 | |||||||
| chr17:38906094 | G | A | 194 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0092 others(191): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.357+7575G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38906094 | |||||||
| chr17:38906256 | G | A | 83 | a0001c0001t0001g0011 a0001c0001t0001g0138 a0001c0001t0001g0161 others(80): Show |
83 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.357+7737G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38906256 | |||||||
| chr17:38906330 | T | C | 40 | a0001c0001t0001g0073 a0001c0001t0001g0078 a0001c0001t0001g0189 others(37): Show |
40 | HG00673.hp2 HG01884.hp1 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.357+7811T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38906330 | |||||||
| chr17:38906331 | C | CA | 3 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0007t0002g0141 |
3 | HG01081.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.357+7813dupA | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38906331 | ||||||
| chr17:38906388 | G | A | 26 | a0001c0001t0001g0078 a0001c0001t0001g0189 a0001c0001t0001g0261 others(23): Show |
26 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.357+7869G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38906388 | |||||||
| chr17:38906496 | T | C | 10 | a0001c0001t0001g0011 a0001c0001t0001g0073 a0001c0001t0002g0190 others(7): Show |
10 | HG01891.hp2 HG02109.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.358-7829T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38906496 | |||||||
| chr17:38906527 | A | AAAAT | 3 | a0001c0002t0003g0239 a0001c0003t0001g0241 a0001c0005t0003g0380 |
3 | HG02738.hp1 HG03831.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.358-7774_358-7771d others(6): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38906527 | ||||||
| chr17:38906527 | A | AAAATAAA others(1): Show |
3 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0007t0002g0141 |
3 | HG01081.hp1 HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.358-7778_358-7771d others(10): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38906527 | ||||||
| chr17:38906527 | AAAAT | A | 17 | a0001c0001t0004g0188 a0001c0001t0004g0325 a0001c0001t0004g0382 others(14): Show |
17 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.358-7774_358-7771d others(6): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38906527 | ||||||
| chr17:38906594 | A | G | 81 | a0001c0001t0001g0138 a0001c0001t0001g0161 a0001c0001t0001g0306 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.358-7731A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38906594 | |||||||
| chr17:38906793 | C | T | 1 | a0001c0002t0003g0228 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.358-7532C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38906793 | |||||||
| chr17:38906798 | A | C | 1 | a0001c0001t0028g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.358-7527A>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38906798 | |||||||
| chr17:38906944 | C | A | 7 | a0001c0001t0001g0256 a0001c0001t0004g0267 a0001c0001t0014g0269 others(4): Show |
7 | HG02622.hp1 HG02922.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.358-7381C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38906944 | |||||||
| chr17:38907032 | C | T | 1 | a0001c0001t0002g0190 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.358-7293C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907032 | |||||||
| chr17:38907093 | A | G | 1 | a0001c0011t0002g0298 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.358-7232A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907093 | |||||||
| chr17:38907218 | A | C | 102 | a0001c0001t0001g0040 a0001c0001t0001g0078 a0001c0001t0001g0092 others(99): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.358-7107A>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907218 | |||||||
| chr17:38907251 | C | T | 2 | a0001c0001t0006g0018 a0001c0001t0006g0371 |
2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.358-7074C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907251 | |||||||
| chr17:38907252 | G | A | 15 | a0001c0001t0004g0084 a0001c0001t0004g0325 a0001c0001t0004g0382 others(12): Show |
15 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.358-7073G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907252 | |||||||
| chr17:38907292 | T | C | 110 | a0001c0001t0001g0073 a0001c0001t0001g0138 a0001c0001t0001g0161 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.358-7033T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907292 | |||||||
| chr17:38907341 | A | T | 5 | a0001c0001t0015g0265 a0001c0001t0028g0178 a0001c0003t0004g0047 others(2): Show |
5 | HG02615.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.358-6984A>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907341 | |||||||
| chr17:38907379 | A | G | 2 | a0001c0001t0002g0010 a0001c0001t0014g0074 |
2 | HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.358-6946A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907379 | |||||||
| chr17:38907553 | G | T | 24 | a0001c0001t0004g0084 a0001c0001t0004g0104 a0001c0001t0004g0105 others(21): Show |
24 | HG01081.hp1 HG01109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.358-6772G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907553 | |||||||
| chr17:38907573 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358-6752C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907573 | |||||||
| chr17:38907574 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.358-6751G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907574 | |||||||
| chr17:38907872 | T | C | 12 | a0001c0001t0006g0018 a0001c0001t0006g0371 a0001c0001t0008g0021 others(9): Show |
12 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.358-6453T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907872 | |||||||
| chr17:38907874 | T | C | 130 | a0001c0001t0001g0073 a0001c0001t0001g0078 a0001c0001t0001g0138 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.358-6451T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907874 | |||||||
