Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 427 |
| ensemblid | ENSG00000104763.20 |
| hgncid | 735 |
| symbol | ASAH1 |
| name | N-acylsphingosine amidohydrolase 1 |
| refseq_nuc | NM_177924.5 |
| refseq_prot | NP_808592.2 |
| ensembl_nuc | ENST00000637790.2 |
| ensembl_prot | ENSP00000490272.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 18055992 |
| end | 18084107 |
| strand | - |
| ver | v1.2 |
| region | chr8:18055992-18084107 |
| region5000 | chr8:18050992-18089107 |
| regionname0 | ASAH1_chr8_18055992_18084107 |
| regionname5000 | ASAH1_chr8_18050992_18089107 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 395 | 173 | 23 | 45 | 76 | 10 | 18 | 60 | ASAH1_chr8_18050992_18089107 | ASAH1 | MPGRS others(390): Show |
chr8 | 18050992 | 18089107 |
| a0002 | 0/0 | 395 | 163 | 32 | 25 | 81 | 8 | 17 | 67 | ASAH1_chr8_18050992_18089107 | ASAH1 | MPGRS others(390): Show |
chr8 | 18050992 | 18089107 |
| a0003 | 1/0 | 395 | 67 | 39 | 3 | 20 | 0 | 4 | 13 | ASAH1_chr8_18050992_18089107 | ASAH1 | MPGRS others(390): Show |
chr8 | 18050992 | 18089107 |
| a0004 | 0/0 | 395 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | ASAH1_chr8_18050992_18089107 | ASAH1 | MPGRS others(390): Show |
chr8 | 18050992 | 18089107 |
| a0005 | 0/0 | 395 | 5 | 0 | 1 | 4 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | MPGRS others(390): Show |
chr8 | 18050992 | 18089107 |
| a0006 | 0/0 | 395 | 5 | 0 | 0 | 0 | 0 | 5 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | MPGRS others(390): Show |
chr8 | 18050992 | 18089107 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1185 | 170 | 22 | 45 | 75 | 10 | 17 | ASAH1_chr8_18050992_18089107 | ASAH1 | ATGCC others(1180): Show |
chr8 | 18050992 | 18089107 | ||
| a0001c0007 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | ATGCC others(1180): Show |
chr8 | 18050992 | 18089107 | ||
| a0001c0008 | 0/0 | 1185 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | ATGCC others(1180): Show |
chr8 | 18050992 | 18089107 | ||
| a0001c0009 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | ATGCC others(1180): Show |
chr8 | 18050992 | 18089107 | ||
| a0002c0002 | 0/0 | 1185 | 163 | 32 | 25 | 81 | 8 | 17 | ASAH1_chr8_18050992_18089107 | ASAH1 | ATGCC others(1180): Show |
chr8 | 18050992 | 18089107 | ||
| a0003c0003 | 1/0 | 1185 | 67 | 39 | 3 | 20 | 0 | 4 | ASAH1_chr8_18050992_18089107 | ASAH1 | ATGCC others(1180): Show |
chr8 | 18050992 | 18089107 | ||
| a0004c0004 | 0/0 | 1185 | 7 | 0 | 0 | 7 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | ATGCC others(1180): Show |
chr8 | 18050992 | 18089107 | ||
| a0005c0006 | 0/0 | 1185 | 5 | 0 | 1 | 4 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | ATGCC others(1180): Show |
chr8 | 18050992 | 18089107 | ||
| a0006c0005 | 0/0 | 1185 | 5 | 0 | 0 | 0 | 0 | 5 | ASAH1_chr8_18050992_18089107 | ASAH1 | ATGCC others(1180): Show |
chr8 | 18050992 | 18089107 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2779 | 94 | 5 | 27 | 42 | 7 | 12 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0002 | 0/0 | 2779 | 15 | 4 | 7 | 2 | 2 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0003 | 0/0 | 2775 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2770): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0004 | 0/0 | 2773 | 24 | 5 | 7 | 12 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2768): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0006 | 0/0 | 2779 | 10 | 0 | 0 | 8 | 0 | 2 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0007 | 0/0 | 2773 | 10 | 4 | 3 | 1 | 1 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2768): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0012 | 0/0 | 2779 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0013 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0014 | 0/0 | 2779 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0015 | 0/0 | 2779 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0016 | 0/0 | 2779 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0020 | 0/0 | 2773 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2768): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0021 | 0/0 | 2773 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2768): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0022 | 0/0 | 2773 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2768): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0031 | 0/0 | 2779 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0032 | 0/0 | 2779 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0001c0001t0034 | 0/0 | 2779 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0001c0007t0023 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0001c0008t0006 | 0/0 | 2779 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0001c0009t0001 | 0/0 | 2779 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0001 | 0/0 | 2779 | 8 | 0 | 0 | 8 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0002 | 0/0 | 2779 | 77 | 16 | 21 | 27 | 7 | 6 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0003 | 0/0 | 2775 | 66 | 11 | 4 | 40 | 1 | 10 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2770): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0004 | 0/0 | 2773 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2768): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0005 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0006 | 0/0 | 2779 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0018 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0019 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2770): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0025 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0027 | 0/0 | 2775 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2770): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0028 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2770): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0029 | 0/0 | 2775 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2770): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0030 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0033 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2770): Show |
chr8 | 18050992 | 18089107 |
| a0002c0002t0035 | 0/0 | 2779 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0003c0003t0001 | 1/0 | 2779 | 26 | 0 | 2 | 20 | 0 | 3 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0003c0003t0002 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0003c0003t0005 | 0/0 | 2779 | 15 | 15 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0003c0003t0008 | 0/0 | 2773 | 9 | 8 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2768): Show |
chr8 | 18050992 | 18089107 |
| a0003c0003t0009 | 0/0 | 2775 | 8 | 8 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2770): Show |
chr8 | 18050992 | 18089107 |
| a0003c0003t0010 | 0/0 | 2779 | 4 | 4 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0003c0003t0013 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0003c0003t0017 | 0/0 | 2779 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0003c0003t0024 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0003c0003t0026 | 0/0 | 2779 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0004c0004t0003 | 0/0 | 2775 | 7 | 0 | 0 | 7 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2770): Show |
chr8 | 18050992 | 18089107 |
| a0005c0006t0003 | 0/0 | 2775 | 5 | 0 | 1 | 4 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2770): Show |
chr8 | 18050992 | 18089107 |
| a0006c0005t0001 | 0/0 | 2779 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| a0006c0005t0011 | 0/0 | 2779 | 4 | 0 | 0 | 0 | 0 | 4 | ASAH1_chr8_18050992_18089107 | ASAH1 | CTTCT others(2774): Show |
chr8 | 18050992 | 18089107 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 4 | 2 | 0 | 6 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0012 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0006g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0007g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0007g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0007g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0012g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0012g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0013g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0014g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0015g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0015g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0016g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0020g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0021g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0022g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0031g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0032g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0001t0034g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0007t0023g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0008t0006g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0001c0009t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0001 | 0/0 | 16 | 2 | 4 | 7 | 0 | 3 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0008 | 0/0 | 6 | 0 | 3 | 0 | 3 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0004 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0005 | 0/0 | 7 | 0 | 0 | 6 | 1 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0018g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0019g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0025g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0027g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0028g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0029g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0030g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0033g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0002c0002t0035g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0010 | 1/0 | 5 | 0 | 0 | 4 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0005g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0005g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0008g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0008g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0009g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0009g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0009g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0010g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0013g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0017g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0024g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0003c0003t0026g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0004c0004t0003g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0004c0004t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0005c0006t0003g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0005c0006t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0005c0006t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0006c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0006c0005t0011g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0006c0005t0011g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| a0006c0005t0011g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0192 | EUR | GBR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0185 | EUR | GBR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0140 | EUR | GBR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0143 | EUR | FIN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0038 | EUR | FIN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0072 | EUR | FIN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00423 | hp1 | a0001 | c0001 | t0012 | g0050 | EAS | CHS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0249 | EAS | CHS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00438 | hp1 | a0005 | c0006 | t0003 | g0127 | EAS | CHS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | CHS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00558 | hp1 | a0005 | c0006 | t0003 | g0023 | EAS | CHS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0160 | EAS | CHS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00597 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | CHS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0224 | EAS | CHS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | CHS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00621 | hp1 | a0005 | c0006 | t0003 | g0023 | EAS | CHS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | CHS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01099 | hp1 | a0003 | c0003 | t0008 | g0022 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01099 | hp2 | a0003 | c0003 | t0001 | g0120 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0090 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01167 | hp1 | a0001 | c0001 | t0007 | g0074 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0132 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0073 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0118 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0149 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0033 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0038 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0092 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0153 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0154 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0076 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01358 | hp1 | a0002 | c0002 | t0003 | g0031 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0039 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | IBS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | IBS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0008 | EUR | IBS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0008 | EUR | IBS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01884 | hp1 | a0003 | c0003 | t0008 | g0030 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0077 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01891 | hp1 | a0003 | c0003 | t0010 | g0279 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01891 | hp2 | a0003 | c0003 | t0005 | g0026 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0095 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01952 | hp1 | a0001 | c0001 | t0021 | g0057 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01975 | hp2 | a0002 | c0002 | t0003 | g0241 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02027 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02040 | hp1 | a0002 | c0002 | t0003 | g0242 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02083 | hp1 | a0001 | c0001 | t0007 | g0064 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02083 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02135 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02145 | hp2 | a0002 | c0002 | t0003 | g0270 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02148 | hp1 | a0005 | c0006 | t0003 | g0023 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02165 | hp2 | a0002 | c0002 | t0003 | g0104 | EAS | CDX | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02257 | hp2 | a0001 | c0007 | t0023 | g0275 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02258 | hp1 | a0003 | c0003 | t0005 | g0024 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02258 | hp2 | a0003 | c0003 | t0005 | g0203 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0088 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02280 | hp2 | a0003 | c0003 | t0008 | g0087 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0082 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02451 | hp1 | a0003 | c0003 | t0013 | g0267 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02523 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | KHV | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0021 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02572 | hp2 | a0002 | c0002 | t0030 | g0250 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02602 | hp1 | a0002 | c0002 | t0003 | g0235 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0226 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0134 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02622 | hp2 | a0003 | c0003 | t0026 | g0264 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0225 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02630 | hp2 | a0003 | c0003 | t0005 | g0026 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02647 | hp1 | a0003 | c0003 | t0005 | g0260 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02647 | hp2 | a0003 | c0003 | t0009 | g0216 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02683 | hp1 | a0001 | c0008 | t0006 | g0215 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02683 | hp2 | a0003 | c0003 | t0001 | g0051 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02698 | hp1 | a0006 | c0005 | t0001 | g0210 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02698 | hp2 | a0006 | c0005 | t0011 | g0209 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02717 | hp1 | a0003 | c0003 | t0005 | g0272 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02717 | hp2 | a0002 | c0002 | t0003 | g0025 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02723 | hp1 | a0003 | c0003 | t0009 | g0014 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0214 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02735 | hp2 | a0003 | c0003 | t0001 | g0051 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02738 | hp2 | a0002 | c0002 | t0003 | g0244 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02809 | hp1 | a0003 | c0003 | t0005 | g0026 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02809 | hp2 | a0003 | c0003 | t0002 | g0220 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02818 | hp1 | a0003 | c0003 | t0009 | g0014 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02818 | hp2 | a0003 | c0003 | t0005 | g0056 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0262 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02886 | hp2 | a0003 | c0003 | t0008 | g0022 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02895 | hp1 | a0002 | c0002 | t0003 | g0271 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0027 