Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23176 |
| ensemblid | ENSG00000164402.14 |
| hgncid | 16511 |
| symbol | SEPTIN8 |
| name | septin 8 |
| refseq_nuc | NM_001098811.2 |
| refseq_prot | NP_001092281.1 |
| ensembl_nuc | ENST00000378719.7 |
| ensembl_prot | ENSP00000367991.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 132750819 |
| end | 132777239 |
| strand | - |
| ver | v1.2 |
| region | chr5:132750819-132777239 |
| region5000 | chr5:132745819-132782239 |
| regionname0 | SEPTIN8_chr5_132750819_132777239 |
| regionname5000 | SEPTIN8_chr5_132745819_132782239 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 483 | 318 | 89 | 53 | 144 | 4 | 26 | 108 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | MAATD others(478): Show |
chr5 | 132745819 | 132782239 |
| a0002 | 0/0 | 483 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | MAATD others(478): Show |
chr5 | 132745819 | 132782239 |
| a0003 | 0/0 | 483 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | MAATD others(478): Show |
chr5 | 132745819 | 132782239 |
| a0004 | 0/0 | 483 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | MAATD others(478): Show |
chr5 | 132745819 | 132782239 |
| a0005 | 0/0 | 483 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | MAATD others(478): Show |
chr5 | 132745819 | 132782239 |
| a0006 | 0/0 | 483 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | MAATD others(478): Show |
chr5 | 132745819 | 132782239 |
| a0007 | 0/0 | 483 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | MAATD others(478): Show |
chr5 | 132745819 | 132782239 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1449 | 214 | 79 | 22 | 106 | 0 | 7 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATGGC others(1444): Show |
chr5 | 132745819 | 132782239 | ||
| a0001c0002 | 1/1 | 1449 | 97 | 5 | 30 | 37 | 4 | 19 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATGGC others(1444): Show |
chr5 | 132745819 | 132782239 | ||
| a0001c0003 | 0/0 | 1449 | 5 | 4 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATGGC others(1444): Show |
chr5 | 132745819 | 132782239 | ||
| a0001c0007 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATGGC others(1444): Show |
chr5 | 132745819 | 132782239 | ||
| a0001c0010 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATGGC others(1444): Show |
chr5 | 132745819 | 132782239 | ||
| a0002c0004 | 0/0 | 1449 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATGGC others(1444): Show |
chr5 | 132745819 | 132782239 | ||
| a0003c0005 | 0/0 | 1449 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATGGC others(1444): Show |
chr5 | 132745819 | 132782239 | ||
| a0004c0008 | 0/0 | 1449 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATGGC others(1444): Show |
chr5 | 132745819 | 132782239 | ||
| a0005c0011 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATGGC others(1444): Show |
chr5 | 132745819 | 132782239 | ||
| a0006c0009 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATGGC others(1444): Show |
chr5 | 132745819 | 132782239 | ||
| a0007c0006 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATGGC others(1444): Show |
chr5 | 132745819 | 132782239 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2751 | 169 | 57 | 20 | 86 | 0 | 6 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0001c0001t0002 | 0/0 | 2751 | 12 | 5 | 1 | 6 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0001c0001t0003 | 0/0 | 2745 | 7 | 7 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2740): Show |
chr5 | 132745819 | 132782239 |
| a0001c0001t0004 | 0/0 | 2751 | 10 | 9 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0001c0001t0005 | 0/0 | 2751 | 9 | 0 | 0 | 9 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0001c0001t0006 | 0/0 | 2751 | 6 | 0 | 0 | 5 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0001c0001t0008 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0001c0002t0002 | 1/1 | 2751 | 94 | 5 | 28 | 36 | 4 | 19 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0001c0002t0007 | 0/0 | 2751 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0001c0002t0009 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0001c0003t0003 | 0/0 | 2745 | 5 | 4 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2740): Show |
chr5 | 132745819 | 132782239 |
| a0001c0007t0001 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0001c0010t0004 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0002c0004t0001 | 0/0 | 2751 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0003c0005t0002 | 0/0 | 2751 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0004c0008t0001 | 0/0 | 2751 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0005c0011t0002 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0006c0009t0002 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| a0007c0006t0001 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | ATTCA others(2746): Show |
chr5 | 132745819 | 132782239 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0009 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0004g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0005g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0001t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0001 | 0/0 | 13 | 2 | 6 | 1 | 1 | 3 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0003 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0011 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0012 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0013 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0020 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0022 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0218 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0007g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0002t0009g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0003t0003g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0003t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0007t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0001c0010t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0002c0004t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0003c0005t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0004c0008t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0005c0011t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0006c0009t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| a0007c0006t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0050 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0047 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0178 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00642 | hp1 | a0001 | c0003 | t0003 | g0151 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0214 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0179 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0181 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01167 | hp2 | a0002 | c0004 | t0001 | g0030 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0199 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01168 | hp2 | a0001 | c0002 | t0007 | g0044 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01169 | hp1 | a0002 | c0004 | t0001 | g0030 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01169 | hp2 | a0001 | c0002 | t0007 | g0044 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0194 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0203 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01346 | hp1 | a0004 | c0008 | t0001 | g0171 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0180 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0170 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0217 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0022 | EUR | IBS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0200 | EUR | IBS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0182 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0020 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0051 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0021 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0225 | EAS | CDX | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0183 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02717 | hp1 | a0001 | c0003 | t0003 | g0010 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02723 | hp1 | a0001 | c0010 | t0004 | g0146 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0195 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0222 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02895 | hp1 | a0001 | c0003 | t0003 | g0010 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0010 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0229 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0068 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0144 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0216 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0043 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0043 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03540 | hp1 | a0001 | c0003 | t0003 | g0010 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0213 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0215 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0202 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0205 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0190 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0020 | SAS | BEB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0021 | SAS | STU | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0012 | SAS | BEB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0013 | SAS | STU | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | STU | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18747 | hp2 | a0001 | c0007 | t0001 | g0110 | EAS | CHB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | YRI | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18947 | hp1 | a0001 | c0002 | t0009 | g0204 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0228 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18952 | hp2 | a0003 | c0005 | t0002 | g0040 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18968 | hp2 | a0005 | c0011 | t0002 | g0192 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0226 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18986 | hp2 | a0006 | c0009 | t0002 | g0191 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18991 | hp2 | a0001 | c0001 | t0006 | g0224 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0227 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19066 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA19240 | hp2 | a0007 | c0006 | t0001 | g0127 | AFR | YRI | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ASW | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ASW | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | TSI | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0013 | EUR | TSI | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0189 | SAS | GIH | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0197 | SAS | GIH | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0083 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0172 | AFR | USA | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18955 | hp1 | a0003 | c0005 | t0002 | g0040 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | USA | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0212 | REF | REF | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0218 | REF | REF | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:132761584 | A | G | 1 | a0006 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.836T>C | p.Met279Thr | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 7/10 | 938/2751 | 836/1452 | 279/483 | chr5 | 132761584 | |||
| chr5:132761600 | C | T | 1 | a0004 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.820G>A | p.Val274Met | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 7/10 | 922/2751 | 820/1452 | 274/483 | chr5 | 132761600 | |||
| chr5:132763867 | C | T | 1 | a0003 | 2 | NA18952.hp2 NA18955.hp1 |
missense_variant | MODERATE | c.373G>A | p.Asp125Asn | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/10 | 475/2751 | 373/1452 | 125/483 | chr5 | 132763867 | |||
| chr5:132764270 | T | C | 1 | a0005 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.301A>G | p.Ile101Val | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 3/10 | 403/2751 | 301/1452 | 101/483 | chr5 | 132764270 | |||
| chr5:132764278 | T | A | 1 | a0002 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.293A>T | p.Lys98Met | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 3/10 | 395/2751 | 293/1452 | 98/483 | chr5 | 132764278 | |||
| chr5:132764320 | C | T | 1 | a0007 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.251G>A | p.Arg84Gln | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 3/10 | 353/2751 | 251/1452 | 84/483 | chr5 | 132764320 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:132752040 | C | T | 1 | a0001c0003 | 5 | HG00642.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
synonymous_variant | LOW | c.1428G>A | p.Ala476Ala | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 1530/2751 | 1428/1452 | 476/483 | chr5 | 132752040 | |||
| chr5:132760876 | C | T | 1 | a0001c0010 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1212G>A | p.Ala404Ala | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/10 | 1314/2751 | 1212/1452 | 404/483 | chr5 | 132760876 | |||
| chr5:132763766 | C | T | 1 | a0001c0007 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.474G>A | p.Thr158Thr | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/10 | 576/2751 | 474/1452 | 158/483 | chr5 | 132763766 | |||
| chr5:132764307 | A | G | 9 | a0001c0001 a0001c0003 a0001c0007 others(6): Show |
227 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(224): Show |
synonymous_variant | LOW | c.264T>C | p.Tyr88Tyr | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 3/10 | 366/2751 | 264/1452 | 88/483 | chr5 | 132764307 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:132750906 | C | T | 1 | a0001c0002t0009 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1110G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 1110 | chr5 | 132750906 | ||||||
| chr5:132751125 | G | C | 12 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(9): Show |
213 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*891C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 891 | chr5 | 132751125 | ||||||
| chr5:132751440 | GTTTGTA | G | 2 | a0001c0001t0003 a0001c0003t0003 |
12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*570_*575delTACAAA | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 570 | chr5 | 132751440 | ||||||
| chr5:132751601 | C | T | 1 | a0001c0001t0008 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 415 | chr5 | 132751601 | ||||||
| chr5:132751623 | G | A | 1 | a0001c0002t0007 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 393 | chr5 | 132751623 | ||||||
| chr5:132751902 | T | C | 2 | a0001c0001t0004 a0001c0010t0004 |
11 | HG01243.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*114A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 114 | chr5 | 132751902 | ||||||
| chr5:132777186 | G | T | 1 | a0001c0001t0005 | 9 | HG00408.hp1 HG00408.hp2 HG02027.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-49C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/10 | 49 | chr5 | 132777186 | ||||||
| chr5:132777203 | T | C | 1 | a0001c0001t0006 | 6 | HG02155.hp1 HG03017.hp1 NA18951.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-66A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/10 | 66 | chr5 | 132777203 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:132752256 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1287-75G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132752256 | |||||||
| chr5:132752361 | G | A | 12 | a0001c0001t0001g0015 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1287-180C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132752361 | |||||||
| chr5:132752821 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1287-640A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132752821 | |||||||
| chr5:132752885 | G | T | 1 | a0001c0001t0004g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1287-704C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132752885 | |||||||
| chr5:132752989 | G | A | 1 | a0001c0001t0008g0068 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1287-808C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132752989 | |||||||
| chr5:132753175 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0052 others(4): Show |
10 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.1287-994C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753175 | |||||||
| chr5:132753263 | G | T | 18 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0037 others(15): Show |
24 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1287-1082C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753263 | |||||||
| chr5:132753287 | G | C | 9 | a0001c0001t0003g0063 a0001c0001t0003g0150 a0001c0001t0003g0152 others(6): Show |
12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1287-1106C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753287 | |||||||
| chr5:132753508 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0001g0087 others(5): Show |
10 | HG01069.hp2 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1287-1327G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753508 | |||||||
| chr5:132753534 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1287-1353T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753534 | |||||||
| chr5:132753584 | A | C | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1287-1403T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753584 | |||||||
| chr5:132753785 | G | A | 1 | a0001c0002t0002g0188 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1287-1604C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753785 | |||||||
| chr5:132753795 | C | T | 9 | a0001c0001t0003g0063 a0001c0001t0003g0150 a0001c0001t0003g0152 others(6): Show |
12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1287-1614G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753795 | |||||||
| chr5:132753877 | G | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1287-1696C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753877 | |||||||
| chr5:132753956 | G | GT | 26 | a0001c0001t0001g0055 a0001c0001t0001g0126 a0001c0001t0002g0065 others(23): Show |
36 | HG00639.hp2 HG00642.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.1287-1776dupA | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | |||||||
| chr5:132753956 | G | GTT | 26 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0037 others(23): Show |
34 | HG00621.hp1 HG00735.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1287-1777_1287-177 others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | |||||||
| chr5:132753956 | G | GTTT | 17 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0058 others(14): Show |
20 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1287-1778_1287-177 others(7): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | |||||||
| chr5:132753956 | G | GTTTT | 6 | a0001c0001t0001g0091 a0001c0001t0004g0083 a0001c0001t0004g0144 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287-1779_1287-177 others(8): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | |||||||
| chr5:132753956 | GT | G | 19 | a0001c0001t0001g0016 a0001c0001t0001g0070 a0001c0001t0001g0079 others(16): Show |
21 | HG00438.hp2 HG00597.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-1776delA | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | |||||||
| chr5:132753956 | GTT | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
126 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1287-1777_1287-177 others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | |||||||
| chr5:132753956 | GTTT | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0129 others(1): Show |