| chr17:38907903 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0016g0262 |
2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.358-6422A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907903 | |||||||
| chr17:38907908 | C | T | 65 | a0001c0001t0001g0138 a0001c0001t0001g0161 a0001c0001t0001g0306 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.358-6417C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38907908 | |||||||
| chr17:38908095 | G | A | 348 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(345): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.358-6230G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908095 | |||||||
| chr17:38908196 | G | A | 6 | a0001c0006t0003g0389 a0001c0006t0005g0029 a0001c0006t0005g0165 others(3): Show |
6 | HG00673.hp2 HG02135.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.358-6129G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908196 | |||||||
| chr17:38908224 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0149 |
2 | HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.358-6101C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908224 | |||||||
| chr17:38908317 | C | G | 6 | a0001c0006t0003g0389 a0001c0006t0005g0029 a0001c0006t0005g0165 others(3): Show |
6 | HG00673.hp2 HG02135.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.358-6008C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908317 | |||||||
| chr17:38908420 | A | G | 349 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(346): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.358-5905A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908420 | |||||||
| chr17:38908500 | G | A | 1 | a0001c0001t0030g0020 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.358-5825G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908500 | |||||||
| chr17:38908545 | C | T | 145 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0050 others(142): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.358-5780C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908545 | |||||||
| chr17:38908563 | C | T | 2 | a0001c0001t0008g0021 a0001c0001t0008g0263 |
2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.358-5762C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908563 | |||||||
| chr17:38908689 | C | T | 250 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.358-5636C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908689 | |||||||
| chr17:38908755 | T | C | 253 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(250): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.358-5570T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908755 | |||||||
| chr17:38908791 | G | T | 2 | a0001c0002t0003g0148 a0001c0002t0003g0365 |
2 | HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.358-5534G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908791 | |||||||
| chr17:38908953 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0050 |
2 | HG03239.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.358-5372C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908953 | |||||||
| chr17:38908971 | G | A | 13 | a0001c0001t0001g0155 a0001c0002t0001g0028 a0001c0002t0001g0091 others(10): Show |
13 | HG00735.hp1 HG01261.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.358-5354G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908971 | |||||||
| chr17:38908985 | C | T | 1 | a0001c0001t0004g0267 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.358-5340C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38908985 | |||||||
| chr17:38909125 | G | A | 2 | a0001c0001t0001g0306 a0001c0002t0003g0307 |
2 | NA18962.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.358-5200G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38909125 | |||||||
| chr17:38909262 | A | G | 256 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(253): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.358-5063A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38909262 | |||||||
| chr17:38909412 | G | T | 1 | a0001c0004t0002g0128 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.358-4913G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38909412 | |||||||
| chr17:38909424 | T | C | 255 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(252): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.358-4901T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38909424 | |||||||
| chr17:38909435 | T | C | 273 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(270): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.358-4890T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38909435 | |||||||
| chr17:38909436 | G | A | 6 | a0001c0001t0009g0099 a0001c0001t0009g0110 a0001c0001t0009g0323 others(3): Show |
6 | HG02145.hp2 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.358-4889G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38909436 | |||||||
| chr17:38909484 | A | G | 254 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(251): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.358-4841A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38909484 | |||||||
| chr17:38909728 | C | CTCAT | 157 | a0001c0001t0001g0037 a0001c0001t0001g0050 a0001c0001t0001g0073 others(154): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.358-4567_358-4564d others(6): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38909728 | ||||||
| chr17:38909728 | C | CTCATTCA others(1): Show |
20 | a0001c0001t0001g0127 a0001c0001t0001g0155 a0001c0001t0001g0242 others(17): Show |
20 | HG00609.hp1 HG01070.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.358-4571_358-4564d others(10): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38909728 | ||||||
| chr17:38909728 | C | CTCATTCA others(5): Show |
1 | a0001c0005t0003g0041 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.358-4575_358-4564d others(14): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38909728 | ||||||
| chr17:38909728 | CTCAT | C | 42 | a0001c0001t0001g0256 a0001c0001t0001g0335 a0001c0001t0002g0374 others(39): Show |