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02896 | hp1 | a0003 | c0003 | t0009 | g0014 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02897 | hp1 | a0001 | c0001 | t0014 | g0027 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02897 | hp2 | a0003 | c0003 | t0009 | g0014 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0141 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0135 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0254 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0137 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0021 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0206 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02976 | hp1 | a0003 | c0003 | t0008 | g0084 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02976 | hp2 | a0001 | c0001 | t0013 | g0277 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03017 | hp1 | a0006 | c0005 | t0011 | g0208 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03041 | hp1 | a0003 | c0003 | t0005 | g0259 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0256 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03098 | hp1 | a0002 | c0002 | t0003 | g0060 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0028 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03130 | hp1 | a0003 | c0003 | t0008 | g0030 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03130 | hp2 | a0002 | c0002 | t0003 | g0025 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03139 | hp1 | a0003 | c0003 | t0010 | g0161 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03139 | hp2 | a0002 | c0002 | t0003 | g0263 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0078 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03195 | hp2 | a0003 | c0003 | t0010 | g0052 | AFR | ESN | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03225 | hp1 | a0001 | c0001 | t0022 | g0081 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03225 | hp2 | a0002 | c0002 | t0005 | g0238 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0039 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03239 | hp2 | a0002 | c0002 | t0027 | g0239 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03453 | hp1 | a0003 | c0003 | t0005 | g0273 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03453 | hp2 | a0003 | c0003 | t0009 | g0062 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0028 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0055 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03491 | hp1 | a0002 | c0002 | t0003 | g0234 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03540 | hp2 | a0002 | c0002 | t0018 | g0266 | AFR | GWD | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03579 | hp1 | a0002 | c0002 | t0003 | g0269 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03579 | hp2 | a0003 | c0003 | t0008 | g0085 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03669 | hp2 | a0002 | c0002 | t0003 | g0004 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | STU | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | STU | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0004 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03710 | hp2 | a0003 | c0003 | t0017 | g0268 | SAS | PJL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03831 | hp1 | a0002 | c0002 | t0003 | g0207 | SAS | BEB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0152 | SAS | BEB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03834 | hp1 | a0006 | c0005 | t0011 | g0046 | SAS | BEB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0157 | SAS | BEB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0219 | SAS | BEB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0156 | SAS | BEB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0193 | SAS | BEB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG04115 | hp1 | a0001 | c0001 | t0007 | g0058 | SAS | STU | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG04115 | hp2 | a0002 | c0002 | t0003 | g0116 | SAS | STU | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG04204 | hp1 | a0001 | c0001 | t0020 | g0075 | SAS | STU | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG04204 | hp2 | a0002 | c0002 | t0003 | g0233 | SAS | STU | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG04228 | hp1 | a0003 | c0003 | t0001 | g0265 | SAS | STU | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG04228 | hp2 | a0006 | c0005 | t0011 | g0046 | SAS | STU | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18522 | hp1 | a0003 | c0003 | t0005 | g0165 | AFR | YRI | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18522 | hp2 | a0002 | c0002 | t0003 | g0025 | AFR | YRI | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CHB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18612 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | CHB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | CHB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18906 | hp1 | a0003 | c0003 | t0008 | g0022 | AFR | YRI | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18906 | hp2 | a0003 | c0003 | t0005 | g0024 | AFR | YRI | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18939 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18940 | hp2 | a0001 | c0001 | t0006 | g0222 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18941 | hp2 | a0002 | c0002 | t0028 | g0245 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18943 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18944 | hp1 | a0004 | c0004 | t0003 | g0007 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18945 | hp1 | a0001 | c0001 | t0012 | g0050 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18947 | hp1 | a0002 | c0002 | t0003 | g0031 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18947 | hp2 | a0001 | c0001 | t0012 | g0258 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18948 | hp1 | a0002 | c0002 | t0029 | g0105 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18948 | hp2 | a0004 | c0004 | t0003 | g0007 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18949 | hp1 | a0002 | c0002 | t0003 | g0049 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18950 | hp1 | a0002 | c0002 | t0003 | g0097 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18950 | hp2 | a0001 | c0001 | t0032 | g0173 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18952 | hp1 | a0002 | c0002 | t0003 | g0094 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18953 | hp1 | a0001 | c0001 | t0031 | g0115 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18953 | hp2 | a0002 | c0002 | t0003 | g0049 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18954 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18956 | hp2 | a0002 | c0002 | t0003 | g0100 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18959 | hp2 | a0001 | c0001 | t0015 | g0178 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18960 | hp2 | a0002 | c0002 | t0019 | g0240 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18962 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18962 | hp2 | a0002 | c0002 | t0003 | g0111 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18963 | hp2 | a0003 | c0003 | t0001 | g0033 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18965 | hp2 | a0002 | c0002 | t0003 | g0131 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18966 | hp1 | a0002 | c0002 | t0003 | g0114 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18968 | hp1 | a0003 | c0003 | t0001 | g0119 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18975 | hp1 | a0001 | c0001 | t0016 | g0043 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18977 | hp1 | a0002 | c0002 | t0006 | g0144 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18977 | hp2 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18978 | hp2 | a0002 | c0002 | t0003 | g0243 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18979 | hp1 | a0002 | c0002 | t0003 | g0230 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18979 | hp2 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18981 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18982 | hp1 | a0003 | c0003 | t0001 | g0126 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0125 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18984 | hp1 | a0004 | c0004 | t0003 | g0007 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18986 | hp1 | a0004 | c0004 | t0003 | g0112 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18986 | hp2 | a0001 | c0001 | t0006 | g0221 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18988 | hp1 | a0002 | c0002 | t0003 | g0248 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18988 | hp2 | a0003 | c0003 | t0001 | g0124 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18991 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18991 | hp2 | a0002 | c0002 | t0003 | g0108 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18992 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18998 | hp1 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18999 | hp2 | a0002 | c0002 | t0003 | g0102 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19001 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19004 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19006 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19007 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19007 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19010 | hp1 | a0005 | c0006 | t0003 | g0231 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19010 | hp2 | a0003 | c0003 | t0001 | g0276 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0096 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | LWK | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19043 | hp2 | a0003 | c0003 | t0005 | g0063 | AFR | LWK | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19055 | hp1 | a0002 | c0002 | t0003 | g0106 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19055 | hp2 | a0001 | c0009 | t0001 | g0093 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19057 | hp1 | a0002 | c0002 | t0004 | g0110 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19060 | hp2 | a0001 | c0001 | t0006 | g0218 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19062 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19062 | hp2 | a0001 | c0001 | t0016 | g0043 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19063 | hp2 | a0002 | c0002 | t0003 | g0246 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19064 | hp1 | a0002 | c0002 | t0003 | g0236 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19066 | hp1 | a0001 | c0001 | t0034 | g0183 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19067 | hp1 | a0002 | c0002 | t0003 | g0251 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19068 | hp1 | a0004 | c0004 | t0003 | g0007 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19068 | hp2 | a0002 | c0002 | t0035 | g0282 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19074 | hp2 | a0003 | c0003 | t0001 | g0123 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19076 | hp1 | a0003 | c0003 | t0001 | g0117 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19081 | hp2 | a0002 | c0002 | t0003 | g0048 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19082 | hp1 | a0004 | c0004 | t0003 | g0007 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19083 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19084 | hp1 | a0002 | c0002 | t0003 | g0113 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19087 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19090 | hp1 | a0001 | c0001 | t0015 | g0159 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19240 | hp1 | a0003 | c0003 | t0009 | g0195 | AFR | YRI | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA19240 | hp2 | a0003 | c0003 | t0024 | g0278 | AFR | YRI | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA20129 | hp1 | a0003 | c0003 | t0008 | g0086 | AFR | ASW | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA20129 | hp2 | a0002 | c0002 | t0003 | g0059 | AFR | ASW | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA20752 | hp1 | a0002 | c0002 | t0003 | g0005 | EUR | TSI | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | TSI | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0136 | EUR | TSI | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0008 | EUR | TSI | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0229 | SAS | GIH | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02109 | hp1 | a0003 | c0003 | t0010 | g0052 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02109 | hp2 | a0003 | c0003 | t0009 | g0196 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0139 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02559 | hp1 | a0003 | c0003 | t0005 | g0024 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG02559 | hp2 | a0002 | c0002 | t0033 | g0053 | AFR | ACB | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0061 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG03471 | hp2 | a0003 | c0003 | t0005 | g0261 | AFR | MSL | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | USA | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0036 | AFR | USA | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18955 | hp1 | a0004 | c0004 | t0003 | g0007 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA18955 | hp2 | a0002 | c0002 | t0003 | g0107 | EAS | JPT | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0142 | AFR | LWK | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| NA21309 | hp2 | a0002 | c0002 | t0025 | g0054 | AFR | LWK | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0177 | REF | REF | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0010 | REF | REF | ASAH1_chr8_18050992_18089107 | ASAH1 | chr8 | 18050992 | 18089107 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:18057617 | C | T | 1 | a0005 | 5 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(2): Show |
missense_variant | MODERATE | c.1105G>A | p.Val369Ile | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 1154/2779 | 1105/1188 | 369/395 | chr8 | 18057617 | |||
| chr8:18059579 | C | G | 1 | a0004 | 7 | NA18944.hp1 NA18948.hp2 NA18955.hp1 others(4): Show |
missense_variant | MODERATE | c.910G>C | p.Val304Leu | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 11/14 | 959/2779 | 910/1188 | 304/395 | chr8 | 18059579 | |||
| chr8:18061425 | A | G | 5 | a0001 a0002 a0004 others(2): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
missense_variant | MODERATE | c.737T>C | p.Val246Ala | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/14 | 786/2779 | 737/1188 | 246/395 | chr8 | 18061425 | |||
| chr8:18067230 | A | T | 1 | a0006 | 5 | HG02698.hp1 HG02698.hp2 HG03017.hp1 others(2): Show |
missense_variant | MODERATE | c.372T>A | p.Asp124Glu | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/14 | 421/2779 | 372/1188 | 124/395 | chr8 | 18067230 | |||
| chr8:18069818 | T | C | 2 | a0001 a0006 |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
missense_variant | MODERATE | c.277A>G | p.Ile93Val | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/14 | 326/2779 | 277/1188 | 93/395 | chr8 | 18069818 | |||
| chr8:18071302 | C | T | 2 | a0001 a0006 |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
missense_variant&splice_region_variant | MODERATE | c.214G>A | p.Val72Met | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/14 | 263/2779 | 214/1188 | 72/395 | chr8 | 18071302 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:18061723 | T | C | 1 | a0001c0007 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.666A>G | p.Thr222Thr | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 9/14 | 715/2779 | 666/1188 | 222/395 | chr8 | 18061723 | |||
| chr8:18067221 | T | C | 1 | a0001c0008 | 1 | HG02683.hp1 | splice_region_variant&synonymous_variant | LOW | c.381A>G | p.Leu127Leu | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/14 | 430/2779 | 381/1188 | 127/395 | chr8 | 18067221 | |||
| chr8:18069834 | G | A | 1 | a0001c0009 | 1 | NA19055.hp2 | synonymous_variant | LOW | c.261C>T | p.Phe87Phe | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/14 | 310/2779 | 261/1188 | 87/395 | chr8 | 18069834 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:18056042 | C | T | 1 | a0002c0002t0029 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1492G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 1492 | chr8 | 18056042 | ||||||
| chr8:18056145 | C | T | 3 | a0001c0001t0014 a0002c0002t0018 a0002c0002t0025 |
4 | HG02895.hp2 HG02897.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1389G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 1389 | chr8 | 18056145 | ||||||
| chr8:18056166 | A | G | 1 | a0001c0001t0020 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1368T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 1368 | chr8 | 18056166 | ||||||
| chr8:18056186 | A | G | 1 | a0003c0003t0024 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1348T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 1348 | chr8 | 18056186 | ||||||
| chr8:18056244 | T | C | 5 | a0001c0001t0013 a0001c0001t0032 a0003c0003t0013 others(2): Show |
8 | HG02451.hp1 HG02698.hp2 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1290A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 1290 | chr8 | 18056244 | ||||||
| chr8:18056289 | A | G | 2 | a0001c0001t0013 a0003c0003t0013 |
2 | HG02451.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1245T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 1245 | chr8 | 18056289 | ||||||
| chr8:18056302 | C | G | 2 | a0003c0003t0010 a0003c0003t0024 |
5 | HG01891.hp1 HG02109.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1232G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 1232 | chr8 | 18056302 | ||||||
| chr8:18056304 | G | A | 11 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0013 others(8): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1230C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 1230 | chr8 | 18056304 | ||||||
| chr8:18056431 | G | A | 8 | a0001c0001t0003 a0002c0002t0003 a0002c0002t0019 others(5): Show |
83 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1103C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 1103 | chr8 | 18056431 | ||||||
| chr8:18056461 | G | A | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(32): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1073C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 1073 | chr8 | 18056461 | ||||||