6 | HG02451.hp2 HG02630.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1287-1778_1287-177 others(7): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | |||||||
| chr5:132754149 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0001g0087 |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287-1968T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754149 | |||||||
| chr5:132754428 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1287-2247G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754428 | |||||||
| chr5:132754602 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1287-2421A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754602 | |||||||
| chr5:132754615 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1287-2434A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754615 | |||||||
| chr5:132754690 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1287-2509G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754690 | |||||||
| chr5:132754764 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0008g0068 |
3 | HG02630.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1287-2583G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754764 | |||||||
| chr5:132754946 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1287-2765G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754946 | |||||||
| chr5:132755136 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1287-2955A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132755136 | |||||||
| chr5:132755257 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1287-3076G>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132755257 | |||||||
| chr5:132755959 | C | CTT | 164 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1287-3779_1287-377 others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132755959 | |||||||
| chr5:132756251 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0001g0087 |
5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287-4070C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132756251 | |||||||
| chr5:132756374 | G | T | 31 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0066 others(28): Show |
37 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1287-4193C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132756374 | |||||||
| chr5:132756386 | A | G | 1 | a0001c0002t0002g0209 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1287-4205T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132756386 | |||||||
| chr5:132756438 | T | C | 1 | a0001c0002t0002g0205 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1287-4257A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132756438 | |||||||
| chr5:132756716 | G | A | 1 | a0001c0002t0009g0204 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1286+4086C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132756716 | |||||||
| chr5:132756792 | G | A | 8 | a0001c0001t0005g0023 a0001c0001t0005g0045 a0001c0001t0005g0046 others(5): Show |
9 | HG00408.hp1 HG00408.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1286+4010C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132756792 | |||||||
| chr5:132757112 | T | A | 1 | a0001c0001t0001g0129 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1286+3690A>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757112 | |||||||
| chr5:132757121 | G | T | 1 | a0001c0002t0002g0198 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1286+3681C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757121 | |||||||
| chr5:132757345 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
155 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1286+3457C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757345 | |||||||
| chr5:132757357 | C | T | 9 | a0001c0001t0003g0063 a0001c0001t0003g0150 a0001c0001t0003g0152 others(6): Show |
12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1286+3445G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757357 | |||||||
| chr5:132757568 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1286+3234C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757568 | |||||||
| chr5:132757590 | T | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0001g0087 others(5): Show |
10 | HG01069.hp2 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1286+3212A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757590 | |||||||
| chr5:132757628 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1286+3174C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757628 | |||||||
| chr5:132757720 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1286+3082G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757720 | |||||||
| chr5:132757723 | G | A | 1 | a0001c0002t0002g0200 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1286+3079C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757723 | |||||||
| chr5:132757957 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1286+2845A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757957 | |||||||
| chr5:132757967 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1286+2835A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757967 | |||||||
| chr5:132758043 | A | C | 1 | a0007c0006t0001g0127 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1286+2759T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758043 | |||||||
| chr5:132758302 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
166 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.1286+2500G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758302 | |||||||
| chr5:132758313 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0133 a0001c0001t0001g0141 |
5 | HG01243.hp2 HG02809.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1286+2489T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758313 | |||||||
| chr5:132758411 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1286+2391C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758411 | |||||||
| chr5:132758513 | G | A | 17 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0082 others(14): Show |
21 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.1286+2289C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758513 | |||||||
| chr5:132758634 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1286+2168C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758634 | |||||||
| chr5:132758664 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1286+2138G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758664 | |||||||
| chr5:132758665 | G | A | 7 | a0001c0001t0001g0109 a0001c0001t0004g0144 a0001c0001t0004g0145 others(4): Show |
7 | HG02145.hp2 HG02300.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1286+2137C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758665 | |||||||
| chr5:132758718 | G | A | 2 | a0001c0002t0002g0194 a0001c0002t0002g0202 |
2 | HG01175.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1286+2084C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758718 | |||||||
| chr5:132759036 | T | G | 5 | a0001c0001t0001g0105 a0001c0001t0001g0111 a0001c0001t0001g0113 others(2): Show |
5 | HG02040.hp1 HG02155.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+1766A>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759036 | |||||||
| chr5:132759060 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1286+1742G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759060 | |||||||
| chr5:132759089 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1286+1713C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759089 | |||||||
| chr5:132759200 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1286+1602G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759200 | |||||||
| chr5:132759218 | G | GTCATGGG others(10): Show |
1 | a0001c0001t0002g0174 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1286+1567_1286+158 others(21): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759218 | |||||||
| chr5:132759225 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1286+1577C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759225 | |||||||
| chr5:132759230 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1286+1572C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759230 | |||||||
| chr5:132759282 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1286+1520C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759282 | |||||||
| chr5:132759350 | A | G | 1 | a0001c0002t0002g0209 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1286+1452T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759350 | |||||||
| chr5:132759467 | CCT | C | 9 | a0001c0001t0003g0063 a0001c0001t0003g0150 a0001c0001t0003g0152 others(6): Show |
12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1286+1333_1286+133 others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759467 | |||||||
| chr5:132759554 | G | A | 1 | a0001c0002t0002g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1286+1248C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759554 | |||||||
| chr5:132759916 | G | T | 1 | a0001c0002t0002g0207 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1286+886C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759916 | |||||||
| chr5:132760074 | G | T | 1 | a0001c0002t0002g0184 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1286+728C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760074 | |||||||
| chr5:132760431 | A | G | 37 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0024 others(34): Show |
45 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.1286+371T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760431 | |||||||
| chr5:132760603 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1286+199C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760603 | |||||||
| chr5:132760631 | A | AAAAG | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.1286+167_1286+170d others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760631 | |||||||
| chr5:132760779 | C | T | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0138 others(3): Show |