42 | HG00673.hp2 HG01346.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.358-4567_358-4564d others(6): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38909728 | ||||||
| chr17:38909891 | G | A | 12 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0001t0006g0018 others(9): Show |
12 | HG01081.hp1 HG01109.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.358-4434G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38909891 | |||||||
| chr17:38909915 | G | T | 10 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0001t0006g0175 others(7): Show |
10 | HG01081.hp1 HG01109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.358-4410G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38909915 | |||||||
| chr17:38909920 | G | A | 1 | a0001c0001t0007g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.358-4405G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38909920 | |||||||
| chr17:38910076 | G | A | 2 | a0001c0001t0004g0017 a0001c0001t0004g0383 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.358-4249G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910076 | |||||||
| chr17:38910085 | T | C | 56 | a0001c0001t0001g0138 a0001c0001t0001g0243 a0001c0001t0001g0264 others(53): Show |
56 | HG00280.hp2 HG00408.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.358-4240T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910085 | |||||||
| chr17:38910153 | G | A | 2 | a0001c0001t0002g0124 a0001c0001t0002g0142 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.358-4172G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910153 | |||||||
| chr17:38910169 | T | G | 1 | a0001c0004t0002g0377 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.358-4156T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910169 | |||||||
| chr17:38910197 | A | G | 146 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(143): Show |
148 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.358-4128A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910197 | |||||||
| chr17:38910202 | A | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0162 a0001c0003t0001g0205 |
3 | HG02056.hp1 NA18940.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.358-4123A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910202 | |||||||
| chr17:38910555 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0016g0262 others(4): Show |
7 | HG02486.hp1 HG02559.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.358-3770C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910555 | |||||||
| chr17:38910571 | G | A | 100 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(97): Show |
102 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.358-3754G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910571 | |||||||
| chr17:38910577 | A | G | 3 | a0001c0001t0002g0190 a0001c0001t0006g0018 a0001c0001t0006g0371 |
3 | HG02630.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.358-3748A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910577 | |||||||
| chr17:38910733 | C | CTTTTTTT others(6): Show |
14 | a0001c0001t0001g0138 a0001c0001t0001g0335 a0001c0001t0002g0353 others(11): Show |
14 | HG00280.hp2 HG01070.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.358-3584_358-3583i others(15): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38910733 | ||||||
| chr17:38910733 | C | CTTTTTTT others(7): Show |
103 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0001g0189 others(100): Show |
103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.358-3584_358-3583i others(16): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38910733 | ||||||
| chr17:38910733 | C | CTTTTTTT others(8): Show |
99 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(96): Show |
101 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.358-3584_358-3583i others(17): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38910733 | ||||||
| chr17:38910733 | C | CTTTTTTT others(9): Show |
27 | a0001c0001t0001g0092 a0001c0001t0001g0161 a0001c0001t0001g0162 others(24): Show |
27 | HG00738.hp1 HG01106.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.358-3584_358-3583i others(18): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38910733 | ||||||
| chr17:38910733 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0003g0174 a0001c0003t0001g0203 a0001c0004t0002g0377 |
3 | HG02818.hp2 NA18981.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.358-3584_358-3583i others(19): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38910733 | ||||||
| chr17:38910759 | G | C | 52 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0002g0010 others(49): Show |
52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.358-3566G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910759 | |||||||
| chr17:38910767 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0322 |
2 | HG02027.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.358-3558G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910767 | |||||||
| chr17:38910801 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.358-3524C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910801 | |||||||
| chr17:38910808 | C | T | 245 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.358-3517C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910808 | |||||||
| chr17:38910832 | C | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0001g0335 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.358-3493C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910832 | |||||||
| chr17:38910912 | G | A | 99 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(96): Show |
101 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.358-3413G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910912 | |||||||
| chr17:38910913 | G | A | 2 | a0001c0001t0006g0018 a0001c0001t0006g0371 |
2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.358-3412G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910913 | |||||||
| chr17:38910914 | C | G | 99 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(96): Show |
101 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.358-3411C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910914 | |||||||
