| geneid | 56624 |
|---|---|
| ensemblid | ENSG00000188611.17 |
| hgncid | 18860 |
| symbol | ASAH2 |
| name | N-acylsphingosine amidohydrolase 2 |
| refseq_nuc | NM_019893.4 |
| refseq_prot | NP_063946.2 |
| ensembl_nuc | ENST00000682911.1 |
| ensembl_prot | ENSP00000506746.1 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 50184861 |
| end | 50251516 |
| strand | - |
| ver | v1.2 |
| region | chr10:50184861-50251516 |
| region5000 | chr10:50179861-50256516 |
| regionname0 | ASAH2_chr10_50184861_50251516 |
| regionname5000 | ASAH2_chr10_50179861_50256516 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 780 | 174 | 70 | 23 | 68 | 0 | 12 | 54 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002 | 0/1 | 780 | 132 | 19 | 31 | 61 | 7 | 13 | 44 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003 | 0/0 | 780 | 91 | 3 | 20 | 56 | 8 | 4 | 45 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0004 | 0/0 | 780 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0005 | 0/0 | 780 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0006 | 0/0 | 82 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0007 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0008 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0009 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0010 | 0/0 | 780 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0011 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0012 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2343 | 122 | 15 | 30 | 56 | 7 | 13 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0002 | 0/0 | 2343 | 87 | 27 | 8 | 44 | 0 | 8 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0003 | 0/0 | 2343 | 87 | 3 | 20 | 52 | 8 | 4 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0004 | 0/0 | 2343 | 37 | 8 | 6 | 20 | 0 | 3 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0005 | 1/0 | 2343 | 34 | 23 | 6 | 3 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0006 | 0/0 | 2343 | 7 | 3 | 0 | 4 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0007 | 0/0 | 2343 | 5 | 4 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0008 | 0/0 | 2343 | 4 | 0 | 0 | 4 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0009 | 0/0 | 2343 | 3 | 1 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0010 | 0/0 | 2343 | 3 | 3 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0011 | 0/0 | 2343 | 3 | 2 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0012 | 0/0 | 2343 | 2 | 1 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0013 | 0/0 | 2343 | 2 | 1 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0014 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0015 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0016 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0017 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0018 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0019 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0020 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0021 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0022 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0023 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0024 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| c0025 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2610 | 47 | 1 | 7 | 32 | 4 | 3 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0002 | 0/0 | 2617 | 25 | 0 | 10 | 13 | 2 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0003 | 0/0 | 2610 | 22 | 0 | 0 | 22 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0004 | 0/0 | 2615 | 15 | 0 | 2 | 12 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0005 | 0/0 | 2606 | 14 | 4 | 7 | 3 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0006 | 0/0 | 2615 | 11 | 2 | 2 | 5 | 0 | 2 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0007 | 0/0 | 2601 | 11 | 9 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0008 | 0/0 | 2619 | 10 | 1 | 6 | 0 | 0 | 3 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0009 | 1/0 | 2613 | 10 | 8 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0010 | 0/0 | 2610 | 9 | 2 | 3 | 4 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0011 | 0/0 | 2612 | 8 | 1 | 4 | 3 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0012 | 0/0 | 2603 | 8 | 0 | 0 | 8 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0013 | 0/0 | 2614 | 7 | 0 | 0 | 5 | 0 | 2 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0014 | 0/0 | 2610 | 7 | 0 | 0 | 7 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0015 | 0/0 | 2610 | 7 | 0 | 2 | 0 | 4 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0016 | 0/0 | 2613 | 7 | 1 | 0 | 3 | 0 | 3 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0017 | 0/0 | 2613 | 6 | 0 | 0 | 6 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0018 | 0/0 | 2617 | 6 | 0 | 1 | 1 | 3 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0019 | 0/0 | 2617 | 6 | 5 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0020 | 0/0 | 2620 | 6 | 5 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0021 | 0/0 | 2613 | 5 | 0 | 1 | 4 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0022 | 0/0 | 2616 | 5 | 0 | 0 | 5 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0023 | 0/0 | 2612 | 5 | 0 | 0 | 5 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0024 | 0/0 | 2612 | 5 | 0 | 3 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0025 | 0/0 | 2619 | 5 | 5 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0026 | 0/0 | 2619 | 5 | 0 | 5 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0027 | 0/0 | 2615 | 4 | 1 | 1 | 0 | 0 | 2 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0028 | 0/0 | 2613 | 4 | 3 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0029 | 0/0 | 2615 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0030 | 0/0 | 2623 | 3 | 0 | 1 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0031 | 0/0 | 2610 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0032 | 0/0 | 2608 | 3 | 0 | 3 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0033 | 0/0 | 2613 | 3 | 1 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0034 | 0/0 | 2611 | 3 | 0 | 3 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0035 | 0/0 | 2611 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0036 | 0/0 | 2619 | 3 | 0 | 1 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0037 | 0/0 | 2615 | 3 | 3 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0038 | 0/0 | 2612 | 3 | 2 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0039 | 0/0 | 2625 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0040 | 0/0 | 2621 | 2 | 0 | 1 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0041 | 0/0 | 2601 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0042 | 0/0 | 2621 | 2 | 0 | 0 | 0 | 1 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0043 | 0/0 | 2597 | 2 | 0 | 0 | 1 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0044 | 0/0 | 2606 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0045 | 0/0 | 2618 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0046 | 0/0 | 2613 | 2 | 1 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0047 | 0/0 | 2604 | 2 | 1 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0048 | 0/0 | 2615 | 2 | 0 | 0 | 1 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0049 | 0/0 | 2613 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0050 | 0/0 | 2606 | 2 | 0 | 1 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0051 | 0/0 | 2617 | 2 | 0 | 0 | 0 | 0 | 2 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0052 | 0/0 | 2609 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0053 | 0/0 | 2617 | 2 | 0 | 0 | 1 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0054 | 0/0 | 2613 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0055 | 0/0 | 2617 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0056 | 0/0 | 2610 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0057 | 0/0 | 2621 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0058 | 0/0 | 2617 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0059 | 0/0 | 2611 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0060 | 0/0 | 2617 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0061 | 0/0 | 2619 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0062 | 0/0 | 2617 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0063 | 0/1 | 2613 | 1 | 0 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0064 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0065 | 0/0 | 2616 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0066 | 0/0 | 2612 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0067 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0068 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0069 | 0/0 | 2602 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0070 | 0/0 | 2618 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0071 | 0/0 | 2617 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0072 | 0/0 | 2616 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0073 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0074 | 0/0 | 2615 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0075 | 0/0 | 2614 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0076 | 0/0 | 2612 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0077 | 0/0 | 2612 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0078 | 0/0 | 2612 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0079 | 0/0 | 2612 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0080 | 0/0 | 2611 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0081 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0082 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0083 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0084 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0085 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0086 | 0/0 | 2602 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0087 | 0/0 | 2612 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0088 | 0/0 | 2614 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0089 | 0/0 | 2614 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0090 | 0/0 | 2611 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0091 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0092 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0093 | 0/0 | 2607 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0094 | 0/0 | 2606 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0095 | 0/0 | 2619 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0096 | 0/0 | 2617 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0097 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0098 | 0/0 | 2612 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0099 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0100 | 0/0 | 2610 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0101 | 0/0 | 2607 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0102 | 0/0 | 2596 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0103 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0104 | 0/0 | 2613 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0105 | 0/0 | 2617 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0106 | 0/0 | 2612 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0107 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0108 | 0/0 | 2617 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0109 | 0/0 | 2620 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0110 | 0/0 | 2624 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0111 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0112 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0113 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0114 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0115 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0116 | 0/0 | 2603 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0117 | 0/0 | 2606 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| t0118 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 2343 | 87 | 27 | 8 | 44 | 0 | 8 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004 | 0/0 | 2343 | 37 | 8 | 6 | 20 | 0 | 3 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005 | 1/0 | 2343 | 34 | 23 | 6 | 3 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0007 | 0/0 | 2343 | 5 | 4 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0009 | 0/0 | 2343 | 3 | 1 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0010 | 0/0 | 2343 | 3 | 3 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0011 | 0/0 | 2343 | 3 | 2 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0015 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0018 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001 | 0/1 | 2343 | 122 | 15 | 30 | 56 | 7 | 13 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0006 | 0/0 | 2343 | 7 | 3 | 0 | 4 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0016 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0022 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0024 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003 | 0/0 | 2343 | 87 | 3 | 20 | 52 | 8 | 4 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0008 | 0/0 | 2343 | 4 | 0 | 0 | 4 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0004c0013 | 0/0 | 2343 | 2 | 1 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0005c0012 | 0/0 | 2343 | 2 | 1 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0006c0020 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0007c0017 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0008c0023 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0009c0021 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0010c0025 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0011c0019 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0012c0014 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 4952 | 4 | 0 | 1 | 2 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0003 | 0/0 | 4952 | 15 | 0 | 0 | 15 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0004 | 0/0 | 4957 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0005 | 0/0 | 4948 | 6 | 2 | 3 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0006 | 0/0 | 4957 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0009 | 0/0 | 4955 | 4 | 3 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0010 | 0/0 | 4952 | 6 | 1 | 1 | 4 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0011 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0013 | 0/0 | 4956 | 5 | 0 | 0 | 4 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0014 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0019 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0022 | 0/0 | 4958 | 5 | 0 | 0 | 5 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0023 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0025 | 0/0 | 4961 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0028 | 0/0 | 4955 | 4 | 3 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0044 | 0/0 | 4948 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0045 | 0/0 | 4960 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0047 | 0/0 | 4946 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0049 | 0/0 | 4955 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0050 | 0/0 | 4948 | 2 | 0 | 1 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0051 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0052 | 0/0 | 4951 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0053 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0056 | 0/0 | 4952 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0064 | 0/0 | 4955 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0065 | 0/0 | 4958 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0066 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0068 | 0/0 | 4950 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0071 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0074 | 0/0 | 4957 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0076 | 0/0 | 4954 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0077 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0080 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0082 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0083 | 0/0 | 4952 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0084 | 0/0 | 4951 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0085 | 0/0 | 4951 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0091 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0096 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0103 | 0/0 | 4955 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0002t0118 | 0/0 | 4955 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0006 | 0/0 | 4957 | 8 | 2 | 2 | 3 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0012 | 0/0 | 4945 | 8 | 0 | 0 | 8 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0013 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0020 | 0/0 | 4962 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0033 | 0/0 | 4955 | 3 | 1 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0034 | 0/0 | 4953 | 3 | 0 | 3 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0036 | 0/0 | 4961 | 3 | 0 | 1 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0046 | 0/0 | 4955 | 2 | 1 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0048 | 0/0 | 4957 | 2 | 0 | 0 | 1 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0051 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0053 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0090 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0095 | 0/0 | 4961 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0004t0097 | 0/0 | 4955 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0003 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0008 | 0/0 | 4961 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0009 | 1/0 | 4955 | 5 | 4 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0011 | 0/0 | 4954 | 6 | 1 | 4 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0013 | 0/0 | 4956 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0019 | 0/0 | 4959 | 4 | 3 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0025 | 0/0 | 4961 | 4 | 4 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0037 | 0/0 | 4957 | 3 | 3 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0052 | 0/0 | 4951 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0055 | 0/0 | 4959 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0093 | 0/0 | 4949 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0098 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0099 | 0/0 | 4952 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0107 | 0/0 | 4955 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0116 | 0/0 | 4945 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0005t0117 | 0/0 | 4948 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0007t0020 | 0/0 | 4962 | 3 | 2 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0007t0038 | 0/0 | 4954 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0009t0010 | 0/0 | 4952 | 3 | 1 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0010t0069 | 0/0 | 4944 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0010t0087 | 0/0 | 4954 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0010t0102 | 0/0 | 4938 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0011t0006 | 0/0 | 4957 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0011t0020 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0011t0109 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0015t0094 | 0/0 | 4948 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0001c0018t0009 | 0/0 | 4955 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0002 | 0/0 | 4959 | 23 | 0 | 10 | 11 | 2 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0003 | 0/0 | 4952 | 4 | 0 | 0 | 4 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0004 | 0/0 | 4957 | 12 | 0 | 2 | 9 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0007 | 0/0 | 4943 | 11 | 9 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0008 | 0/0 | 4961 | 9 | 0 | 6 | 0 | 0 | 3 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0011 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0016 | 0/0 | 4955 | 5 | 0 | 0 | 3 | 0 | 2 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0017 | 0/0 | 4955 | 6 | 0 | 0 | 6 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0018 | 0/0 | 4959 | 6 | 0 | 1 | 1 | 3 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0021 | 0/0 | 4955 | 5 | 0 | 1 | 4 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0026 | 0/0 | 4961 | 5 | 0 | 5 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0027 | 0/0 | 4957 | 4 | 1 | 1 | 0 | 0 | 2 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0029 | 0/0 | 4957 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0030 | 0/0 | 4965 | 3 | 0 | 1 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0035 | 0/0 | 4953 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0039 | 0/0 | 4967 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0040 | 0/0 | 4963 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0041 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0042 | 0/0 | 4963 | 2 | 0 | 0 | 0 | 1 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0043 | 0/0 | 4939 | 2 | 0 | 0 | 1 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0054 | 0/0 | 4955 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0057 | 0/0 | 4963 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0058 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0059 | 0/0 | 4953 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0060 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0062 | 0/0 | 4959 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0063 | 0/1 | 4955 | 1 | 0 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0104 | 0/0 | 4955 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0105 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0108 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0111 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0112 | 0/0 | 4939 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0113 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0001t0115 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0006t0002 | 0/0 | 4959 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0006t0004 | 0/0 | 4957 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0006t0101 | 0/0 | 4949 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0006t0106 | 0/0 | 4954 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0006t0114 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0016t0003 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0022t0040 | 0/0 | 4963 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0002c0024t0041 | 0/0 | 4943 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0001 | 0/0 | 4952 | 39 | 1 | 6 | 26 | 4 | 2 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0005 | 0/0 | 4948 | 6 | 1 | 3 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0014 | 0/0 | 4952 | 5 | 0 | 0 | 5 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0015 | 0/0 | 4952 | 7 | 0 | 2 | 0 | 4 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0023 | 0/0 | 4954 | 4 | 0 | 0 | 4 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0024 | 0/0 | 4954 | 5 | 0 | 3 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0031 | 0/0 | 4952 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0032 | 0/0 | 4950 | 3 | 0 | 3 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0039 | 0/0 | 4967 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0047 | 0/0 | 4946 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0067 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0070 | 0/0 | 4960 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0072 | 0/0 | 4958 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0073 | 0/0 | 4958 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0075 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0078 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0079 | 0/0 | 4954 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0081 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0086 | 0/0 | 4944 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0088 | 0/0 | 4956 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0089 | 0/0 | 4956 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0092 | 0/0 | 4950 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0003t0100 | 0/0 | 4952 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0008t0001 | 0/0 | 4952 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0003c0008t0014 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0004c0013t0005 | 0/0 | 4948 | 2 | 1 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0005c0012t0016 | 0/0 | 4955 | 2 | 1 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0006c0020t0038 | 0/0 | 4954 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0007c0017t0003 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0008c0023t0110 | 0/0 | 4966 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0009c0021t0019 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0010c0025t0061 | 0/0 | 4961 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0011c0019t0006 | 0/0 | 4957 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| a0012c0014t0001 | 0/0 | 4952 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | copy fasta | chr10 | 50179861 | 50256516 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0006g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0009g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0009g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0009g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0009g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0010g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0010g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0010g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0011g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0013g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0013g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0013g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0013g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0013g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0014g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0019g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0022g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0022g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0022g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0022g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0023g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0025g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0028g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0028g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0044g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0045g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0045g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0047g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0049g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0050g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0050g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0051g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0052g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0053g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0056g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0056g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0064g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0065g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0066g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0068g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0071g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0074g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0076g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0077g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0080g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0082g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0083g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0084g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0085g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0091g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0096g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0103g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0002t0118g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0006g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0006g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0006g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0006g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0012g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0012g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0013g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0020g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0020g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0033g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0033g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0033g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0034g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0034g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0034g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0036g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0036g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0036g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0046g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0046g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0048g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0048g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0051g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0053g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0090g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0095g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0004t0097g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0009g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0009g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0009g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0011g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0011g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0011g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0011g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0013g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0019g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0019g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0019g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0025g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0025g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0025g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0037g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0037g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0052g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0055g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0055g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0093g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0098g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0099g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0107g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0116g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0005t0117g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0007t0020g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0007t0020g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0007t0020g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0007t0038g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0007t0038g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0009t0010g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0009t0010g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0009t0010g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0010t0069g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0010t0087g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0010t0102g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0011t0006g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0011t0020g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0011t0109g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0015t0094g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0001c0018t0009g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0004g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0004g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0007g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0007g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0007g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0008g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0008g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0008g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0008g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0008g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0008g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0008g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0008g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0008g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0011g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0016g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0016g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0016g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0016g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0016g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0017g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0017g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0017g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0017g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0017g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0018g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0018g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0018g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0018g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0018g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0018g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0021g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0021g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0021g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0021g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0021g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0026g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0026g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0026g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0026g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0027g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0027g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0027g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0029g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0029g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0029g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0030g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0030g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0030g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0035g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0035g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0035g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0039g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0040g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0041g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0042g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0042g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0043g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0043g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0054g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0054g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0057g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0058g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0059g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0060g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0062g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0063g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0104g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0105g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0108g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0111g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0112g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0113g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0001t0115g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0006t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0006t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0006t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0006t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0006t0101g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0006t0106g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0006t0114g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0016t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0022t0040g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0002c0024t0041g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0014g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0014g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0014g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0014g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0014g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0015g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0015g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0015g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0015g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0015g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0015g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0023g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0023g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0023g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0023g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0024g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0024g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0024g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0024g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0024g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0031g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0031g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0032g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0032g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0039g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0047g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0067g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0070g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0072g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0073g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0075g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0078g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0079g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0081g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0086g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0088g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0089g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0092g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0003t0100g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0008t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0008t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0003c0008t0014g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0004c0013t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0004c0013t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0005c0012t0016g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0006c0020t0038g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0007c0017t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0008c0023t0110g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0009c0021t0019g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0010c0025t0061g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0011c0019t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| a0012c0014t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0042 | g0332 | EUR | GBR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00099 | hp2 | a0003 | c0003 | t0015 | g0197 | EUR | GBR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0135 | EUR | GBR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00140 | hp2 | a0010 | c0025 | t0061 | g0318 | EUR | GBR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00280 | hp1 | a0003 | c0003 | t0001 | g0152 | EUR | FIN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00280 | hp2 | a0002 | c0001 | t0018 | g0324 | EUR | FIN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00323 | hp1 | a0002 | c0001 | t0060 | g0317 | EUR | FIN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00323 | hp2 | a0003 | c0003 | t0015 | g0192 | EUR | FIN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00423 | hp1 | a0003 | c0003 | t0014 | g0163 | EAS | CHS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00423 | hp2 | a0001 | c0002 | t0056 | g0363 | EAS | CHS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00438 | hp1 | a0003 | c0003 | t0001 | g0138 | EAS | CHS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00438 | hp2 | a0002 | c0001 | t0002 | g0221 | EAS | CHS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00544 | hp1 | a0002 | c0001 | t0002 | g0253 | EAS | CHS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00544 | hp2 | a0002 | c0001 | t0030 | g0193 | EAS | CHS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00558 | hp1 | a0002 | c0001 | t0035 | g0256 | EAS | CHS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0077 | EAS | CHS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00597 | hp1 | a0002 | c0006 | t0002 | g0277 | EAS | CHS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00597 | hp2 | a0001 | c0002 | t0005 | g0086 | EAS | CHS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00609 | hp1 | a0003 | c0008 | t0001 | g0075 | EAS | CHS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00609 | hp2 | a0003 | c0003 | t0001 | g0148 | EAS | CHS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00639 | hp1 | a0002 | c0001 | t0007 | g0047 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00639 | hp2 | a0003 | c0003 | t0001 | g0137 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00642 | hp1 | a0001 | c0009 | t0010 | g0306 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00642 | hp2 | a0002 | c0001 | t0027 | g0224 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00733 | hp1 | a0003 | c0003 | t0005 | g0115 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00733 | hp2 | a0001 | c0002 | t0005 | g0114 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00735 | hp1 | a0003 | c0003 | t0100 | g0172 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00735 | hp2 | a0006 | c0020 | t0038 | g0059 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00738 | hp1 | a0002 | c0001 | t0008 | g0323 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00738 | hp2 | a0001 | c0004 | t0034 | g0280 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00741 | hp1 | a0001 | c0004 | t0036 | g0055 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG00741 | hp2 | a0002 | c0001 | t0030 | g0328 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01069 | hp1 | a0001 | c0009 | t0010 | g0305 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01069 | hp2 | a0003 | c0003 | t0032 | g0019 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01070 | hp1 | a0001 | c0005 | t0011 | g0010 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01071 | hp1 | a0001 | c0005 | t0011 | g0010 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01071 | hp2 | a0003 | c0003 | t0032 | g0019 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01081 | hp1 | a0001 | c0002 | t0005 | g0063 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01081 | hp2 | a0003 | c0003 | t0015 | g0198 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01106 | hp1 | a0001 | c0004 | t0006 | g0293 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01106 | hp2 | a0002 | c0001 | t0008 | g0316 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01109 | hp1 | a0001 | c0002 | t0009 | g0352 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01109 | hp2 | a0002 | c0001 | t0008 | g0330 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01167 | hp1 | a0003 | c0003 | t0015 | g0022 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01167 | hp2 | a0001 | c0002 | t0028 | g0303 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01175 | hp1 | a0003 | c0003 | t0024 | g0165 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01175 | hp2 | a0002 | c0001 | t0008 | g0309 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01192 | hp1 | a0001 | c0007 | t0020 | g0359 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01192 | hp2 | a0003 | c0003 | t0001 | g0119 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01243 | hp1 | a0002 | c0001 | t0007 | g0049 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01243 | hp2 | a0001 | c0005 | t0019 | g0026 | AMR | PUR | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01255 | hp1 | a0003 | c0003 | t0005 | g0173 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01255 | hp2 | a0002 | c0001 | t0026 | g0234 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01256 | hp1 | a0002 | c0022 | t0040 | g0132 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01256 | hp2 | a0002 | c0001 | t0004 | g0023 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01257 | hp1 | a0001 | c0005 | t0011 | g0009 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01257 | hp2 | a0003 | c0003 | t0001 | g0136 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01258 | hp1 | a0001 | c0005 | t0011 | g0009 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01258 | hp2 | a0002 | c0001 | t0004 | g0023 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01346 | hp1 | a0002 | c0001 | t0002 | g0231 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01346 | hp2 | a0003 | c0003 | t0024 | g0145 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01358 | hp1 | a0002 | c0001 | t0002 | g0264 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01358 | hp2 | a0001 | c0002 | t0005 | g0066 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01361 | hp1 | a0002 | c0001 | t0008 | g0123 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01361 | hp2 | a0003 | c0003 | t0092 | g0117 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01433 | hp1 | a0001 | c0002 | t0050 | g0065 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0201 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01496 | hp1 | a0002 | c0001 | t0002 | g0183 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01496 | hp2 | a0002 | c0001 | t0062 | g0320 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01515 | hp1 | a0003 | c0003 | t0001 | g0020 | EUR | IBS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01515 | hp2 | a0002 | c0001 | t0018 | g0202 | EUR | IBS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01517 | hp1 | a0002 | c0001 | t0002 | g0229 | EUR | IBS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0020 | EUR | IBS | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01884 | hp1 | a0001 | c0004 | t0006 | g0298 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01884 | hp2 | a0001 | c0018 | t0009 | g0353 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01891 | hp1 | a0002 | c0001 | t0113 | g0046 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01891 | hp2 | a0001 | c0005 | t0009 | g0025 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01928 | hp1 | a0002 | c0001 | t0021 | g0345 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01928 | hp2 | a0002 | c0001 | t0002 | g0024 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01934 | hp1 | a0003 | c0003 | t0005 | g0191 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01934 | hp2 | a0002 | c0001 | t0026 | g0262 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01943 | hp1 | a0002 | c0001 | t0002 | g0024 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01943 | hp2 | a0001 | c0004 | t0034 | g0276 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0168 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01952 | hp2 | a0002 | c0001 | t0026 | g0029 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01975 | hp1 | a0002 | c0001 | t0018 | g0312 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01975 | hp2 | a0002 | c0001 | t0002 | g0182 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01978 | hp1 | a0001 | c0004 | t0006 | g0294 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01978 | hp2 | a0002 | c0001 | t0002 | g0185 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01981 | hp1 | a0002 | c0001 | t0002 | g0239 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01981 | hp2 | a0001 | c0005 | t0117 | g0266 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01993 | hp1 | a0002 | c0001 | t0026 | g0029 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01993 | hp2 | a0003 | c0003 | t0024 | g0181 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02004 | hp1 | a0002 | c0001 | t0002 | g0233 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02004 | hp2 | a0002 | c0001 | t0008 | g0313 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02015 | hp1 | a0001 | c0005 | t0003 | g0261 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02015 | hp2 | a0002 | c0001 | t0004 | g0260 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02027 | hp1 | a0002 | c0001 | t0035 | g0254 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02027 | hp2 | a0002 | c0001 | t0039 | g0327 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0091 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02040 | hp2 | a0002 | c0001 | t0004 | g0030 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02055 | hp1 | a0001 | c0005 | t0037 | g0027 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02055 | hp2 | a0001 | c0002 | t0009 | g0347 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02056 | hp1 | a0001 | c0002 | t0011 | g0081 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02056 | hp2 | a0003 | c0003 | t0001 | g0129 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02074 | hp1 | a0001 | c0004 | t0013 | g0289 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02074 | hp2 | a0001 | c0002 | t0010 | g0017 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02080 | hp1 | a0001 | c0005 | t0098 | g0037 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02080 | hp2 | a0002 | c0001 | t0004 | g0258 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02083 | hp1 | a0002 | c0001 | t0004 | g0249 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02083 | hp2 | a0001 | c0002 | t0014 | g0100 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02129 | hp1 | a0002 | c0001 | t0035 | g0251 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02129 | hp2 | a0001 | c0002 | t0013 | g0071 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02132 | hp1 | a0001 | c0004 | t0012 | g0001 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02132 | hp2 | a0003 | c0003 | t0067 | g0189 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02135 | hp1 | a0003 | c0003 | t0079 | g0157 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02135 | hp2 | a0002 | c0006 | t0002 | g0105 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02145 | hp1 | a0002 | c0001 | t0041 | g0329 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02145 | hp2 | a0002 | c0001 | t0007 | g0003 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02148 | hp1 | a0002 | c0001 | t0026 | g0184 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02148 | hp2 | a0001 | c0002 | t0010 | g0099 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02155 | hp1 | a0002 | c0001 | t0021 | g0053 | EAS | CDX | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0016 | EAS | CDX | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02165 | hp1 | a0002 | c0001 | t0002 | g0259 | EAS | CDX | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02165 | hp2 | a0003 | c0003 | t0047 | g0150 | EAS | CDX | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02257 | hp1 | a0001 | c0002 | t0049 | g0031 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02257 | hp2 | a0001 | c0004 | t0033 | g0297 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02258 | hp1 | a0002 | c0001 | t0007 | g0003 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02258 | hp2 | a0001 | c0004 | t0020 | g0290 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02280 | hp1 | a0001 | c0005 | t0011 | g0180 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02280 | hp2 | a0002 | c0001 | t0112 | g0043 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02293 | hp1 | a0002 | c0001 | t0002 | g0244 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02293 | hp2 | a0003 | c0003 | t0086 | g0188 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02300 | hp1 | a0001 | c0004 | t0034 | g0279 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02300 | hp2 | a0003 | c0003 | t0001 | g0124 | AMR | PEL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02451 | hp1 | a0001 | c0007 | t0038 | g0360 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02451 | hp2 | a0001 | c0002 | t0052 | g0350 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02523 | hp1 | a0002 | c0001 | t0002 | g0248 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | KHV | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02572 | hp1 | a0001 | c0002 | t0074 | g0271 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02572 | hp2 | a0001 | c0005 | t0025 | g0007 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02615 | hp1 | a0003 | c0003 | t0073 | g0141 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02615 | hp2 | a0001 | c0011 | t0109 | g0355 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02622 | hp1 | a0001 | c0002 | t0118 | g0301 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02622 | hp2 | a0001 | c0005 | t0025 | g0206 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02630 | hp1 | a0002 | c0001 | t0007 | g0045 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02630 | hp2 | a0001 | c0005 | t0009 | g0214 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02647 | hp1 | a0001 | c0002 | t0028 | g0006 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02647 | hp2 | a0002 | c0006 | t0114 | g0302 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02683 | hp1 | a0002 | c0001 | t0016 | g0263 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02683 | hp2 | a0001 | c0002 | t0050 | g0064 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02698 | hp1 | a0003 | c0003 | t0001 | g0130 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02698 | hp2 | a0002 | c0001 | t0042 | g0331 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02717 | hp1 | a0001 | c0005 | t0055 | g0220 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02717 | hp2 | a0002 | c0001 | t0007 | g0038 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02723 | hp1 | a0001 | c0005 | t0107 | g0219 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02723 | hp2 | a0001 | c0005 | t0025 | g0034 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02735 | hp1 | a0003 | c0003 | t0015 | g0131 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02735 | hp2 | a0001 | c0004 | t0006 | g0292 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02738 | hp1 | a0003 | c0003 | t0089 | g0153 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02738 | hp2 | a0002 | c0001 | t0027 | g0033 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02818 | hp1 | a0001 | c0005 | t0037 | g0207 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02818 | hp2 | a0001 | c0002 | t0028 | g0006 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02886 | hp1 | a0001 | c0002 | t0080 | g0274 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02886 | hp2 | a0002 | c0001 | t0111 | g0039 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02895 | hp1 | a0001 | c0002 | t0044 | g0011 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02895 | hp2 | a0002 | c0001 | t0007 | g0044 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02896 | hp1 | a0001 | c0005 | t0008 | g0215 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02896 | hp2 | a0002 | c0001 | t0007 | g0003 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02897 | hp1 | a0001 | c0002 | t0044 | g0011 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02897 | hp2 | a0002 | c0001 | t0007 | g0054 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02922 | hp1 | a0001 | c0002 | t0005 | g0061 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02922 | hp2 | a0001 | c0009 | t0010 | g0307 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02965 | hp1 | a0001 | c0005 | t0019 | g0217 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02965 | hp2 | a0001 | c0002 | t0064 | g0268 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02976 | hp1 | a0008 | c0023 | t0110 | g0361 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02976 | hp2 | a0001 | c0010 | t0102 | g0362 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03017 | hp1 | a0002 | c0001 | t0008 | g0315 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03017 | hp2 | a0002 | c0001 | t0004 | g0116 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03041 | hp1 | a0001 | c0002 | t0019 | g0349 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03041 | hp2 | a0001 | c0002 | t0103 | g0060 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03098 | hp1 | a0004 | c0013 | t0005 | g0067 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03098 | hp2 | a0001 | c0005 | t0052 | g0216 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03130 | hp1 | a0001 | c0007 | t0020 | g0357 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03130 | hp2 | a0002 | c0001 | t0115 | g0042 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03139 | hp1 | a0001 | c0007 | t0038 | g0358 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03139 | hp2 | a0001 | c0005 | t0116 | g0213 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03195 | hp1 | a0001 | c0004 | t0006 | g0295 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03195 | hp2 | a0001 | c0002 | t0049 | g0031 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03209 | hp1 | a0001 | c0002 | t0025 | g0346 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03209 | hp2 | a0001 | c0002 | t0009 | g0272 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03225 | hp1 | a0001 | c0010 | t0087 | g0050 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03225 | hp2 | a0001 | c0005 | t0099 | g0040 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03239 | hp1 | a0002 | c0001 | t0008 | g0319 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03239 | hp2 | a0001 | c0002 | t0006 | g0079 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03453 | hp1 | a0001 | c0015 | t0094 | g0036 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03453 | hp2 | a0001 | c0005 | t0009 | g0203 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03486 | hp1 | a0001 | c0004 | t0097 | g0304 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03486 | hp2 | a0001 | c0004 | t0090 | g0348 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03491 | hp1 | a0003 | c0003 | t0001 | g0121 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03491 | hp2 | a0002 | c0001 | t0008 | g0343 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03516 | hp1 | a0001 | c0002 | t0076 | g0056 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03516 | hp2 | a0001 | c0005 | t0019 | g0205 | AFR | ESN | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03540 | hp1 | a0001 | c0002 | t0083 | g0057 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03540 | hp2 | a0001 | c0002 | t0028 | g0006 | AFR | GWD | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03579 | hp1 | a0001 | c0005 | t0037 | g0027 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03579 | hp2 | a0001 | c0004 | t0046 | g0296 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03654 | hp1 | a0002 | c0001 | t0016 | g0133 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03654 | hp2 | a0001 | c0002 | t0068 | g0104 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03688 | hp1 | a0002 | c0001 | t0040 | g0310 | SAS | STU | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03688 | hp2 | a0001 | c0004 | t0048 | g0113 | SAS | STU | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03704 | hp1 | a0002 | c0001 | t0018 | g0326 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03704 | hp2 | a0001 | c0002 | t0051 | g0112 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03710 | hp1 | a0001 | c0002 | t0053 | g0078 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03710 | hp2 | a0002 | c0001 | t0104 | g0227 | SAS | PJL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03831 | hp1 | a0001 | c0004 | t0051 | g0300 | SAS | BEB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03831 | hp2 | a0002 | c0001 | t0027 | g0033 | SAS | BEB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | BEB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03834 | hp2 | a0001 | c0002 | t0013 | g0103 | SAS | BEB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03927 | hp1 | a0005 | c0012 | t0016 | g0028 | SAS | BEB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03927 | hp2 | a0001 | c0005 | t0013 | g0035 | SAS | BEB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03942 | hp1 | a0002 | c0001 | t0043 | g0308 | SAS | BEB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03942 | hp2 | a0001 | c0002 | t0096 | g0074 | SAS | BEB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18522 | hp1 | a0001 | c0002 | t0005 | g0267 | AFR | YRI | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18522 | hp2 | a0002 | c0006 | t0101 | g0273 | AFR | YRI | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18612 | hp1 | a0003 | c0003 | t0001 | g0222 | EAS | CHB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18612 | hp2 | a0002 | c0006 | t0004 | g0076 | EAS | CHB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0126 | EAS | CHB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18747 | hp2 | a0003 | c0003 | t0001 | g0052 | EAS | CHB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18906 | hp1 | a0002 | c0006 | t0106 | g0058 | AFR | YRI | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18906 | hp2 | a0001 | c0002 | t0085 | g0270 | AFR | YRI | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18941 | hp1 | a0002 | c0001 | t0017 | g0340 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18942 | hp1 | a0001 | c0002 | t0003 | g0088 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18942 | hp2 | a0003 | c0003 | t0023 | g0142 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18944 | hp1 | a0002 | c0001 | t0004 | g0211 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18944 | hp2 | a0011 | c0019 | t0006 | g0285 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18945 | hp1 | a0002 | c0001 | t0054 | g0243 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18945 | hp2 | a0002 | c0001 | t0017 | g0032 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18947 | hp1 | a0002 | c0001 | t0021 | g0339 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18947 | hp2 | a0001 | c0002 | t0004 | g0082 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18948 | hp1 | a0001 | c0011 | t0006 | g0342 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18948 | hp2 | a0003 | c0003 | t0039 | g0149 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18950 | hp1 | a0001 | c0002 | t0022 | g0108 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18950 | hp2 | a0003 | c0003 | t0001 | g0171 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18952 | hp1 | a0001 | c0002 | t0077 | g0109 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18952 | hp2 | a0003 | c0003 | t0005 | g0209 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18954 | hp1 | a0002 | c0001 | t0002 | g0237 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18954 | hp2 | a0001 | c0002 | t0010 | g0017 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18956 | hp1 | a0001 | c0002 | t0003 | g0092 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18956 | hp2 | a0002 | c0001 | t0002 | g0005 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18957 | hp1 | a0001 | c0002 | t0045 | g0096 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18957 | hp2 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18960 | hp1 | a0003 | c0003 | t0031 | g0021 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18960 | hp2 | a0002 | c0001 | t0003 | g0235 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18962 | hp2 | a0002 | c0001 | t0017 | g0334 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18963 | hp1 | a0002 | c0001 | t0004 | g0030 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18963 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18965 | hp1 | a0001 | c0004 | t0006 | g0282 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18965 | hp2 | a0001 | c0004 | t0006 | g0018 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18966 | hp1 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18966 | hp2 | a0001 | c0004 | t0006 | g0018 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18967 | hp1 | a0001 | c0002 | t0066 | g0098 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18967 | hp2 | a0003 | c0003 | t0088 | g0177 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18968 | hp1 | a0003 | c0003 | t0001 | g0210 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18968 | hp2 | a0003 | c0003 | t0001 | g0186 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18969 | hp1 | a0002 | c0001 | t0016 | g0250 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0190 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18970 | hp1 | a0012 | c0014 | t0001 | g0118 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18970 | hp2 | a0002 | c0001 | t0043 | g0335 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18973 | hp1 | a0003 | c0003 | t0081 | g0139 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18973 | hp2 | a0002 | c0001 | t0017 | g0032 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18974 | hp1 | a0001 | c0002 | t0003 | g0089 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18974 | hp2 | a0003 | c0003 | t0014 | g0170 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18975 | hp1 | a0001 | c0002 | t0010 | g0008 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18975 | hp2 | a0002 | c0001 | t0058 | g0336 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18977 | hp1 | a0001 | c0005 | t0011 | g0041 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18977 | hp2 | a0001 | c0002 | t0013 | g0070 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18978 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18978 | hp2 | a0002 | c0001 | t0105 | g0225 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18980 | hp1 | a0001 | c0002 | t0023 | g0084 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18980 | hp2 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18984 | hp1 | a0001 | c0002 | t0010 | g0008 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18984 | hp2 | a0003 | c0003 | t0023 | g0140 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18986 | hp1 | a0003 | c0003 | t0001 | g0158 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18986 | hp2 | a0002 | c0001 | t0059 | g0341 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18988 | hp1 | a0003 | c0003 | t0023 | g0159 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18989 | hp1 | a0002 | c0001 | t0030 | g0178 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18989 | hp2 | a0003 | c0003 | t0024 | g0122 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18990 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18990 | hp2 | a0002 | c0001 | t0054 | g0257 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18991 | hp1 | a0003 | c0003 | t0070 | g0127 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18991 | hp2 | a0001 | c0002 | t0056 | g0364 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18992 | hp1 | a0001 | c0002 | t0003 | g0093 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0144 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18994 | hp1 | a0001 | c0004 | t0033 | g0275 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18994 | hp2 | a0001 | c0002 | t0045 | g0107 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18995 | hp1 | a0001 | c0002 | t0013 | g0094 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18995 | hp2 | a0003 | c0003 | t0001 | g0169 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18997 | hp1 | a0003 | c0003 | t0023 | g0166 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18997 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18999 | hp1 | a0001 | c0004 | t0046 | g0287 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA18999 | hp2 | a0002 | c0001 | t0002 | g0005 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19000 | hp1 | a0002 | c0001 | t0002 | g0245 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19000 | hp2 | a0001 | c0002 | t0065 | g0102 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19001 | hp1 | a0002 | c0001 | t0003 | g0242 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19001 | hp2 | a0003 | c0003 | t0024 | g0154 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19002 | hp1 | a0002 | c0001 | t0004 | g0179 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19002 | hp2 | a0001 | c0002 | t0022 | g0015 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19003 | hp1 | a0003 | c0003 | t0031 | g0199 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19003 | hp2 | a0003 | c0003 | t0014 | g0161 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19004 | hp1 | a0001 | c0004 | t0012 | g0001 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19004 | hp2 | a0001 | c0002 | t0013 | g0069 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19005 | hp1 | a0002 | c0001 | t0016 | g0255 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19005 | hp2 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19006 | hp1 | a0003 | c0003 | t0078 | g0187 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19006 | hp2 | a0001 | c0002 | t0022 | g0087 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19007 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19007 | hp2 | a0001 | c0004 | t0012 | g0001 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19010 | hp1 | a0002 | c0006 | t0004 | g0085 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19010 | hp2 | a0007 | c0017 | t0003 | g0106 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19011 | hp1 | a0001 | c0004 | t0048 | g0281 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19011 | hp2 | a0001 | c0004 | t0012 | g0001 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19012 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19012 | hp2 | a0001 | c0004 | t0033 | g0278 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19030 | hp1 | a0001 | c0005 | t0019 | g0026 | AFR | LWK | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19030 | hp2 | a0001 | c0011 | t0020 | g0344 | AFR | LWK | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19043 | hp1 | a0009 | c0021 | t0019 | g0208 | AFR | LWK | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19043 | hp2 | a0001 | c0005 | t0025 | g0007 | AFR | LWK | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19054 | hp1 | a0002 | c0001 | t0057 | g0338 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0110 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19056 | hp1 | a0002 | c0001 | t0016 | g0246 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19056 | hp2 | a0002 | c0001 | t0017 | g0333 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19058 | hp1 | a0001 | c0004 | t0036 | g0072 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19058 | hp2 | a0002 | c0001 | t0003 | g0236 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19060 | hp1 | a0002 | c0001 | t0021 | g0175 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19060 | hp2 | a0001 | c0004 | t0012 | g0001 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19062 | hp1 | a0002 | c0001 | t0029 | g0337 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19062 | hp2 | a0002 | c0001 | t0002 | g0232 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19065 | hp1 | a0003 | c0008 | t0001 | g0013 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19065 | hp2 | a0001 | c0002 | t0003 | g0090 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19066 | hp1 | a0001 | c0002 | t0091 | g0111 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19066 | hp2 | a0003 | c0003 | t0005 | g0147 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19068 | hp1 | a0002 | c0001 | t0029 | g0322 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19068 | hp2 | a0002 | c0001 | t0003 | g0241 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19070 | hp1 | a0002 | c0001 | t0011 | g0238 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19070 | hp2 | a0003 | c0003 | t0014 | g0151 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19072 | hp1 | a0001 | c0004 | t0036 | g0288 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19072 | hp2 | a0003 | c0003 | t0001 | g0143 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19074 | hp1 | a0001 | c0004 | t0095 | g0284 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19074 | hp2 | a0003 | c0003 | t0072 | g0223 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19075 | hp1 | a0003 | c0008 | t0014 | g0286 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19075 | hp2 | a0001 | c0002 | t0022 | g0073 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19076 | hp1 | a0002 | c0001 | t0021 | g0195 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19076 | hp2 | a0002 | c0001 | t0004 | g0247 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19077 | hp1 | a0003 | c0008 | t0001 | g0013 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19077 | hp2 | a0002 | c0001 | t0017 | g0321 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19079 | hp1 | a0003 | c0003 | t0075 | g0176 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19080 | hp1 | a0003 | c0003 | t0031 | g0021 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19080 | hp2 | a0001 | c0004 | t0053 | g0283 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19081 | hp1 | a0001 | c0004 | t0012 | g0299 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19081 | hp2 | a0002 | c0001 | t0029 | g0325 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19082 | hp1 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19082 | hp2 | a0002 | c0001 | t0002 | g0005 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19083 | hp1 | a0001 | c0002 | t0082 | g0080 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19083 | hp2 | a0001 | c0004 | t0012 | g0001 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19084 | hp1 | a0001 | c0002 | t0022 | g0015 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19084 | hp2 | a0001 | c0004 | t0012 | g0001 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19085 | hp1 | a0002 | c0001 | t0002 | g0230 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19085 | hp2 | a0003 | c0003 | t0014 | g0128 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19088 | hp1 | a0003 | c0003 | t0001 | g0167 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19088 | hp2 | a0002 | c0001 | t0004 | g0226 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19089 | hp1 | a0003 | c0003 | t0001 | g0164 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19089 | hp2 | a0002 | c0001 | t0108 | g0252 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19091 | hp1 | a0002 | c0001 | t0018 | g0194 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19091 | hp2 | a0002 | c0016 | t0003 | g0097 | EAS | JPT | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19240 | hp1 | a0001 | c0004 | t0020 | g0291 | AFR | YRI | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA19240 | hp2 | a0001 | c0005 | t0093 | g0212 | AFR | YRI | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA20129 | hp1 | a0005 | c0012 | t0016 | g0028 | AFR | ASW | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA20129 | hp2 | a0001 | c0002 | t0009 | g0351 | AFR | ASW | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA20752 | hp1 | a0002 | c0001 | t0002 | g0228 | EUR | TSI | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA20752 | hp2 | a0003 | c0003 | t0015 | g0134 | EUR | TSI | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA20805 | hp1 | a0002 | c0001 | t0018 | g0265 | EUR | TSI | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA20805 | hp2 | a0003 | c0003 | t0015 | g0022 | EUR | TSI | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01123 | hp1 | a0004 | c0013 | t0005 | g0068 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG01123 | hp2 | a0003 | c0003 | t0032 | g0125 | AMR | CLM | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02109 | hp1 | a0001 | c0005 | t0055 | g0218 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02109 | hp2 | a0003 | c0003 | t0005 | g0196 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02486 | hp1 | a0002 | c0024 | t0041 | g0314 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02486 | hp2 | a0001 | c0005 | t0009 | g0025 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02559 | hp1 | a0001 | c0002 | t0084 | g0354 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG02559 | hp2 | a0001 | c0007 | t0020 | g0356 | AFR | ACB | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03471 | hp1 | a0001 | c0010 | t0069 | g0200 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG03471 | hp2 | a0001 | c0002 | t0071 | g0269 | AFR | MSL | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG06807 | hp1 | a0002 | c0001 | t0007 | g0048 | AFR | USA | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| HG06807 | hp2 | a0002 | c0001 | t0027 | g0311 | AFR | USA | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA20300 | hp1 | a0002 | c0001 | t0007 | g0051 | AFR | USA | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA20300 | hp2 | a0001 | c0002 | t0010 | g0101 | AFR | USA | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA21309 | hp1 | a0001 | c0002 | t0047 | g0062 | AFR | LWK | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0120 | AFR | LWK | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0063 | g0240 | REF | REF | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| homoSapiens_grch38 | hp1 | a0001 | c0005 | t0009 | g0204 | REF | REF | ASAH2_chr10_50179861_50256516 | ASAH2 | chr10 | 50179861 | 50256516 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:50187320
|
T | A | 1 | a0008 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.2338A>T | p.Ile780Phe | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2496/4955 | 2338/2343 | 780/780 | chr10 | 50187320 | ||
| chr10:50187409
|
T | C | 1 | a0005 | 2 | HG03927.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.2249A>G | p.Tyr750Cys | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2407/4955 | 2249/2343 | 750/780 | chr10 | 50187409 | ||
| chr10:50187430
|
G | A | 1 | a0007 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.2228C>T | p.Pro743Leu | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2386/4955 | 2228/2343 | 743/780 | chr10 | 50187430 | ||
| chr10:50189523
|
C | T | 2 | a0003a0012 | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
missense_variant | MODERATE | c.2129G>A | p.Cys710Tyr | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/21 | 2287/4955 | 2129/2343 | 710/780 | chr10 | 50189523 | ||
| chr10:50189563
|
C | T | 1 | a0009 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.2089G>A | p.Glu697Lys | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/21 | 2247/4955 | 2089/2343 | 697/780 | chr10 | 50189563 | ||
| chr10:50189586
|
G | T | 5 | a0002a0003a0005others(2): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
missense_variant&splice_region_variant | MODERATE | c.2066C>A | p.Thr689Asn | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/21 | 2224/4955 | 2066/2343 | 689/780 | chr10 | 50189586 | ||
| chr10:50214847
|
C | A | 1 | a0010 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1036G>T | p.Ala346Ser | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/21 | 1194/4955 | 1036/2343 | 346/780 | chr10 | 50214847 | ||
| chr10:50245233
|
C | A | 1 | a0011 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.349G>T | p.Asp117Tyr | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/21 | 507/4955 | 349/2343 | 117/780 | chr10 | 50245233 | ||
| chr10:50245335
|
G | A | 1 | a0006 | 1 | HG00735.hp2 | stop_gained | HIGH | c.247C>T | p.Gln83* | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/21 | 405/4955 | 247/2343 | 83/780 | chr10 | 50245335 | ||
| chr10:50245431
|
T | C | 1 | a0004 | 2 | HG01123.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.151A>G | p.Thr51Ala | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/21 | 309/4955 | 151/2343 | 51/780 | chr10 | 50245431 | ||
| chr10:50248498
|
A | G | 1 | a0012 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.113T>C | p.Ile38Thr | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/21 | 271/4955 | 113/2343 | 38/780 | chr10 | 50248498 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:50192704
|
A | C | 1 | a0002c0022 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.2013T>G | p.Val671Val | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/21 | 2171/4955 | 2013/2343 | 671/780 | chr10 | 50192704 | ||
| chr10:50199108
|
C | T | 2 | a0001c0010a0001c0015 | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
synonymous_variant | LOW | c.1800G>A | p.Pro600Pro | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/21 | 1958/4955 | 1800/2343 | 600/780 | chr10 | 50199108 | ||
| chr10:50202868
|
G | A | 2 | a0001c0010a0001c0015 | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
synonymous_variant | LOW | c.1722C>T | p.Asn574Asn | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/21 | 1880/4955 | 1722/2343 | 574/780 | chr10 | 50202868 | ||
| chr10:50205988
|
G | A | 1 | a0002c0024 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1524C>T | p.Thr508Thr | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 13/21 | 1682/4955 | 1524/2343 | 508/780 | chr10 | 50205988 | ||
| chr10:50210866
|
T | C | 14 | a0001c0004a0001c0007a0001c0011others(11): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
synonymous_variant | LOW | c.1371A>G | p.Ala457Ala | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/21 | 1529/4955 | 1371/2343 | 457/780 | chr10 | 50210866 | ||
| chr10:50235909
|
G | A | 1 | a0007c0017 | 1 | NA19010.hp2 | synonymous_variant | LOW | c.666C>T | p.His222His | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/21 | 824/4955 | 666/2343 | 222/780 | chr10 | 50235909 | ||
| chr10:50235999
|
G | A | 1 | a0001c0018 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.576C>T | p.Gly192Gly | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/21 | 734/4955 | 576/2343 | 192/780 | chr10 | 50235999 | ||
| chr10:50243220
|
T | G | 10 | a0001c0002a0001c0004a0001c0018others(7): Show | 142 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(139): Show |
synonymous_variant | LOW | c.492A>C | p.Ser164Ser | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/21 | 650/4955 | 492/2343 | 164/780 | chr10 | 50243220 | ||
| chr10:50245393
|
A | G | 13 | a0001c0002a0001c0004a0001c0007others(10): Show | 151 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(148): Show |
synonymous_variant | LOW | c.189T>C | p.Ala63Ala | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/21 | 347/4955 | 189/2343 | 63/780 | chr10 | 50245393 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:50184869
|
G | A | 3 | a0001c0002t0014a0003c0003t0014a0003c0008t0014 | 7 | HG00423.hp1 HG02083.hp2 NA18974.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2446C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2446 | chr10 | 50184869 | |||||
| chr10:50184947
|
T | C | 1 | a0001c0004t0097 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2368A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2368 | chr10 | 50184947 | |||||
| chr10:50184999
|
C | T | 1 | a0003c0003t0031 | 3 | NA18960.hp1 NA19003.hp1 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2316G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2316 | chr10 | 50184999 | |||||
| chr10:50185035
|
T | C | 13 | a0001c0004t0020a0001c0005t0117a0001c0007t0020others(10): Show | 17 | HG00735.hp2 HG01192.hp1 HG01981.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2280A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2280 | chr10 | 50185035 | |||||
| chr10:50185075
|
CCT | C | 1 | a0001c0004t0034 | 3 | HG00738.hp2 HG01943.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2238_*2239delAG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2238 | chr10 | 50185075 | |||||
| chr10:50185124
|
T | C | 5 | a0001c0004t0020a0001c0007t0020a0001c0007t0038others(2): Show | 9 | HG00735.hp2 HG01192.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2191A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2191 | chr10 | 50185124 | |||||
| chr10:50185152
|
G | T | 1 | a0002c0006t0101 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2163C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2163 | chr10 | 50185152 | |||||
| chr10:50185156
|
C | G | 1 | a0003c0003t0088 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2159G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2159 | chr10 | 50185156 | |||||
| chr10:50185174
|
T | C | 13 | a0001c0004t0020a0001c0005t0117a0001c0007t0020others(10): Show | 17 | HG00735.hp2 HG01192.hp1 HG01981.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2141A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2141 | chr10 | 50185174 | |||||
| chr10:50185225
|
T | C | 1 | a0001c0005t0117 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2090A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2090 | chr10 | 50185225 | |||||
| chr10:50185277
|
T | C | 1 | a0002c0006t0114 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2038A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2038 | chr10 | 50185277 | |||||
| chr10:50185280
|
A | G | 23 | a0001c0005t0008a0002c0001t0008a0002c0001t0017others(20): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2035T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2035 | chr10 | 50185280 | |||||
| chr10:50185284
|
T | C | 13 | a0001c0004t0020a0001c0005t0117a0001c0007t0020others(10): Show | 17 | HG00735.hp2 HG01192.hp1 HG01981.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2031A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 2031 | chr10 | 50185284 | |||||
| chr10:50185358
|
C | A | 1 | a0002c0001t0060 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1957G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1957 | chr10 | 50185358 | |||||
| chr10:50185389
|
T | A | 130 | a0001c0002t0001a0001c0002t0003a0001c0002t0005others(127): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*1926A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1926 | chr10 | 50185389 | |||||
| chr10:50185476
|
T | C | 13 | a0001c0002t0004a0002c0001t0002a0002c0001t0004others(10): Show | 60 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1839A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1839 | chr10 | 50185476 | |||||
| chr10:50185553
|
A | G | 129 | a0001c0002t0001a0001c0002t0003a0001c0002t0005others(126): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*1762T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1762 | chr10 | 50185553 | |||||
| chr10:50185562
|
T | C | 1 | a0002c0001t0115 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1753A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1753 | chr10 | 50185562 | |||||
| chr10:50185645
|
A | G | 120 | a0001c0002t0001a0001c0002t0003a0001c0002t0005others(117): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*1670T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1670 | chr10 | 50185645 | |||||
| chr10:50185650
|
C | T | 119 | a0001c0002t0001a0001c0002t0003a0001c0002t0005others(116): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*1665G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1665 | chr10 | 50185650 | |||||
| chr10:50185652
|
GA | G | 13 | a0001c0004t0020a0001c0005t0117a0001c0007t0020others(10): Show | 17 | HG00735.hp2 HG01192.hp1 HG01981.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1662delT | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1662 | chr10 | 50185652 | |||||
| chr10:50185701
|
G | A | 1 | a0001c0002t0083 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1614C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1614 | chr10 | 50185701 | |||||
| chr10:50185706
|
T | G | 9 | a0001c0002t0082a0001c0004t0012a0001c0005t0116others(6): Show | 26 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1609A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1609 | chr10 | 50185706 | |||||
| chr10:50185707
|
G | A | 4 | a0002c0001t0007a0002c0001t0111a0002c0001t0112others(1): Show | 14 | HG00639.hp1 HG01243.hp1 HG02145.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1608C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1608 | chr10 | 50185707 | |||||
| chr10:50185824
|
G | T | 3 | a0001c0002t0096a0001c0005t0117a0002c0001t0108 | 3 | HG01981.hp2 HG03942.hp2 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1491C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1491 | chr10 | 50185824 | |||||
| chr10:50185863
|
A | G | 13 | a0001c0004t0020a0001c0005t0117a0001c0007t0020others(10): Show | 17 | HG00735.hp2 HG01192.hp1 HG01981.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1452T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1452 | chr10 | 50185863 | |||||
| chr10:50185960
|
G | C | 118 | a0001c0002t0001a0001c0002t0003a0001c0002t0005others(115): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*1355C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1355 | chr10 | 50185960 | |||||
| chr10:50186025
|
A | G | 1 | a0001c0005t0117 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1290T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1290 | chr10 | 50186025 | |||||
| chr10:50186101
|
C | T | 63 | a0001c0002t0001a0001c0002t0003a0001c0002t0005others(60): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1214G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1214 | chr10 | 50186101 | |||||
| chr10:50186120
|
C | T | 13 | a0001c0004t0020a0001c0005t0117a0001c0007t0020others(10): Show | 17 | HG00735.hp2 HG01192.hp1 HG01981.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1195G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1195 | chr10 | 50186120 | |||||
| chr10:50186122
|
C | G | 1 | a0003c0003t0078 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1193G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1193 | chr10 | 50186122 | |||||
| chr10:50186179
|
T | G | 35 | a0001c0002t0001a0001c0002t0005a0001c0002t0014others(32): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1136A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1136 | chr10 | 50186179 | |||||
| chr10:50186184
|
A | G | 1 | a0003c0003t0081 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1131T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1131 | chr10 | 50186184 | |||||
| chr10:50186190
|
T | C | 121 | a0001c0002t0001a0001c0002t0003a0001c0002t0005others(118): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*1125A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1125 | chr10 | 50186190 | |||||
| chr10:50186215
|
G | A | 13 | a0001c0004t0020a0001c0005t0117a0001c0007t0020others(10): Show | 17 | HG00735.hp2 HG01192.hp1 HG01981.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1100C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1100 | chr10 | 50186215 | |||||
| chr10:50186298
|
G | T | 13 | a0001c0004t0020a0001c0005t0117a0001c0007t0020others(10): Show | 17 | HG00735.hp2 HG01192.hp1 HG01981.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1017C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 1017 | chr10 | 50186298 | |||||
| chr10:50186455
|
A | G | 121 | a0001c0002t0001a0001c0002t0003a0001c0002t0005others(118): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*860T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 860 | chr10 | 50186455 | |||||
| chr10:50186504
|
G | C | 23 | a0001c0005t0008a0002c0001t0008a0002c0001t0017others(20): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*811C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 811 | chr10 | 50186504 | |||||
| chr10:50186574
|
A | G | 14 | a0001c0002t0076a0001c0004t0020a0001c0005t0117others(11): Show | 18 | HG00735.hp2 HG01192.hp1 HG01981.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*741T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 741 | chr10 | 50186574 | |||||
| chr10:50186586
|
G | A | 1 | a0001c0002t0049 | 2 | HG02257.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*729C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 729 | chr10 | 50186586 | |||||
| chr10:50186638
|
C | T | 13 | a0001c0004t0020a0001c0005t0117a0001c0007t0020others(10): Show | 17 | HG00735.hp2 HG01192.hp1 HG01981.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*677G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 677 | chr10 | 50186638 | |||||
| chr10:50186713
|
T | C | 1 | a0002c0001t0063 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*602A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 602 | chr10 | 50186713 | |||||
| chr10:50186726
|
G | T | 2 | a0001c0002t0028a0001c0002t0049 | 6 | HG01167.hp2 HG02257.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*589C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 589 | chr10 | 50186726 | |||||
| chr10:50186910
|
T | A | 8 | a0001c0004t0012a0001c0005t0116a0002c0001t0007others(5): Show | 25 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*405A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 405 | chr10 | 50186910 | |||||
| chr10:50187031
|
T | C | 1 | a0002c0001t0043 | 2 | HG03942.hp1 NA18970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*284A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 284 | chr10 | 50187031 | |||||
| chr10:50187065
|
G | A | 19 | a0001c0002t0064a0001c0002t0071a0001c0002t0074others(16): Show | 24 | HG00735.hp2 HG01192.hp1 HG01981.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*250C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 250 | chr10 | 50187065 | |||||
| chr10:50187075
|
T | C | 22 | a0001c0005t0008a0002c0001t0008a0002c0001t0017others(19): Show | 52 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*240A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 240 | chr10 | 50187075 | |||||
| chr10:50187083
|
AC | A | 22 | a0001c0002t0005a0001c0002t0011a0001c0002t0023others(19): Show | 49 | HG00597.hp2 HG00733.hp1 HG00733.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*231delG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 231 | chr10 | 50187083 | |||||
| chr10:50187083
|
ACCT | A | 25 | a0001c0002t0001a0001c0002t0003a0001c0002t0010others(22): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*229_*231delAGG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 229 | chr10 | 50187083 | |||||
| chr10:50187084
|
C | CCT | 8 | a0001c0002t0006a0001c0002t0074a0001c0004t0006others(5): Show | 21 | HG00642.hp2 HG01106.hp1 HG01884.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*229_*230dupAG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 230 | chr10 | 50187084 | |||||
| chr10:50187084
|
C | CCTCT | 10 | a0001c0002t0051a0001c0002t0053a0001c0002t0071others(7): Show | 15 | HG00280.hp2 HG00323.hp1 HG01496.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*227_*230dupAGAG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 230 | chr10 | 50187084 | |||||
| chr10:50187084
|
C | CCTCTCT | 5 | a0001c0004t0036a0001c0004t0095a0001c0005t0008others(2): Show | 15 | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*225_*230dupAGAGAG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 230 | chr10 | 50187084 | |||||
| chr10:50187084
|
C | CCTCTCTC others(1): Show |
4 | a0002c0001t0040a0002c0001t0042a0002c0001t0057others(1): Show | 5 | HG00099.hp1 HG01256.hp1 HG02698.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*223_*230dupAGAGAG others(2): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 230 | chr10 | 50187084 | |||||
| chr10:50187084
|
C | CCTCTCTC others(3): Show |
1 | a0002c0001t0030 | 3 | HG00544.hp2 HG00741.hp2 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*221_*230dupAGAGAG others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 230 | chr10 | 50187084 | |||||
| chr10:50187084
|
C | CCTCTCTC others(5): Show |
2 | a0002c0001t0039a0003c0003t0039 | 2 | HG02027.hp2 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*219_*230dupAGAGAG others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 230 | chr10 | 50187084 | |||||
| chr10:50187084
|
C | CT | 6 | a0001c0002t0013a0001c0004t0013a0001c0005t0013others(3): Show | 10 | HG02074.hp1 HG02129.hp2 HG02738.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*230_*231insA | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 230 | chr10 | 50187084 | |||||
| chr10:50187084
|
C | CTCT | 4 | a0001c0002t0022a0001c0002t0065a0003c0003t0072others(1): Show | 8 | HG02615.hp1 NA18950.hp1 NA19000.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*230_*231insAGA | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 230 | chr10 | 50187084 | |||||
| chr10:50187084
|
C | CTCTCT | 2 | a0001c0002t0045a0003c0003t0070 | 3 | NA18957.hp1 NA18991.hp1 NA18994.hp2 |
3_prime_UTR_variant | MODIFIER | c.*230_*231insAGAGA | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 230 | chr10 | 50187084 | |||||
| chr10:50187084
|
CCTCTCT | C | 3 | a0001c0005t0117a0001c0015t0094a0002c0006t0101 | 3 | HG01981.hp2 HG03453.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*225_*230delAGAGAG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 225 | chr10 | 50187084 | |||||
| chr10:50187084
|
CCTCTCTC others(9): Show |
C | 1 | a0001c0010t0102 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*215_*230delAGAGAG others(10): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 215 | chr10 | 50187084 | |||||
| chr10:50187110
|
TCTCTCTC others(9): Show |
T | 1 | a0002c0001t0043 | 2 | HG03942.hp1 NA18970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*189_*204delTGTGTG others(10): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 189 | chr10 | 50187110 | |||||
| chr10:50187112
|
T | A | 1 | a0001c0005t0107 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*203A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 203 | chr10 | 50187112 | |||||
| chr10:50187112
|
TCTCTCTC others(3): Show |
T | 1 | a0001c0010t0069 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*193_*202delTGTGAG others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 193 | chr10 | 50187112 | |||||
| chr10:50187114
|
T | A | 1 | a0001c0005t0107 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*201A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 201 | chr10 | 50187114 | |||||
| chr10:50187114
|
TCTCTCAC others(3): Show |
T | 1 | a0001c0005t0116 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191_*200delTGTGTG others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 191 | chr10 | 50187114 | |||||
| chr10:50187115
|
C | T | 1 | a0001c0005t0107 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 200 | chr10 | 50187115 | |||||
| chr10:50187116
|
T | A | 1 | a0001c0005t0107 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*199A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 199 | chr10 | 50187116 | |||||
| chr10:50187116
|
T | TCACATAC others(1): Show |
4 | a0001c0004t0020a0001c0007t0020a0001c0011t0020others(1): Show | 7 | HG01192.hp1 HG02258.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*198_*199insTGTATG others(2): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 198 | chr10 | 50187116 | |||||
| chr10:50187116
|
T | TCACATAC others(5): Show |
1 | a0008c0023t0110 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*198_*199insTGTGTG others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 198 | chr10 | 50187116 | |||||
| chr10:50187116
|
TCTCACAC others(3): Show |
T | 1 | a0001c0004t0012 | 8 | HG02132.hp1 NA19004.hp1 NA19007.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*189_*198delTGTGTG others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 189 | chr10 | 50187116 | |||||
| chr10:50187116
|
TCTCACAC others(5): Show |
T | 5 | a0002c0001t0007a0002c0001t0111a0002c0001t0113others(2): Show | 15 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*187_*198delTGTGTG others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 187 | chr10 | 50187116 | |||||
| chr10:50187116
|
TCTCACAC others(9): Show |
T | 1 | a0002c0001t0112 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*183_*198delTGTGTG others(10): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 183 | chr10 | 50187116 | |||||
| chr10:50187118
|
T | A | 13 | a0001c0004t0020a0001c0005t0107a0001c0005t0117others(10): Show | 18 | HG00735.hp2 HG01192.hp1 HG01981.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*197A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 197 | chr10 | 50187118 | |||||
| chr10:50187118
|
T | TCA | 4 | a0001c0002t0004a0001c0005t0037a0002c0001t0004others(1): Show | 18 | HG01256.hp2 HG01258.hp2 HG02015.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*195_*196dupTG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 196 | chr10 | 50187118 | |||||
| chr10:50187118
|
T | TCACA | 4 | a0001c0005t0055a0002c0001t0002a0002c0001t0108others(1): Show | 28 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*193_*196dupTGTG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 196 | chr10 | 50187118 | |||||
| chr10:50187118
|
T | TCACACA | 1 | a0002c0001t0026 | 5 | HG01255.hp2 HG01934.hp2 HG01952.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*191_*196dupTGTGTG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 196 | chr10 | 50187118 | |||||
| chr10:50187118
|
T | TCTCA | 4 | a0001c0002t0019a0001c0005t0019a0002c0001t0105others(1): Show | 7 | HG01243.hp2 HG02965.hp1 HG03041.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*196_*197insTGAG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 196 | chr10 | 50187118 | |||||
| chr10:50187118
|
T | TCTCTCA | 2 | a0001c0002t0025a0001c0005t0025 | 5 | HG02572.hp2 HG02622.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*196_*197insTGAGAG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 196 | chr10 | 50187118 | |||||
| chr10:50187118
|
TCA | T | 4 | a0001c0002t0080a0001c0004t0090a0002c0001t0035others(1): Show | 6 | HG00558.hp1 HG02027.hp1 HG02129.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*195_*196delTG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 195 | chr10 | 50187118 | |||||
| chr10:50187118
|
TCACA | T | 7 | a0001c0002t0052a0001c0002t0068a0001c0002t0084others(4): Show | 9 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*193_*196delTGTG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 193 | chr10 | 50187118 | |||||
| chr10:50187118
|
TCACACA | T | 6 | a0001c0002t0005a0001c0002t0044a0001c0002t0050others(3): Show | 19 | HG00597.hp2 HG00733.hp1 HG00733.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*191_*196delTGTGTG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 191 | chr10 | 50187118 | |||||
| chr10:50187118
|
TCACACAC others(1): Show |
T | 3 | a0001c0002t0047a0003c0003t0047a0003c0003t0086 | 3 | HG02165.hp2 HG02293.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*189_*196delTGTGTG others(2): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 189 | chr10 | 50187118 | |||||
| chr10:50187118
|
TCACACAC others(5): Show |
T | 2 | a0002c0001t0041a0002c0024t0041 | 2 | HG02145.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*185_*196delTGTGTG others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 185 | chr10 | 50187118 | |||||
| chr10:50187120
|
A | T | 90 | a0001c0002t0001a0001c0002t0003a0001c0002t0006others(87): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*195T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 195 | chr10 | 50187120 | |||||
| chr10:50187121
|
C | T | 3 | a0001c0005t0117a0001c0010t0102a0002c0006t0101 | 3 | HG01981.hp2 HG02976.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*194G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 194 | chr10 | 50187121 | |||||
| chr10:50187122
|
A | T | 89 | a0001c0002t0001a0001c0002t0003a0001c0002t0006others(86): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*193T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 193 | chr10 | 50187122 | |||||
| chr10:50187123
|
C | T | 1 | a0001c0015t0094 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*192G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 192 | chr10 | 50187123 | |||||
| chr10:50187124
|
A | T | 80 | a0001c0002t0001a0001c0002t0003a0001c0002t0010others(77): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*191T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 191 | chr10 | 50187124 | |||||
| chr10:50187125
|
C | T | 1 | a0001c0010t0087 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*190G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 190 | chr10 | 50187125 | |||||
| chr10:50187126
|
A | T | 70 | a0001c0002t0001a0001c0002t0003a0001c0002t0005others(67): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*189T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 189 | chr10 | 50187126 | |||||
| chr10:50187127
|
C | T | 1 | a0001c0010t0069 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 188 | chr10 | 50187127 | |||||
| chr10:50187128
|
A | T | 28 | a0001c0002t0010a0001c0002t0044a0001c0002t0064others(25): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*187T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 187 | chr10 | 50187128 | |||||
| chr10:50187130
|
A | T | 22 | a0001c0002t0044a0001c0002t0064a0001c0005t0008others(19): Show | 53 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*185T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 185 | chr10 | 50187130 | |||||
| chr10:50187131
|
C | T | 1 | a0002c0001t0043 | 2 | HG03942.hp1 NA18970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*184G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 184 | chr10 | 50187131 | |||||
| chr10:50187132
|
A | T | 22 | a0001c0005t0008a0002c0001t0008a0002c0001t0017others(19): Show | 52 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*183T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 183 | chr10 | 50187132 | |||||
| chr10:50187134
|
A | T | 18 | a0001c0005t0008a0002c0001t0008a0002c0001t0017others(15): Show | 47 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*181T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 181 | chr10 | 50187134 | |||||
| chr10:50187135
|
C | T | 1 | a0002c0001t0111 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*180G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 180 | chr10 | 50187135 | |||||
| chr10:50187136
|
A | T | 5 | a0002c0001t0017a0002c0001t0029a0002c0001t0057others(2): Show | 12 | NA18941.hp1 NA18945.hp2 NA18962.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*179T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 179 | chr10 | 50187136 | |||||
| chr10:50187138
|
A | T | 2 | a0002c0001t0057a0002c0001t0058 | 2 | NA18975.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*177T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 177 | chr10 | 50187138 | |||||
| chr10:50187266
|
T | C | 9 | a0001c0004t0012a0001c0005t0116a0001c0005t0117others(6): Show | 26 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*49A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 49 | chr10 | 50187266 | |||||
| chr10:50187275
|
G | C | 1 | a0001c0002t0118 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*40C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 21/21 | 40 | chr10 | 50187275 | |||||
| chr10:50251503
|
T | C | 1 | a0001c0002t0056 | 2 | HG00423.hp2 NA18991.hp2 |
5_prime_UTR_variant | MODIFIER | c.-145A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/21 | 2893 | chr10 | 50251503 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:50187545