| chr8:18056602 | G | A | 2 | a0003c0003t0008 a0003c0003t0009 |
17 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*932C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 932 | chr8 | 18056602 | ||||||
| chr8:18056608 | T | A | 1 | a0001c0001t0012 | 3 | HG00423.hp1 NA18945.hp1 NA18947.hp2 |
3_prime_UTR_variant | MODIFIER | c.*926A>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 926 | chr8 | 18056608 | ||||||
| chr8:18056608 | T | G | 11 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0014 others(8): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*926A>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 926 | chr8 | 18056608 | ||||||
| chr8:18056795 | C | T | 1 | a0001c0001t0031 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*739G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 739 | chr8 | 18056795 | ||||||
| chr8:18056796 | G | C | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(14): Show |
139 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*738C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 738 | chr8 | 18056796 | ||||||
| chr8:18056805 | A | G | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(14): Show |
139 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*729T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 729 | chr8 | 18056805 | ||||||
| chr8:18056822 | ACTTC | A | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(14): Show |
139 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*708_*711delGAAG | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 708 | chr8 | 18056822 | ||||||
| chr8:18056839 | G | A | 6 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0020 others(3): Show |
38 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*695C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 695 | chr8 | 18056839 | ||||||
| chr8:18056847 | G | C | 16 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(13): Show |
138 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*687C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 687 | chr8 | 18056847 | ||||||
| chr8:18057075 | A | G | 1 | a0003c0003t0017 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*459T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 459 | chr8 | 18057075 | ||||||
| chr8:18057166 | G | A | 1 | a0002c0002t0030 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*368C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 368 | chr8 | 18057166 | ||||||
| chr8:18057178 | G | C | 1 | a0001c0001t0015 | 2 | NA18959.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*356C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 356 | chr8 | 18057178 | ||||||
| chr8:18057200 | C | T | 2 | a0001c0001t0007 a0001c0001t0020 |
11 | HG00323.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*334G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 334 | chr8 | 18057200 | ||||||
| chr8:18057290 | G | A | 7 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0020 others(4): Show |
47 | HG00323.hp2 HG00438.hp2 HG01099.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*244C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 244 | chr8 | 18057290 | ||||||
| chr8:18057334 | G | A | 3 | a0001c0001t0006 a0001c0008t0006 a0002c0002t0006 |
12 | HG00597.hp2 HG02683.hp1 HG02735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*200C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 200 | chr8 | 18057334 | ||||||
| chr8:18057350 | A | T | 7 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0020 others(4): Show |
47 | HG00323.hp2 HG00438.hp2 HG01099.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*184T>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 184 | chr8 | 18057350 | ||||||
| chr8:18057356 | TAG | T | 7 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0020 others(4): Show |
47 | HG00323.hp2 HG00438.hp2 HG01099.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*176_*177delCT | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 176 | chr8 | 18057356 | ||||||
| chr8:18057363 | A | G | 7 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0020 others(4): Show |
47 | HG00323.hp2 HG00438.hp2 HG01099.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*171T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 171 | chr8 | 18057363 | ||||||
| chr8:18057374 | A | G | 7 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0020 others(4): Show |
47 | HG00323.hp2 HG00438.hp2 HG01099.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*160T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 160 | chr8 | 18057374 | ||||||
| chr8:18057398 | C | T | 1 | a0002c0002t0019 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*136G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 136 | chr8 | 18057398 | ||||||
| chr8:18057410 | A | T | 28 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(25): Show |
163 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*124T>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 124 | chr8 | 18057410 | ||||||
| chr8:18057476 | C | T | 1 | a0002c0002t0018 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*58G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 58 | chr8 | 18057476 | ||||||
| chr8:18057509 | C | T | 1 | a0003c0003t0017 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 25 | chr8 | 18057509 | ||||||
| chr8:18057510 | G | A | 1 | a0001c0001t0034 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*24C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 24 | chr8 | 18057510 | ||||||
| chr8:18057528 | G | A | 1 | a0001c0001t0016 | 2 | NA18975.hp1 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 14/14 | 6 | chr8 | 18057528 | ||||||
| chr8:18084096 | G | A | 1 | a0002c0002t0035 | 1 | NA19068.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-38C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/14 | chr8 | 18084096 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:18057681 | T | C | 1 | a0001c0001t0002g0186 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1099-58A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18057681 | |||||||
| chr8:18057696 | A | G | 1 | a0002c0002t0004g0110 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1099-73T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18057696 | |||||||
| chr8:18057744 | C | CTG | 66 | a0001c0001t0004g0009 a0001c0001t0004g0012 a0001c0001t0004g0029 others(63): Show |
86 | HG00323.hp2 HG00438.hp2 HG01099.hp1 others(83): Show |
intron_variant | MODIFIER | c.1099-122_1099-121i others(4): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18057744 | |||||||
| chr8:18057790 | T | C | 26 | a0001c0001t0013g0277 a0001c0007t0023g0275 a0002c0002t0018g0266 others(23): Show |
32 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1099-167A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18057790 | |||||||
| chr8:18057832 | A | G | 26 | a0001c0001t0013g0277 a0001c0007t0023g0275 a0002c0002t0018g0266 others(23): Show |
32 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1099-209T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18057832 | |||||||
| chr8:18057906 | C | T | 26 | a0001c0001t0013g0277 a0001c0007t0023g0275 a0002c0002t0018g0266 others(23): Show |
32 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1099-283G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18057906 | |||||||
| chr8:18058010 | C | T | 2 | a0002c0002t0002g0143 a0002c0002t0002g0193 |
2 | HG00280.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1099-387G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058010 | |||||||
| chr8:18058017 | C | T | 21 | a0001c0007t0023g0275 a0002c0002t0018g0266 a0002c0002t0025g0054 others(18): Show |
26 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1099-394G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058017 | |||||||
| chr8:18058041 | T | C | 3 | a0002c0002t0003g0059 a0002c0002t0003g0060 a0002c0002t0003g0061 |
3 | HG03098.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1099-418A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058041 | |||||||
| chr8:18058048 | T | C | 1 | a0002c0002t0003g0271 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1099-425A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058048 | |||||||
| chr8:18058089 | C | T | 1 | a0002c0002t0003g0095 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1099-466G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058089 | |||||||
| chr8:18058111 | C | A | 106 | a0001c0001t0003g0156 a0001c0001t0004g0009 a0001c0001t0004g0012 others(103): Show |
145 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1099-488G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058111 | |||||||
| chr8:18058112 | A | C | 106 | a0001c0001t0003g0156 a0001c0001t0004g0009 a0001c0001t0004g0012 others(103): Show |
145 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1099-489T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058112 | |||||||
| chr8:18058160 | G | C | 4 | a0003c0003t0005g0026 a0003c0003t0005g0056 a0003c0003t0005g0165 others(1): Show |
6 | HG01891.hp2 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-537C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058160 | |||||||
| chr8:18058269 | C | T | 2 | a0002c0002t0018g0266 a0002c0002t0025g0054 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1098+566G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058269 | |||||||
| chr8:18058274 | T | C | 1 | a0002c0002t0002g0028 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1098+561A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058274 | |||||||
| chr8:18058330 | A | T | 130 | a0001c0001t0003g0156 a0001c0001t0004g0009 a0001c0001t0004g0012 others(127): Show |
177 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.1098+505T>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058330 | |||||||
| chr8:18058387 | G | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0198 |
3 | HG00639.hp1 HG01934.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1098+448C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058387 | |||||||
| chr8:18058413 | A | G | 1 | a0001c0001t0013g0277 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1098+422T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058413 | |||||||
| chr8:18058419 | C | T | 35 | a0001c0007t0023g0275 a0002c0002t0018g0266 a0002c0002t0025g0054 others(32): Show |
47 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.1098+416G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058419 | |||||||
| chr8:18058466 | C | G | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(231): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1098+369G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058466 | |||||||
| chr8:18058484 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1098+351C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058484 | |||||||
| chr8:18058715 | A | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(142): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1098+120T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058715 | |||||||
| chr8:18058799 | C | T | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1098+36G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 13/13 | chr8 | 18058799 | |||||||
| chr8:18058936 | A | G | 1 | a0002c0002t0003g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1042-45T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 12/13 | chr8 | 18058936 | |||||||
| chr8:18059044 | C | T | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(231): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1042-153G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 12/13 | chr8 | 18059044 | |||||||
| chr8:18059089 | CT | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(231): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1042-199delA | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 12/13 | chr8 | 18059089 | |||||||
| chr8:18059219 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1041+122C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 12/13 | chr8 | 18059219 | |||||||
| chr8:18059243 | G | A | 61 | a0001c0001t0003g0156 a0002c0002t0002g0237 a0002c0002t0003g0004 others(58): Show |
87 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1041+98C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 12/13 | chr8 | 18059243 | |||||||
| chr8:18059322 | G | T | 2 | a0001c0001t0004g0066 a0001c0001t0004g0067 |
2 | NA18949.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1041+19C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 12/13 | chr8 | 18059322 | |||||||
| chr8:18059500 | A | C | 5 | a0003c0003t0005g0272 a0003c0003t0010g0052 a0003c0003t0010g0161 others(2): Show |
6 | HG01891.hp1 HG02109.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.918-36T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 11/13 | chr8 | 18059500 | |||||||
| chr8:18059752 | G | A | 1 | a0001c0001t0013g0277 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.786-49C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18059752 | |||||||
| chr8:18059837 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(108): Show |
162 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.786-134G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18059837 | |||||||
| chr8:18059853 | G | C | 1 | a0003c0003t0013g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.786-150C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18059853 | |||||||
| chr8:18059919 | C | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(110): Show |
165 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.786-216G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18059919 | |||||||
| chr8:18059942 | CCT | C | 15 | a0003c0003t0001g0051 a0003c0003t0001g0265 a0003c0003t0002g0220 others(12): Show |
22 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.786-241_786-240del others(2): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18059942 | |||||||
| chr8:18059944 | T | C | 62 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(59): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.786-241A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18059944 | |||||||
| chr8:18059984 | C | T | 1 | a0002c0002t0002g0021 | 3 | HG01109.hp2 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.786-281G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18059984 | |||||||
| chr8:18060125 | A | G | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.786-422T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18060125 | |||||||
| chr8:18060182 | G | C | 1 | a0002c0002t0003g0269 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.786-479C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18060182 | |||||||
| chr8:18060357 | T | C | 3 | a0002c0002t0002g0008 a0002c0002t0002g0035 a0002c0002t0002g0149 |
9 | HG00741.hp2 HG01106.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.786-654A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18060357 | |||||||
| chr8:18060379 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(173): Show |
254 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.786-676G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18060379 | |||||||
| chr8:18060546 | G | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG01515.hp2 HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.785+831C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18060546 | |||||||
| chr8:18060641 | T | G | 1 | a0003c0003t0008g0030 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.785+736A>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18060641 | |||||||
| chr8:18060682 | T | C | 1 | a0001c0001t0013g0277 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.785+695A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18060682 | |||||||
| chr8:18060730 | T | C | 2 | a0002c0002t0018g0266 a0002c0002t0025g0054 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.785+647A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18060730 | |||||||
| chr8:18060801 | G | A | 1 | a0001c0001t0013g0277 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.785+576C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18060801 | |||||||
| chr8:18060826 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(109): Show |
163 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.785+551G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18060826 | |||||||
| chr8:18060889 | C | T | 3 | a0003c0003t0001g0051 a0003c0003t0001g0265 a0003c0003t0017g0268 |
4 | HG02683.hp2 HG02735.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+488G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18060889 | |||||||
| chr8:18060945 | G | T | 61 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(58): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.785+432C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18060945 | |||||||
| chr8:18060967 | G | C | 1 | a0001c0001t0007g0076 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.785+410C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18060967 | |||||||
| chr8:18061018 | G | A | 90 | a0001c0001t0003g0156 a0001c0001t0004g0009 a0001c0001t0004g0012 others(87): Show |
124 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.785+359C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18061018 | |||||||
| chr8:18061079 | AC | A | 4 | a0002c0002t0003g0048 a0002c0002t0003g0096 a0002c0002t0003g0236 others(1): Show |
5 | NA18960.hp2 NA18998.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+297delG | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18061079 | |||||||
| chr8:18061104 | G | A | 2 | a0002c0002t0002g0132 a0002c0002t0002g0140 |
2 | HG00140.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.785+273C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18061104 | |||||||
| chr8:18061138 | T | C | 9 | a0001c0001t0004g0009 a0001c0001t0004g0065 a0001c0001t0004g0068 others(6): Show |
13 | HG00438.hp2 HG01257.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.785+239A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18061138 | |||||||
| chr8:18061217 | G | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(170): Show |
250 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.785+160C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18061217 | |||||||
| chr8:18061224 | A | G | 2 | a0002c0002t0003g0097 a0002c0002t0003g0100 |