| chr17:38910915 | A | G | 99 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(96): Show |
101 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.358-3410A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910915 | |||||||
| chr17:38910961 | G | A | 1 | a0001c0002t0003g0134 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.358-3364G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38910961 | |||||||
| chr17:38911003 | G | A | 1 | a0001c0001t0002g0152 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.358-3322G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911003 | |||||||
| chr17:38911008 | T | C | 246 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(243): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.358-3317T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911008 | |||||||
| chr17:38911013 | G | A | 1 | a0001c0002t0003g0196 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.358-3312G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911013 | |||||||
| chr17:38911019 | G | A | 1 | a0001c0002t0003g0307 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.358-3306G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911019 | |||||||
| chr17:38911055 | G | T | 13 | a0001c0006t0001g0210 a0001c0006t0001g0229 a0001c0006t0003g0389 others(10): Show |
13 | HG00673.hp2 HG02015.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.358-3270G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911055 | |||||||
| chr17:38911109 | C | T | 246 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(243): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.358-3216C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911109 | |||||||
| chr17:38911114 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.358-3211C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911114 | |||||||
| chr17:38911121 | A | T | 1 | a0001c0001t0015g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.358-3204A>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911121 | |||||||
| chr17:38911186 | G | T | 1 | a0002c0015t0001g0386 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.358-3139G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911186 | |||||||
| chr17:38911198 | C | T | 1 | a0001c0001t0004g0245 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.358-3127C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911198 | |||||||
| chr17:38911228 | A | T | 50 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0002g0010 others(47): Show |
50 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(47): Show |
intron_variant | MODIFIER | c.358-3097A>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911228 | |||||||
| chr17:38911429 | G | A | 1 | a0001c0002t0003g0313 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.358-2896G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911429 | |||||||
| chr17:38911444 | C | CT | 248 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.358-2880dupT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38911444 | ||||||
| chr17:38911497 | T | C | 1 | a0001c0002t0006g0016 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.358-2828T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911497 | |||||||
| chr17:38911586 | G | A | 104 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(101): Show |
106 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.358-2739G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911586 | |||||||
| chr17:38911681 | G | A | 66 | a0001c0001t0001g0011 a0001c0001t0001g0073 a0001c0001t0001g0078 others(63): Show |
66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.358-2644G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911681 | |||||||
| chr17:38911787 | C | CT | 131 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(128): Show |
133 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.358-2528dupT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38911787 | ||||||
| chr17:38911817 | G | A | 2 | a0001c0007t0002g0172 a0001c0007t0002g0373 |
2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.358-2508G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911817 | |||||||
| chr17:38911875 | C | T | 130 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(127): Show |
132 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.358-2450C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911875 | |||||||
| chr17:38911921 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.358-2404G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911921 | |||||||
| chr17:38911929 | G | A | 1 | a0001c0001t0007g0327 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.358-2396G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38911929 | |||||||
| chr17:38912067 | T | A | 1 | a0001c0001t0001g0335 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.358-2258T>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38912067 | |||||||
| chr17:38912103 | G | A | 246 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(243): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.358-2222G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38912103 | |||||||
| chr17:38912104 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.358-2221C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38912104 | |||||||
| chr17:38912177 | G | A | 1 | a0001c0001t0015g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.358-2148G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38912177 | |||||||
| chr17:38912207 | C | G | 108 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(105): Show |
110 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.358-2118C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38912207 | |||||||
| chr17:38912236 | C | T | 1 | a0001c0001t0002g0312 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.358-2089C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38912236 | |||||||
| chr17:38912238 | G | A | 131 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(128): Show |
133 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.358-2087G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38912238 | |||||||