|
A | G | 79 | a0001c0002t0001g0012a0001c0002t0001g0095a0001c0002t0003g0004others(76): Show | 90 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.2154-41T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50187545 | ||||||
| chr10:50187685
|
A | G | 4 | a0001c0005t0117g0266a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2154-181T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50187685 | ||||||
| chr10:50187719
|
C | T | 174 | a0001c0002t0001g0012a0001c0002t0001g0095a0001c0002t0003g0004others(171): Show | 203 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2154-215G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50187719 | ||||||
| chr10:50187875
|
C | CTA | 99 | a0001c0002t0064g0268a0001c0002t0084g0354a0001c0004t0006g0018others(96): Show | 109 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.2154-373_2154-372d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50187875 | ||||||
| chr10:50187885
|
A | ATATG | 4 | a0001c0005t0117g0266a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2154-382_2154-381i others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50187885 | ||||||
| chr10:50187887
|
G | A | 249 | a0001c0002t0001g0012a0001c0002t0005g0061a0001c0002t0005g0063others(246): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.2154-383C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50187887 | ||||||
| chr10:50187895
|
G | A | 4 | a0001c0005t0117g0266a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2154-391C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50187895 | ||||||
| chr10:50187897
|
A | G | 323 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(320): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.2154-393T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50187897 | ||||||
| chr10:50187902
|
T | C | 320 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(317): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.2154-398A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50187902 | ||||||
| chr10:50187915
|
A | G | 3 | a0001c0002t0044g0011a0001c0002t0076g0056a0001c0002t0083g0057 | 4 | HG02895.hp1 HG02897.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2154-411T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50187915 | ||||||
| chr10:50188068
|
A | C | 1 | a0002c0001t0112g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2154-564T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188068 | ||||||
| chr10:50188120
|
T | C | 4 | a0003c0003t0014g0128a0003c0003t0014g0151a0003c0003t0014g0161others(1): Show | 4 | NA18974.hp2 NA19003.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154-616A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188120 | ||||||
| chr10:50188135
|
C | A | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2154-631G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188135 | ||||||
| chr10:50188171
|
A | T | 1 | a0001c0004t0033g0297 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2154-667T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188171 | ||||||
| chr10:50188174
|
T | C | 37 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(34): Show | 38 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.2154-670A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188174 | ||||||
| chr10:50188205
|
G | A | 1 | a0001c0011t0109g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2154-701C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188205 | ||||||
| chr10:50188384
|
C | T | 5 | a0001c0002t0010g0101a0001c0002t0019g0349a0001c0002t0025g0346others(2): Show | 5 | HG01192.hp1 HG03041.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154-880G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188384 | ||||||
| chr10:50188385
|
G | A | 1 | a0002c0001t0029g0322 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2154-881C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188385 | ||||||
| chr10:50188389
|
TA | T | 3 | a0001c0002t0009g0347a0001c0005t0025g0007a0001c0005t0025g0034 | 4 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154-886delT | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188389 | ||||||
| chr10:50188555
|
A | G | 26 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(23): Show | 27 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.2153+944T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188555 | ||||||
| chr10:50188589
|
C | G | 11 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0004t0046g0296others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2153+910G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188589 | ||||||
| chr10:50188636
|
A | G | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2153+863T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188636 | ||||||
| chr10:50188637
|
C | T | 1 | a0003c0003t0001g0222 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2153+862G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188637 | ||||||
| chr10:50188891
|
T | A | 1 | a0001c0002t0001g0012 | 2 | HG01070.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2153+608A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188891 | ||||||
| chr10:50188904
|
A | G | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2153+595T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188904 | ||||||
| chr10:50188934
|
A | G | 328 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(325): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.2153+565T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188934 | ||||||
| chr10:50188976
|
C | T | 328 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(325): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.2153+523G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188976 | ||||||
| chr10:50188977
|
G | A | 3 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0015t0094g0036 | 3 | HG03225.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2153+522C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50188977 | ||||||
| chr10:50189038
|
T | C | 123 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(120): Show | 138 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.2153+461A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50189038 | ||||||
| chr10:50189197
|
T | C | 118 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(115): Show | 133 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.2153+302A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50189197 | ||||||
| chr10:50189224
|
G | A | 46 | a0001c0002t0001g0083a0001c0002t0001g0095a0001c0002t0003g0004others(43): Show | 53 | HG00423.hp2 HG00558.hp2 HG02015.hp1 others(50): Show |
intron_variant | MODIFIER | c.2153+275C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50189224 | ||||||
| chr10:50189321
|
C | T | 122 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(119): Show | 137 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.2153+178G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50189321 | ||||||
| chr10:50189345
|
C | G | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2153+154G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50189345 | ||||||
| chr10:50189439
|
C | T | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2153+60G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50189439 | ||||||
| chr10:50189448
|
C | T | 1 | a0002c0001t0029g0337 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2153+51G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50189448 | ||||||
| chr10:50189460
|
G | A | 206 | a0002c0001t0002g0005a0002c0001t0002g0024a0002c0001t0002g0182others(203): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2153+39C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50189460 | ||||||
| chr10:50189478
|
A | G | 2 | a0002c0006t0106g0058a0002c0006t0114g0302 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2153+21T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 20/20 | chr10 | 50189478 | ||||||
| chr10:50189782
|
A | G | 1 | a0001c0011t0020g0344 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2065-195T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50189782 | ||||||
| chr10:50189951
|
G | A | 118 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(115): Show | 133 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.2065-364C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50189951 | ||||||
| chr10:50189966
|
C | T | 122 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(119): Show | 137 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.2065-379G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50189966 | ||||||
| chr10:50189974
|
G | T | 122 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(119): Show | 137 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.2065-387C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50189974 | ||||||
| chr10:50190062
|
T | C | 2 | a0002c0001t0027g0224a0002c0001t0062g0320 | 2 | HG00642.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2065-475A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190062 | ||||||
| chr10:50190086
|
T | C | 1 | a0002c0001t0035g0251 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2065-499A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190086 | ||||||
| chr10:50190224
|
C | G | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2065-637G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190224 | ||||||
| chr10:50190274
|
C | A | 118 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(115): Show | 133 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.2065-687G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190274 | ||||||
| chr10:50190306
|
G | T | 1 | a0002c0006t0101g0273 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2065-719C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190306 | ||||||
| chr10:50190318
|
G | C | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2065-731C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190318 | ||||||
| chr10:50190318
|
G | T | 1 | a0002c0006t0114g0302 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2065-731C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190318 | ||||||
| chr10:50190344
|
A | C | 102 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0007g0003others(99): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.2065-757T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190344 | ||||||
| chr10:50190398
|
T | C | 5 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(2): Show | 8 | HG01167.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2065-811A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190398 | ||||||
| chr10:50190418
|
G | A | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2065-831C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190418 | ||||||
| chr10:50190443
|
C | T | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2065-856G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190443 | ||||||
| chr10:50190503
|
T | C | 329 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.2065-916A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190503 | ||||||
| chr10:50190616
|
T | C | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2065-1029A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190616 | ||||||
| chr10:50190674
|
C | T | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2065-1087G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190674 | ||||||
| chr10:50190704
|
C | G | 14 | a0001c0002t0009g0272a0001c0002t0009g0351a0001c0002t0009g0352others(11): Show | 15 | HG00735.hp2 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2065-1117G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190704 | ||||||
| chr10:50190756
|
G | A | 211 | a0001c0004t0012g0001a0001c0004t0012g0299a0001c0005t0117g0266others(208): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.2065-1169C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190756 | ||||||
| chr10:50190773
|
G | A | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2065-1186C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190773 | ||||||
| chr10:50190776
|
A | G | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2065-1189T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190776 | ||||||
| chr10:50190777
|
G | A | 3 | a0001c0002t0044g0011a0001c0002t0076g0056a0001c0002t0083g0057 | 4 | HG02895.hp1 HG02897.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2065-1190C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190777 | ||||||
| chr10:50190797
|
T | C | 4 | a0001c0002t0009g0347a0001c0002t0025g0346a0001c0005t0025g0007others(1): Show | 5 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2065-1210A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190797 | ||||||
| chr10:50190800
|
G | A | 329 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.2065-1213C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190800 | ||||||
| chr10:50190807
|
G | A | 208 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0002g0005others(205): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2065-1220C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190807 | ||||||
| chr10:50190929
|
G | A | 1 | a0001c0004t0033g0275 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2065-1342C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190929 | ||||||
| chr10:50190959
|
G | A | 332 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(329): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.2065-1372C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50190959 | ||||||
| chr10:50191130
|
G | A | 332 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(329): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.2064+1523C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191130 | ||||||
| chr10:50191135
|
C | T | 332 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(329): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.2064+1518G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191135 | ||||||
| chr10:50191185
|
G | C | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+1468C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191185 | ||||||
| chr10:50191230
|
A | G | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2064+1423T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191230 | ||||||
| chr10:50191256
|
A | G | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2064+1397T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191256 | ||||||
| chr10:50191260
|
T | C | 274 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(271): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.2064+1393A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191260 | ||||||
| chr10:50191263
|
T | C | 59 | a0002c0001t0002g0005a0002c0001t0002g0024a0002c0001t0002g0182others(56): Show | 66 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2064+1390A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191263 | ||||||
| chr10:50191352
|
G | A | 5 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(2): Show | 8 | HG01167.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2064+1301C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191352 | ||||||
| chr10:50191442
|
C | T | 1 | a0002c0001t0004g0023 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2064+1211G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191442 | ||||||
| chr10:50191452
|
T | G | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2064+1201A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191452 | ||||||
| chr10:50191455
|
T | C | 4 | a0001c0005t0019g0217a0001c0005t0055g0218a0001c0005t0055g0220others(1): Show | 4 | HG02109.hp1 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+1198A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191455 | ||||||
| chr10:50191534
|
C | G | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2064+1119G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191534 | ||||||
| chr10:50191576
|
T | C | 59 | a0002c0001t0002g0005a0002c0001t0002g0024a0002c0001t0002g0182others(56): Show | 66 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2064+1077A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191576 | ||||||
| chr10:50191577
|
A | G | 1 | a0001c0002t0003g0088 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2064+1076T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191577 | ||||||
| chr10:50191587
|
A | G | 1 | a0002c0001t0018g0312 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2064+1066T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191587 | ||||||
| chr10:50191614
|
A | G | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2064+1039T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191614 | ||||||
| chr10:50191620
|
C | T | 5 | a0003c0003t0001g0130a0003c0003t0001g0158a0003c0003t0001g0160others(2): Show | 5 | HG02698.hp1 NA18941.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.2064+1033G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191620 | ||||||
| chr10:50191674
|
G | A | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+979C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191674 | ||||||
| chr10:50191785
|
T | C | 5 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(2): Show | 8 | HG01167.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2064+868A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191785 | ||||||
| chr10:50191807
|
C | T | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+846G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191807 | ||||||
| chr10:50191808
|
A | G | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2064+845T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191808 | ||||||
| chr10:50191828
|
A | G | 1 | a0003c0003t0032g0019 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2064+825T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191828 | ||||||
| chr10:50191865
|
T | C | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2064+788A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191865 | ||||||
| chr10:50191872
|
C | G | 3 | a0003c0003t0039g0149a0003c0003t0088g0177a0003c0008t0001g0075 | 3 | HG00609.hp1 NA18948.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.2064+781G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191872 | ||||||
| chr10:50191896
|
G | A | 1 | a0001c0004t0034g0276 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2064+757C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50191896 | ||||||
| chr10:50192007
|
A | G | 1 | a0002c0001t0035g0251 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2064+646T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192007 | ||||||
| chr10:50192133
|
T | TACAC | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2064+519_2064+520i others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192133 | ||||||
| chr10:50192139
|
G | A | 1 | a0002c0001t0035g0254 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2064+514C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192139 | ||||||
| chr10:50192151
|
T | C | 329 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.2064+502A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192151 | ||||||
| chr10:50192157
|
G | A | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2064+496C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192157 | ||||||
| chr10:50192168
|
G | T | 1 | a0002c0001t0042g0331 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2064+485C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192168 | ||||||
| chr10:50192203
|
G | A | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2064+450C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192203 | ||||||
| chr10:50192259
|
G | A | 329 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(326): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.2064+394C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192259 | ||||||
| chr10:50192279
|
G | A | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+374C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192279 | ||||||
| chr10:50192298
|
C | T | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2064+355G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192298 | ||||||
| chr10:50192353
|
T | A | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+300A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192353 | ||||||
| chr10:50192353
|
T | C | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.2064+300A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192353 | ||||||
| chr10:50192355
|
C | G | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064+298G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192355 | ||||||
| chr10:50192356
|
A | G | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2064+297T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192356 | ||||||
| chr10:50192410
|
A | G | 1 | a0002c0001t0002g0231 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2064+243T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192410 | ||||||
| chr10:50192447
|
G | A | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2064+206C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192447 | ||||||
| chr10:50192454
|
TTA | T | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2064+197_2064+198d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192454 | ||||||
| chr10:50192469
|
G | T | 5 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(2): Show | 8 | HG01167.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2064+184C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192469 | ||||||
| chr10:50192481
|
A | G | 1 | a0003c0003t0023g0159 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2064+172T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192481 | ||||||
| chr10:50192519
|
C | T | 2 | a0001c0004t0006g0298a0001c0004t0033g0297 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2064+134G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 19/20 | chr10 | 50192519 | ||||||
| chr10:50192738
|
T | C | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2005-26A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50192738 | ||||||
| chr10:50192749
|
C | A | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2005-37G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50192749 | ||||||
| chr10:50192751
|
GT | G | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2005-40delA | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50192751 | ||||||
| chr10:50192776
|
G | C | 1 | a0001c0007t0038g0360 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2005-64C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50192776 | ||||||
| chr10:50192777
|
A | T | 1 | a0001c0007t0038g0360 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2005-65T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50192777 | ||||||
| chr10:50192876
|
A | T | 1 | a0008c0023t0110g0361 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2005-164T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50192876 | ||||||
| chr10:50192916
|
A | G | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2005-204T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50192916 | ||||||
| chr10:50192933
|
A | G | 1 | a0003c0003t0001g0158 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2005-221T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50192933 | ||||||
| chr10:50193026
|
A | G | 4 | a0001c0002t0006g0079a0001c0002t0051g0112a0001c0002t0053g0078others(1): Show | 4 | HG03239.hp2 HG03704.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.2005-314T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50193026 | ||||||
| chr10:50193100
|
C | G | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2005-388G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50193100 | ||||||
| chr10:50193155
|
C | A | 2 | a0001c0002t0091g0111a0001c0005t0117g0266 | 2 | HG01981.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2005-443G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50193155 | ||||||
| chr10:50193231
|
T | A | 1 | a0002c0024t0041g0314 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2005-519A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50193231 | ||||||
| chr10:50193434
|
A | G | 113 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(110): Show | 125 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.2005-722T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50193434 | ||||||
| chr10:50193462
|
C | T | 1 | a0002c0001t0002g0229 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2005-750G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50193462 | ||||||
| chr10:50193481
|
G | C | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2005-769C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50193481 | ||||||
| chr10:50193499
|
A | G | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.2005-787T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50193499 | ||||||
| chr10:50193699
|
A | G | 1 | a0001c0011t0109g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2005-987T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50193699 | ||||||
| chr10:50193944
|
C | G | 1 | a0001c0010t0102g0362 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2005-1232G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50193944 | ||||||
| chr10:50193994
|
T | G | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2005-1282A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50193994 | ||||||
| chr10:50194010
|
G | T | 1 | a0003c0003t0005g0209 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2005-1298C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194010 | ||||||
| chr10:50194071
|
G | T | 2 | a0001c0010t0087g0050a0001c0015t0094g0036 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2005-1359C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194071 | ||||||
| chr10:50194254
|
C | CCT | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2005-1543_2005-154 others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194254 | ||||||
| chr10:50194322
|
G | A | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2005-1610C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194322 | ||||||
| chr10:50194326
|
T | C | 113 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(110): Show | 125 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.2005-1614A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194326 | ||||||
| chr10:50194355
|
T | C | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2005-1643A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194355 | ||||||
| chr10:50194548
|
C | A | 122 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(119): Show | 137 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.2005-1836G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194548 | ||||||
| chr10:50194562
|
A | G | 112 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(109): Show | 124 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.2005-1850T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194562 | ||||||
| chr10:50194644
|
A | C | 1 | a0002c0001t0004g0247 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2005-1932T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194644 | ||||||
| chr10:50194758
|
G | T | 210 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0002g0005others(207): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2004+2015C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194758 | ||||||
| chr10:50194800
|
C | T | 49 | a0002c0001t0008g0123a0002c0001t0008g0309a0002c0001t0008g0313others(46): Show | 51 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.2004+1973G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194800 | ||||||
| chr10:50194933
|
A | G | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+1840T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194933 | ||||||
| chr10:50194968
|
A | G | 46 | a0001c0002t0001g0083a0001c0002t0001g0095a0001c0002t0003g0004others(43): Show | 53 | HG00423.hp2 HG00558.hp2 HG02015.hp1 others(50): Show |
intron_variant | MODIFIER | c.2004+1805T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194968 | ||||||
| chr10:50194981
|
C | T | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+1792G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50194981 | ||||||
| chr10:50195069
|
G | A | 5 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(2): Show | 8 | HG01167.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2004+1704C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50195069 | ||||||
| chr10:50195097
|
G | A | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2004+1676C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50195097 | ||||||
| chr10:50195099
|
G | A | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2004+1674C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50195099 | ||||||
| chr10:50195216
|
C | T | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+1557G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50195216 | ||||||
| chr10:50195266
|
C | T | 59 | a0002c0001t0002g0005a0002c0001t0002g0024a0002c0001t0002g0182others(56): Show | 66 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2004+1507G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50195266 | ||||||
| chr10:50195314
|
C | T | 1 | a0001c0005t0019g0205 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2004+1459G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50195314 | ||||||
| chr10:50195505
|
A | T | 1 | a0001c0004t0006g0293 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2004+1268T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50195505 | ||||||
| chr10:50195649
|
T | C | 1 | a0002c0001t0115g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2004+1124A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50195649 | ||||||
| chr10:50195778
|
A | G | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+995T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50195778 | ||||||
| chr10:50195833
|
C | T | 1 | a0002c0001t0003g0235 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2004+940G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50195833 | ||||||
| chr10:50195837
|
C | A | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+936G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50195837 | ||||||
| chr10:50195956
|
G | C | 1 | a0001c0004t0006g0295 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2004+817C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50195956 | ||||||
| chr10:50196079
|
T | C | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2004+694A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50196079 | ||||||
| chr10:50196152
|
G | A | 122 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(119): Show | 137 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.2004+621C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50196152 | ||||||
| chr10:50196198
|
T | A | 1 | a0002c0001t0043g0335 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2004+575A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50196198 | ||||||
| chr10:50196216
|
A | T | 113 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(110): Show | 125 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.2004+557T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50196216 | ||||||
| chr10:50196228
|
G | A | 14 | a0001c0002t0001g0012a0001c0002t0005g0061a0001c0002t0005g0063others(11): Show | 16 | HG00733.hp2 HG01070.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.2004+545C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50196228 | ||||||
| chr10:50196242
|
G | A | 123 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(120): Show | 138 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.2004+531C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50196242 | ||||||
| chr10:50196248
|
G | A | 1 | a0001c0002t0096g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2004+525C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50196248 | ||||||
| chr10:50196268
|
T | C | 1 | a0001c0005t0008g0215 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2004+505A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50196268 | ||||||
| chr10:50196673
|
A | G | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2004+100T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50196673 | ||||||
| chr10:50196733
|
A | AT | 26 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(23): Show | 27 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.2004+39dupA | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 18/20 | chr10 | 50196733 | ||||||
| chr10:50196961
|
C | T | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1858-42G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50196961 | ||||||
| chr10:50197051
|
A | C | 2 | a0001c0004t0046g0296a0001c0004t0090g0348 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1858-132T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50197051 | ||||||
| chr10:50197154
|
C | T | 113 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(110): Show | 125 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.1858-235G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50197154 | ||||||
| chr10:50197259
|
T | C | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1858-340A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50197259 | ||||||
| chr10:50197339
|
C | T | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1858-420G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50197339 | ||||||
| chr10:50197370
|
T | C | 118 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(115): Show | 133 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.1858-451A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50197370 | ||||||
| chr10:50197458
|
A | C | 1 | a0003c0003t0024g0145 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1858-539T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50197458 | ||||||
| chr10:50197564
|
C | T | 1 | a0001c0002t0006g0079 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1858-645G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50197564 | ||||||
| chr10:50197779
|
CA | C | 5 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(2): Show | 8 | HG01167.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1858-861delT | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50197779 | ||||||
| chr10:50197872
|
T | G | 122 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(119): Show | 137 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.1858-953A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50197872 | ||||||
| chr10:50197927
|
T | A | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1858-1008A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50197927 | ||||||
| chr10:50197994
|
A | G | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857+1057T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50197994 | ||||||
| chr10:50198005
|
A | C | 5 | a0001c0005t0008g0215a0001c0005t0009g0214a0001c0005t0052g0216others(2): Show | 5 | HG02630.hp2 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1857+1046T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198005 | ||||||
| chr10:50198030
|
G | A | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1857+1021C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198030 | ||||||
| chr10:50198064
|
AAC | A | 49 | a0002c0001t0008g0123a0002c0001t0008g0309a0002c0001t0008g0313others(46): Show | 51 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1857+985_1857+986d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198064 | ||||||
| chr10:50198111
|
T | A | 1 | a0009c0021t0019g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1857+940A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198111 | ||||||
| chr10:50198156
|
C | T | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857+895G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198156 | ||||||
| chr10:50198240
|
C | T | 2 | a0001c0004t0020g0290a0001c0004t0020g0291 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1857+811G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198240 | ||||||
| chr10:50198276
|
CTCTTTA | C | 12 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0004t0046g0296others(9): Show | 12 | HG01192.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1857+769_1857+774d others(8): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198276 | ||||||
| chr10:50198282
|