2 | NA18950.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.785+153T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18061224 | |||||||
| chr8:18061234 | T | C | 61 | a0001c0001t0003g0156 a0002c0002t0002g0237 a0002c0002t0003g0004 others(58): Show |
87 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.785+143A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18061234 | |||||||
| chr8:18061259 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(109): Show |
163 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.785+118G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 10/13 | chr8 | 18061259 | |||||||
| chr8:18061477 | A | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(77): Show |
122 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.704-19T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 9/13 | chr8 | 18061477 | |||||||
| chr8:18061489 | G | A | 3 | a0003c0003t0001g0051 a0003c0003t0001g0265 a0003c0003t0017g0268 |
4 | HG02683.hp2 HG02735.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-31C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 9/13 | chr8 | 18061489 | |||||||
| chr8:18061522 | C | T | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(68): Show |
111 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.704-64G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 9/13 | chr8 | 18061522 | |||||||
| chr8:18061748 | A | G | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | splice_region_variant&intron_variant | LOW | c.649-8T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 8/13 | chr8 | 18061748 | |||||||
| chr8:18061961 | A | C | 61 | a0001c0001t0003g0156 a0002c0002t0002g0237 a0002c0002t0003g0004 others(58): Show |
87 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.649-221T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 8/13 | chr8 | 18061961 | |||||||
| chr8:18062059 | G | A | 6 | a0003c0003t0002g0220 a0003c0003t0008g0022 a0003c0003t0008g0030 others(3): Show |
9 | HG01099.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.648+220C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 8/13 | chr8 | 18062059 | |||||||
| chr8:18062259 | T | G | 1 | a0003c0003t0005g0273 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.648+20A>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 8/13 | chr8 | 18062259 | |||||||
| chr8:18062533 | G | A | 1 | a0001c0001t0012g0258 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.504-110C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18062533 | |||||||
| chr8:18062568 | T | A | 53 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0001c0007t0023g0275 others(50): Show |
90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.504-145A>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18062568 | |||||||
| chr8:18062645 | T | C | 1 | a0001c0001t0001g0019 | 3 | HG02071.hp2 HG02080.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.504-222A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18062645 | |||||||
| chr8:18062761 | A | G | 2 | a0002c0002t0018g0266 a0002c0002t0025g0054 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.504-338T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18062761 | |||||||
| chr8:18062828 | C | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(112): Show |
166 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.503+357G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18062828 | |||||||
| chr8:18062846 | C | G | 1 | a0001c0001t0002g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.503+339G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18062846 | |||||||
| chr8:18062850 | C | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(112): Show |
166 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.503+335G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18062850 | |||||||
| chr8:18062852 | A | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(112): Show |
166 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.503+333T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18062852 | |||||||
| chr8:18062864 | T | C | 1 | a0002c0002t0003g0242 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.503+321A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18062864 | |||||||
| chr8:18062868 | CT | C | 65 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(62): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.503+316delA | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18062868 | |||||||
| chr8:18062868 | CTT | C | 38 | a0001c0001t0002g0247 a0001c0001t0004g0009 a0001c0001t0004g0012 others(35): Show |
50 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.503+315_503+316del others(2): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18062868 | |||||||
| chr8:18062868 | CTTT | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(78): Show |
124 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.503+314_503+316del others(3): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18062868 | |||||||
| chr8:18062975 | A | C | 1 | a0003c0003t0005g0272 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.503+210T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18062975 | |||||||
| chr8:18063058 | C | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(111): Show |
164 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.503+127G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18063058 | |||||||
| chr8:18063060 | G | T | 1 | a0001c0001t0014g0027 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.503+125C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18063060 | |||||||
| chr8:18063114 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(113): Show |
167 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.503+71G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18063114 | |||||||
| chr8:18063159 | T | C | 1 | a0001c0001t0002g0247 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.503+26A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 7/13 | chr8 | 18063159 | |||||||
| chr8:18063271 | A | G | 8 | a0003c0003t0001g0051 a0003c0003t0001g0265 a0003c0003t0009g0014 others(5): Show |
12 | HG02109.hp2 HG02647.hp2 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.458-41T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063271 | |||||||
| chr8:18063274 | T | C | 8 | a0003c0003t0001g0051 a0003c0003t0001g0265 a0003c0003t0009g0014 others(5): Show |
12 | HG02109.hp2 HG02647.hp2 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.458-44A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063274 | |||||||
| chr8:18063298 | A | G | 60 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(57): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.458-68T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063298 | |||||||
| chr8:18063308 | ATTAAT | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0204 a0001c0001t0001g0205 |
6 | HG00280.hp2 HG00642.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-83_458-79delAT others(3): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063308 | |||||||
| chr8:18063311 | A | T | 48 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0002c0002t0001g0013 others(45): Show |
84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.458-81T>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063311 | |||||||
| chr8:18063398 | G | A | 1 | a0003c0003t0010g0161 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.458-168C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063398 | |||||||
| chr8:18063399 | G | A | 1 | a0002c0002t0030g0250 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.458-169C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063399 | |||||||
| chr8:18063431 | G | A | 55 | a0001c0001t0001g0171 a0002c0002t0002g0237 a0002c0002t0003g0004 others(52): Show |
79 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.458-201C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063431 | |||||||
| chr8:18063467 | C | A | 1 | a0001c0001t0001g0045 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.458-237G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063467 | |||||||
| chr8:18063470 | C | CT | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(84): Show |
133 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.458-241dupA | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063470 | |||||||
| chr8:18063470 | C | CTT | 8 | a0001c0001t0001g0171 a0001c0001t0001g0187 a0001c0001t0013g0277 others(5): Show |
9 | HG02451.hp1 HG02698.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-242_458-241dup others(2): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063470 | |||||||
| chr8:18063485 | T | TTG | 29 | a0001c0001t0002g0247 a0001c0001t0004g0009 a0001c0001t0004g0012 others(26): Show |
37 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.458-256_458-255ins others(2): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063485 | |||||||
| chr8:18063566 | G | A | 30 | a0001c0001t0002g0247 a0001c0001t0004g0009 a0001c0001t0004g0012 others(27): Show |
38 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.458-336C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063566 | |||||||
| chr8:18063587 | G | A | 1 | a0002c0002t0002g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.458-357C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063587 | |||||||
| chr8:18063644 | C | A | 2 | a0002c0002t0002g0132 a0002c0002t0002g0140 |
2 | HG00140.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.458-414G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063644 | |||||||
| chr8:18063705 | T | C | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.458-475A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063705 | |||||||
| chr8:18063721 | G | A | 151 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(148): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.458-491C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063721 | |||||||
| chr8:18063874 | A | G | 1 | a0003c0003t0026g0264 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.457+583T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063874 | |||||||
| chr8:18063943 | C | A | 13 | a0001c0001t0004g0009 a0001c0001t0004g0012 a0001c0001t0004g0065 others(10): Show |
20 | HG00438.hp2 HG01257.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.457+514G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18063943 | |||||||
| chr8:18064157 | C | T | 153 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(150): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.457+300G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18064157 | |||||||
| chr8:18064164 | G | T | 153 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(150): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.457+293C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18064164 | |||||||
| chr8:18064301 | G | C | 83 | a0002c0002t0002g0237 a0002c0002t0003g0004 a0002c0002t0003g0005 others(80): Show |
117 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.457+156C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18064301 | |||||||
| chr8:18064319 | A | G | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.457+138T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18064319 | |||||||
| chr8:18064344 | A | G | 1 | a0001c0001t0007g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.457+113T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18064344 | |||||||
| chr8:18064364 | G | C | 1 | a0003c0003t0013g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.457+93C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18064364 | |||||||
| chr8:18064412 | T | C | 146 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(143): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.457+45A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 6/13 | chr8 | 18064412 | |||||||
| chr8:18064598 | G | A | 1 | a0003c0003t0013g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.383-67C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18064598 | |||||||
| chr8:18064603 | AGTTTCAG others(1): Show |
A | 4 | a0003c0003t0005g0024 a0003c0003t0005g0259 a0003c0003t0005g0260 others(1): Show |
6 | HG02258.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-80_383-73delAC others(6): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18064603 | |||||||
| chr8:18064620 | T | C | 1 | a0001c0001t0013g0277 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.383-89A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18064620 | |||||||
| chr8:18064645 | G | A | 29 | a0001c0001t0002g0247 a0001c0001t0004g0009 a0001c0001t0004g0012 others(26): Show |
37 | HG00323.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.383-114C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18064645 | |||||||
| chr8:18064652 | T | C | 4 | a0002c0002t0002g0028 a0002c0002t0002g0055 a0002c0002t0002g0254 others(1): Show |
5 | HG02559.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-121A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18064652 | |||||||
| chr8:18064664 | C | T | 2 | a0003c0003t0001g0051 a0003c0003t0001g0265 |
3 | HG02683.hp2 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.383-133G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18064664 | |||||||
| chr8:18064744 | C | T | 1 | a0003c0003t0013g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.383-213G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18064744 | |||||||
| chr8:18064778 | C | T | 2 | a0002c0002t0018g0266 a0002c0002t0025g0054 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.383-247G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18064778 | |||||||
| chr8:18064819 | G | C | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.383-288C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18064819 | |||||||
| chr8:18064887 | T | C | 153 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(150): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.383-356A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18064887 | |||||||
| chr8:18064905 | A | G | 146 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(143): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.383-374T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18064905 | |||||||
| chr8:18064943 | C | T | 2 | a0001c0001t0002g0217 a0001c0001t0002g0232 |
2 | HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.383-412G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18064943 | |||||||
| chr8:18065165 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.383-634C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065165 | |||||||
| chr8:18065179 | T | C | 1 | a0002c0002t0002g0028 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.383-648A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065179 | |||||||
| chr8:18065376 | G | T | 181 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0001c0001t0002g0247 others(178): Show |
265 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.383-845C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065376 | |||||||
| chr8:18065473 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.383-942A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065473 | |||||||
| chr8:18065509 | G | T | 1 | a0002c0002t0003g0242 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.383-978C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065509 | |||||||
| chr8:18065511 | T | C | 2 | a0001c0001t0002g0042 a0001c0001t0002g0198 |
3 | HG00639.hp1 HG01934.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.383-980A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065511 | |||||||
| chr8:18065531 | G | A | 1 | a0002c0002t0025g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.383-1000C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065531 | |||||||
| chr8:18065577 | A | C | 1 | a0002c0002t0003g0236 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.383-1046T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065577 | |||||||
| chr8:18065633 | G | A | 154 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(151): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.383-1102C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065633 | |||||||
| chr8:18065638 | T | C | 154 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(151): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.383-1107A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065638 | |||||||
| chr8:18065664 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.383-1133T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065664 | |||||||
| chr8:18065764 | A | C | 1 | a0003c0003t0001g0117 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.383-1233T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065764 | |||||||
| chr8:18065830 | C | T | 144 | a0001c0001t0002g0192 a0001c0001t0002g0197 a0002c0002t0001g0013 others(141): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.383-1299G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065830 | |||||||
| chr8:18065859 | C | T | 1 | a0002c0002t0002g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.383-1328G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065859 | |||||||
| chr8:18065882 | T | TTG | 93 | a0001c0001t0001g0045 a0001c0001t0002g0042 a0001c0001t0002g0162 others(90): Show |
131 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.382+1336_382+1337d others(4): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065882 | |||||||
| chr8:18065882 | T | TTGTG | 45 | a0001c0001t0002g0192 a0001c0001t0002g0198 a0001c0001t0004g0029 others(42): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.382+1334_382+1337d others(6): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065882 | |||||||
| chr8:18065882 | T | TTGTGTG | 15 | a0001c0001t0001g0169 a0001c0001t0001g0180 a0001c0001t0002g0163 others(12): Show |
26 | HG00323.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.382+1332_382+1337d others(8): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065882 | |||||||
| chr8:18065882 | T | TTGTGTGT others(1): Show |
7 | a0001c0001t0002g0197 a0002c0002t0001g0032 a0002c0002t0001g0133 others(4): Show |
11 | HG01167.hp2 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+1330_382+1337d others(10): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065882 | |||||||
| chr8:18065882 | TTG | T | 12 | a0001c0001t0001g0182 a0001c0001t0006g0214 a0001c0001t0006g0219 others(9): Show |