| chr17:38912354 | G | C | 1 | a0001c0006t0005g0165 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.358-1971G>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38912354 | |||||||
| chr17:38912682 | G | T | 110 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(107): Show |
112 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.358-1643G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38912682 | |||||||
| chr17:38912690 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.358-1635G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38912690 | |||||||
| chr17:38912842 | G | A | 7 | a0001c0001t0002g0013 a0001c0001t0002g0079 a0001c0001t0002g0081 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.358-1483G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38912842 | |||||||
| chr17:38912992 | C | T | 1 | a0001c0001t0008g0263 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.358-1333C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38912992 | |||||||
| chr17:38913034 | C | T | 3 | a0001c0002t0004g0014 a0001c0002t0006g0016 a0001c0002t0015g0339 |
3 | HG02486.hp1 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.358-1291C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38913034 | |||||||
| chr17:38913099 | C | G | 1 | a0001c0003t0003g0057 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.358-1226C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38913099 | |||||||
| chr17:38913114 | C | T | 14 | a0001c0006t0001g0210 a0001c0006t0001g0229 a0001c0006t0002g0347 others(11): Show |
14 | HG00673.hp2 HG02015.hp2 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.358-1211C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38913114 | |||||||
| chr17:38913141 | A | G | 136 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(133): Show |
138 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.358-1184A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38913141 | |||||||
| chr17:38913306 | C | A | 1 | a0001c0002t0029g0324 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.358-1019C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38913306 | |||||||
| chr17:38913312 | C | T | 4 | a0001c0001t0001g0189 a0001c0001t0001g0242 a0001c0001t0001g0326 others(1): Show |
4 | HG02055.hp2 HG02896.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-1013C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38913312 | |||||||
| chr17:38913332 | A | G | 1 | a0001c0004t0001g0359 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.358-993A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38913332 | |||||||
| chr17:38913455 | A | T | 1 | a0001c0002t0001g0028 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.358-870A>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38913455 | |||||||
| chr17:38913729 | C | T | 3 | a0001c0002t0004g0014 a0001c0002t0006g0016 a0001c0002t0015g0339 |
3 | HG02486.hp1 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.358-596C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38913729 | |||||||
| chr17:38913837 | A | AC | 248 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.358-488_358-487ins others(1): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38913837 | |||||||
| chr17:38913839 | T | A | 248 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.358-486T>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38913839 | |||||||
| chr17:38913942 | C | T | 48 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0002g0010 others(45): Show |
48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.358-383C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38913942 | |||||||
| chr17:38914002 | G | GA | 51 | a0001c0001t0001g0138 a0001c0001t0001g0306 a0001c0001t0001g0341 others(48): Show |
51 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.358-308dupA | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 38914002 | ||||||
| chr17:38914137 | A | C | 1 | a0001c0002t0003g0248 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.358-188A>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38914137 | |||||||
| chr17:38914148 | T | C | 1 | a0001c0001t0002g0284 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.358-177T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 4/6 | chr17 | 38914148 | |||||||
| chr17:38914484 | A | G | 246 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(243): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.508+9A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/6 | chr17 | 38914484 | |||||||
| chr17:38914640 | G | A | 62 | a0001c0001t0001g0138 a0001c0001t0001g0306 a0001c0001t0001g0341 others(59): Show |
62 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.508+165G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/6 | chr17 | 38914640 | |||||||
| chr17:38914677 | G | GAC | 8 | a0001c0002t0001g0362 a0001c0002t0002g0240 a0001c0002t0002g0348 others(5): Show |
8 | HG00280.hp1 HG00733.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.508+238_508+239dup others(2): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 38914677 | ||||||
| chr17:38914677 | GAC | G | 68 | a0001c0001t0001g0106 a0001c0001t0001g0295 a0001c0001t0001g0296 others(65): Show |
71 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.508+238_508+239del others(2): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 38914677 | ||||||
| chr17:38914677 | GACAC | G | 55 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0001g0150 others(52): Show |
55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.508+236_508+239del others(4): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 38914677 | ||||||
| chr17:38914677 | GACACAC | G | 203 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(200): Show |
205 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.508+234_508+239del others(6): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 38914677 | ||||||
| chr17:38914677 | GACACACA others(3): Show |
G | 2 | a0001c0002t0004g0014 a0001c0002t0006g0016 |
2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.508+230_508+239del others(10): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 38914677 | ||||||