AT | A | 106 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(103): Show | 121 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.1857+768delA | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198282 | ||||||
| chr10:50198336
|
G | A | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857+715C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198336 | ||||||
| chr10:50198395
|
C | T | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857+656G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198395 | ||||||
| chr10:50198603
|
C | T | 1 | a0001c0004t0006g0295 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1857+448G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198603 | ||||||
| chr10:50198615
|
C | A | 1 | a0001c0002t0083g0057 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1857+436G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198615 | ||||||
| chr10:50198849
|
T | G | 122 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(119): Show | 137 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.1857+202A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198849 | ||||||
| chr10:50198927
|
G | A | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857+124C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198927 | ||||||
| chr10:50198991
|
TAC | T | 7 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(4): Show | 10 | HG01167.hp2 HG02257.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1857+58_1857+59del others(2): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198991 | ||||||
| chr10:50198991
|
TACACAC | T | 113 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(110): Show | 125 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.1857+54_1857+59del others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50198991 | ||||||
| chr10:50199004
|
A | T | 1 | a0001c0002t0083g0057 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1857+47T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50199004 | ||||||
| chr10:50199017
|
C | T | 7 | a0003c0003t0001g0052a0003c0003t0001g0129a0003c0003t0001g0156others(4): Show | 8 | HG02056.hp2 HG02135.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.1857+34G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50199017 | ||||||
| chr10:50199020
|
G | A | 122 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(119): Show | 137 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.1857+31C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 17/20 | chr10 | 50199020 | ||||||
| chr10:50199171
|
T | C | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1762-25A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199171 | ||||||
| chr10:50199172
|
A | C | 113 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(110): Show | 125 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.1762-26T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199172 | ||||||
| chr10:50199248
|
A | T | 1 | a0001c0002t0080g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1762-102T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199248 | ||||||
| chr10:50199365
|
G | T | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762-219C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199365 | ||||||
| chr10:50199407
|
C | G | 332 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(329): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1762-261G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199407 | ||||||
| chr10:50199514
|
A | G | 1 | a0002c0024t0041g0314 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1762-368T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199514 | ||||||
| chr10:50199637
|
T | C | 75 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(72): Show | 86 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1762-491A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199637 | ||||||
| chr10:50199671
|
A | G | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1762-525T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199671 | ||||||
| chr10:50199713
|
C | G | 1 | a0002c0001t0054g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1762-567G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199713 | ||||||
| chr10:50199808
|
C | T | 5 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(2): Show | 5 | HG01243.hp1 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762-662G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199808 | ||||||
| chr10:50199899
|
A | G | 3 | a0001c0002t0022g0108a0001c0002t0045g0107a0001c0002t0077g0109 | 3 | NA18950.hp1 NA18952.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1762-753T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199899 | ||||||
| chr10:50199913
|
C | T | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762-767G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199913 | ||||||
| chr10:50199942
|
G | A | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762-796C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199942 | ||||||
| chr10:50199956
|
C | T | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1762-810G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50199956 | ||||||
| chr10:50200139
|
T | G | 1 | a0002c0001t0063g0240 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1762-993A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50200139 | ||||||
| chr10:50200369
|
T | A | 1 | a0001c0002t0003g0004 | 3 | NA18963.hp2 NA18983.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1762-1223A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50200369 | ||||||
| chr10:50200397
|
G | T | 73 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(70): Show | 84 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1762-1251C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50200397 | ||||||
| chr10:50200554
|
C | A | 1 | a0002c0006t0106g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1762-1408G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50200554 | ||||||
| chr10:50200615
|
G | A | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1762-1469C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50200615 | ||||||
| chr10:50200622
|
A | C | 1 | a0001c0004t0046g0296 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1762-1476T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50200622 | ||||||
| chr10:50200691
|
A | C | 1 | a0003c0003t0001g0156 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1762-1545T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50200691 | ||||||
| chr10:50200703
|
A | G | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1762-1557T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50200703 | ||||||
| chr10:50200720
|
G | T | 1 | a0001c0002t0051g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1762-1574C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50200720 | ||||||
| chr10:50200755
|
G | C | 38 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(35): Show | 39 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.1762-1609C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50200755 | ||||||
| chr10:50200787
|
T | C | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762-1641A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50200787 | ||||||
| chr10:50200895
|
C | A | 2 | a0002c0001t0027g0224a0002c0001t0062g0320 | 2 | HG00642.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1762-1749G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50200895 | ||||||
| chr10:50201004
|
G | A | 49 | a0002c0001t0008g0123a0002c0001t0008g0309a0002c0001t0008g0313others(46): Show | 51 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1761+1825C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201004 | ||||||
| chr10:50201067
|
G | A | 1 | a0001c0002t0003g0092 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1761+1762C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201067 | ||||||
| chr10:50201090
|
C | T | 12 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0004t0046g0296others(9): Show | 12 | HG01192.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1761+1739G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201090 | ||||||
| chr10:50201188
|
C | T | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1761+1641G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201188 | ||||||
| chr10:50201364
|
A | G | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1761+1465T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201364 | ||||||
| chr10:50201425
|
A | T | 1 | a0003c0003t0001g0174 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1761+1404T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201425 | ||||||
| chr10:50201541
|
A | T | 1 | a0002c0001t0016g0250 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1761+1288T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201541 | ||||||
| chr10:50201722
|
T | C | 2 | a0002c0001t0027g0224a0002c0001t0062g0320 | 2 | HG00642.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1761+1107A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201722 | ||||||
| chr10:50201745
|
T | C | 1 | a0002c0001t0011g0238 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1761+1084A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201745 | ||||||
| chr10:50201788
|
G | T | 1 | a0003c0003t0015g0197 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1761+1041C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201788 | ||||||
| chr10:50201844
|
G | A | 1 | a0002c0001t0008g0315 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1761+985C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201844 | ||||||
| chr10:50201865
|
T | A | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1761+964A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201865 | ||||||
| chr10:50201928
|
A | C | 5 | a0003c0003t0001g0155a0003c0003t0001g0186a0003c0003t0005g0115others(2): Show | 5 | HG00733.hp1 HG02165.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1761+901T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201928 | ||||||
| chr10:50201991
|
A | G | 1 | a0001c0004t0006g0295 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1761+838T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50201991 | ||||||
| chr10:50202008
|
T | C | 2 | a0001c0010t0087g0050a0001c0015t0094g0036 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1761+821A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50202008 | ||||||
| chr10:50202046
|
C | A | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1761+783G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50202046 | ||||||
| chr10:50202143
|
G | A | 59 | a0002c0001t0002g0005a0002c0001t0002g0024a0002c0001t0002g0182others(56): Show | 66 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1761+686C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50202143 | ||||||
| chr10:50202157
|
T | C | 1 | a0002c0001t0008g0319 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1761+672A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50202157 | ||||||
| chr10:50202376
|
G | A | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1761+453C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50202376 | ||||||
| chr10:50202569
|
G | T | 1 | a0001c0005t0025g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1761+260C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50202569 | ||||||
| chr10:50202685
|
T | TTA | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1761+142_1761+143d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50202685 | ||||||
| chr10:50202703
|
T | C | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1761+126A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50202703 | ||||||
| chr10:50202715
|
C | T | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1761+114G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50202715 | ||||||
| chr10:50202773
|
A | C | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1761+56T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 16/20 | chr10 | 50202773 | ||||||
| chr10:50202970
|
C | A | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1666-46G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 15/20 | chr10 | 50202970 | ||||||
| chr10:50203047
|
T | A | 2 | a0002c0001t0041g0329a0002c0024t0041g0314 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1666-123A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 15/20 | chr10 | 50203047 | ||||||
| chr10:50203096
|
C | T | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1666-172G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 15/20 | chr10 | 50203096 | ||||||
| chr10:50203577
|
A | AATCCTAT others(7): Show |
102 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0007g0003others(99): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1665+62_1665+63ins others(14): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 15/20 | chr10 | 50203577 | ||||||
| chr10:50203578
|
G | A | 106 | a0001c0004t0012g0001a0001c0004t0012g0299a0001c0010t0069g0200others(103): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1665+62C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 15/20 | chr10 | 50203578 | ||||||
| chr10:50203580
|
A | G | 102 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0007g0003others(99): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1665+60T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 15/20 | chr10 | 50203580 | ||||||
| chr10:50203581
|
T | G | 102 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0007g0003others(99): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1665+59A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 15/20 | chr10 | 50203581 | ||||||
| chr10:50203609
|
A | G | 1 | a0002c0001t0027g0311 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1665+31T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 15/20 | chr10 | 50203609 | ||||||
| chr10:50203694
|
A | C | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1626-15T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50203694 | ||||||
| chr10:50203735
|
A | G | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1626-56T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50203735 | ||||||
| chr10:50203746
|
G | T | 5 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(2): Show | 5 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1626-67C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50203746 | ||||||
| chr10:50203798
|
T | C | 4 | a0001c0002t0003g0014a0001c0002t0003g0089a0001c0002t0003g0090others(1): Show | 5 | NA18974.hp1 NA18997.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.1626-119A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50203798 | ||||||
| chr10:50204024
|
A | G | 1 | a0001c0010t0102g0362 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1626-345T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50204024 | ||||||
| chr10:50204102
|
G | C | 1 | a0002c0001t0026g0184 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1626-423C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50204102 | ||||||
| chr10:50204321
|
C | A | 1 | a0001c0002t0003g0090 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1625+540G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50204321 | ||||||
| chr10:50204321
|
C | T | 4 | a0001c0010t0069g0200a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG02976.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1625+540G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50204321 | ||||||
| chr10:50204368
|
A | C | 2 | a0002c0006t0106g0058a0002c0006t0114g0302 | 2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1625+493T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50204368 | ||||||
| chr10:50204394
|
A | T | 1 | a0002c0006t0101g0273 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1625+467T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50204394 | ||||||
| chr10:50204627
|
TA | T | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1625+233delT | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50204627 | ||||||
| chr10:50204629
|
A | C | 2 | a0001c0005t0117g0266a0001c0010t0069g0200 | 2 | HG01981.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1625+232T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50204629 | ||||||
| chr10:50204630
|
G | C | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1625+231C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50204630 | ||||||
| chr10:50204654
|
C | T | 1 | a0007c0017t0003g0106 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1625+207G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50204654 | ||||||
| chr10:50204833
|
T | C | 1 | a0001c0002t0005g0066 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1625+28A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 14/20 | chr10 | 50204833 | ||||||
| chr10:50205060
|
A | G | 27 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(24): Show | 28 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1531-105T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 13/20 | chr10 | 50205060 | ||||||
| chr10:50205145
|
C | A | 1 | a0003c0003t0001g0168 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1531-190G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 13/20 | chr10 | 50205145 | ||||||
| chr10:50205224
|
G | A | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1531-269C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 13/20 | chr10 | 50205224 | ||||||
| chr10:50205325
|
C | A | 27 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(24): Show | 28 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1531-370G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 13/20 | chr10 | 50205325 | ||||||
| chr10:50205454
|
G | GA | 31 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(28): Show | 32 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1531-500dupT | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 13/20 | chr10 | 50205454 | ||||||
| chr10:50205550
|
C | T | 7 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(4): Show | 10 | HG01167.hp2 HG02257.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1530+432G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 13/20 | chr10 | 50205550 | ||||||
| chr10:50205620
|
C | T | 1 | a0001c0002t0001g0012 | 2 | HG01070.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1530+362G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 13/20 | chr10 | 50205620 | ||||||
| chr10:50205621
|
A | G | 27 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(24): Show | 28 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1530+361T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 13/20 | chr10 | 50205621 | ||||||
| chr10:50205687
|
G | A | 27 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(24): Show | 28 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1530+295C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 13/20 | chr10 | 50205687 | ||||||
| chr10:50205726
|
T | G | 1 | a0001c0002t0003g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1530+256A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 13/20 | chr10 | 50205726 | ||||||
| chr10:50205822
|
T | C | 30 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(27): Show | 31 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1530+160A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 13/20 | chr10 | 50205822 | ||||||
| chr10:50205908
|
A | G | 15 | a0001c0002t0001g0012a0001c0002t0005g0061a0001c0002t0005g0063others(12): Show | 17 | HG00597.hp2 HG00733.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1530+74T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 13/20 | chr10 | 50205908 | ||||||
| chr10:50206106
|
A | C | 1 | a0001c0002t0096g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1415-9T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206106 | ||||||
| chr10:50206187
|
A | G | 3 | a0002c0001t0008g0313a0002c0001t0018g0312a0002c0001t0021g0345 | 3 | HG01928.hp1 HG01975.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1415-90T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206187 | ||||||
| chr10:50206254
|
G | A | 210 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0002g0005others(207): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1415-157C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206254 | ||||||
| chr10:50206274
|
T | C | 1 | a0001c0002t0056g0364 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1415-177A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206274 | ||||||
| chr10:50206275
|
A | G | 30 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(27): Show | 31 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1415-178T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206275 | ||||||
| chr10:50206484
|
A | G | 1 | a0001c0005t0011g0009 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1415-387T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206484 | ||||||
| chr10:50206517
|
T | C | 1 | a0001c0002t0022g0108 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1415-420A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206517 | ||||||
| chr10:50206535
|
T | C | 13 | a0001c0007t0038g0358a0002c0001t0007g0003a0002c0001t0007g0038others(10): Show | 15 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1415-438A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206535 | ||||||
| chr10:50206537
|
T | TAC | 58 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(55): Show | 72 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.1415-442_1415-441d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206537 | ||||||
| chr10:50206537
|
T | TACAC | 73 | a0001c0002t0006g0079a0001c0002t0009g0347a0001c0002t0025g0346others(70): Show | 84 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1415-444_1415-441d others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206537 | ||||||
| chr10:50206537
|
T | TACACAC | 85 | a0001c0002t0022g0108a0001c0002t0045g0107a0001c0002t0053g0078others(82): Show | 91 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1415-446_1415-441d others(8): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206537 | ||||||
| chr10:50206537
|
T | TACACACA others(1): Show |
52 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(49): Show | 58 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(55): Show |
intron_variant | MODIFIER | c.1415-448_1415-441d others(10): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206537 | ||||||
| chr10:50206537
|
T | TACACACA others(3): Show |
27 | a0001c0002t0080g0274a0001c0002t0118g0301a0001c0004t0090g0348others(24): Show | 28 | HG00639.hp1 HG01433.hp2 HG01515.hp1 others(25): Show |
intron_variant | MODIFIER | c.1415-450_1415-441d others(12): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206537 | ||||||
| chr10:50206537
|
T | TACACACA others(5): Show |
5 | a0001c0002t0077g0109a0001c0005t0117g0266a0002c0001t0008g0319others(2): Show | 5 | HG01515.hp2 HG01981.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1415-452_1415-441d others(14): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206537 | ||||||
| chr10:50206537
|
T | TACACACA others(7): Show |
5 | a0001c0007t0038g0358a0002c0001t0007g0003a0002c0001t0007g0048others(2): Show | 7 | HG01256.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1415-454_1415-441d others(16): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206537 | ||||||
| chr10:50206537
|
TAC | T | 6 | a0001c0002t0003g0093a0001c0004t0033g0278a0001c0004t0034g0276others(3): Show | 6 | HG00738.hp2 HG01943.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1415-442_1415-441d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206537 | ||||||
| chr10:50206537
|
TACAC | T | 7 | a0001c0004t0033g0275a0001c0005t0008g0215a0001c0005t0009g0214others(4): Show | 7 | HG02630.hp2 HG02896.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1415-444_1415-441d others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206537 | ||||||
| chr10:50206537
|
TACACACA others(3): Show |
T | 1 | a0002c0006t0106g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1415-450_1415-441d others(12): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206537 | ||||||
| chr10:50206578
|
A | ACACACAC others(4): Show |
1 | a0002c0001t0021g0339 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1415-482_1415-481i others(13): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206578 | ||||||
| chr10:50206579
|
A | C | 1 | a0001c0002t0051g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1415-482T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206579 | ||||||
| chr10:50206646
|
C | T | 2 | a0001c0004t0012g0001a0001c0004t0012g0299 | 8 | HG02132.hp1 NA19004.hp1 NA19007.hp2 others(5): Show |
intron_variant | MODIFIER | c.1415-549G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206646 | ||||||
| chr10:50206647
|
T | G | 2 | a0003c0003t0001g0052a0003c0008t0001g0013 | 3 | NA18747.hp2 NA19065.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1415-550A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206647 | ||||||
| chr10:50206658
|
G | T | 1 | a0003c0003t0001g0152 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1415-561C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206658 | ||||||
| chr10:50206662
|
C | A | 30 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(27): Show | 31 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1415-565G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206662 | ||||||
| chr10:50206665
|
T | C | 211 | a0001c0004t0012g0001a0001c0004t0012g0299a0001c0007t0038g0358others(208): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1415-568A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206665 | ||||||
| chr10:50206766
|
A | G | 2 | a0003c0003t0014g0151a0003c0003t0014g0170 | 2 | NA18974.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1415-669T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206766 | ||||||
| chr10:50206784
|
C | T | 10 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0004t0090g0348others(7): Show | 10 | HG01192.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1415-687G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206784 | ||||||
| chr10:50206787
|
A | G | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1415-690T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206787 | ||||||
| chr10:50206799
|
A | G | 30 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(27): Show | 31 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1415-702T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206799 | ||||||
| chr10:50206893
|
C | T | 84 | a0003c0003t0001g0002a0003c0003t0001g0020a0003c0003t0001g0052others(81): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1415-796G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206893 | ||||||
| chr10:50206910
|
A | G | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1415-813T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50206910 | ||||||
| chr10:50207039
|
G | A | 5 | a0001c0004t0033g0275a0001c0004t0033g0278a0001c0004t0034g0276others(2): Show | 5 | HG00738.hp2 HG01943.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.1415-942C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50207039 | ||||||
| chr10:50207092
|
G | T | 30 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(27): Show | 31 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1415-995C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50207092 | ||||||
| chr10:50207211
|
C | T | 2 | a0001c0004t0012g0001a0001c0004t0012g0299 | 8 | HG02132.hp1 NA19004.hp1 NA19007.hp2 others(5): Show |
intron_variant | MODIFIER | c.1415-1114G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50207211 | ||||||
| chr10:50207270
|
T | A | 1 | a0001c0002t0076g0056 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1415-1173A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50207270 | ||||||
| chr10:50207364
|
A | G | 30 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(27): Show | 31 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1415-1267T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50207364 | ||||||
| chr10:50207530
|
A | G | 75 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(72): Show | 86 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1415-1433T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50207530 | ||||||
| chr10:50207631
|
TC | T | 9 | a0002c0001t0002g0248a0002c0001t0004g0030a0002c0001t0004g0211others(6): Show | 10 | HG02015.hp2 HG02040.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1415-1535delG | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50207631 | ||||||
| chr10:50207632
|
C | G | 5 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(2): Show | 8 | HG01167.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1415-1535G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50207632 | ||||||
| chr10:50207633
|
TA | T | 241 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(238): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1415-1537delT | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50207633 | ||||||
| chr10:50207634
|
A | T | 9 | a0002c0001t0002g0248a0002c0001t0004g0030a0002c0001t0004g0211others(6): Show | 10 | HG02015.hp2 HG02040.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1415-1537T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50207634 | ||||||
| chr10:50207801
|
G | C | 30 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(27): Show | 31 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1415-1704C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50207801 | ||||||
| chr10:50207815
|
G | A | 30 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(27): Show | 31 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1415-1718C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50207815 | ||||||
| chr10:50208267
|
T | C | 252 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(249): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1415-2170A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50208267 | ||||||
| chr10:50208313
|
C | A | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1415-2216G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50208313 | ||||||
| chr10:50208473
|
G | A | 1 | a0002c0001t0111g0039 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1414+2350C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50208473 | ||||||
| chr10:50208590
|
C | CTT | 330 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(327): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.1414+2232_1414+223 others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50208590 | ||||||
| chr10:50208689
|
T | C | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1414+2134A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50208689 | ||||||
| chr10:50208768
|
A | G | 11 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0004t0090g0348others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1414+2055T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50208768 | ||||||
| chr10:50208879
|
A | G | 81 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(78): Show | 95 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.1414+1944T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50208879 | ||||||
| chr10:50208924
|
C | T | 1 | a0002c0001t0042g0332 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1414+1899G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50208924 | ||||||
| chr10:50208967
|
G | C | 2 | a0001c0002t0005g0061a0001c0002t0047g0062 | 2 | HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1414+1856C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50208967 | ||||||
| chr10:50209028
|
A | G | 1 | a0001c0011t0020g0344 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1414+1795T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209028 | ||||||
| chr10:50209082
|
G | C | 1 | a0001c0002t0049g0031 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1414+1741C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209082 | ||||||
| chr10:50209088
|
T | C | 31 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(28): Show | 32 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1414+1735A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209088 | ||||||
| chr10:50209217
|
T | G | 1 | a0001c0002t0003g0088 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1414+1606A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209217 | ||||||
| chr10:50209236
|
C | T | 1 | a0001c0004t0090g0348 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1414+1587G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209236 | ||||||
| chr10:50209442
|
C | T | 221 | a0001c0004t0012g0001a0001c0004t0012g0299a0001c0004t0020g0290others(218): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1414+1381G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209442 | ||||||
| chr10:50209445
|
T | G | 252 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(249): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1414+1378A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209445 | ||||||
| chr10:50209455
|
T | C | 1 | a0003c0003t0001g0020 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1414+1368A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209455 | ||||||
| chr10:50209531
|
T | C | 1 | a0002c0001t0016g0133 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1414+1292A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209531 | ||||||
| chr10:50209730
|
C | T | 75 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(72): Show | 86 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1414+1093G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209730 | ||||||
| chr10:50209773
|
C | T | 30 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(27): Show | 31 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1414+1050G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209773 | ||||||
| chr10:50209779
|
T | C | 1 | a0001c0004t0095g0284 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1414+1044A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209779 | ||||||
| chr10:50209826
|
A | G | 3 | a0001c0002t0003g0014a0001c0002t0003g0089a0001c0002t0003g0090 | 4 | NA18974.hp1 NA18997.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414+997T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209826 | ||||||
| chr10:50209842
|
C | T | 221 | a0001c0004t0012g0001a0001c0004t0012g0299a0001c0004t0020g0290others(218): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1414+981G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50209842 | ||||||
| chr10:50210002
|
A | G | 1 | a0002c0001t0054g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1414+821T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50210002 | ||||||
| chr10:50210080
|
C | T | 221 | a0001c0004t0012g0001a0001c0004t0012g0299a0001c0004t0020g0290others(218): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1414+743G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50210080 | ||||||
| chr10:50210134
|
C | G | 1 | a0002c0001t0030g0178 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1414+689G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50210134 | ||||||
| chr10:50210361
|
G | A | 30 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(27): Show | 31 | HG00738.hp2 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1414+462C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50210361 | ||||||
| chr10:50210508
|
T | A | 250 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(247): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1414+315A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50210508 | ||||||
| chr10:50210518
|
C | T | 1 | a0001c0018t0009g0353 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1414+305G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50210518 | ||||||
| chr10:50210525
|
A | G | 251 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(248): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1414+298T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50210525 | ||||||
| chr10:50210743
|
C | T | 3 | a0002c0001t0002g0233a0002c0001t0026g0234a0002c0001t0026g0262 | 3 | HG01255.hp2 HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1414+80G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 12/20 | chr10 | 50210743 | ||||||
| chr10:50210927
|
A | G | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1333-23T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 11/20 | chr10 | 50210927 | ||||||
| chr10:50211182
|