16 | HG02109.hp2 HG02647.hp2 HG02683.hp1 others(13): Show |
intron_variant | MODIFIER | c.382+1336_382+1337d others(4): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065882 | |||||||
| chr8:18065882 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0007g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.382+1328_382+1337d others(12): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065882 | |||||||
| chr8:18065910 | G | A | 8 | a0003c0003t0001g0051 a0003c0003t0001g0265 a0003c0003t0009g0014 others(5): Show |
12 | HG02109.hp2 HG02647.hp2 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.382+1310C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065910 | |||||||
| chr8:18065910 | GTA | G | 6 | a0003c0003t0002g0220 a0003c0003t0008g0022 a0003c0003t0008g0030 others(3): Show |
9 | HG01099.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.382+1308_382+1309d others(4): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065910 | |||||||
| chr8:18065912 | A | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0175 a0001c0001t0001g0179 others(140): Show |
211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.382+1308T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065912 | |||||||
| chr8:18065914 | A | G | 60 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(57): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.382+1306T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065914 | |||||||
| chr8:18065916 | A | G | 2 | a0002c0002t0002g0021 a0002c0002t0002g0138 |
4 | HG01109.hp2 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+1304T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065916 | |||||||
| chr8:18065944 | A | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0181 a0001c0001t0001g0255 |
4 | NA18747.hp2 NA18954.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+1276T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065944 | |||||||
| chr8:18065990 | C | G | 152 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(149): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.382+1230G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18065990 | |||||||
| chr8:18066048 | T | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0168 |
2 | HG01928.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.382+1172A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066048 | |||||||
| chr8:18066080 | T | C | 12 | a0001c0001t0001g0169 a0001c0001t0001g0223 a0001c0001t0006g0047 others(9): Show |
13 | HG00597.hp2 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.382+1140A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066080 | |||||||
| chr8:18066177 | A | G | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.382+1043T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066177 | |||||||
| chr8:18066245 | C | T | 1 | a0002c0002t0002g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.382+975G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066245 | |||||||
| chr8:18066283 | A | C | 1 | a0001c0001t0013g0277 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.382+937T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066283 | |||||||
| chr8:18066404 | A | C | 2 | a0003c0003t0009g0062 a0003c0003t0009g0196 |
2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.382+816T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066404 | |||||||
| chr8:18066422 | C | CA | 30 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0019 others(27): Show |
55 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.382+797dupT | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066422 | |||||||
| chr8:18066422 | CA | C | 93 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(90): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.382+797delT | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066422 | |||||||
| chr8:18066422 | CAA | C | 93 | a0001c0001t0002g0247 a0001c0001t0004g0080 a0001c0001t0007g0058 others(90): Show |
127 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.382+796_382+797del others(2): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066422 | |||||||
| chr8:18066517 | A | C | 1 | a0002c0002t0002g0137 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.382+703T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066517 | |||||||
| chr8:18066546 | CA | C | 136 | a0001c0001t0002g0042 a0001c0001t0002g0162 a0001c0001t0002g0163 others(133): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.382+673delT | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066546 | |||||||
| chr8:18066546 | CAA | C | 9 | a0002c0002t0033g0053 a0003c0003t0001g0051 a0003c0003t0001g0265 others(6): Show |
13 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.382+672_382+673del others(2): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066546 | |||||||
| chr8:18066555 | A | G | 2 | a0002c0002t0018g0266 a0002c0002t0025g0054 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.382+665T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066555 | |||||||
| chr8:18066557 | G | A | 2 | a0002c0002t0018g0266 a0002c0002t0025g0054 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.382+663C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066557 | |||||||
| chr8:18066595 | A | C | 2 | a0006c0005t0011g0208 a0006c0005t0011g0209 |
2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.382+625T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066595 | |||||||
| chr8:18066871 | C | T | 1 | a0002c0002t0003g0108 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.382+349G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066871 | |||||||
| chr8:18066899 | C | A | 8 | a0003c0003t0001g0051 a0003c0003t0001g0265 a0003c0003t0009g0014 others(5): Show |
12 | HG02109.hp2 HG02647.hp2 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.382+321G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18066899 | |||||||
| chr8:18067071 | G | A | 4 | a0003c0003t0005g0026 a0003c0003t0005g0056 a0003c0003t0005g0165 others(1): Show |
6 | HG01891.hp2 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+149C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18067071 | |||||||
| chr8:18067100 | T | TGCACCTG others(22): Show |
53 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0170 others(50): Show |
90 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.382+91_382+119dupT others(28): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18067100 | |||||||
| chr8:18067100 | T | TGCACCTG others(51): Show |
2 | a0001c0001t0002g0042 a0001c0001t0002g0198 |
3 | HG00639.hp1 HG01934.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.382+119_382+120ins others(58): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18067100 | |||||||
| chr8:18067103 | ACCTGTGC others(23): Show |
A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(113): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.382+87_382+116delG others(29): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18067103 | |||||||
| chr8:18067136 | G | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(113): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.382+84C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18067136 | |||||||
| chr8:18067161 | T | C | 12 | a0001c0001t0001g0169 a0001c0001t0001g0223 a0001c0001t0006g0047 others(9): Show |
13 | HG00597.hp2 HG02683.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.382+59A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 5/13 | chr8 | 18067161 | |||||||
| chr8:18067340 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.304-42G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067340 | |||||||
| chr8:18067357 | T | C | 1 | a0003c0003t0013g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.304-59A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067357 | |||||||
| chr8:18067479 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.304-181A>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067479 | |||||||
| chr8:18067575 | T | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0176 |
2 | HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.304-277A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067575 | |||||||
| chr8:18067605 | C | T | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.304-307G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067605 | |||||||
| chr8:18067622 | C | T | 1 | a0003c0003t0001g0124 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.304-324G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067622 | |||||||
| chr8:18067642 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.304-344G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067642 | |||||||
| chr8:18067646 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.304-348T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067646 | |||||||
| chr8:18067657 | T | C | 1 | a0001c0009t0001g0093 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.304-359A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067657 | |||||||
| chr8:18067754 | A | G | 2 | a0003c0003t0005g0063 a0003c0003t0008g0084 |
2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.304-456T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067754 | |||||||
| chr8:18067822 | A | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(114): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.304-524T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067822 | |||||||
| chr8:18067897 | C | T | 1 | a0005c0006t0003g0127 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.304-599G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067897 | |||||||
| chr8:18067901 | A | G | 1 | a0003c0003t0001g0265 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.304-603T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067901 | |||||||
| chr8:18067981 | T | C | 1 | a0003c0003t0008g0086 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.304-683A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067981 | |||||||
| chr8:18067999 | T | A | 1 | a0003c0003t0005g0272 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.304-701A>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18067999 | |||||||
| chr8:18068009 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(120): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.304-711G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068009 | |||||||
| chr8:18068031 | C | A | 2 | a0002c0002t0003g0049 a0002c0002t0028g0245 |
3 | NA18941.hp2 NA18949.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.304-733G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068031 | |||||||
| chr8:18068077 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.304-779A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068077 | |||||||
| chr8:18068227 | C | A | 2 | a0002c0002t0018g0266 a0002c0002t0025g0054 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.304-929G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068227 | |||||||
| chr8:18068236 | C | T | 8 | a0003c0003t0001g0051 a0003c0003t0001g0265 a0003c0003t0009g0014 others(5): Show |
12 | HG02109.hp2 HG02647.hp2 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.304-938G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068236 | |||||||
| chr8:18068282 | G | A | 2 | a0002c0002t0003g0107 a0002c0002t0003g0248 |
2 | NA18955.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.304-984C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068282 | |||||||
| chr8:18068477 | C | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.304-1179G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068477 | |||||||
| chr8:18068480 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.304-1182C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068480 | |||||||
| chr8:18068572 | C | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(86): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.303+1220G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068572 | |||||||
| chr8:18068651 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.303+1141C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068651 | |||||||
| chr8:18068794 | C | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG01515.hp2 HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.303+998G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068794 | |||||||
| chr8:18068812 | G | T | 1 | a0001c0001t0002g0247 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.303+980C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068812 | |||||||
| chr8:18068848 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(87): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.303+944C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068848 | |||||||
| chr8:18068864 | A | G | 2 | a0001c0001t0002g0217 a0001c0001t0002g0232 |
2 | HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.303+928T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068864 | |||||||
| chr8:18068923 | G | A | 30 | a0001c0001t0002g0247 a0001c0001t0004g0009 a0001c0001t0004g0012 others(27): Show |
38 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.303+869C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18068923 | |||||||
| chr8:18069128 | G | A | 1 | a0002c0002t0002g0135 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.303+664C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069128 | |||||||
| chr8:18069140 | CA | C | 7 | a0001c0001t0001g0187 a0001c0001t0002g0188 a0001c0007t0023g0275 others(4): Show |
7 | HG00738.hp2 HG02257.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.303+651delT | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069140 | |||||||
| chr8:18069140 | CAA | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(83): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.303+650_303+651del others(2): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069140 | |||||||
| chr8:18069140 | CAAA | C | 10 | a0001c0001t0001g0172 a0001c0001t0001g0174 a0001c0001t0001g0189 others(7): Show |
11 | HG01256.hp2 HG03225.hp1 HG03491.hp2 others(8): Show |
intron_variant | MODIFIER | c.303+649_303+651del others(3): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069140 | |||||||
| chr8:18069140 | CAAAA | C | 24 | a0001c0001t0002g0247 a0001c0001t0004g0009 a0001c0001t0004g0012 others(21): Show |
31 | HG00323.hp2 HG00438.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.303+648_303+651del others(4): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069140 | |||||||
| chr8:18069188 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.303+604C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069188 | |||||||
| chr8:18069281 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.303+511C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069281 | |||||||
| chr8:18069486 | C | A | 1 | a0002c0002t0003g0263 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.303+306G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069486 | |||||||
| chr8:18069497 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(122): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.303+295T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069497 | |||||||
| chr8:18069552 | G | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.303+240C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069552 | |||||||
| chr8:18069573 | T | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(122): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.303+219A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069573 | |||||||
| chr8:18069623 | A | G | 5 | a0003c0003t0005g0024 a0003c0003t0005g0063 a0003c0003t0005g0259 others(2): Show |
7 | HG02258.hp1 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.303+169T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069623 | |||||||
| chr8:18069675 | A | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(92): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.303+117T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069675 | |||||||
| chr8:18069704 | C | T | 3 | a0001c0001t0007g0072 a0001c0001t0007g0073 a0001c0001t0007g0074 |
3 | HG00323.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.303+88G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069704 | |||||||
| chr8:18069739 | A | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(122): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.303+53T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069739 | |||||||
| chr8:18069771 | G | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(92): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.303+21C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069771 | |||||||
| chr8:18069785 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(122): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
splice_region_variant&intron_variant | LOW | c.303+7G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 4/13 | chr8 | 18069785 | |||||||
| chr8:18069954 | T | A | 4 | a0006c0005t0001g0210 a0006c0005t0011g0046 a0006c0005t0011g0208 others(1): Show |
5 | HG02698.hp1 HG02698.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-76A>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18069954 | |||||||
| chr8:18069965 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.217-87C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18069965 | |||||||
| chr8:18069994 | T | A | 1 | a0003c0003t0010g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.217-116A>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18069994 | |||||||
| chr8:18070007 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(122): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.217-129T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070007 | |||||||
| chr8:18070043 | C | A | 1 | a0002c0002t0002g0145 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.217-165G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070043 | |||||||
| chr8:18070100 | C | T | 14 | a0001c0001t0004g0009 a0001c0001t0004g0012 a0001c0001t0004g0065 others(11): Show |
21 | HG00438.hp2 HG01257.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.217-222G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070100 | |||||||
| chr8:18070125 | T | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.217-247A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070125 | |||||||
| chr8:18070140 | C | T | 1 | a0002c0002t0003g0233 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.217-262G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070140 | |||||||