8 | HG02055.hp1 HG02155.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286+23G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760779 | |||||||
| chr5:132760785 | C | T | 10 | a0001c0001t0001g0017 a0001c0001t0001g0032 a0001c0001t0001g0094 others(7): Show |
13 | HG00438.hp2 HG02015.hp1 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.1286+17G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760785 | |||||||
| chr5:132760786 | G | A | 6 | a0001c0001t0004g0144 a0001c0001t0004g0145 a0001c0001t0004g0147 others(3): Show |
6 | HG02145.hp2 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1286+16C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760786 | |||||||
| chr5:132761010 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1096-18C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 8/9 | chr5 | 132761010 | |||||||
| chr5:132761104 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1095+29G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 8/9 | chr5 | 132761104 | |||||||
| chr5:132761110 | C | G | 1 | a0001c0002t0002g0043 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1095+23G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 8/9 | chr5 | 132761110 | |||||||
| chr5:132761359 | G | T | 38 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0024 others(35): Show |
46 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.963-94C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 7/9 | chr5 | 132761359 | |||||||
| chr5:132761733 | T | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0165 others(2): Show |
5 | HG00639.hp1 HG01358.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+67A>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 6/9 | chr5 | 132761733 | |||||||
| chr5:132761902 | A | G | 1 | a0001c0002t0002g0197 | 1 | NA20905.hp2 | splice_region_variant&intron_variant | LOW | c.697-6T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 5/9 | chr5 | 132761902 | |||||||
| chr5:132762071 | G | A | 1 | a0001c0002t0002g0203 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.697-175C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 5/9 | chr5 | 132762071 | |||||||
| chr5:132762225 | G | T | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.696+259C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 5/9 | chr5 | 132762225 | |||||||
| chr5:132762226 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.696+258G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 5/9 | chr5 | 132762226 | |||||||
| chr5:132762728 | A | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
210 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.535-83T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132762728 | |||||||
| chr5:132762841 | A | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0075 others(1): Show |
6 | NA18954.hp1 NA18991.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.535-196T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132762841 | |||||||
| chr5:132762874 | TC | T | 9 | a0001c0001t0003g0063 a0001c0001t0003g0150 a0001c0001t0003g0152 others(6): Show |
12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.535-230delG | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132762874 | |||||||
| chr5:132763074 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0008g0068 others(1): Show |
6 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.535-429G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132763074 | |||||||
| chr5:132763433 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0008g0068 others(1): Show |
6 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.534+273C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132763433 | |||||||
| chr5:132763443 | C | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.534+263G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132763443 | |||||||
| chr5:132763546 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.534+160T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132763546 | |||||||
| chr5:132763559 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.534+147G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132763559 | |||||||
| chr5:132763687 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.534+19G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132763687 | |||||||
| chr5:132764206 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.347+18C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 3/9 | chr5 | 132764206 | |||||||
| chr5:132764448 | G | A | 10 | a0001c0001t0001g0134 a0001c0001t0001g0161 a0001c0001t0001g0162 others(7): Show |
10 | HG00639.hp1 HG01358.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-29C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 2/9 | chr5 | 132764448 | |||||||
| chr5:132764668 | T | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0008g0068 others(1): Show |
6 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-249A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 2/9 | chr5 | 132764668 | |||||||
| chr5:132764780 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.152-361A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 2/9 | chr5 | 132764780 | |||||||
| chr5:132764807 | A | G | 1 | a0001c0001t0005g0047 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.152-388T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 2/9 | chr5 | 132764807 | |||||||
| chr5:132764913 | A | G | 50 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0024 others(47): Show |
61 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.152-494T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 2/9 | chr5 | 132764913 | |||||||
| chr5:132765036 | A | G | 9 | a0001c0001t0003g0063 a0001c0001t0003g0150 a0001c0001t0003g0152 others(6): Show |
12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.151+373T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 2/9 | chr5 | 132765036 | |||||||
| chr5:132765561 | C | T | 6 | a0001c0001t0004g0144 a0001c0001t0004g0145 a0001c0001t0004g0147 others(3): Show |
6 | HG02145.hp2 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-32G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132765561 | |||||||
| chr5:132765649 | A | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0100 |
2 | HG03927.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.31-120T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132765649 | |||||||
| chr5:132765754 | G | A | 1 | a0001c0002t0002g0201 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.31-225C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132765754 | |||||||
| chr5:132765937 | T | C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG01884.hp1 HG01891.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-408A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132765937 | |||||||
| chr5:132765977 | C | G | 9 | a0001c0001t0003g0063 a0001c0001t0003g0150 a0001c0001t0003g0152 others(6): Show |
12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-448G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132765977 | |||||||
| chr5:132766077 | C | T | 1 | a0001c0002t0002g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.31-548G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766077 | |||||||
| chr5:132766184 | G | C | 9 | a0001c0001t0003g0063 a0001c0001t0003g0150 a0001c0001t0003g0152 others(6): Show |
12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-655C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766184 | |||||||
| chr5:132766211 | G | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
195 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.31-682C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766211 | |||||||
| chr5:132766368 | G | A | 1 | a0001c0001t0003g0154 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31-839C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766368 | |||||||
| chr5:132766400 | G | C | 51 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0024 others(48): Show |
62 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.31-871C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766400 | |||||||
| chr5:132766432 | G | A | 5 | a0001c0002t0002g0008 a0001c0002t0002g0184 a0001c0002t0002g0206 others(2): Show |
9 | NA18941.hp1 NA18945.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-903C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766432 | |||||||
| chr5:132766976 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.31-1447T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766976 | |||||||
| chr5:132767095 | C | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0008g0068 others(1): Show |
6 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-1566G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767095 | |||||||
| chr5:132767549 | C | T | 33 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0024 others(30): Show |
41 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.31-2020G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767549 | |||||||
| chr5:132767579 | G | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.31-2050C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767579 | |||||||
| chr5:132767586 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0008g0068 a0002c0004t0001g0030 |
4 | HG01167.hp2 HG01169.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-2057G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767586 | |||||||
| chr5:132767664 | C | T | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.31-2135G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767664 | |||||||
| chr5:132767676 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.31-2147T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767676 | |||||||
| chr5:132767885 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.31-2356C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767885 | |||||||
| chr5:132767916 | C | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0117 |
2 | NA18943.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.31-2387G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767916 | |||||||