T | G | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1228-48A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211182 | ||||||
| chr10:50211183
|
C | T | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1228-49G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211183 | ||||||
| chr10:50211197
|
C | T | 11 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0004t0090g0348others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1228-63G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211197 | ||||||
| chr10:50211223
|
T | C | 1 | a0001c0002t0003g0088 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1228-89A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211223 | ||||||
| chr10:50211322
|
A | G | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1228-188T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211322 | ||||||
| chr10:50211371
|
G | A | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1228-237C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211371 | ||||||
| chr10:50211401
|
A | G | 4 | a0001c0005t0117g0266a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-267T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211401 | ||||||
| chr10:50211473
|
C | T | 1 | a0002c0001t0008g0315 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1228-339G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211473 | ||||||
| chr10:50211477
|
G | T | 57 | a0002c0001t0002g0005a0002c0001t0002g0024a0002c0001t0002g0182others(54): Show | 64 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1228-343C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211477 | ||||||
| chr10:50211601
|
T | C | 86 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(83): Show | 100 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1228-467A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211601 | ||||||
| chr10:50211708
|
A | C | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1228-574T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211708 | ||||||
| chr10:50211842
|
T | A | 76 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(73): Show | 87 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1228-708A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211842 | ||||||
| chr10:50211866
|
A | G | 1 | a0001c0005t0011g0041 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1228-732T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211866 | ||||||
| chr10:50211989
|
C | T | 1 | a0002c0006t0106g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1228-855G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50211989 | ||||||
| chr10:50212182
|
A | AAC | 72 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0004t0033g0275others(69): Show | 79 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1227+788_1227+789d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212182 | ||||||
| chr10:50212182
|
A | AACAC | 38 | a0001c0002t0001g0095a0001c0002t0013g0071a0001c0002t0028g0006others(35): Show | 42 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.1227+786_1227+789d others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212182 | ||||||
| chr10:50212182
|
A | AACACAC | 3 | a0001c0004t0006g0293a0001c0005t0011g0041a0008c0023t0110g0361 | 3 | HG01106.hp1 HG02976.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1227+784_1227+789d others(8): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212182 | ||||||
| chr10:50212182
|
A | AACACACA others(1): Show |
16 | a0001c0002t0003g0016a0001c0002t0003g0093a0001c0002t0005g0086others(13): Show | 19 | HG00597.hp2 HG00642.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.1227+782_1227+789d others(10): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212182 | ||||||
| chr10:50212182
|
A | AACACACA others(3): Show |
40 | a0001c0002t0001g0083a0001c0002t0003g0004a0001c0002t0003g0077others(37): Show | 46 | HG00423.hp2 HG00558.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1227+780_1227+789d others(12): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212182 | ||||||
| chr10:50212182
|
A | AACACACA others(5): Show |
7 | a0001c0002t0003g0014a0001c0002t0003g0088a0001c0002t0005g0267others(4): Show | 8 | HG01123.hp1 HG03098.hp1 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.1227+778_1227+789d others(14): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212182 | ||||||
| chr10:50212182
|
A | AACACACA others(7): Show |
5 | a0001c0002t0006g0079a0001c0002t0051g0112a0001c0002t0091g0111others(2): Show | 5 | HG03239.hp2 HG03471.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+776_1227+789d others(16): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212182 | ||||||
| chr10:50212182
|
A | AACACACA others(9): Show |
3 | a0001c0002t0022g0073a0001c0002t0022g0087a0001c0002t0053g0078 | 3 | HG03710.hp1 NA19006.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1227+774_1227+789d others(18): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212182 | ||||||
| chr10:50212182
|
AAC | A | 5 | a0002c0001t0007g0044a0003c0003t0001g0119a0003c0003t0001g0120others(2): Show | 5 | HG01192.hp2 HG01433.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+788_1227+789d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212182 | ||||||
| chr10:50212182
|
AACACACA others(5): Show |
A | 1 | a0002c0001t0021g0175 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1227+778_1227+789d others(14): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212182 | ||||||
| chr10:50212310
|
A | C | 251 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(248): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1227+662T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212310 | ||||||
| chr10:50212384
|
G | A | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1227+588C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212384 | ||||||
| chr10:50212464
|
C | A | 305 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(302): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1227+508G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212464 | ||||||
| chr10:50212464
|
C | T | 28 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(25): Show | 29 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1227+508G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212464 | ||||||
| chr10:50212697
|
A | C | 76 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(73): Show | 87 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1227+275T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212697 | ||||||
| chr10:50212787
|
C | A | 57 | a0002c0001t0002g0005a0002c0001t0002g0024a0002c0001t0002g0182others(54): Show | 64 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1227+185G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212787 | ||||||
| chr10:50212964
|
T | G | 1 | a0001c0002t0045g0096 | 1 | NA18957.hp1 | splice_region_variant&intron_variant | LOW | c.1227+8A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 10/20 | chr10 | 50212964 | ||||||
| chr10:50213091
|
C | T | 18 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0013g0289others(15): Show | 19 | HG00597.hp1 HG00738.hp2 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.1141-33G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50213091 | ||||||
| chr10:50213116
|
T | C | 82 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(79): Show | 96 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.1141-58A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50213116 | ||||||
| chr10:50213215
|
T | G | 4 | a0001c0002t0009g0347a0001c0002t0025g0346a0001c0005t0025g0007others(1): Show | 5 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1141-157A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50213215 | ||||||
| chr10:50213233
|
G | C | 332 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(329): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1141-175C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50213233 | ||||||
| chr10:50213394
|
C | T | 1 | a0001c0010t0102g0362 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1141-336G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50213394 | ||||||
| chr10:50213434
|
C | T | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1141-376G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50213434 | ||||||
| chr10:50213443
|
G | A | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1141-385C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50213443 | ||||||
| chr10:50213648
|
G | C | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1141-590C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50213648 | ||||||
| chr10:50213702
|
T | C | 4 | a0001c0004t0033g0278a0001c0004t0034g0276a0001c0004t0034g0279others(1): Show | 4 | HG00738.hp2 HG01943.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141-644A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50213702 | ||||||
| chr10:50213851
|
A | G | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1141-793T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50213851 | ||||||
| chr10:50213888
|
G | A | 1 | a0003c0003t0001g0137 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1141-830C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50213888 | ||||||
| chr10:50214058
|
A | G | 1 | a0002c0006t0101g0273 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1140+685T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50214058 | ||||||
| chr10:50214168
|
G | T | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1140+575C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50214168 | ||||||
| chr10:50214174
|
G | A | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1140+569C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50214174 | ||||||
| chr10:50214183
|
G | A | 1 | a0001c0004t0006g0018 | 2 | NA18965.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1140+560C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50214183 | ||||||
| chr10:50214184
|
G | A | 1 | a0002c0006t0101g0273 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1140+559C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50214184 | ||||||
| chr10:50214237
|
T | C | 4 | a0001c0005t0117g0266a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140+506A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50214237 | ||||||
| chr10:50214534
|
C | A | 251 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(248): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1140+209G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50214534 | ||||||
| chr10:50214566
|
T | C | 4 | a0002c0001t0002g0221a0002c0001t0002g0259a0002c0001t0016g0246others(1): Show | 4 | HG00438.hp2 HG02165.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140+177A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50214566 | ||||||
| chr10:50214715
|
A | G | 8 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0007t0020g0356others(5): Show | 8 | HG01192.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1140+28T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50214715 | ||||||
| chr10:50214729
|
T | C | 251 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(248): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1140+14A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50214729 | ||||||
| chr10:50214734
|
A | T | 1 | a0003c0003t0023g0140 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1140+9T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 9/20 | chr10 | 50214734 | ||||||
| chr10:50214925
|
C | T | 102 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0007g0003others(99): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1015-57G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50214925 | ||||||
| chr10:50214965
|
T | C | 7 | a0001c0002t0010g0008a0001c0002t0010g0017a0001c0002t0010g0099others(4): Show | 9 | HG02074.hp2 HG02083.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.1015-97A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50214965 | ||||||
| chr10:50215018
|
C | T | 84 | a0003c0003t0001g0002a0003c0003t0001g0020a0003c0003t0001g0052others(81): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1015-150G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215018 | ||||||
| chr10:50215057
|
G | A | 1 | a0003c0003t0032g0125 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1015-189C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215057 | ||||||
| chr10:50215249
|
G | A | 1 | a0003c0003t0001g0168 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1015-381C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215249 | ||||||
| chr10:50215256
|
G | A | 5 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(2): Show | 8 | HG01167.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1015-388C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215256 | ||||||
| chr10:50215384
|
C | T | 1 | a0003c0003t0001g0137 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1015-516G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215384 | ||||||
| chr10:50215476
|
A | G | 1 | a0001c0002t0003g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1015-608T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215476 | ||||||
| chr10:50215479
|
A | C | 2 | a0001c0005t0093g0212a0001c0005t0116g0213 | 2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1015-611T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215479 | ||||||
| chr10:50215481
|
G | A | 5 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(2): Show | 8 | HG01167.hp2 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1015-613C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215481 | ||||||
| chr10:50215514
|
A | G | 1 | a0008c0023t0110g0361 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1015-646T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215514 | ||||||
| chr10:50215529
|
T | C | 1 | a0002c0001t0007g0048 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1015-661A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215529 | ||||||
| chr10:50215612
|
A | T | 2 | a0002c0001t0002g0228a0002c0001t0104g0227 | 2 | HG03710.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1015-744T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215612 | ||||||
| chr10:50215750
|
C | T | 1 | a0001c0004t0051g0300 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1015-882G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215750 | ||||||
| chr10:50215816
|
T | C | 11 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0004t0090g0348others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1015-948A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215816 | ||||||
| chr10:50215879
|
C | T | 208 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0002g0005others(205): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1015-1011G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50215879 | ||||||
| chr10:50216010
|
A | C | 1 | a0002c0001t0008g0319 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1015-1142T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50216010 | ||||||
| chr10:50216036
|
T | G | 1 | a0001c0007t0020g0359 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1015-1168A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50216036 | ||||||
| chr10:50216197
|
C | T | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1015-1329G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50216197 | ||||||
| chr10:50216308
|
TAA | T | 241 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(238): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1015-1442_1015-144 others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50216308 | ||||||
| chr10:50216673
|
TTC | T | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1015-1807_1015-180 others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50216673 | ||||||
| chr10:50216884
|
C | G | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1014+1626G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50216884 | ||||||
| chr10:50216929
|
C | T | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1014+1581G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50216929 | ||||||
| chr10:50216939
|
A | G | 11 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0004t0090g0348others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1014+1571T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50216939 | ||||||
| chr10:50217001
|
T | C | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1014+1509A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217001 | ||||||
| chr10:50217046
|
C | T | 2 | a0001c0009t0010g0305a0001c0009t0010g0306 | 2 | HG00642.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1014+1464G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217046 | ||||||
| chr10:50217175
|
C | T | 1 | a0002c0001t0008g0313 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1014+1335G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217175 | ||||||
| chr10:50217195
|
C | T | 1 | a0002c0001t0004g0116 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1014+1315G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217195 | ||||||
| chr10:50217229
|
C | CT | 240 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(237): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.1014+1280dupA | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217229 | ||||||
| chr10:50217233
|
T | C | 1 | a0001c0002t0080g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1014+1277A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217233 | ||||||
| chr10:50217353
|
A | T | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1014+1157T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217353 | ||||||
| chr10:50217387
|
C | A | 2 | a0002c0001t0042g0332a0010c0025t0061g0318 | 2 | HG00099.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.1014+1123G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217387 | ||||||
| chr10:50217462
|
C | T | 1 | a0002c0001t0002g0232 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1014+1048G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217462 | ||||||
| chr10:50217463
|
A | G | 246 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(243): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1014+1047T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217463 | ||||||
| chr10:50217478
|
C | T | 8 | a0001c0010t0069g0200a0002c0001t0002g0248a0002c0001t0004g0030others(5): Show | 9 | HG02040.hp2 HG02080.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1014+1032G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217478 | ||||||
| chr10:50217532
|
G | T | 250 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(247): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1014+978C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217532 | ||||||
| chr10:50217543
|
G | A | 250 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(247): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1014+967C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217543 | ||||||
| chr10:50217615
|
A | C | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1014+895T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217615 | ||||||
| chr10:50217775
|
T | C | 1 | a0003c0003t0001g0169 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1014+735A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217775 | ||||||
| chr10:50217956
|
C | T | 1 | a0003c0003t0047g0150 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1014+554G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217956 | ||||||
| chr10:50217985
|
C | G | 1 | a0003c0003t0005g0147 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1014+525G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217985 | ||||||
| chr10:50217985
|
C | T | 1 | a0002c0001t0054g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1014+525G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50217985 | ||||||
| chr10:50218011
|
G | C | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1014+499C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50218011 | ||||||
| chr10:50218082
|
C | T | 1 | a0002c0001t0004g0116 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1014+428G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50218082 | ||||||
| chr10:50218089
|
T | A | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1014+421A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50218089 | ||||||
| chr10:50218130
|
T | TA | 328 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(325): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1014+379dupT | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50218130 | ||||||
| chr10:50218223
|
C | A | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1014+287G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50218223 | ||||||
| chr10:50218292
|
T | C | 208 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0002g0005others(205): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1014+218A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50218292 | ||||||
| chr10:50218362
|
A | T | 1 | a0001c0002t0076g0056 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1014+148T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50218362 | ||||||
| chr10:50218381
|
C | T | 3 | a0003c0003t0001g0148a0003c0003t0039g0149a0003c0003t0088g0177 | 3 | HG00609.hp2 NA18948.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1014+129G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50218381 | ||||||
| chr10:50218382
|
A | G | 208 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0002g0005others(205): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1014+128T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50218382 | ||||||
| chr10:50218417
|
T | C | 1 | a0001c0015t0094g0036 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1014+93A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 8/20 | chr10 | 50218417 | ||||||
| chr10:50218643
|
A | G | 1 | a0003c0003t0005g0147 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.894-13T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50218643 | ||||||
| chr10:50218644
|
A | G | 249 | a0001c0002t0076g0056a0001c0002t0083g0057a0001c0004t0006g0018others(246): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.894-14T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50218644 | ||||||
| chr10:50218670
|
G | C | 249 | a0001c0002t0076g0056a0001c0002t0083g0057a0001c0004t0006g0018others(246): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.894-40C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50218670 | ||||||
| chr10:50218730
|
A | G | 76 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(73): Show | 87 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.894-100T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50218730 | ||||||
| chr10:50218772
|
T | C | 1 | a0001c0005t0011g0180 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.894-142A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50218772 | ||||||
| chr10:50218844
|
A | T | 76 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(73): Show | 87 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.894-214T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50218844 | ||||||
| chr10:50218993
|
A | T | 1 | a0002c0001t0002g0182 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.894-363T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50218993 | ||||||
| chr10:50219008
|
C | T | 11 | a0001c0002t0001g0012a0001c0002t0005g0061a0001c0002t0005g0063others(8): Show | 12 | HG00733.hp2 HG01070.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.894-378G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50219008 | ||||||
| chr10:50219268
|
G | A | 1 | a0002c0001t0002g0231 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.894-638C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50219268 | ||||||
| chr10:50219372
|
A | G | 2 | a0002c0001t0057g0338a0002c0001t0058g0336 | 2 | NA18975.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.894-742T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50219372 | ||||||
| chr10:50219487
|
G | A | 28 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(25): Show | 29 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.894-857C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50219487 | ||||||
| chr10:50219546
|
A | G | 251 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(248): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.894-916T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50219546 | ||||||
| chr10:50219553
|
A | G | 354 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(351): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.894-923T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50219553 | ||||||
| chr10:50219583
|
T | A | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.894-953A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50219583 | ||||||
| chr10:50219701
|
A | T | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.894-1071T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50219701 | ||||||
| chr10:50219904
|
A | C | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.894-1274T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50219904 | ||||||
| chr10:50219936
|
G | T | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.894-1306C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50219936 | ||||||
| chr10:50220040
|
C | T | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.894-1410G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220040 | ||||||
| chr10:50220057
|
T | C | 1 | a0001c0004t0006g0295 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.894-1427A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220057 | ||||||
| chr10:50220061
|
A | G | 1 | a0003c0003t0001g0146 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.894-1431T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220061 | ||||||
| chr10:50220170
|
G | A | 3 | a0002c0001t0105g0225a0002c0001t0111g0039a0002c0006t0004g0085 | 3 | HG02886.hp2 NA18978.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.894-1540C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220170 | ||||||
| chr10:50220497
|
GCT | G | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.894-1869_894-1868d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220497 | ||||||
| chr10:50220502
|
ATTTG | A | 333 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(330): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.894-1876_894-1873d others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220502 | ||||||
| chr10:50220541
|
C | CA | 4 | a0001c0005t0117g0266a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.894-1912dupT | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220541 | ||||||
| chr10:50220580
|
A | G | 251 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(248): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.894-1950T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220580 | ||||||
| chr10:50220588
|
C | T | 4 | a0001c0005t0117g0266a0001c0010t0087g0050a0001c0010t0102g0362others(1): Show | 4 | HG01981.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.894-1958G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220588 | ||||||
| chr10:50220836
|
C | CA | 24 | a0001c0002t0009g0272a0001c0002t0009g0347a0001c0002t0009g0351others(21): Show | 27 | HG00735.hp2 HG01109.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.894-2207dupT | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220836 | ||||||
| chr10:50220836
|
CA | C | 9 | a0001c0002t0005g0066a0001c0002t0013g0069a0001c0002t0013g0071others(6): Show | 9 | HG00642.hp1 HG01358.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.894-2207delT | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220836 | ||||||
| chr10:50220836
|
CAA | C | 67 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(64): Show | 80 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.894-2208_894-2207d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220836 | ||||||
| chr10:50220836
|
CAAA | C | 29 | a0001c0002t0028g0303a0001c0002t0049g0031a0001c0002t0080g0274others(26): Show | 30 | HG00438.hp2 HG00735.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.894-2209_894-2207d others(5): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220836 | ||||||
| chr10:50220836
|
CAAAA | C | 211 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(208): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.894-2210_894-2207d others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220836 | ||||||
| chr10:50220836
|
CAAAAA | C | 15 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0004t0090g0348others(12): Show | 15 | HG01192.hp1 HG01361.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.894-2211_894-2207d others(7): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220836 | ||||||
| chr10:50220981
|
C | A | 5 | a0001c0004t0006g0282a0001c0004t0013g0289a0001c0004t0053g0283others(2): Show | 5 | HG02074.hp1 NA18944.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.894-2351G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50220981 | ||||||
| chr10:50221071
|
G | A | 1 | a0001c0010t0102g0362 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.894-2441C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221071 | ||||||
| chr10:50221073
|
C | T | 247 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(244): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.894-2443G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221073 | ||||||
| chr10:50221125
|
A | G | 82 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(79): Show | 96 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.894-2495T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221125 | ||||||
| chr10:50221171
|
T | C | 82 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(79): Show | 96 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.894-2541A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221171 | ||||||
| chr10:50221239
|
T | C | 1 | a0001c0005t0011g0041 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.894-2609A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221239 | ||||||
| chr10:50221285
|
T | A | 1 | a0003c0003t0005g0173 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.894-2655A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221285 | ||||||
| chr10:50221627
|
T | TTG | 189 | a0001c0005t0117g0266a0001c0010t0069g0200a0001c0010t0087g0050others(186): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.894-2999_894-2998d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221627 | ||||||
| chr10:50221627
|
T | TTGTG | 15 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0007g0003others(12): Show | 23 | HG00639.hp1 HG01243.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.894-2998_894-2997i others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221627 | ||||||
| chr10:50221627
|
TTGTA | T | 53 | a0001c0002t0001g0083a0001c0002t0001g0095a0001c0002t0003g0004others(50): Show | 63 | HG00423.hp2 HG00558.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.894-3001_894-2998d others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221627 | ||||||
| chr10:50221629
|
GTA | G | 28 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(25): Show | 29 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.894-3001_894-3000d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221629 | ||||||
| chr10:50221631
|
A | G | 252 | a0001c0002t0001g0012a0001c0002t0005g0061a0001c0002t0005g0063others(249): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.894-3001T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221631 | ||||||
| chr10:50221631
|
ATG | A | 4 | a0001c0002t0009g0347a0001c0002t0025g0346a0001c0005t0025g0007others(1): Show | 5 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.894-3003_894-3002d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221631 | ||||||
| chr10:50221639
|
G | A | 11 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0004t0090g0348others(8): Show | 11 | HG01192.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.894-3009C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221639 | ||||||
| chr10:50221660
|
TATAG | T | 5 | a0001c0004t0090g0348a0001c0007t0020g0357a0001c0007t0020g0359others(2): Show | 5 | HG01192.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.894-3034_894-3031d others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221660 | ||||||
| chr10:50221661
|
A | G | 6 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0007t0020g0356others(3): Show | 6 | HG02258.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.894-3031T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221661 | ||||||
| chr10:50221662
|
TAG | T | 6 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0007t0020g0356others(3): Show | 6 | HG02258.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.894-3034_894-3033d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221662 | ||||||
| chr10:50221674
|
TGATA | T | 19 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0013g0289others(16): Show | 20 | HG00597.hp1 HG00738.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.894-3048_894-3045d others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221674 | ||||||
| chr10:50221679
|
G | C | 1 | a0001c0002t0028g0303 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.894-3049C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221679 | ||||||
| chr10:50221686
|
A | G | 1 | a0001c0011t0109g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.894-3056T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221686 | ||||||
| chr10:50221690
|
A | G | 1 | a0001c0011t0109g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.894-3060T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221690 | ||||||
| chr10:50221694
|
G | A | 1 | a0001c0011t0109g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.894-3064C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221694 | ||||||
| chr10:50221698
|
G | A | 1 | a0001c0011t0109g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.894-3068C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221698 | ||||||
| chr10:50221698
|
G | GGATA | 26 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(23): Show | 31 | HG00280.hp2 HG00642.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.894-3072_894-3069d others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221698 | ||||||
| chr10:50221698
|
G | GGATAGAT others(1): Show |
15 | a0002c0001t0008g0309a0002c0001t0008g0330a0002c0001t0017g0340others(12): Show | 15 | HG00099.hp1 HG00544.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.894-3076_894-3069d others(10): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221698 | ||||||
| chr10:50221698
|
GGATA | G | 218 | a0001c0002t0001g0012a0001c0002t0001g0095a0001c0002t0003g0004others(215): Show | 250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.894-3072_894-3069d others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221698 | ||||||
| chr10:50221698
|
GGATAGAT others(1): Show |
G | 40 | a0001c0002t0001g0083a0001c0004t0006g0018a0001c0004t0006g0282others(37): Show | 41 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.894-3076_894-3069d others(10): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221698 | ||||||
| chr10:50221698
|
GGATAGAT others(5): Show |
G | 1 | a0005c0012t0016g0028 | 2 | HG03927.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.894-3080_894-3069d others(14): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221698 | ||||||
| chr10:50221706
|
A | G | 1 | a0002c0001t0002g0228 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.894-3076T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221706 | ||||||
| chr10:50221710
|
A | G | 1 | a0002c0001t0104g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.894-3080T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221710 | ||||||
| chr10:50221741
|
G | C | 49 | a0002c0001t0008g0123a0002c0001t0008g0309a0002c0001t0008g0313others(46): Show | 51 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.894-3111C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221741 | ||||||
| chr10:50221765
|
C | T | 1 | a0003c0003t0001g0222 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.894-3135G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221765 | ||||||
| chr10:50221797
|
C | A | 2 | a0001c0004t0020g0290a0001c0004t0020g0291 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.894-3167G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221797 | ||||||