| chr8:18070155 | A | AT | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(120): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.217-278dupA | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070155 | |||||||
| chr8:18070175 | G | A | 4 | a0006c0005t0001g0210 a0006c0005t0011g0046 a0006c0005t0011g0208 others(1): Show |
5 | HG02698.hp1 HG02698.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-297C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070175 | |||||||
| chr8:18070189 | G | T | 143 | a0002c0002t0001g0013 a0002c0002t0001g0032 a0002c0002t0001g0133 others(140): Show |
218 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.217-311C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070189 | |||||||
| chr8:18070205 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.217-327T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070205 | |||||||
| chr8:18070213 | G | A | 1 | a0001c0001t0013g0277 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.217-335C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070213 | |||||||
| chr8:18070336 | G | A | 8 | a0003c0003t0001g0051 a0003c0003t0001g0265 a0003c0003t0009g0014 others(5): Show |
12 | HG02109.hp2 HG02647.hp2 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.217-458C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070336 | |||||||
| chr8:18070416 | G | A | 2 | a0002c0002t0002g0143 a0002c0002t0002g0193 |
2 | HG00280.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.217-538C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070416 | |||||||
| chr8:18070423 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.217-545G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070423 | |||||||
| chr8:18070500 | T | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(122): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.217-622A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070500 | |||||||
| chr8:18070514 | T | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(122): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.217-636A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070514 | |||||||
| chr8:18070543 | C | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(122): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.217-665G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070543 | |||||||
| chr8:18070562 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(122): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.217-684T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070562 | |||||||
| chr8:18070580 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.217-702C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070580 | |||||||
| chr8:18070585 | G | C | 1 | a0001c0001t0002g0247 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.217-707C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070585 | |||||||
| chr8:18070690 | G | C | 1 | a0001c0001t0007g0226 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.216+610C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070690 | |||||||
| chr8:18070722 | G | A | 1 | a0002c0002t0002g0145 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.216+578C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070722 | |||||||
| chr8:18070757 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0103 a0001c0001t0001g0155 others(2): Show |
7 | HG00741.hp1 HG01433.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.216+543C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070757 | |||||||
| chr8:18070762 | G | A | 1 | a0001c0001t0004g0079 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.216+538C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070762 | |||||||
| chr8:18070938 | C | A | 10 | a0002c0002t0018g0266 a0002c0002t0025g0054 a0003c0003t0001g0051 others(7): Show |
14 | HG02109.hp2 HG02647.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.216+362G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070938 | |||||||
| chr8:18070938 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.216+362G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18070938 | |||||||
| chr8:18071018 | G | C | 1 | a0003c0003t0026g0264 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.216+282C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18071018 | |||||||
| chr8:18071117 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(173): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.216+183T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18071117 | |||||||
| chr8:18071139 | G | A | 1 | a0003c0003t0005g0056 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.216+161C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18071139 | |||||||
| chr8:18071163 | T | C | 10 | a0002c0002t0018g0266 a0002c0002t0025g0054 a0003c0003t0001g0051 others(7): Show |
14 | HG02109.hp2 HG02647.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.216+137A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18071163 | |||||||
| chr8:18071180 | C | G | 10 | a0002c0002t0018g0266 a0002c0002t0025g0054 a0003c0003t0001g0051 others(7): Show |
14 | HG02109.hp2 HG02647.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.216+120G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18071180 | |||||||
| chr8:18071202 | G | A | 51 | a0002c0002t0001g0013 a0002c0002t0001g0032 a0002c0002t0001g0133 others(48): Show |
88 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.216+98C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18071202 | |||||||
| chr8:18071211 | C | CA | 59 | a0002c0002t0002g0237 a0002c0002t0003g0004 a0002c0002t0003g0005 others(56): Show |
85 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.216+88dupT | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18071211 | |||||||
| chr8:18071227 | C | A | 4 | a0003c0003t0005g0024 a0003c0003t0005g0259 a0003c0003t0005g0260 others(1): Show |
6 | HG02258.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+73G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18071227 | |||||||
| chr8:18071244 | G | GAAATA | 62 | a0002c0002t0001g0013 a0002c0002t0001g0032 a0002c0002t0001g0133 others(59): Show |
103 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.216+51_216+55dupTA others(3): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18071244 | |||||||
| chr8:18071253 | T | TATA | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(122): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.216+46_216+47insTA others(1): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 3/13 | chr8 | 18071253 | |||||||
| chr8:18071411 | T | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(122): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.126-21A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071411 | |||||||
| chr8:18071490 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.126-100C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071490 | |||||||
| chr8:18071567 | C | G | 3 | a0003c0003t0001g0051 a0003c0003t0001g0265 a0003c0003t0017g0268 |
4 | HG02683.hp2 HG02735.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-177G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071567 | |||||||
| chr8:18071599 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.126-209A>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071599 | |||||||
| chr8:18071605 | G | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(83): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.126-215C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071605 | |||||||
| chr8:18071647 | A | T | 1 | a0003c0003t0005g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.126-257T>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071647 | |||||||
| chr8:18071688 | A | T | 3 | a0002c0002t0003g0031 a0002c0002t0003g0094 a0002c0002t0003g0095 |
4 | HG01358.hp1 HG01943.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.126-298T>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071688 | |||||||
| chr8:18071689 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0166 a0001c0001t0001g0168 |
7 | HG01928.hp1 HG01981.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.126-299G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071689 | |||||||
| chr8:18071699 | C | G | 1 | a0002c0002t0003g0157 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.126-309G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071699 | |||||||
| chr8:18071704 | A | AT | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(107): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.126-315dupA | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071704 | |||||||
| chr8:18071727 | T | C | 7 | a0001c0001t0001g0223 a0001c0001t0006g0047 a0001c0001t0006g0151 others(4): Show |
8 | HG00597.hp2 NA18939.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.126-337A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071727 | |||||||
| chr8:18071767 | G | A | 3 | a0003c0003t0001g0051 a0003c0003t0001g0265 a0003c0003t0017g0268 |
4 | HG02683.hp2 HG02735.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-377C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071767 | |||||||
| chr8:18071895 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.126-505G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071895 | |||||||
| chr8:18071966 | C | T | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(181): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.126-576G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18071966 | |||||||
| chr8:18072013 | T | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(85): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.126-623A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072013 | |||||||
| chr8:18072076 | G | A | 4 | a0006c0005t0001g0210 a0006c0005t0011g0046 a0006c0005t0011g0208 others(1): Show |
5 | HG02698.hp1 HG02698.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-686C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072076 | |||||||
| chr8:18072189 | G | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(120): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.126-799C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072189 | |||||||
| chr8:18072248 | C | A | 1 | a0002c0002t0003g0109 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.126-858G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072248 | |||||||
| chr8:18072393 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.126-1003T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072393 | |||||||
| chr8:18072505 | C | CAGAAA | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.126-1120_126-1116d others(7): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072505 | |||||||
| chr8:18072520 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.126-1130C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072520 | |||||||
| chr8:18072559 | G | A | 1 | a0003c0003t0005g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.126-1169C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072559 | |||||||
| chr8:18072639 | T | C | 1 | a0002c0002t0002g0118 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.126-1249A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072639 | |||||||
| chr8:18072653 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(120): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.126-1263T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072653 | |||||||
| chr8:18072704 | T | G | 1 | a0003c0003t0008g0030 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.126-1314A>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072704 | |||||||
| chr8:18072835 | C | T | 4 | a0003c0003t0005g0024 a0003c0003t0005g0259 a0003c0003t0005g0260 others(1): Show |
6 | HG02258.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.126-1445G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072835 | |||||||
| chr8:18072845 | A | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(122): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.126-1455T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072845 | |||||||
| chr8:18072878 | T | C | 30 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(27): Show |
38 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.126-1488A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072878 | |||||||
| chr8:18072926 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.126-1536G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072926 | |||||||
| chr8:18072990 | C | T | 30 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(27): Show |
38 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.126-1600G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072990 | |||||||
| chr8:18072992 | C | T | 1 | a0002c0002t0003g0104 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.126-1602G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18072992 | |||||||
| chr8:18073040 | T | G | 1 | a0001c0001t0001g0044 | 2 | HG00639.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.126-1650A>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073040 | |||||||
| chr8:18073096 | A | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(123): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.126-1706T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073096 | |||||||
| chr8:18073218 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.126-1828C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073218 | |||||||
| chr8:18073219 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.126-1829G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073219 | |||||||
| chr8:18073225 | C | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(120): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.126-1835G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073225 | |||||||
| chr8:18073263 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(120): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.126-1873G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073263 | |||||||
| chr8:18073467 | T | C | 1 | a0002c0002t0002g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.125+2074A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073467 | |||||||
| chr8:18073490 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(121): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.125+2051T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073490 | |||||||
| chr8:18073582 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(120): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.125+1959G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073582 | |||||||
| chr8:18073608 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(91): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.125+1933G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073608 | |||||||
| chr8:18073702 | G | A | 3 | a0002c0002t0003g0230 a0002c0002t0003g0246 a0002c0002t0003g0251 |
3 | NA18979.hp1 NA19063.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.125+1839C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073702 | |||||||
| chr8:18073807 | A | G | 1 | a0002c0002t0002g0148 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.125+1734T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073807 | |||||||
| chr8:18073931 | T | C | 30 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(27): Show |
38 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.125+1610A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073931 | |||||||
| chr8:18073937 | C | T | 1 | a0003c0003t0010g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.125+1604G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073937 | |||||||
| chr8:18073965 | T | A | 4 | a0002c0002t0002g0028 a0002c0002t0002g0055 a0002c0002t0002g0254 others(1): Show |
5 | HG02559.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.125+1576A>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18073965 | |||||||
| chr8:18074027 | A | AG | 36 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(33): Show |
45 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.125+1513dupC | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074027 | |||||||
| chr8:18074055 | G | C | 1 | a0002c0002t0004g0110 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.125+1486C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074055 | |||||||
| chr8:18074094 | T | G | 37 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(34): Show |
46 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.125+1447A>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074094 | |||||||
| chr8:18074195 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(133): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.125+1346G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074195 | |||||||
| chr8:18074196 | A | T | 36 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(33): Show |
45 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.125+1345T>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074196 | |||||||
| chr8:18074225 | C | G | 1 | a0001c0001t0002g0162 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.125+1316G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074225 | |||||||
| chr8:18074252 | G | A | 36 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(33): Show |
45 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.125+1289C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074252 | |||||||
| chr8:18074273 | C | G | 10 | a0002c0002t0018g0266 a0002c0002t0025g0054 a0003c0003t0001g0051 others(7): Show |
14 | HG02109.hp2 HG02647.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.125+1268G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074273 | |||||||
| chr8:18074296 | A | AAC | 36 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(33): Show |
45 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.125+1243_125+1244d others(4): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074296 | |||||||
| chr8:18074379 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.125+1162C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074379 | |||||||
| chr8:18074391 | AACTT | A | 36 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(33): Show |
45 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.125+1146_125+1149d others(6): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074391 | |||||||
| chr8:18074397 | G | T | 36 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(33): Show |