| chr17:38914735 | A | T | 251 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.508+260A>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/6 | chr17 | 38914735 | |||||||
| chr17:38914741 | A | G | 265 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(262): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.508+266A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/6 | chr17 | 38914741 | |||||||
| chr17:38914833 | G | A | 1 | a0001c0004t0002g0370 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.509-210G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/6 | chr17 | 38914833 | |||||||
| chr17:38914936 | C | T | 248 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(245): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.509-107C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/6 | chr17 | 38914936 | |||||||
| chr17:38914976 | C | T | 4 | a0001c0003t0001g0002 a0001c0003t0001g0067 a0001c0003t0001g0276 others(1): Show |
5 | HG00735.hp2 HG01175.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-67C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/6 | chr17 | 38914976 | |||||||
| chr17:38914982 | C | G | 1 | a0001c0001t0001g0319 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.509-61C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 5/6 | chr17 | 38914982 | |||||||
| chr17:38915182 | CA | C | 3 | a0001c0002t0004g0014 a0001c0002t0006g0016 a0001c0002t0015g0339 |
3 | HG02486.hp1 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.612+37delA | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38915182 | |||||||
| chr17:38915330 | G | A | 1 | a0001c0004t0020g0042 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.612+184G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38915330 | |||||||
| chr17:38915508 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.612+362G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38915508 | |||||||
| chr17:38915699 | A | T | 1 | a0001c0001t0001g0304 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.612+553A>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38915699 | |||||||
| chr17:38915742 | T | C | 263 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(260): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.612+596T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38915742 | |||||||
| chr17:38915743 | G | A | 1 | a0001c0001t0006g0371 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.612+597G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38915743 | |||||||
| chr17:38915820 | G | A | 73 | a0001c0001t0001g0138 a0001c0001t0001g0306 a0001c0001t0001g0335 others(70): Show |
73 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.612+674G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38915820 | |||||||
| chr17:38915838 | T | C | 3 | a0001c0001t0006g0018 a0001c0001t0006g0371 a0001c0001t0030g0020 |
3 | HG02630.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.612+692T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38915838 | |||||||
| chr17:38915861 | C | T | 2 | a0001c0001t0027g0095 a0001c0001t0028g0178 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.612+715C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38915861 | |||||||
| chr17:38915871 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.612+725C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38915871 | |||||||
| chr17:38915939 | T | G | 74 | a0001c0001t0001g0138 a0001c0001t0001g0306 a0001c0001t0001g0335 others(71): Show |
74 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.612+793T>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38915939 | |||||||
| chr17:38916018 | G | A | 1 | a0001c0003t0005g0215 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.612+872G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916018 | |||||||
| chr17:38916076 | A | G | 2 | a0001c0002t0017g0086 a0001c0002t0017g0332 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.612+930A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916076 | |||||||
| chr17:38916203 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.612+1057G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916203 | |||||||
| chr17:38916281 | C | T | 2 | a0001c0006t0002g0347 a0001c0006t0005g0029 |
2 | HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.612+1135C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916281 | |||||||
| chr17:38916297 | C | T | 2 | a0001c0002t0017g0086 a0001c0002t0017g0332 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.612+1151C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916297 | |||||||
| chr17:38916344 | G | T | 1 | a0001c0001t0002g0281 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.612+1198G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916344 | |||||||
| chr17:38916372 | C | G | 115 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(112): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.612+1226C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916372 | |||||||
| chr17:38916388 | C | T | 114 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(111): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.612+1242C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916388 | |||||||
| chr17:38916441 | C | A | 1 | a0001c0003t0003g0057 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.612+1295C>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916441 | |||||||
| chr17:38916459 | C | T | 6 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0001t0006g0175 others(3): Show |
6 | HG02280.hp2 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.612+1313C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916459 | |||||||
| chr17:38916492 | G | A | 4 | a0001c0001t0007g0275 a0001c0003t0004g0047 a0001c0003t0004g0077 others(1): Show |
4 | HG02615.hp1 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+1346G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916492 | |||||||
| chr17:38916523 | CACTATTG others(4): Show |
C | 14 | a0001c0002t0003g0001 a0001c0002t0003g0134 a0001c0002t0003g0192 others(11): Show |