| chr10:50221997
|
C | T | 1 | a0001c0002t0005g0086 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.894-3367G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50221997 | ||||||
| chr10:50222058
|
C | T | 2 | a0001c0002t0013g0069a0001c0002t0013g0070 | 2 | NA18977.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.894-3428G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50222058 | ||||||
| chr10:50222501
|
A | T | 1 | a0003c0003t0023g0140 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.894-3871T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50222501 | ||||||
| chr10:50222835
|
G | A | 208 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0002g0005others(205): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.894-4205C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50222835 | ||||||
| chr10:50222973
|
T | A | 76 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(73): Show | 87 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.894-4343A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50222973 | ||||||
| chr10:50223017
|
G | C | 1 | a0003c0003t0075g0176 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.894-4387C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50223017 | ||||||
| chr10:50223024
|
G | T | 327 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(324): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.894-4394C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50223024 | ||||||
| chr10:50223065
|
A | G | 246 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(243): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.894-4435T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50223065 | ||||||
| chr10:50223162
|
C | G | 246 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(243): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.894-4532G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50223162 | ||||||
| chr10:50223168
|
T | C | 80 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(77): Show | 91 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.894-4538A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50223168 | ||||||
| chr10:50223266
|
C | T | 325 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(322): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.894-4636G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50223266 | ||||||
| chr10:50223457
|
G | A | 1 | a0002c0001t0004g0260 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.894-4827C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50223457 | ||||||
| chr10:50223464
|
T | C | 2 | a0001c0002t0001g0083a0001c0002t0023g0084 | 2 | HG02523.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.894-4834A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50223464 | ||||||
| chr10:50223502
|
C | T | 2 | a0002c0001t0004g0211a0002c0001t0004g0226 | 2 | NA18944.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.894-4872G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50223502 | ||||||
| chr10:50223559
|
C | T | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.894-4929G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50223559 | ||||||
| chr10:50223690
|
T | C | 93 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(90): Show | 106 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.894-5060A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50223690 | ||||||
| chr10:50223911
|
G | C | 193 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0002g0005others(190): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.894-5281C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50223911 | ||||||
| chr10:50224066
|
C | T | 3 | a0002c0001t0004g0179a0002c0001t0105g0225a0002c0006t0004g0085 | 3 | NA18978.hp2 NA19002.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.894-5436G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224066 | ||||||
| chr10:50224192
|
C | G | 1 | a0003c0003t0001g0020 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.894-5562G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224192 | ||||||
| chr10:50224305
|
T | A | 28 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(25): Show | 29 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.894-5675A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224305 | ||||||
| chr10:50224407
|
T | C | 327 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(324): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.894-5777A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224407 | ||||||
| chr10:50224534
|
C | T | 1 | a0003c0003t0081g0139 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.894-5904G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224534 | ||||||
| chr10:50224580
|
C | G | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.894-5950G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224580 | ||||||
| chr10:50224582
|
T | A | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.894-5952A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224582 | ||||||
| chr10:50224583
|
TTGCAAGG others(9): Show |
T | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.894-5969_894-5954d others(18): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224583 | ||||||
| chr10:50224597
|
G | T | 10 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0007t0020g0356others(7): Show | 10 | HG01192.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.894-5967C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224597 | ||||||
| chr10:50224600
|
T | A | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.894-5970A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224600 | ||||||
| chr10:50224645
|
C | G | 10 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0007t0020g0356others(7): Show | 10 | HG01192.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.894-6015G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224645 | ||||||
| chr10:50224683
|
A | G | 120 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(117): Show | 134 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.894-6053T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224683 | ||||||
| chr10:50224704
|
T | C | 1 | a0002c0006t0106g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.894-6074A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224704 | ||||||
| chr10:50224752
|
C | T | 1 | a0001c0002t0091g0111 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.894-6122G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224752 | ||||||
| chr10:50224768
|
A | C | 324 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(321): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.894-6138T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50224768 | ||||||
| chr10:50225172
|
T | C | 342 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(339): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.894-6542A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225172 | ||||||
| chr10:50225195
|
G | A | 9 | a0002c0001t0017g0333a0002c0001t0017g0334a0002c0001t0017g0340others(6): Show | 9 | NA18941.hp1 NA18947.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.894-6565C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225195 | ||||||
| chr10:50225224
|
T | C | 1 | a0003c0003t0088g0177 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.894-6594A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225224 | ||||||
| chr10:50225400
|
A | T | 1 | a0001c0004t0048g0281 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.894-6770T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225400 | ||||||
| chr10:50225419
|
C | A | 121 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(118): Show | 135 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.894-6789G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225419 | ||||||
| chr10:50225448
|
T | C | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.894-6818A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225448 | ||||||
| chr10:50225605
|
C | A | 121 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(118): Show | 135 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.894-6975G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225605 | ||||||
| chr10:50225609
|
C | T | 1 | a0002c0006t0114g0302 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.894-6979G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225609 | ||||||
| chr10:50225837
|
T | C | 1 | a0002c0001t0004g0179 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.894-7207A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225837 | ||||||
| chr10:50225843
|
T | C | 121 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(118): Show | 135 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.894-7213A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225843 | ||||||
| chr10:50225868
|
A | G | 87 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0021g0175others(84): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.894-7238T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225868 | ||||||
| chr10:50225950
|
G | A | 121 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(118): Show | 135 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.893+7234C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225950 | ||||||
| chr10:50225964
|
G | A | 121 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(118): Show | 135 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.893+7220C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225964 | ||||||
| chr10:50225978
|
A | C | 1 | a0001c0004t0012g0299 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.893+7206T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50225978 | ||||||
| chr10:50226293
|
T | G | 1 | a0002c0001t0018g0202 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.893+6891A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50226293 | ||||||
| chr10:50226332
|
A | G | 1 | a0002c0001t0004g0179 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.893+6852T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50226332 | ||||||
| chr10:50226349
|
G | T | 121 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(118): Show | 135 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.893+6835C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50226349 | ||||||
| chr10:50226459
|
A | C | 28 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(25): Show | 29 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.893+6725T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50226459 | ||||||
| chr10:50226523
|
A | T | 1 | a0003c0003t0001g0138 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.893+6661T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50226523 | ||||||
| chr10:50226559
|
A | G | 1 | a0002c0001t0043g0308 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.893+6625T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50226559 | ||||||
| chr10:50226602
|
G | C | 4 | a0001c0002t0009g0347a0001c0002t0025g0346a0001c0005t0025g0007others(1): Show | 5 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+6582C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50226602 | ||||||
| chr10:50226709
|
A | T | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.893+6475T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50226709 | ||||||
| chr10:50226760
|
C | T | 1 | a0002c0001t0018g0312 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.893+6424G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50226760 | ||||||
| chr10:50226774
|
G | A | 8 | a0001c0004t0020g0290a0001c0004t0020g0291a0001c0007t0020g0356others(5): Show | 8 | HG01192.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.893+6410C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50226774 | ||||||
| chr10:50226831
|
A | C | 3 | a0001c0010t0087g0050a0001c0010t0102g0362a0001c0015t0094g0036 | 3 | HG02976.hp2 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.893+6353T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50226831 | ||||||
| chr10:50227047
|
A | G | 27 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(24): Show | 28 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.893+6137T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50227047 | ||||||
| chr10:50227112
|
C | T | 134 | a0001c0004t0012g0001a0001c0004t0012g0299a0002c0001t0008g0123others(131): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.893+6072G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50227112 | ||||||
| chr10:50227288
|
A | G | 1 | a0002c0001t0111g0039 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.893+5896T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50227288 | ||||||
| chr10:50227311
|
G | T | 1 | a0003c0003t0001g0119 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.893+5873C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50227311 | ||||||
| chr10:50227339
|
G | GA | 332 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(329): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.893+5844_893+5845i others(3): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50227339 | ||||||
| chr10:50227341
|
T | G | 332 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(329): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.893+5843A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50227341 | ||||||
| chr10:50227342
|
T | G | 332 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(329): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.893+5842A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50227342 | ||||||
| chr10:50227344
|
T | C | 332 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(329): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.893+5840A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50227344 | ||||||
| chr10:50227345
|
G | T | 332 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(329): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.893+5839C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50227345 | ||||||
| chr10:50227349
|
T | TA | 332 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(329): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.893+5834_893+5835i others(3): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50227349 | ||||||
| chr10:50227350
|
G | C | 332 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(329): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.893+5834C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50227350 | ||||||
| chr10:50227606
|
C | G | 1 | a0002c0001t0004g0116 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.893+5578G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50227606 | ||||||
| chr10:50227644
|
A | T | 230 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0006g0292others(227): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.893+5540T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50227644 | ||||||
| chr10:50228164
|
T | A | 1 | a0001c0005t0098g0037 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.893+5020A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50228164 | ||||||
| chr10:50228225
|
A | C | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.893+4959T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50228225 | ||||||
| chr10:50228764
|
A | G | 307 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(304): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.893+4420T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50228764 | ||||||
| chr10:50228797
|
G | T | 50 | a0001c0004t0012g0001a0001c0004t0012g0299a0001c0011t0006g0342others(47): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.893+4387C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50228797 | ||||||
| chr10:50228906
|
C | T | 43 | a0001c0005t0117g0266a0001c0011t0006g0342a0002c0001t0008g0123others(40): Show | 45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.893+4278G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50228906 | ||||||
| chr10:50228907
|
G | A | 6 | a0001c0004t0012g0001a0001c0004t0012g0299a0001c0011t0109g0355others(3): Show | 12 | HG02132.hp1 HG02615.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.893+4277C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50228907 | ||||||
| chr10:50228907
|
G | C | 3 | a0001c0004t0006g0298a0001c0004t0033g0297a0001c0004t0046g0296 | 3 | HG01884.hp1 HG02257.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.893+4277C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50228907 | ||||||
| chr10:50229071
|
A | G | 3 | a0001c0002t0005g0267a0004c0013t0005g0067a0004c0013t0005g0068 | 3 | HG01123.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.893+4113T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50229071 | ||||||
| chr10:50229101
|
G | A | 1 | a0002c0001t0008g0343 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.893+4083C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50229101 | ||||||
| chr10:50229153
|
G | C | 1 | a0001c0002t0068g0104 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.893+4031C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50229153 | ||||||
| chr10:50229554
|
C | T | 1 | a0001c0002t0080g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.893+3630G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50229554 | ||||||
| chr10:50229564
|
A | G | 220 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(217): Show | 248 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.893+3620T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50229564 | ||||||
| chr10:50229797
|
T | C | 1 | a0001c0005t0098g0037 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.893+3387A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50229797 | ||||||
| chr10:50229952
|
T | A | 220 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(217): Show | 248 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.893+3232A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50229952 | ||||||
| chr10:50230297
|
G | T | 1 | a0001c0002t0096g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.893+2887C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50230297 | ||||||
| chr10:50230298
|
C | T | 1 | a0007c0017t0003g0106 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.893+2886G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50230298 | ||||||
| chr10:50230327
|
T | G | 18 | a0001c0004t0006g0018a0001c0004t0006g0282a0001c0004t0013g0289others(15): Show | 19 | HG00597.hp1 HG00738.hp2 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.893+2857A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50230327 | ||||||
| chr10:50230348
|
A | G | 158 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(155): Show | 175 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.893+2836T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50230348 | ||||||
| chr10:50231117
|
A | T | 324 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(321): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.893+2067T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50231117 | ||||||
| chr10:50231641
|
T | C | 61 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(58): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.893+1543A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50231641 | ||||||
| chr10:50231644
|
G | C | 1 | a0001c0004t0020g0291 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.893+1540C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50231644 | ||||||
| chr10:50231727
|
C | G | 300 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(297): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.893+1457G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50231727 | ||||||
| chr10:50232052
|
A | T | 158 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(155): Show | 175 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.893+1132T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50232052 | ||||||
| chr10:50232414
|
C | G | 13 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(10): Show | 16 | HG01106.hp1 HG01167.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.893+770G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50232414 | ||||||
| chr10:50232583
|
T | C | 1 | a0001c0002t0005g0066 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.893+601A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50232583 | ||||||
| chr10:50232657
|
A | G | 1 | a0008c0023t0110g0361 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.893+527T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50232657 | ||||||
| chr10:50232820
|
C | T | 158 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(155): Show | 175 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.893+364G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50232820 | ||||||
| chr10:50232838
|
C | T | 57 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(54): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.893+346G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50232838 | ||||||
| chr10:50232854
|
A | G | 5 | a0001c0002t0005g0063a0001c0002t0005g0066a0001c0002t0005g0114others(2): Show | 5 | HG00733.hp2 HG01081.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.893+330T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50232854 | ||||||
| chr10:50232858
|
G | A | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.893+326C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50232858 | ||||||
| chr10:50232957
|
T | C | 1 | a0002c0001t0018g0265 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.893+227A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 7/20 | chr10 | 50232957 | ||||||
| chr10:50233355
|
G | A | 1 | a0001c0004t0097g0304 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.816-94C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 6/20 | chr10 | 50233355 | ||||||
| chr10:50233431
|
A | G | 1 | a0004c0013t0005g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.816-170T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 6/20 | chr10 | 50233431 | ||||||
| chr10:50233441
|
C | T | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.816-180G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 6/20 | chr10 | 50233441 | ||||||
| chr10:50233588
|
T | C | 1 | a0002c0006t0106g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.816-327A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 6/20 | chr10 | 50233588 | ||||||
| chr10:50233673
|
T | C | 82 | a0002c0001t0018g0194a0002c0001t0021g0175a0002c0001t0021g0195others(79): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.816-412A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 6/20 | chr10 | 50233673 | ||||||
| chr10:50234210
|
A | G | 158 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(155): Show | 175 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.815+215T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 6/20 | chr10 | 50234210 | ||||||
| chr10:50234224
|
T | C | 158 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(155): Show | 175 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.815+201A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 6/20 | chr10 | 50234224 | ||||||
| chr10:50234285
|
C | T | 57 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(54): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.815+140G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 6/20 | chr10 | 50234285 | ||||||
| chr10:50234337
|
TA | T | 3 | a0003c0003t0001g0135a0003c0003t0001g0136a0003c0003t0015g0134 | 3 | HG00140.hp1 HG01257.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.815+87delT | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 6/20 | chr10 | 50234337 | ||||||
| chr10:50234688
|
G | A | 53 | a0001c0002t0009g0347a0001c0002t0025g0346a0001c0002t0080g0274others(50): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.688-136C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50234688 | ||||||
| chr10:50234760
|
C | T | 4 | a0001c0002t0009g0347a0001c0002t0025g0346a0001c0005t0025g0007others(1): Show | 5 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.688-208G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50234760 | ||||||
| chr10:50234761
|
G | A | 24 | a0001c0005t0011g0009a0001c0005t0011g0010a0001c0005t0011g0041others(21): Show | 28 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.688-209C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50234761 | ||||||
| chr10:50234770
|
G | A | 11 | a0001c0004t0006g0292a0001c0004t0006g0293a0001c0004t0006g0294others(8): Show | 11 | HG01106.hp1 HG01884.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.688-218C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50234770 | ||||||
| chr10:50234855
|
C | T | 184 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(181): Show | 204 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.688-303G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50234855 | ||||||
| chr10:50234899
|
A | G | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.688-347T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50234899 | ||||||
| chr10:50234992
|
C | T | 8 | a0001c0002t0080g0274a0001c0007t0020g0356a0001c0007t0020g0357others(5): Show | 8 | HG01192.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.688-440G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50234992 | ||||||
| chr10:50235077
|
C | T | 57 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(54): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.688-525G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50235077 | ||||||
| chr10:50235085
|
G | A | 1 | a0001c0011t0109g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.688-533C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50235085 | ||||||
| chr10:50235184
|
A | C | 153 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(150): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.688-632T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50235184 | ||||||
| chr10:50235296
|
A | G | 15 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(12): Show | 18 | HG01106.hp1 HG01167.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.687+592T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50235296 | ||||||
| chr10:50235630
|
T | C | 1 | a0003c0003t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.687+258A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50235630 | ||||||
| chr10:50235784
|
C | G | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.687+104G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50235784 | ||||||
| chr10:50235823
|
C | T | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.687+65G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 5/20 | chr10 | 50235823 | ||||||
| chr10:50236201
|
C | T | 86 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0004g0179others(83): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.511-137G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50236201 | ||||||
| chr10:50236203
|
T | C | 1 | a0001c0002t0080g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.511-139A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50236203 | ||||||
| chr10:50236284
|
T | C | 10 | a0001c0002t0009g0272a0001c0002t0009g0347a0001c0002t0009g0351others(7): Show | 10 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.511-220A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50236284 | ||||||
| chr10:50236319
|
C | T | 86 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0004g0179others(83): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.511-255G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50236319 | ||||||
| chr10:50236388
|
T | C | 7 | a0001c0007t0020g0356a0001c0007t0020g0357a0001c0007t0020g0359others(4): Show | 7 | HG01192.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.511-324A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50236388 | ||||||
| chr10:50236439
|
C | T | 1 | a0003c0003t0001g0052 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.511-375G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50236439 | ||||||
| chr10:50236495
|
C | T | 43 | a0001c0002t0009g0272a0001c0002t0009g0347a0001c0002t0009g0351others(40): Show | 52 | HG00597.hp1 HG00738.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.511-431G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50236495 | ||||||
| chr10:50236518
|
G | T | 4 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(1): Show | 7 | HG01167.hp2 HG02257.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-454C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50236518 | ||||||
| chr10:50236522
|
A | G | 93 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(90): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.511-458T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50236522 | ||||||
| chr10:50236675
|
T | C | 5 | a0001c0007t0020g0356a0001c0007t0020g0357a0001c0007t0020g0359others(2): Show | 5 | HG01192.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-611A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50236675 | ||||||
| chr10:50236722
|
A | G | 266 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(263): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.511-658T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50236722 | ||||||
| chr10:50236899
|
T | C | 292 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(289): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.511-835A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50236899 | ||||||
| chr10:50236912
|
A | T | 2 | a0002c0001t0021g0053a0003c0003t0001g0052 | 2 | HG02155.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.511-848T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50236912 | ||||||
| chr10:50237004
|
T | G | 1 | a0003c0003t0001g0186 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.511-940A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237004 | ||||||
| chr10:50237083
|
G | T | 93 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(90): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.511-1019C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237083 | ||||||
| chr10:50237102
|
G | A | 1 | a0003c0003t0078g0187 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.511-1038C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237102 | ||||||
| chr10:50237135
|
G | C | 4 | a0001c0005t0117g0266a0001c0009t0010g0305a0001c0009t0010g0306others(1): Show | 4 | HG00642.hp1 HG01069.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-1071C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237135 | ||||||
| chr10:50237175
|
G | A | 35 | a0001c0002t0001g0095a0001c0002t0003g0014a0001c0002t0003g0016others(32): Show | 42 | HG00597.hp2 HG02040.hp1 HG02074.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-1111C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237175 | ||||||
| chr10:50237269
|
A | G | 1 | a0001c0004t0034g0276 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.511-1205T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237269 | ||||||
| chr10:50237292
|
C | A | 54 | a0001c0002t0009g0272a0001c0002t0009g0347a0001c0002t0009g0351others(51): Show | 63 | HG00597.hp1 HG00642.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.511-1228G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237292 | ||||||
| chr10:50237390
|
A | C | 266 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(263): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.511-1326T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237390 | ||||||
| chr10:50237397
|
G | A | 1 | a0003c0003t0001g0121 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.511-1333C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237397 | ||||||
| chr10:50237444
|
C | T | 93 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(90): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.511-1380G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237444 | ||||||
| chr10:50237675
|
C | T | 43 | a0001c0002t0009g0272a0001c0002t0009g0347a0001c0002t0009g0351others(40): Show | 52 | HG00597.hp1 HG00738.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.511-1611G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237675 | ||||||
| chr10:50237695
|
C | G | 94 | a0001c0002t0080g0274a0001c0005t0011g0180a0001c0010t0069g0200others(91): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.511-1631G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237695 | ||||||
| chr10:50237722
|
T | C | 172 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(169): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.511-1658A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237722 | ||||||
| chr10:50237722
|
T | G | 1 | a0003c0003t0015g0131 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.511-1658A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237722 | ||||||
| chr10:50237822
|
C | T | 133 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(130): Show | 153 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.511-1758G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50237822 | ||||||
| chr10:50238054
|
T | C | 40 | a0001c0011t0006g0342a0001c0011t0020g0344a0002c0001t0008g0309others(37): Show | 42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-1990A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238054 | ||||||
| chr10:50238080
|
G | T | 1 | a0002c0001t0007g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.511-2016C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238080 | ||||||
| chr10:50238144
|
G | C | 4 | a0001c0005t0117g0266a0001c0009t0010g0305a0001c0009t0010g0306others(1): Show | 4 | HG00642.hp1 HG01069.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-2080C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238144 | ||||||
| chr10:50238251
|
A | G | 94 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(91): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.511-2187T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238251 | ||||||
| chr10:50238324
|
C | T | 3 | a0001c0009t0010g0305a0001c0009t0010g0306a0001c0009t0010g0307 | 3 | HG00642.hp1 HG01069.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.511-2260G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238324 | ||||||
| chr10:50238328
|
C | T | 1 | a0002c0001t0027g0311 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.511-2264G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238328 | ||||||
| chr10:50238387
|
T | C | 94 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(91): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.511-2323A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238387 | ||||||
| chr10:50238406
|
A | T | 1 | a0001c0002t0022g0073 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.511-2342T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238406 | ||||||
| chr10:50238467
|
G | A | 23 | a0001c0005t0011g0009a0001c0005t0011g0010a0001c0005t0011g0041others(20): Show | 27 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.511-2403C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238467 | ||||||
| chr10:50238470
|
T | C | 1 | a0002c0001t0026g0262 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.511-2406A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238470 | ||||||
| chr10:50238508
|
A | C | 1 | a0002c0001t0018g0202 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.511-2444T>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238508 | ||||||
| chr10:50238562
|
G | GTC | 94 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(91): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.511-2499_511-2498i others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238562 | ||||||
| chr10:50238682
|
G | A | 94 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(91): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.511-2618C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238682 | ||||||
| chr10:50238768
|
A | G | 94 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(91): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.511-2704T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238768 | ||||||
| chr10:50238910
|
C | G | 94 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(91): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.511-2846G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238910 | ||||||
| chr10:50238913
|
G | A | 1 | a0001c0004t0051g0300 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.511-2849C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238913 | ||||||