| chr5:132767941 | A | C | 1 | a0001c0002t0002g0190 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-2412T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767941 | |||||||
| chr5:132767942 | A | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0122 |
2 | NA18982.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.31-2413T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767942 | |||||||
| chr5:132767943 | C | CACACACA others(6): Show |
1 | a0001c0001t0001g0125 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.31-2415_31-2414ins others(13): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | C | CACACACA others(8): Show |
1 | a0001c0001t0001g0124 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.31-2415_31-2414ins others(15): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | C | CACACACA others(10): Show |
3 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0122 |
3 | NA18968.hp1 NA18982.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.31-2415_31-2414ins others(17): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | C | CCA | 14 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0024 others(11): Show |
23 | HG01069.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.31-2416_31-2415dup others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | C | CCACA | 43 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(40): Show |
66 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.31-2418_31-2415dup others(4): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | C | CCACACA | 27 | a0001c0001t0001g0061 a0001c0001t0001g0081 a0001c0001t0001g0096 others(24): Show |
39 | HG00735.hp2 HG01257.hp1 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.31-2420_31-2415dup others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | C | CCACACAC others(1): Show |
25 | a0001c0001t0001g0004 a0001c0001t0001g0066 a0001c0001t0001g0106 others(22): Show |
33 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.31-2422_31-2415dup others(8): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | C | CCACACAC others(3): Show |
25 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0072 others(22): Show |
34 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.31-2424_31-2415dup others(10): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | C | CCACACAC others(5): Show |
17 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0032 others(14): Show |
24 | HG00408.hp1 HG00438.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.31-2426_31-2415dup others(12): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | C | CCACACAC others(7): Show |
10 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0025 others(7): Show |
18 | HG00544.hp2 HG00597.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.31-2428_31-2415dup others(14): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | C | CCACACAC others(9): Show |
9 | a0001c0001t0001g0002 a0001c0001t0001g0069 a0001c0001t0001g0071 others(6): Show |
14 | HG00438.hp2 HG01975.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.31-2430_31-2415dup others(16): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | C | CCACACAC others(11): Show |
4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0026 others(1): Show |
9 | HG02015.hp1 NA18612.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-2432_31-2415dup others(18): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | C | CCACACAC others(13): Show |
3 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0123 |
5 | HG02027.hp2 HG04115.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-2434_31-2415dup others(20): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | C | CCACACAC others(17): Show |
1 | a0001c0001t0001g0077 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.31-2438_31-2415dup others(24): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | CCA | C | 2 | a0001c0001t0001g0036 a0007c0006t0001g0127 |
3 | HG02965.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.31-2416_31-2415del others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | CCACA | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0138 a0001c0001t0001g0159 others(1): Show |
5 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-2418_31-2415del others(4): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | CCACACA | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
6 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-2420_31-2415del others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | CCACACAC others(1): Show |
C | 4 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 others(1): Show |
4 | HG02451.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-2422_31-2415del others(8): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132767943 | CCACACAC others(5): Show |
C | 4 | a0001c0001t0001g0080 a0001c0001t0004g0029 a0001c0001t0004g0083 others(1): Show |
5 | HG01243.hp1 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-2426_31-2415del others(12): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | |||||||
| chr5:132768045 | T | G | 1 | a0001c0001t0001g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.31-2516A>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768045 | |||||||
| chr5:132768181 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.31-2652C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768181 | |||||||
| chr5:132768299 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.31-2770C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768299 | |||||||
| chr5:132768410 | T | C | 1 | a0001c0003t0003g0151 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.31-2881A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768410 | |||||||
| chr5:132768464 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
152 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.31-2935G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768464 | |||||||
| chr5:132768690 | C | T | 1 | a0001c0002t0002g0189 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-3161G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768690 | |||||||
| chr5:132768983 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.31-3454C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768983 | |||||||
| chr5:132769176 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.31-3647T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769176 | |||||||
| chr5:132769405 | T | C | 2 | a0001c0001t0004g0148 a0001c0001t0004g0149 |
2 | HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.31-3876A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769405 | |||||||
| chr5:132769592 | A | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0052 others(10): Show |
16 | HG01167.hp1 HG02258.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-4063T>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769592 | |||||||
| chr5:132769683 | C | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
153 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.31-4154G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769683 | |||||||
| chr5:132769704 | G | C | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4175C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769704 | |||||||
| chr5:132769708 | A | C | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4179T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769708 | |||||||
| chr5:132769798 | A | T | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4269T>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769798 | |||||||
| chr5:132769815 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4286C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769815 | |||||||
| chr5:132769825 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4296C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769825 | |||||||
| chr5:132769829 | A | T | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4300T>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769829 | |||||||
| chr5:132769831 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4302C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769831 | |||||||
| chr5:132769833 | GGGAATGG others(18): Show |
G | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4329_31-4305del others(25): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769833 | |||||||
| chr5:132769867 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4338C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769867 | |||||||
| chr5:132769877 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4348A>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769877 | |||||||
| chr5:132769878 | G | C | 17 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0082 others(14): Show |
21 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.31-4349C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769878 | |||||||
| chr5:132769879 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4350C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769879 | |||||||
| chr5:132769913 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4384C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769913 | |||||||
| chr5:132769915 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4386T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769915 | |||||||
| chr5:132769924 | T | TATGTGCC others(41): Show |
1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4396_31-4395ins others(48): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769924 | |||||||
| chr5:132769926 | G | C | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4397C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769926 | |||||||
| chr5:132769937 | T | A | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4408A>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769937 | |||||||
| chr5:132769939 | T | A | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4410A>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769939 | |||||||
| chr5:132769940 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4411A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769940 | |||||||