45 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.125+1144C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074397 | |||||||
| chr8:18074401 | A | G | 30 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(27): Show |
38 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.125+1140T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074401 | |||||||
| chr8:18074468 | C | A | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.125+1073G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074468 | |||||||
| chr8:18074491 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.125+1050G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074491 | |||||||
| chr8:18074497 | G | A | 36 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(33): Show |
45 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.125+1044C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074497 | |||||||
| chr8:18074528 | T | C | 36 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(33): Show |
45 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.125+1013A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074528 | |||||||
| chr8:18074879 | G | A | 5 | a0002c0002t0001g0013 a0002c0002t0001g0032 a0002c0002t0001g0133 others(2): Show |
9 | HG02080.hp2 NA18941.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.125+662C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074879 | |||||||
| chr8:18074907 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.125+634T>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074907 | |||||||
| chr8:18074967 | G | C | 1 | a0001c0001t0001g0194 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.125+574C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074967 | |||||||
| chr8:18074983 | G | A | 1 | a0001c0001t0014g0027 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.125+558C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074983 | |||||||
| chr8:18074986 | G | C | 1 | a0001c0001t0001g0194 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.125+555C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18074986 | |||||||
| chr8:18075001 | C | CTTTTTTT others(7): Show |
26 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(23): Show |
34 | HG00323.hp2 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.125+539_125+540ins others(14): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075001 | |||||||
| chr8:18075001 | C | CTTTTTTT others(8): Show |
4 | a0001c0001t0004g0065 a0001c0001t0004g0066 a0001c0001t0004g0067 others(1): Show |
4 | HG00438.hp2 NA18949.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+539_125+540ins others(15): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075001 | |||||||
| chr8:18075001 | C | CTTTTTTT others(11): Show |
3 | a0006c0005t0001g0210 a0006c0005t0011g0046 a0006c0005t0011g0209 |
4 | HG02698.hp1 HG02698.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+539_125+540ins others(18): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075001 | |||||||
| chr8:18075001 | C | CTTTTTTT others(12): Show |
1 | a0006c0005t0011g0208 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.125+539_125+540ins others(19): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075001 | |||||||
| chr8:18075002 | C | T | 34 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(31): Show |
43 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.125+539G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075002 | |||||||
| chr8:18075020 | G | T | 34 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(31): Show |
43 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.125+521C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075020 | |||||||
| chr8:18075035 | G | A | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.125+506C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075035 | |||||||
| chr8:18075041 | A | G | 36 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(33): Show |
45 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.125+500T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075041 | |||||||
| chr8:18075055 | G | A | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.125+486C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075055 | |||||||
| chr8:18075056 | T | C | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.125+485A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075056 | |||||||
| chr8:18075088 | C | T | 5 | a0001c0007t0023g0275 a0006c0005t0001g0210 a0006c0005t0011g0046 others(2): Show |
6 | HG02257.hp2 HG02698.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+453G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075088 | |||||||
| chr8:18075089 | G | A | 31 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(28): Show |
41 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.125+452C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075089 | |||||||
| chr8:18075097 | G | T | 30 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(27): Show |
38 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.125+444C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075097 | |||||||
| chr8:18075098 | C | T | 1 | a0003c0003t0005g0165 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.125+443G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075098 | |||||||
| chr8:18075120 | A | C | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.125+421T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075120 | |||||||
| chr8:18075121 | G | C | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.125+420C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075121 | |||||||
| chr8:18075140 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.125+401G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075140 | |||||||
| chr8:18075206 | C | G | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.125+335G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075206 | |||||||
| chr8:18075215 | G | T | 34 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(31): Show |
43 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.125+326C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075215 | |||||||
| chr8:18075228 | T | C | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.125+313A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075228 | |||||||
| chr8:18075269 | A | C | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.125+272T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075269 | |||||||
| chr8:18075313 | T | C | 5 | a0002c0002t0002g0037 a0002c0002t0002g0098 a0002c0002t0002g0099 others(2): Show |
6 | HG02056.hp2 HG02523.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.125+228A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075313 | |||||||
| chr8:18075344 | A | G | 1 | a0002c0002t0002g0136 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.125+197T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 2/13 | chr8 | 18075344 | |||||||
| chr8:18075590 | G | A | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
splice_region_variant&intron_variant | LOW | c.79-3C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18075590 | |||||||
| chr8:18075627 | T | C | 2 | a0002c0002t0003g0102 a0002c0002t0003g0111 |
2 | NA18962.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.79-40A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18075627 | |||||||
| chr8:18075637 | C | T | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.79-50G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18075637 | |||||||
| chr8:18075736 | T | C | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.79-149A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18075736 | |||||||
| chr8:18075949 | C | T | 118 | a0001c0001t0001g0071 a0001c0001t0001g0150 a0001c0001t0001g0223 others(115): Show |
173 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.79-362G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18075949 | |||||||
| chr8:18075961 | G | A | 34 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(31): Show |
43 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.79-374C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18075961 | |||||||
| chr8:18076248 | C | G | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.79-661G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076248 | |||||||
| chr8:18076257 | G | A | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.79-670C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076257 | |||||||
| chr8:18076265 | T | C | 13 | a0003c0003t0002g0220 a0003c0003t0005g0063 a0003c0003t0008g0022 others(10): Show |
19 | HG01099.hp1 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.79-678A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076265 | |||||||
| chr8:18076356 | C | T | 27 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(24): Show |
35 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.79-769G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076356 | |||||||
| chr8:18076411 | T | G | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.79-824A>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076411 | |||||||
| chr8:18076452 | G | C | 1 | a0001c0001t0002g0247 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.79-865C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076452 | |||||||
| chr8:18076453 | T | C | 3 | a0002c0002t0002g0038 a0002c0002t0002g0153 a0002c0002t0002g0154 |
4 | HG00323.hp1 HG01192.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-866A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076453 | |||||||
| chr8:18076520 | T | C | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.79-933A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076520 | |||||||
| chr8:18076540 | C | G | 1 | a0003c0003t0008g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.79-953G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076540 | |||||||
| chr8:18076552 | C | CT | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.79-966dupA | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076552 | |||||||
| chr8:18076655 | C | G | 1 | a0002c0002t0003g0102 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.79-1068G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076655 | |||||||
| chr8:18076668 | C | T | 1 | a0005c0006t0003g0231 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.79-1081G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076668 | |||||||
| chr8:18076670 | T | G | 35 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
44 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.79-1083A>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076670 | |||||||
| chr8:18076678 | G | T | 1 | a0003c0003t0005g0273 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.79-1091C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076678 | |||||||
| chr8:18076699 | T | G | 1 | a0003c0003t0013g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79-1112A>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076699 | |||||||
| chr8:18076746 | C | T | 2 | a0002c0002t0002g0134 a0002c0002t0002g0135 |
2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.79-1159G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076746 | |||||||
| chr8:18076813 | C | T | 32 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(29): Show |
41 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.79-1226G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076813 | |||||||
| chr8:18076878 | C | T | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.79-1291G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076878 | |||||||
| chr8:18076907 | T | C | 1 | a0002c0002t0002g0281 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.79-1320A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076907 | |||||||
| chr8:18076950 | G | A | 1 | a0001c0001t0006g0221 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.79-1363C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076950 | |||||||
| chr8:18076951 | T | C | 1 | a0002c0002t0002g0028 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.79-1364A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18076951 | |||||||
| chr8:18077133 | GGATATCC others(13): Show |
G | 1 | a0002c0002t0002g0038 | 2 | HG00323.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.79-1566_79-1547del others(20): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18077133 | |||||||
| chr8:18077344 | C | T | 4 | a0006c0005t0001g0210 a0006c0005t0011g0046 a0006c0005t0011g0208 others(1): Show |
5 | HG02698.hp1 HG02698.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-1757G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18077344 | |||||||
| chr8:18077520 | A | T | 107 | a0001c0001t0001g0150 a0001c0001t0001g0223 a0001c0001t0001g0253 others(104): Show |
161 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.79-1933T>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18077520 | |||||||
| chr8:18077570 | G | A | 3 | a0001c0001t0004g0029 a0001c0001t0004g0080 a0001c0001t0022g0081 |
4 | HG03225.hp1 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-1983C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18077570 | |||||||
| chr8:18077595 | C | A | 107 | a0001c0001t0001g0150 a0001c0001t0001g0223 a0001c0001t0001g0253 others(104): Show |
161 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.79-2008G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18077595 | |||||||
| chr8:18077654 | A | G | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.79-2067T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18077654 | |||||||
| chr8:18077890 | T | A | 1 | a0002c0002t0002g0146 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.79-2303A>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18077890 | |||||||
| chr8:18077916 | A | T | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01081.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.79-2329T>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18077916 | |||||||
| chr8:18077983 | T | C | 109 | a0001c0001t0001g0150 a0001c0001t0001g0223 a0001c0001t0001g0253 others(106): Show |
163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.79-2396A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18077983 | |||||||
| chr8:18078060 | A | G | 1 | a0002c0002t0003g0269 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.79-2473T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078060 | |||||||
| chr8:18078061 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.79-2474A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078061 | |||||||
| chr8:18078088 | A | C | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.79-2501T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078088 | |||||||
| chr8:18078133 | A | C | 107 | a0001c0001t0001g0150 a0001c0001t0001g0223 a0001c0001t0001g0253 others(104): Show |
161 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.79-2546T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078133 | |||||||
| chr8:18078158 | C | T | 107 | a0001c0001t0001g0150 a0001c0001t0001g0223 a0001c0001t0001g0253 others(104): Show |
161 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.79-2571G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078158 | |||||||
| chr8:18078159 | G | T | 6 | a0003c0003t0005g0272 a0003c0003t0010g0052 a0003c0003t0010g0161 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-2572C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078159 | |||||||
| chr8:18078168 | C | G | 106 | a0001c0001t0001g0150 a0001c0001t0001g0223 a0001c0001t0001g0253 others(103): Show |
160 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.79-2581G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078168 | |||||||
| chr8:18078194 | G | A | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.79-2607C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078194 | |||||||
| chr8:18078199 | C | G | 1 | a0001c0001t0007g0064 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.79-2612G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078199 | |||||||
| chr8:18078373 | T | C | 5 | a0002c0002t0001g0013 a0002c0002t0001g0032 a0002c0002t0001g0133 others(2): Show |
9 | HG02080.hp2 NA18941.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-2786A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078373 | |||||||
| chr8:18078442 | G | A | 138 | a0001c0001t0001g0071 a0001c0001t0001g0150 a0001c0001t0001g0223 others(135): Show |
201 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.79-2855C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078442 | |||||||
| chr8:18078455 | T | C | 2 | a0004c0004t0003g0007 a0004c0004t0003g0112 |
7 | NA18944.hp1 NA18948.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.79-2868A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078455 | |||||||
| chr8:18078520 | G | A | 106 | a0001c0001t0001g0150 a0001c0001t0001g0223 a0001c0001t0001g0253 others(103): Show |
160 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.79-2933C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078520 | |||||||
| chr8:18078576 | C | G | 5 | a0002c0002t0001g0013 a0002c0002t0001g0032 a0002c0002t0001g0133 others(2): Show |
9 | HG02080.hp2 NA18941.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-2989G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078576 | |||||||
| chr8:18078682 | C | A | 1 | a0002c0002t0002g0130 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.79-3095G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078682 | |||||||
| chr8:18078711 | A | C | 41 | a0001c0001t0001g0101 a0001c0001t0001g0253 a0001c0001t0002g0232 others(38): Show |
54 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.79-3124T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078711 | |||||||
| chr8:18078892 | CTCTCCCT others(15): Show |
C | 7 | a0002c0002t0003g0025 a0002c0002t0003g0262 a0002c0002t0003g0263 others(4): Show |
11 | HG02258.hp1 HG02559.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-3327_79-3306del others(22): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078892 | |||||||
| chr8:18078956 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.79-3369C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078956 | |||||||
| chr8:18078978 | G | T | 3 | a0003c0003t0001g0033 a0003c0003t0001g0119 a0003c0003t0001g0120 |
4 | HG01099.hp2 HG01192.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-3391C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18078978 | |||||||