| chr10:50238914
|
G | T | 1 | a0001c0002t0080g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.511-2850C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238914 | ||||||
| chr10:50238919
|
A | G | 94 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(91): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.511-2855T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238919 | ||||||
| chr10:50238935
|
A | G | 1 | a0002c0001t0040g0310 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.511-2871T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50238935 | ||||||
| chr10:50239033
|
A | G | 1 | a0008c0023t0110g0361 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.511-2969T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239033 | ||||||
| chr10:50239079
|
G | A | 3 | a0001c0002t0022g0108a0001c0002t0045g0107a0001c0002t0077g0109 | 3 | NA18950.hp1 NA18952.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.511-3015C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239079 | ||||||
| chr10:50239447
|
C | T | 1 | a0001c0010t0069g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.511-3383G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239447 | ||||||
| chr10:50239499
|
G | A | 266 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(263): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.511-3435C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239499 | ||||||
| chr10:50239518
|
G | A | 93 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(90): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.511-3454C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239518 | ||||||
| chr10:50239523
|
C | G | 135 | a0001c0002t0080g0274a0001c0005t0011g0180a0001c0010t0069g0200others(132): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.511-3459G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239523 | ||||||
| chr10:50239600
|
C | T | 133 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(130): Show | 153 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.511-3536G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239600 | ||||||
| chr10:50239612
|
T | C | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.511-3548A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239612 | ||||||
| chr10:50239828
|
A | ATT | 39 | a0001c0011t0006g0342a0002c0001t0008g0309a0002c0001t0008g0313others(36): Show | 41 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+3372_510+3373d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239828 | ||||||
| chr10:50239828
|
A | ATTTT | 9 | a0001c0010t0069g0200a0002c0001t0018g0194a0002c0001t0030g0193others(6): Show | 9 | HG00323.hp2 HG00544.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.510+3370_510+3373d others(6): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239828 | ||||||
| chr10:50239828
|
A | ATTTTT | 78 | a0001c0005t0011g0180a0002c0001t0002g0024a0002c0001t0002g0182others(75): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.510+3369_510+3373d others(7): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239828 | ||||||
| chr10:50239828
|
A | ATTTTTT | 6 | a0002c0001t0008g0123a0003c0003t0001g0129a0003c0003t0001g0130others(3): Show | 6 | HG01361.hp1 HG01361.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+3368_510+3373d others(8): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239828 | ||||||
| chr10:50239828
|
AT | A | 68 | a0001c0002t0009g0272a0001c0002t0009g0347a0001c0002t0009g0351others(65): Show | 81 | HG00597.hp1 HG00639.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.510+3373delA | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239828 | ||||||
| chr10:50239828
|
ATT | A | 10 | a0001c0002t0022g0073a0001c0002t0080g0274a0001c0002t0118g0301others(7): Show | 10 | HG01192.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.510+3372_510+3373d others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239828 | ||||||
| chr10:50239828
|
ATTT | A | 79 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(76): Show | 90 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.510+3371_510+3373d others(5): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239828 | ||||||
| chr10:50239975
|
T | A | 40 | a0001c0011t0006g0342a0001c0011t0020g0344a0002c0001t0008g0309others(37): Show | 42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.510+3227A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239975 | ||||||
| chr10:50239975
|
T | G | 98 | a0001c0005t0011g0180a0001c0005t0117g0266a0001c0009t0010g0305others(95): Show | 107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.510+3227A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239975 | ||||||
| chr10:50239979
|
T | G | 267 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(264): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.510+3223A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50239979 | ||||||
| chr10:50240066
|
G | C | 2 | a0001c0010t0087g0050a0001c0015t0094g0036 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.510+3136C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50240066 | ||||||
| chr10:50240124
|
G | A | 1 | a0001c0002t0080g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+3078C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50240124 | ||||||
| chr10:50240340
|
G | C | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.510+2862C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50240340 | ||||||
| chr10:50240404
|
T | A | 267 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(264): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.510+2798A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50240404 | ||||||
| chr10:50240473
|
C | T | 138 | a0001c0005t0011g0180a0001c0005t0117g0266a0001c0009t0010g0305others(135): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.510+2729G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50240473 | ||||||
| chr10:50240519
|
C | T | 2 | a0001c0004t0020g0290a0001c0004t0020g0291 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.510+2683G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50240519 | ||||||
| chr10:50240520
|
G | A | 1 | a0001c0002t0003g0110 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.510+2682C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50240520 | ||||||
| chr10:50240773
|
C | T | 5 | a0001c0007t0020g0356a0001c0007t0020g0357a0001c0007t0020g0359others(2): Show | 5 | HG01192.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+2429G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50240773 | ||||||
| chr10:50240776
|
T | C | 94 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(91): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.510+2426A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50240776 | ||||||
| chr10:50240795
|
T | C | 1 | a0001c0002t0028g0303 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.510+2407A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50240795 | ||||||
| chr10:50240851
|
A | G | 1 | a0001c0002t0080g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+2351T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50240851 | ||||||
| chr10:50240928
|
T | A | 1 | a0001c0002t0091g0111 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.510+2274A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50240928 | ||||||
| chr10:50241053
|
C | A | 1 | a0001c0011t0109g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.510+2149G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50241053 | ||||||
| chr10:50241080
|
G | A | 43 | a0001c0002t0009g0272a0001c0002t0009g0347a0001c0002t0009g0351others(40): Show | 52 | HG00597.hp1 HG00738.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.510+2122C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50241080 | ||||||
| chr10:50241159
|
T | G | 1 | a0002c0006t0106g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.510+2043A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50241159 | ||||||
| chr10:50241208
|
A | G | 1 | a0001c0010t0102g0362 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.510+1994T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50241208 | ||||||
| chr10:50241239
|
G | A | 128 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(125): Show | 148 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.510+1963C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50241239 | ||||||
| chr10:50241320
|
C | T | 1 | a0002c0001t0002g0221 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.510+1882G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50241320 | ||||||
| chr10:50241324
|
T | C | 1 | a0002c0001t0007g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.510+1878A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50241324 | ||||||
| chr10:50241336
|
G | C | 3 | a0001c0009t0010g0305a0001c0009t0010g0306a0001c0009t0010g0307 | 3 | HG00642.hp1 HG01069.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.510+1866C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50241336 | ||||||
| chr10:50241395
|
A | G | 3 | a0001c0002t0005g0061a0001c0002t0047g0062a0001c0002t0103g0060 | 3 | HG02922.hp1 HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.510+1807T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50241395 | ||||||
| chr10:50241543
|
A | G | 128 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(125): Show | 148 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.510+1659T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50241543 | ||||||
| chr10:50241687
|
C | T | 1 | a0001c0005t0009g0203 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.510+1515G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50241687 | ||||||
| chr10:50241735
|
C | T | 1 | a0008c0023t0110g0361 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.510+1467G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50241735 | ||||||
| chr10:50241885
|
G | A | 128 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(125): Show | 148 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.510+1317C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50241885 | ||||||
| chr10:50242029
|
G | A | 129 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(126): Show | 149 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.510+1173C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242029 | ||||||
| chr10:50242044
|
A | T | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.510+1158T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242044 | ||||||
| chr10:50242192
|
C | G | 1 | a0002c0001t0008g0309 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.510+1010G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242192 | ||||||
| chr10:50242206
|
G | GGTA | 129 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(126): Show | 149 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.510+995_510+996ins others(3): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242206 | ||||||
| chr10:50242217
|
T | G | 128 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(125): Show | 148 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.510+985A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242217 | ||||||
| chr10:50242444
|
C | A | 128 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(125): Show | 148 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.510+758G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242444 | ||||||
| chr10:50242523
|
G | C | 1 | a0001c0002t0080g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+679C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242523 | ||||||
| chr10:50242548
|
G | A | 94 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(91): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.510+654C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242548 | ||||||
| chr10:50242595
|
G | A | 1 | a0001c0010t0102g0362 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.510+607C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242595 | ||||||
| chr10:50242611
|
G | A | 1 | a0001c0002t0084g0354 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.510+591C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242611 | ||||||
| chr10:50242630
|
A | ATCTC | 93 | a0001c0005t0011g0180a0002c0001t0002g0024a0002c0001t0002g0182others(90): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.510+568_510+571dup others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242630 | ||||||
| chr10:50242630
|
ATCTC | A | 3 | a0001c0009t0010g0305a0001c0009t0010g0306a0001c0009t0010g0307 | 3 | HG00642.hp1 HG01069.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.510+568_510+571del others(4): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242630 | ||||||
| chr10:50242728
|
T | C | 1 | a0001c0002t0051g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.510+474A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242728 | ||||||
| chr10:50242788
|
G | A | 53 | a0001c0005t0003g0261a0002c0001t0002g0005a0002c0001t0002g0221others(50): Show | 58 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.510+414C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242788 | ||||||
| chr10:50242848
|
G | T | 1 | a0003c0003t0001g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.510+354C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242848 | ||||||
| chr10:50242875
|
A | T | 1 | a0001c0005t0098g0037 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.510+327T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50242875 | ||||||
| chr10:50243040
|
T | C | 122 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(119): Show | 142 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.510+162A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50243040 | ||||||
| chr10:50243048
|
A | G | 1 | a0001c0004t0036g0072 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.510+154T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50243048 | ||||||
| chr10:50243075
|
G | A | 2 | a0001c0005t0025g0007a0001c0005t0025g0034 | 3 | HG02572.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.510+127C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50243075 | ||||||
| chr10:50243083
|
T | C | 1 | a0001c0004t0097g0304 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510+119A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50243083 | ||||||
| chr10:50243092
|
A | G | 122 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(119): Show | 142 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.510+110T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 4/20 | chr10 | 50243092 | ||||||
| chr10:50243431
|
C | T | 5 | a0001c0005t0008g0215a0001c0005t0009g0214a0001c0005t0052g0216others(2): Show | 5 | HG02630.hp2 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-80G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50243431 | ||||||
| chr10:50243433
|
A | G | 3 | a0001c0002t0013g0069a0001c0002t0013g0070a0001c0002t0013g0071 | 3 | HG02129.hp2 NA18977.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.361-82T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50243433 | ||||||
| chr10:50243480
|
G | T | 1 | a0001c0002t0080g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.361-129C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50243480 | ||||||
| chr10:50243592
|
G | A | 1 | a0001c0004t0048g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.361-241C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50243592 | ||||||
| chr10:50243599
|
T | C | 2 | a0002c0001t0021g0053a0003c0003t0001g0052 | 2 | HG02155.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.361-248A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50243599 | ||||||
| chr10:50243700
|
G | A | 1 | a0002c0001t0021g0345 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.361-349C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50243700 | ||||||
| chr10:50243894
|
G | A | 121 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(118): Show | 141 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.361-543C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50243894 | ||||||
| chr10:50243925
|
C | T | 4 | a0002c0001t0008g0123a0003c0003t0001g0124a0003c0003t0032g0019others(1): Show | 5 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-574G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50243925 | ||||||
| chr10:50244087
|
G | A | 7 | a0001c0007t0020g0356a0001c0007t0020g0357a0001c0007t0020g0359others(4): Show | 7 | HG01192.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.361-736C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50244087 | ||||||
| chr10:50244106
|
A | T | 121 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(118): Show | 141 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.361-755T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50244106 | ||||||
| chr10:50244154
|
G | A | 1 | a0001c0002t0080g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.361-803C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50244154 | ||||||
| chr10:50244206
|
T | C | 2 | a0003c0003t0005g0196a0003c0003t0092g0117 | 2 | HG01361.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.361-855A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50244206 | ||||||
| chr10:50244313
|
A | T | 1 | a0003c0003t0024g0122 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.360+909T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50244313 | ||||||
| chr10:50244348
|
TCATAAAA others(6): Show |
T | 10 | a0001c0002t0009g0272a0001c0002t0009g0347a0001c0002t0009g0351others(7): Show | 10 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.360+861_360+873del others(13): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50244348 | ||||||
| chr10:50244508
|
G | A | 124 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(121): Show | 144 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.360+714C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50244508 | ||||||
| chr10:50244555
|
T | C | 135 | a0001c0005t0011g0180a0001c0005t0117g0266a0001c0010t0069g0200others(132): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.360+667A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50244555 | ||||||
| chr10:50244555
|
T | G | 125 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(122): Show | 145 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.360+667A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50244555 | ||||||
| chr10:50244824
|
T | C | 2 | a0003c0003t0015g0197a0003c0003t0015g0198 | 2 | HG00099.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.360+398A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50244824 | ||||||
| chr10:50244839
|
C | CT | 110 | a0001c0002t0001g0083a0001c0002t0001g0095a0001c0002t0003g0004others(107): Show | 128 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(125): Show |
intron_variant | MODIFIER | c.360+382dupA | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50244839 | ||||||
| chr10:50244839
|
C | CTT | 16 | a0001c0002t0001g0012a0001c0002t0005g0061a0001c0002t0005g0063others(13): Show | 18 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.360+381_360+382dup others(2): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50244839 | ||||||
| chr10:50244948
|
G | A | 1 | a0001c0002t0080g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.360+274C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50244948 | ||||||
| chr10:50245002
|
GA | G | 125 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(122): Show | 145 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.360+219delT | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50245002 | ||||||
| chr10:50245101
|
G | T | 1 | a0002c0001t0004g0211 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.360+121C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50245101 | ||||||
| chr10:50245117
|
A | G | 125 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(122): Show | 145 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.360+105T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50245117 | ||||||
| chr10:50245202
|
G | A | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.360+20C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 3/20 | chr10 | 50245202 | ||||||
| chr10:50245511
|
T | G | 79 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(76): Show | 90 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.128-57A>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50245511 | ||||||
| chr10:50245533
|
G | A | 79 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(76): Show | 90 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.128-79C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50245533 | ||||||
| chr10:50245543
|
A | G | 125 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(122): Show | 145 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.128-89T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50245543 | ||||||
| chr10:50245590
|
C | T | 125 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(122): Show | 145 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.128-136G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50245590 | ||||||
| chr10:50245593
|
G | A | 125 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(122): Show | 145 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.128-139C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50245593 | ||||||
| chr10:50245657
|
C | A | 125 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(122): Show | 145 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.128-203G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50245657 | ||||||
| chr10:50245690
|
C | G | 2 | a0001c0005t0025g0007a0001c0005t0025g0034 | 3 | HG02572.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.128-236G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50245690 | ||||||
| chr10:50245835
|
C | T | 4 | a0001c0004t0006g0282a0001c0004t0053g0283a0001c0004t0095g0284others(1): Show | 4 | NA18944.hp2 NA18965.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-381G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50245835 | ||||||
| chr10:50245950
|
C | G | 2 | a0003c0003t0001g0210a0003c0003t0005g0209 | 2 | NA18952.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.128-496G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50245950 | ||||||
| chr10:50246241
|
G | T | 180 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(177): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.128-787C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50246241 | ||||||
| chr10:50246248
|
A | G | 165 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(162): Show | 187 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.128-794T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50246248 | ||||||
| chr10:50246405
|
C | A | 79 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(76): Show | 90 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.128-951G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50246405 | ||||||
| chr10:50246473
|
A | G | 86 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(83): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.128-1019T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50246473 | ||||||
| chr10:50246492
|
C | A | 86 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(83): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.128-1038G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50246492 | ||||||
| chr10:50246742
|
C | A | 86 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(83): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.128-1288G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50246742 | ||||||
| chr10:50246768
|
G | A | 85 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(82): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.128-1314C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50246768 | ||||||
| chr10:50246889
|
G | T | 85 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(82): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.128-1435C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50246889 | ||||||
| chr10:50246921
|
C | T | 93 | a0001c0005t0011g0180a0002c0001t0002g0024a0002c0001t0002g0182others(90): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.128-1467G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50246921 | ||||||
| chr10:50246968
|
C | A | 1 | a0002c0001t0018g0265 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.128-1514G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50246968 | ||||||
| chr10:50246981
|
T | A | 85 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(82): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.127+1503A>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50246981 | ||||||
| chr10:50247011
|
G | C | 85 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(82): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.127+1473C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247011 | ||||||
| chr10:50247214
|
G | A | 1 | a0001c0010t0102g0362 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127+1270C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247214 | ||||||
| chr10:50247256
|
G | A | 11 | a0001c0002t0001g0012a0001c0002t0005g0061a0001c0002t0005g0063others(8): Show | 12 | HG00733.hp2 HG01070.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.127+1228C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247256 | ||||||
| chr10:50247303
|
G | A | 9 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(6): Show | 9 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.127+1181C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247303 | ||||||
| chr10:50247323
|
AT | A | 181 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(178): Show | 201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.127+1160delA | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247323 | ||||||
| chr10:50247323
|
ATTT | A | 86 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(83): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.127+1158_127+1160d others(5): Show |
ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247323 | ||||||
| chr10:50247367
|
G | A | 86 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(83): Show | 97 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.127+1117C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247367 | ||||||
| chr10:50247419
|
T | C | 86 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(83): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.127+1065A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247419 | ||||||
| chr10:50247520
|
T | C | 86 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(83): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.127+964A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247520 | ||||||
| chr10:50247521
|
G | A | 85 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(82): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.127+963C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247521 | ||||||
| chr10:50247537
|
G | C | 1 | a0001c0004t0048g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.127+947C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247537 | ||||||
| chr10:50247587
|
A | G | 86 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(83): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.127+897T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247587 | ||||||
| chr10:50247697
|
C | G | 4 | a0003c0003t0001g0119a0003c0003t0001g0120a0003c0003t0001g0121others(1): Show | 4 | HG01192.hp2 HG01433.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+787G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247697 | ||||||
| chr10:50247827
|
G | T | 1 | a0001c0005t0117g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.127+657C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247827 | ||||||
| chr10:50247866
|
T | C | 86 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(83): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.127+618A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247866 | ||||||
| chr10:50247966
|
C | T | 1 | a0001c0002t0080g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.127+518G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247966 | ||||||
| chr10:50247994
|
C | A | 93 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(90): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.127+490G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247994 | ||||||
| chr10:50247995
|
C | A | 93 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(90): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.127+489G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50247995 | ||||||
| chr10:50248006
|
T | C | 1 | a0003c0003t0031g0199 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.127+478A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50248006 | ||||||
| chr10:50248081
|
A | T | 1 | a0001c0004t0033g0275 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.127+403T>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50248081 | ||||||
| chr10:50248150
|
A | G | 1 | a0001c0005t0013g0035 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127+334T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50248150 | ||||||
| chr10:50248209
|
G | A | 292 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(289): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.127+275C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50248209 | ||||||
| chr10:50248228
|
G | C | 93 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(90): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.127+256C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50248228 | ||||||
| chr10:50248314
|
T | C | 356 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(353): Show | 398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.127+170A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50248314 | ||||||
| chr10:50248355
|
G | A | 1 | a0001c0011t0109g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127+129C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50248355 | ||||||
| chr10:50248380
|
C | T | 92 | a0001c0005t0011g0180a0002c0001t0002g0024a0002c0001t0002g0182others(89): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.127+104G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 2/20 | chr10 | 50248380 | ||||||
| chr10:50248661
|
A | G | 1 | a0003c0003t0092g0117 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-36-15T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50248661 | ||||||
| chr10:50248970
|
G | A | 74 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(71): Show | 85 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.-36-324C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50248970 | ||||||
| chr10:50248988
|
G | A | 85 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(82): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-36-342C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50248988 | ||||||
| chr10:50249002
|
G | C | 1 | a0001c0004t0048g0281 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-36-356C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50249002 | ||||||
| chr10:50249046
|
G | A | 2 | a0001c0005t0025g0007a0001c0005t0025g0034 | 3 | HG02572.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-36-400C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50249046 | ||||||
| chr10:50249063
|
G | A | 1 | a0003c0003t0001g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-36-417C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50249063 | ||||||
| chr10:50249168
|
A | G | 1 | a0002c0001t0018g0202 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-36-522T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50249168 | ||||||
| chr10:50249236
|
G | C | 93 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(90): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-36-590C>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50249236 | ||||||
| chr10:50249301
|
C | T | 85 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(82): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-36-655G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50249301 | ||||||
| chr10:50249700
|
C | G | 1 | a0001c0004t0048g0281 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-36-1054G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50249700 | ||||||
| chr10:50249888
|
A | G | 94 | a0001c0005t0011g0180a0001c0010t0069g0200a0002c0001t0002g0024others(91): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.-36-1242T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50249888 | ||||||
| chr10:50250091
|
C | T | 36 | a0001c0002t0028g0006a0001c0002t0028g0303a0001c0002t0049g0031others(33): Show | 45 | HG00597.hp1 HG00642.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.-37+1304G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50250091 | ||||||
| chr10:50250127
|
T | C | 55 | a0001c0002t0001g0083a0001c0002t0001g0095a0001c0002t0003g0004others(52): Show | 64 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.-37+1268A>G | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50250127 | ||||||
| chr10:50250208
|
C | A | 1 | a0001c0002t0005g0114 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-37+1187G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50250208 | ||||||
| chr10:50250391
|
C | T | 1 | a0001c0011t0109g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-37+1004G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50250391 | ||||||
| chr10:50250533
|
A | G | 6 | a0001c0004t0033g0275a0001c0004t0033g0278a0001c0004t0034g0276others(3): Show | 6 | HG00597.hp1 HG00738.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+862T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50250533 | ||||||
| chr10:50250537
|
C | T | 1 | a0003c0003t0005g0115 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-37+858G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50250537 | ||||||
| chr10:50250597
|
C | T | 1 | a0001c0011t0109g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-37+798G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50250597 | ||||||
| chr10:50250650
|
C | G | 15 | a0001c0004t0006g0282a0001c0004t0013g0289a0001c0004t0033g0275others(12): Show | 15 | HG00597.hp1 HG00738.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.-37+745G>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50250650 | ||||||
| chr10:50250753
|
G | T | 1 | a0001c0002t0080g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-37+642C>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50250753 | ||||||
| chr10:50250881
|
C | A | 1 | a0001c0011t0109g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-37+514G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50250881 | ||||||
| chr10:50250948
|
C | T | 72 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0095others(69): Show | 83 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.-37+447G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50250948 | ||||||
| chr10:50251204
|
G | A | 87 | a0001c0002t0009g0347a0001c0002t0009g0351a0001c0002t0009g0352others(84): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.-37+191C>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50251204 | ||||||
| chr10:50251218
|
C | T | 2 | a0001c0005t0025g0007a0001c0005t0025g0034 | 3 | HG02572.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-37+177G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50251218 | ||||||
| chr10:50251219
|
A | G | 25 | a0001c0005t0011g0009a0001c0005t0011g0010a0001c0005t0011g0041others(22): Show | 30 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-37+176T>C | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50251219 | ||||||
| chr10:50251225
|
C | T | 1 | a0001c0002t0010g0008 | 2 | NA18975.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-37+170G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50251225 | ||||||
| chr10:50251315
|
C | T | 2 | a0001c0005t0025g0007a0001c0005t0025g0034 | 3 | HG02572.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-37+80G>A | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50251315 | ||||||
| chr10:50251326
|
C | A | 7 | a0001c0007t0020g0356a0001c0007t0020g0357a0001c0007t0020g0359others(4): Show | 7 | HG01192.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+69G>T | ASAH2 | ENSG00000188611.17 | transcript | ENST00000682911.1 | protein_coding | 1/20 | chr10 | 50251326 |