| chr5:132769941 | C | A | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4412G>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769941 | |||||||
| chr5:132769944 | G | C | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4415C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769944 | |||||||
| chr5:132769945 | T | A | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4416A>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769945 | |||||||
| chr5:132769946 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4417A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769946 | |||||||
| chr5:132769973 | C | A | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4444G>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769973 | |||||||
| chr5:132769982 | C | CAT | 4 | a0001c0001t0001g0143 a0001c0001t0002g0174 a0001c0002t0002g0176 others(1): Show |
4 | HG03130.hp1 NA18940.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-4455_31-4454dup others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | |||||||
| chr5:132769982 | C | CATAT | 8 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0002t0002g0173 others(5): Show |
8 | HG01496.hp2 HG02080.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-4457_31-4454dup others(4): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | |||||||
| chr5:132769982 | C | CATATATA others(3): Show |
1 | a0001c0002t0002g0184 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.31-4463_31-4454dup others(10): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | |||||||
| chr5:132769982 | CAT | C | 12 | a0001c0001t0001g0080 a0001c0001t0001g0088 a0001c0001t0003g0150 others(9): Show |
16 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-4455_31-4454del others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | |||||||
| chr5:132769982 | CATATAT | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0062 a0001c0001t0003g0152 others(4): Show |
12 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-4459_31-4454del others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | |||||||
| chr5:132769982 | CATATATA others(1): Show |
C | 7 | a0001c0001t0001g0081 a0001c0001t0001g0086 a0001c0001t0001g0087 others(4): Show |
7 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-4461_31-4454del others(8): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | |||||||
| chr5:132769982 | CATATATA others(3): Show |
C | 2 | a0001c0001t0001g0090 a0001c0001t0002g0221 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.31-4463_31-4454del others(10): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | |||||||
| chr5:132769982 | CATATATA others(5): Show |
C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.31-4465_31-4454del others(12): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | |||||||
| chr5:132769982 | CATATATA others(9): Show |
C | 2 | a0001c0001t0005g0023 a0001c0001t0005g0051 |
3 | HG02027.hp1 NA18964.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.31-4469_31-4454del others(16): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | |||||||
| chr5:132769984 | T | C | 1 | a0001c0001t0001g0018 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-4455A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769984 | |||||||
| chr5:132769998 | TATATATA others(19): Show |
T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0098 |
3 | HG02257.hp2 HG02895.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.31-4495_31-4470del others(26): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769998 | |||||||
| chr5:132770002 | TATATATA others(15): Show |
T | 1 | a0001c0001t0002g0039 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.31-4495_31-4474del others(22): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770002 | |||||||
| chr5:132770004 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0096 others(2): Show |
5 | HG01496.hp1 HG02280.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-4475A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770004 | |||||||
| chr5:132770006 | T | C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(62): Show |
91 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.31-4477A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770006 | |||||||
| chr5:132770006 | TATATATA others(11): Show |
T | 2 | a0001c0001t0004g0145 a0001c0002t0002g0216 |
2 | HG02145.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.31-4495_31-4478del others(18): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770006 | |||||||
| chr5:132770008 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(31): Show |
45 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.31-4479A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770008 | |||||||
| chr5:132770008 | T | TAC | 5 | a0001c0001t0001g0027 a0001c0001t0001g0076 a0001c0001t0001g0109 others(2): Show |
6 | HG02300.hp1 HG03017.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-4480_31-4479ins others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770008 | |||||||
| chr5:132770008 | TATATATA others(9): Show |
T | 2 | a0001c0001t0001g0057 a0001c0001t0005g0045 |
2 | HG03195.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.31-4495_31-4480del others(16): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770008 | |||||||
| chr5:132770010 | TATATATA others(7): Show |
T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0052 others(4): Show |
10 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-4495_31-4482del others(14): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770010 | |||||||
| chr5:132770011 | A | C | 1 | a0001c0001t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4482T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770011 | |||||||
| chr5:132770012 | TATATATA others(5): Show |
T | 2 | a0001c0001t0001g0053 a0001c0001t0004g0147 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.31-4495_31-4484del others(12): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770012 | |||||||
| chr5:132770014 | TATATATA others(3): Show |
T | 2 | a0001c0001t0001g0037 a0001c0001t0008g0068 |
3 | HG02630.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.31-4495_31-4486del others(10): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770014 | |||||||
| chr5:132770016 | TATATATA others(1): Show |
T | 13 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0095 others(10): Show |
16 | HG01070.hp1 HG01099.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-4495_31-4488del others(8): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770016 | |||||||
| chr5:132770018 | TATATAC | T | 17 | a0001c0001t0002g0038 a0001c0002t0002g0001 a0001c0002t0002g0003 others(14): Show |
26 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.31-4495_31-4490del others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770018 | |||||||
| chr5:132770020 | TATAC | T | 21 | a0001c0001t0001g0096 a0001c0001t0001g0103 a0001c0001t0001g0132 others(18): Show |
24 | HG00735.hp2 HG00738.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.31-4495_31-4492del others(4): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770020 | |||||||
| chr5:132770022 | TAC | T | 61 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(58): Show |
87 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.31-4495_31-4494del others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770022 | |||||||
| chr5:132770023 | ACACACAC others(51): Show |
A | 1 | a0001c0001t0001g0071 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4552_31-4495del others(58): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770023 | |||||||
| chr5:132770024 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(63): Show |
81 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.31-4495G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770024 | |||||||
| chr5:132770026 | C | T | 5 | a0001c0001t0001g0126 a0001c0001t0001g0139 a0001c0001t0001g0142 others(2): Show |
6 | HG00558.hp1 HG03471.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-4497G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770026 | |||||||
| chr5:132770028 | CACAT | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(11): Show |
17 | HG00621.hp2 HG02055.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.31-4503_31-4500del others(4): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770028 | |||||||
| chr5:132770030 | C | T | 3 | a0001c0002t0002g0173 a0001c0002t0002g0182 a0001c0002t0002g0183 |
3 | HG01975.hp2 HG02300.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.31-4501G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770030 | |||||||
| chr5:132770032 | T | C | 8 | a0001c0001t0001g0085 a0001c0001t0001g0126 a0001c0001t0001g0139 others(5): Show |
10 | HG00558.hp1 HG01243.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-4503A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770032 | |||||||
| chr5:132770034 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.31-4505A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770034 | |||||||
| chr5:132770039 | A | G | 5 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG02280.hp1 HG02630.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-4510T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770039 | |||||||
| chr5:132770041 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
189 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.31-4512T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770041 | |||||||
| chr5:132770043 | G | A | 2 | a0001c0001t0002g0211 a0001c0002t0002g0043 |
3 | HG03491.hp2 HG03492.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.31-4514C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770043 | |||||||
| chr5:132770055 | GTGTGTGT others(75): Show |
G | 1 | a0001c0001t0001g0086 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.31-4608_31-4527del others(82): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770055 | |||||||
| chr5:132770059 | GTGTGTAT others(83): Show |
G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0089 a0001c0001t0002g0102 |