16 | HG00423.hp1 NA18941.hp2 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.612+1378_612+1388d others(13): Show |
LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916523 | |||||||
| chr17:38916585 | G | T | 1 | a0001c0001t0001g0335 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.612+1439G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916585 | |||||||
| chr17:38916590 | G | A | 103 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(100): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.612+1444G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916590 | |||||||
| chr17:38916659 | C | T | 1 | a0001c0007t0002g0141 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.612+1513C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916659 | |||||||
| chr17:38916697 | A | G | 1 | a0001c0002t0003g0208 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.612+1551A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916697 | |||||||
| chr17:38916705 | T | C | 1 | a0001c0002t0010g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.612+1559T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916705 | |||||||
| chr17:38916719 | G | A | 1 | a0001c0001t0007g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.612+1573G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916719 | |||||||
| chr17:38916788 | G | A | 1 | a0001c0003t0004g0120 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.612+1642G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916788 | |||||||
| chr17:38916817 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.612+1671C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916817 | |||||||
| chr17:38916929 | G | A | 62 | a0001c0001t0001g0040 a0001c0001t0001g0092 a0001c0001t0001g0106 others(59): Show |
63 | HG00558.hp1 HG00609.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.613-1676G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916929 | |||||||
| chr17:38916935 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.613-1670C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38916935 | |||||||
| chr17:38917038 | G | A | 1 | a0001c0006t0005g0029 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.613-1567G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38917038 | |||||||
| chr17:38917279 | G | A | 55 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0078 others(52): Show |
55 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.613-1326G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38917279 | |||||||
| chr17:38917283 | T | A | 1 | a0001c0001t0001g0226 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.613-1322T>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38917283 | |||||||
| chr17:38917398 | C | T | 1 | a0001c0002t0002g0206 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.613-1207C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38917398 | |||||||
| chr17:38917423 | T | A | 75 | a0001c0001t0001g0037 a0001c0001t0001g0050 a0001c0001t0001g0127 others(72): Show |
77 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.613-1182T>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38917423 | |||||||
| chr17:38917606 | G | T | 1 | a0001c0008t0002g0255 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.613-999G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38917606 | |||||||
| chr17:38917683 | G | GT | 12 | a0001c0001t0001g0335 a0001c0002t0003g0135 a0001c0002t0005g0194 others(9): Show |
12 | HG00621.hp1 HG01884.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.613-912dupT | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 38917683 | ||||||
| chr17:38917694 | C | T | 1 | a0001c0002t0003g0197 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.613-911C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38917694 | |||||||
| chr17:38917771 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.613-834C>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38917771 | |||||||
| chr17:38917901 | G | A | 3 | a0001c0003t0002g0035 a0001c0003t0002g0075 a0001c0003t0002g0076 |
3 | HG02976.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.613-704G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38917901 | |||||||
| chr17:38917946 | G | A | 1 | a0001c0003t0001g0363 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.613-659G>A | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38917946 | |||||||
| chr17:38918015 | T | C | 304 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(301): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.613-590T>C | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38918015 | |||||||
| chr17:38918056 | C | T | 23 | a0001c0001t0004g0017 a0001c0001t0004g0084 a0001c0001t0004g0104 others(20): Show |
23 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.613-549C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38918056 | |||||||
| chr17:38918139 | C | CA | 10 | a0001c0002t0005g0194 a0001c0002t0005g0198 a0001c0003t0005g0215 others(7): Show |
10 | HG00621.hp1 HG02015.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.613-449dupA | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 38918139 | ||||||
| chr17:38918139 | CA | C | 13 | a0001c0002t0003g0197 a0001c0002t0003g0238 a0001c0002t0003g0310 others(10): Show |
13 | HG00558.hp1 HG02015.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.613-449delA | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 38918139 | ||||||
| chr17:38918157 | G | T | 1 | a0001c0013t0016g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.613-448G>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38918157 | |||||||
| chr17:38918240 | C | T | 1 | a0001c0002t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.613-365C>T | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38918240 | |||||||
| chr17:38918449 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.613-156A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38918449 | |||||||
| chr17:38918592 | A | G | 1 | a0001c0002t0003g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.613-13A>G | LASP1 | ENSG00000002834.19 | transcript | ENST00000318008.11 | protein_coding | 6/6 | chr17 | 38918592 |