| chr8:18079095 | G | T | 1 | a0002c0002t0002g0281 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.79-3508C>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079095 | |||||||
| chr8:18079134 | TG | T | 108 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0223 others(105): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.79-3548delC | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079134 | |||||||
| chr8:18079165 | C | T | 3 | a0001c0001t0001g0280 a0001c0001t0006g0214 a0001c0008t0006g0215 |
3 | HG02683.hp1 HG02735.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.79-3578G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079165 | |||||||
| chr8:18079198 | G | A | 108 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0223 others(105): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.79-3611C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079198 | |||||||
| chr8:18079221 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.79-3634G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079221 | |||||||
| chr8:18079274 | G | GA | 104 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0199 others(101): Show |
157 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.79-3688dupT | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079274 | |||||||
| chr8:18079274 | G | GAA | 11 | a0001c0001t0006g0222 a0002c0002t0001g0147 a0002c0002t0002g0099 others(8): Show |
11 | HG00423.hp2 HG01175.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.79-3689_79-3688dup others(2): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079274 | |||||||
| chr8:18079284 | A | C | 2 | a0001c0001t0015g0159 a0003c0003t0001g0160 |
2 | HG00558.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.79-3697T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079284 | |||||||
| chr8:18079289 | C | A | 108 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0223 others(105): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.79-3702G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079289 | |||||||
| chr8:18079449 | C | A | 107 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0223 others(104): Show |
161 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.79-3862G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079449 | |||||||
| chr8:18079468 | C | CATT | 108 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0223 others(105): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.79-3884_79-3882dup others(3): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079468 | |||||||
| chr8:18079470 | T | A | 8 | a0002c0002t0003g0025 a0002c0002t0003g0262 a0002c0002t0003g0263 others(5): Show |
12 | HG02258.hp1 HG02559.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.79-3883A>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079470 | |||||||
| chr8:18079488 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.79-3901G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079488 | |||||||
| chr8:18079589 | G | A | 108 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0223 others(105): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.79-4002C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079589 | |||||||
| chr8:18079631 | T | C | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.79-4044A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079631 | |||||||
| chr8:18079658 | G | A | 108 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0223 others(105): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.79-4071C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079658 | |||||||
| chr8:18079660 | A | G | 1 | a0002c0002t0003g0230 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.79-4073T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079660 | |||||||
| chr8:18079683 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.79-4096A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079683 | |||||||
| chr8:18079723 | C | A | 106 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0223 others(103): Show |
160 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.79-4136G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079723 | |||||||
| chr8:18079804 | G | A | 107 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0223 others(104): Show |
160 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.78+4177C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079804 | |||||||
| chr8:18079855 | C | T | 108 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0223 others(105): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.78+4126G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18079855 | |||||||
| chr8:18080021 | G | A | 65 | a0001c0001t0001g0150 a0001c0001t0001g0223 a0001c0001t0002g0213 others(62): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.78+3960C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080021 | |||||||
| chr8:18080061 | G | C | 2 | a0001c0001t0001g0223 a0001c0001t0006g0224 |
2 | HG00597.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.78+3920C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080061 | |||||||
| chr8:18080085 | C | T | 105 | a0001c0001t0001g0150 a0001c0001t0001g0223 a0001c0001t0001g0253 others(102): Show |
159 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.78+3896G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080085 | |||||||
| chr8:18080133 | G | C | 1 | a0001c0001t0001g0045 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.78+3848C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080133 | |||||||
| chr8:18080145 | T | A | 1 | a0001c0001t0013g0277 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.78+3836A>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080145 | |||||||
| chr8:18080167 | C | G | 1 | a0003c0003t0001g0276 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.78+3814G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080167 | |||||||
| chr8:18080168 | G | A | 2 | a0003c0003t0001g0276 a0003c0003t0008g0087 |
2 | HG02280.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.78+3813C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080168 | |||||||
| chr8:18080199 | C | G | 27 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(24): Show |
35 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.78+3782G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080199 | |||||||
| chr8:18080214 | T | C | 108 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0223 others(105): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.78+3767A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080214 | |||||||
| chr8:18080222 | C | T | 1 | a0001c0001t0003g0156 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.78+3759G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080222 | |||||||
| chr8:18080233 | A | C | 109 | a0001c0001t0001g0101 a0001c0001t0001g0150 a0001c0001t0001g0223 others(106): Show |
163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.78+3748T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080233 | |||||||
| chr8:18080237 | T | C | 2 | a0001c0001t0013g0277 a0001c0001t0014g0027 |
3 | HG02895.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.78+3744A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080237 | |||||||
| chr8:18080300 | A | G | 7 | a0002c0002t0003g0025 a0002c0002t0003g0262 a0002c0002t0003g0263 others(4): Show |
11 | HG02258.hp1 HG02559.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.78+3681T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080300 | |||||||
| chr8:18080309 | C | G | 27 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(24): Show |
35 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.78+3672G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080309 | |||||||
| chr8:18080417 | C | T | 1 | a0003c0003t0005g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.78+3564G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080417 | |||||||
| chr8:18080458 | T | C | 1 | a0002c0002t0002g0039 | 2 | HG01361.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.78+3523A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080458 | |||||||
| chr8:18080509 | A | C | 107 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0211 others(104): Show |
160 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.78+3472T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080509 | |||||||
| chr8:18080571 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.78+3410A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080571 | |||||||
| chr8:18080590 | G | A | 3 | a0002c0002t0003g0269 a0002c0002t0003g0270 a0002c0002t0003g0271 |
3 | HG02145.hp2 HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.78+3391C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080590 | |||||||
| chr8:18080649 | C | T | 1 | a0002c0002t0002g0028 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.78+3332G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080649 | |||||||
| chr8:18080711 | C | T | 4 | a0002c0002t0002g0034 a0002c0002t0002g0128 a0002c0002t0002g0129 others(1): Show |
5 | HG02129.hp2 HG02135.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+3270G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080711 | |||||||
| chr8:18080748 | G | C | 1 | a0003c0003t0010g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.78+3233C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080748 | |||||||
| chr8:18080880 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0031g0115 |
5 | HG02165.hp1 HG04184.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+3101A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080880 | |||||||
| chr8:18080999 | A | G | 7 | a0002c0002t0003g0025 a0002c0002t0003g0262 a0002c0002t0003g0263 others(4): Show |
11 | HG02258.hp1 HG02559.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.78+2982T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18080999 | |||||||
| chr8:18081065 | C | T | 108 | a0001c0001t0001g0223 a0001c0001t0001g0252 a0001c0001t0001g0253 others(105): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.78+2916G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18081065 | |||||||
| chr8:18081108 | G | C | 1 | a0003c0003t0005g0272 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.78+2873C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18081108 | |||||||
| chr8:18081133 | T | C | 1 | a0001c0001t0004g0088 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.78+2848A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18081133 | |||||||
| chr8:18081194 | A | G | 2 | a0001c0001t0013g0277 a0001c0001t0014g0027 |
3 | HG02895.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.78+2787T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18081194 | |||||||
| chr8:18081372 | A | C | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.78+2609T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18081372 | |||||||
| chr8:18081443 | T | C | 1 | a0002c0002t0003g0116 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.78+2538A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18081443 | |||||||
| chr8:18081634 | G | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(264): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.78+2347C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18081634 | |||||||
| chr8:18081685 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0204 a0001c0001t0001g0205 |
6 | HG00280.hp2 HG00642.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+2296C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18081685 | |||||||
| chr8:18081868 | G | C | 1 | a0003c0003t0005g0026 | 3 | HG01891.hp2 HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.78+2113C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18081868 | |||||||
| chr8:18081884 | A | T | 5 | a0002c0002t0003g0207 a0006c0005t0001g0210 a0006c0005t0011g0046 others(2): Show |
6 | HG02698.hp1 HG02698.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+2097T>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18081884 | |||||||
| chr8:18081889 | A | G | 1 | a0002c0002t0002g0118 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.78+2092T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18081889 | |||||||
| chr8:18081937 | A | T | 1 | a0003c0003t0001g0117 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.78+2044T>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18081937 | |||||||
| chr8:18082007 | C | T | 5 | a0002c0002t0003g0207 a0006c0005t0001g0210 a0006c0005t0011g0046 others(2): Show |
6 | HG02698.hp1 HG02698.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+1974G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082007 | |||||||
| chr8:18082033 | T | G | 1 | a0003c0003t0001g0276 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.78+1948A>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082033 | |||||||
| chr8:18082047 | A | C | 1 | a0002c0002t0003g0229 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.78+1934T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082047 | |||||||
| chr8:18082102 | T | A | 1 | a0002c0002t0002g0206 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.78+1879A>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082102 | |||||||
| chr8:18082128 | A | C | 85 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0211 others(82): Show |
117 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.78+1853T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082128 | |||||||
| chr8:18082166 | A | C | 1 | a0002c0002t0002g0092 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.78+1815T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082166 | |||||||
| chr8:18082203 | T | G | 1 | a0002c0002t0002g0028 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.78+1778A>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082203 | |||||||
| chr8:18082268 | T | C | 1 | a0003c0003t0005g0273 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.78+1713A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082268 | |||||||
| chr8:18082499 | C | G | 33 | a0001c0001t0001g0223 a0001c0001t0001g0227 a0001c0001t0001g0228 others(30): Show |
43 | HG00597.hp2 HG01099.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.78+1482G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082499 | |||||||
| chr8:18082616 | A | G | 1 | a0001c0001t0007g0058 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.78+1365T>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082616 | |||||||
| chr8:18082684 | A | C | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.78+1297T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082684 | |||||||
| chr8:18082703 | T | C | 28 | a0001c0001t0001g0211 a0001c0001t0001g0223 a0001c0001t0001g0227 others(25): Show |
36 | HG00597.hp2 HG01099.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.78+1278A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082703 | |||||||
| chr8:18082719 | C | A | 1 | a0003c0003t0001g0276 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.78+1262G>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082719 | |||||||
| chr8:18082741 | C | T | 1 | a0001c0001t0021g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.78+1240G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082741 | |||||||
| chr8:18082903 | AATTTT | A | 20 | a0001c0001t0001g0223 a0001c0001t0001g0227 a0001c0001t0001g0228 others(17): Show |
25 | HG00597.hp2 HG01099.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.78+1073_78+1077del others(5): Show |
ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18082903 | |||||||
| chr8:18083001 | T | A | 94 | a0001c0001t0001g0071 a0001c0001t0001g0252 a0001c0001t0001g0253 others(91): Show |
122 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.78+980A>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083001 | |||||||
| chr8:18083230 | A | C | 1 | a0002c0002t0002g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.78+751T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083230 | |||||||
| chr8:18083240 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.78+741C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083240 | |||||||
| chr8:18083363 | G | A | 1 | a0003c0003t0005g0026 | 3 | HG01891.hp2 HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.78+618C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083363 | |||||||
| chr8:18083515 | G | C | 1 | a0001c0007t0023g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.78+466C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083515 | |||||||
| chr8:18083605 | A | C | 1 | a0002c0002t0003g0090 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.78+376T>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083605 | |||||||
| chr8:18083626 | T | A | 1 | a0003c0003t0001g0276 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.78+355A>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083626 | |||||||
| chr8:18083636 | T | C | 1 | a0001c0001t0004g0089 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.78+345A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083636 | |||||||
| chr8:18083680 | G | C | 6 | a0001c0001t0013g0277 a0001c0001t0014g0027 a0002c0002t0002g0028 others(3): Show |
8 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.78+301C>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083680 | |||||||
| chr8:18083728 | C | G | 38 | a0001c0001t0001g0071 a0001c0001t0004g0009 a0001c0001t0004g0012 others(35): Show |
47 | HG00323.hp2 HG00438.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.78+253G>C | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083728 | |||||||
| chr8:18083804 | G | A | 3 | a0003c0003t0010g0052 a0003c0003t0010g0279 a0003c0003t0024g0278 |
4 | HG01891.hp1 HG02109.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+177C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083804 | |||||||
| chr8:18083879 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.78+102C>T | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083879 | |||||||
| chr8:18083887 | T | C | 1 | a0002c0002t0002g0281 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.78+94A>G | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083887 | |||||||
| chr8:18083906 | C | T | 5 | a0001c0001t0014g0027 a0002c0002t0002g0028 a0002c0002t0002g0055 others(2): Show |
7 | HG02559.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+75G>A | ASAH1 | ENSG00000104763.20 | transcript | ENST00000637790.2 | protein_coding | 1/13 | chr8 | 18083906 |