3 | HG01361.hp2 HG02027.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.31-4620_31-4531del others(90): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770059 | |||||||
| chr5:132770061 | GTGTA | G | 5 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0002t0002g0001 others(2): Show |
7 | HG00642.hp2 NA18944.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-4536_31-4533del others(4): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770061 | |||||||
| chr5:132770061 | GTGTATAT others(81): Show |
G | 19 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0093 others(16): Show |
20 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.31-4620_31-4533del others(88): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770061 | |||||||
| chr5:132770061 | GTGTATAT others(83): Show |
G | 1 | a0001c0001t0001g0128 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.31-4622_31-4533del others(90): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770061 | |||||||
| chr5:132770063 | G | A | 2 | a0001c0002t0002g0182 a0001c0002t0002g0183 |
2 | HG01975.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.31-4534C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | |||||||
| chr5:132770063 | GTA | G | 28 | a0001c0001t0002g0196 a0001c0001t0002g0211 a0001c0001t0002g0220 others(25): Show |
45 | HG00609.hp2 HG00639.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.31-4536_31-4535del others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | |||||||
| chr5:132770063 | GTATATAT others(67): Show |
G | 1 | a0001c0001t0001g0131 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.31-4608_31-4535del others(74): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | |||||||
| chr5:132770063 | GTATATAT others(77): Show |
G | 21 | a0001c0001t0001g0015 a0001c0001t0001g0080 a0001c0001t0001g0087 others(18): Show |
27 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.31-4618_31-4535del others(84): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | |||||||
| chr5:132770063 | GTATATAT others(79): Show |
G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
142 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.31-4620_31-4535del others(86): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | |||||||
| chr5:132770063 | GTATATAT others(81): Show |
G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0052 others(11): Show |
17 | HG02258.hp2 HG02622.hp2 HG02896.hp2 others(14): Show |
intron_variant | MODIFIER | c.31-4622_31-4535del others(88): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | |||||||
| chr5:132770063 | GTATATAT others(83): Show |
G | 2 | a0001c0001t0001g0095 a0002c0004t0001g0030 |
3 | HG01167.hp2 HG01169.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.31-4624_31-4535del others(90): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | |||||||
| chr5:132770065 | A | G | 4 | a0001c0002t0002g0173 a0001c0002t0002g0187 a0001c0002t0002g0201 others(1): Show |
4 | HG02080.hp1 NA18999.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-4536T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770065 | |||||||
| chr5:132770067 | A | G | 5 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0002t0002g0001 others(2): Show |
5 | HG01069.hp1 HG01515.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-4538T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770067 | |||||||
| chr5:132770089 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4560C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770089 | |||||||
| chr5:132770091 | ATATATAT others(11): Show |
A | 1 | a0001c0002t0002g0008 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.31-4580_31-4563del others(18): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770091 | |||||||
| chr5:132770092 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4563A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770092 | |||||||
| chr5:132770093 | A | G | 1 | a0005c0011t0002g0192 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.31-4564T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770093 | |||||||
| chr5:132770101 | G | A | 3 | a0001c0001t0001g0071 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG01884.hp2 HG02148.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-4572C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770101 | |||||||
| chr5:132770103 | A | G | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-4574T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770103 | |||||||
| chr5:132770107 | ATG | A | 3 | a0001c0002t0002g0001 a0001c0002t0002g0013 a0001c0002t0002g0181 |
3 | HG01099.hp2 HG02273.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.31-4580_31-4579del others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770107 | |||||||
| chr5:132770109 | G | A | 3 | a0001c0001t0001g0071 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG01884.hp2 HG02148.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-4580C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770109 | |||||||
| chr5:132770109 | G | GTA | 54 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0174 others(51): Show |
86 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.31-4582_31-4581dup others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770109 | |||||||
| chr5:132770109 | G | GTATATAT others(41): Show |
1 | a0001c0002t0002g0216 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.31-4581_31-4580ins others(48): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770109 | |||||||
| chr5:132770110 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4581A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770110 | |||||||
| chr5:132770111 | A | G | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-4582T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770111 | |||||||
| chr5:132770112 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4583A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770112 | |||||||
| chr5:132770114 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4585A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770114 | |||||||
| chr5:132770129 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4600T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770129 | |||||||
| chr5:132770131 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4602T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770131 | |||||||
| chr5:132770137 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4608T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770137 | |||||||
| chr5:132770143 | G | A | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-4614C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770143 | |||||||
| chr5:132770145 | G | A | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-4616C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770145 | |||||||
| chr5:132770145 | G | GTA | 5 | a0001c0002t0002g0043 a0001c0002t0002g0213 a0001c0002t0002g0214 others(2): Show |
6 | HG01070.hp1 HG03491.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-4618_31-4617dup others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770145 | |||||||
| chr5:132770147 | A | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0086 a0001c0002t0002g0011 others(3): Show |
9 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-4618T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770147 | |||||||
| chr5:132770149 | A | G | 16 | a0001c0001t0001g0015 a0001c0001t0001g0071 a0001c0001t0001g0080 others(13): Show |
22 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.31-4620T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770149 | |||||||
| chr5:132770151 | A | G | 17 | a0001c0001t0001g0037 a0001c0001t0001g0085 a0001c0001t0001g0142 others(14): Show |
21 | HG00642.hp1 HG02258.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.31-4622T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770151 | |||||||
| chr5:132770153 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.31-4624T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770153 | |||||||
| chr5:132770163 | A | G | 4 | a0001c0002t0002g0001 a0001c0002t0002g0194 a0001c0002t0002g0199 others(1): Show |
4 | HG01099.hp1 HG01168.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-4634T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770163 | |||||||
| chr5:132770333 | C | T | 1 | a0001c0002t0002g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.31-4804G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770333 | |||||||
| chr5:132770552 | T | C | 7 | a0001c0001t0004g0144 a0001c0001t0004g0145 a0001c0001t0004g0147 others(4): Show |
7 | HG02145.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-5023A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770552 | |||||||
| chr5:132770640 | C | T | 3 | a0001c0002t0002g0175 a0001c0002t0002g0176 a0001c0002t0002g0177 |
3 | HG00609.hp2 NA18940.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.31-5111G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770640 | |||||||
| chr5:132770789 | T | C | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-5260A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770789 | |||||||
| chr5:132770856 | C | T | 1 | a0001c0001t0004g0222 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.31-5327G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770856 | |||||||
| chr5:132770869 | A | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(71): Show |
109 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.31-5340T>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770869 | |||||||
| chr5:132771093 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.31-5564G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771093 | |||||||
| chr5:132771333 | C | T | 9 | a0001c0001t0003g0063 a0001c0001t0003g0150 a0001c0001t0003g0152 others(6): Show |
12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.30+5775G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771333 | |||||||
| chr5:132771359 | G | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+5749C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771359 | |||||||
| chr5:132771548 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.30+5560C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771548 | |||||||
| chr5:132771654 | T | C | 1 | a0001c0001t0001g0027 | 2 | NA18961.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.30+5454A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771654 | |||||||
| chr5:132771703 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+5405T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771703 | |||||||
| chr5:132771737 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0141 |
4 | HG01243.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+5371C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771737 | |||||||
| chr5:132771876 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.30+5232G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771876 | |||||||
| chr5:132772008 | T | C | 52 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0024 others(49): Show |
63 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.30+5100A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772008 | |||||||
| chr5:132772015 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | NA18979.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.30+5093T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772015 | |||||||
| chr5:132772086 | TCA | T | 3 | a0001c0001t0001g0095 a0001c0001t0008g0068 a0002c0004t0001g0030 |
4 | HG01167.hp2 HG01169.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+5020_30+5021del others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772086 | |||||||
| chr5:132772302 | G | C | 1 | a0001c0001t0006g0229 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.30+4806C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772302 | |||||||
| chr5:132772315 | G | C | 1 | a0001c0001t0001g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.30+4793C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772315 | |||||||
| chr5:132772334 | G | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
213 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.30+4774C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772334 | |||||||
| chr5:132772537 | C | A | 1 | a0001c0002t0002g0216 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.30+4571G>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772537 | |||||||
| chr5:132772626 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0079 |
3 | NA18954.hp1 NA18991.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.30+4482C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772626 | |||||||
| chr5:132772649 | C | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+4459G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772649 | |||||||
| chr5:132772705 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.30+4403C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772705 | |||||||
| chr5:132772993 | G | A | 25 | a0001c0001t0001g0015 a0001c0001t0001g0062 a0001c0001t0001g0080 others(22): Show |
31 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.30+4115C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772993 | |||||||
| chr5:132773109 | C | A | 1 | a0001c0001t0001g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.30+3999G>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773109 | |||||||
| chr5:132773160 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.30+3948T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773160 | |||||||
| chr5:132773431 | C | T | 16 | a0001c0001t0001g0015 a0001c0001t0001g0062 a0001c0001t0001g0080 others(13): Show |
19 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+3677G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773431 | |||||||
| chr5:132773593 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.30+3515T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773593 | |||||||
| chr5:132773761 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.30+3347A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773761 | |||||||
| chr5:132773793 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+3315T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773793 | |||||||
| chr5:132773882 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.30+3226A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773882 | |||||||
| chr5:132773927 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+3181A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773927 | |||||||
| chr5:132774050 | G | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+3058C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132774050 | |||||||
| chr5:132774274 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+2834A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132774274 | |||||||
| chr5:132774495 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG01884.hp1 HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.30+2613G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132774495 | |||||||
| chr5:132774780 | C | T | 1 | a0001c0002t0002g0173 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.30+2328G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132774780 | |||||||
| chr5:132774937 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.30+2171C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132774937 | |||||||
| chr5:132775046 | G | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(14): Show |
26 | HG00738.hp2 HG01975.hp1 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.30+2062C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775046 | |||||||
| chr5:132775238 | A | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+1870T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775238 | |||||||
| chr5:132775351 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+1757C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775351 | |||||||
| chr5:132775596 | G | T | 1 | a0001c0001t0008g0068 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.30+1512C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775596 | |||||||
| chr5:132775626 | C | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
321 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(318): Show |
intron_variant | MODIFIER | c.30+1482G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775626 | |||||||
| chr5:132775651 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.30+1457T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775651 | |||||||
| chr5:132775889 | T | C | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.30+1219A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775889 | |||||||
| chr5:132775898 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+1210T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775898 | |||||||
| chr5:132775931 | C | G | 1 | a0001c0001t0001g0066 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.30+1177G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775931 | |||||||
| chr5:132776043 | G | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+1065C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776043 | |||||||
| chr5:132776297 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+811A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776297 | |||||||
| chr5:132776313 | C | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.30+795G>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776313 | |||||||
| chr5:132776348 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+760C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776348 | |||||||
| chr5:132776477 | C | G | 1 | a0001c0001t0003g0063 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.30+631G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776477 | |||||||
| chr5:132776558 | TGGGGAGC others(8): Show |
T | 1 | a0001c0002t0002g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+535_30+549delTC others(13): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776558 | |||||||
| chr5:132776699 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.30+409G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776699 | |||||||
| chr5:132776741 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+367T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776741 | |||||||
| chr5:132776773 | G | C | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(6): Show |
9 | HG00639.hp1 HG01358.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+335C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776773 | |||||||
| chr5:132776778 | G | A | 1 | a0001c0002t0002g0219 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.30+330C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776778 | |||||||
| chr5:132776783 | C | T | 1 | a0001c0002t0002g0170 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.30+325G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776783 | |||||||
| chr5:132776868 | A | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
215 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.30+240T>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776868 | |||||||
| chr5:132776922 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.30+186G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776922 | |||||||
| chr5:132776950 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.30+158G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776950 | |||||||
| chr5:132776977 | T | C | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.30+131A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776977 | |||||||
| chr5:132776994 | C | G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0052 others(9): Show |
15 | HG01167.hp1 HG02258.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.30+114G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776994 | |||||||
| chr5:132777015 | T | G | 1 | a0001c0001t0004g0222 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.30+93A>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132777015 | |||||||
| chr5:132777080 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.30+28C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132777080 |