Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 113174 |
| ensemblid | ENSG00000166788.10 |
| hgncid | 25158 |
| symbol | SAAL1 |
| name | serum amyloid A like 1 |
| refseq_nuc | NM_138421.3 |
| refseq_prot | NP_612430.2 |
| ensembl_nuc | ENST00000524803.6 |
| ensembl_prot | ENSP00000432487.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 18080292 |
| end | 18106082 |
| strand | - |
| ver | v1.2 |
| region | chr11:18080292-18106082 |
| region5000 | chr11:18075292-18111082 |
| regionname0 | SAAL1_chr11_18080292_18106082 |
| regionname5000 | SAAL1_chr11_18075292_18111082 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 474 | 161 | 52 | 28 | 57 | 5 | 18 | 37 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(469): Show |
chr11 | 18075292 | 18111082 |
| a0002 | 0/1 | 475 | 49 | 1 | 9 | 26 | 3 | 9 | 20 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(470): Show |
chr11 | 18075292 | 18111082 |
| a0003 | 0/0 | 474 | 29 | 16 | 5 | 2 | 2 | 4 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(469): Show |
chr11 | 18075292 | 18111082 |
| a0004 | 0/0 | 474 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(469): Show |
chr11 | 18075292 | 18111082 |
| a0005 | 0/0 | 476 | 10 | 0 | 0 | 10 | 0 | 0 | 9 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(471): Show |
chr11 | 18075292 | 18111082 |
| a0006 | 0/0 | 474 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(469): Show |
chr11 | 18075292 | 18111082 |
| a0007 | 0/0 | 474 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(469): Show |
chr11 | 18075292 | 18111082 |
| a0008 | 0/0 | 474 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(469): Show |
chr11 | 18075292 | 18111082 |
| a0009 | 0/0 | 474 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(469): Show |
chr11 | 18075292 | 18111082 |
| a0010 | 0/0 | 474 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(469): Show |
chr11 | 18075292 | 18111082 |
| a0011 | 0/0 | 474 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(469): Show |
chr11 | 18075292 | 18111082 |
| a0012 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(469): Show |
chr11 | 18075292 | 18111082 |
| a0013 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(469): Show |
chr11 | 18075292 | 18111082 |
| a0014 | 0/0 | 474 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | MDRNP others(469): Show |
chr11 | 18075292 | 18111082 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1422 | 151 | 43 | 28 | 57 | 5 | 17 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0001c0007 | 0/0 | 1422 | 8 | 8 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0001c0016 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0001c0018 | 0/0 | 1422 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0002c0002 | 0/0 | 1425 | 46 | 1 | 9 | 24 | 3 | 9 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1420): Show |
chr11 | 18075292 | 18111082 | ||
| a0002c0008 | 0/1 | 1425 | 2 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1420): Show |
chr11 | 18075292 | 18111082 | ||
| a0002c0013 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1420): Show |
chr11 | 18075292 | 18111082 | ||
| a0003c0003 | 0/0 | 1422 | 29 | 16 | 5 | 2 | 2 | 4 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0004c0004 | 0/0 | 1422 | 13 | 13 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0005c0005 | 0/0 | 1428 | 10 | 0 | 0 | 10 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1423): Show |
chr11 | 18075292 | 18111082 | ||
| a0006c0006 | 0/0 | 1422 | 10 | 9 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0007c0012 | 0/0 | 1422 | 2 | 0 | 1 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0008c0009 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0009c0010 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0010c0011 | 0/0 | 1422 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0011c0014 | 0/0 | 1422 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0012c0019 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0013c0015 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 | ||
| a0014c0017 | 0/0 | 1422 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | ATGGA others(1417): Show |
chr11 | 18075292 | 18111082 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1573 | 150 | 43 | 28 | 57 | 5 | 16 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0001c0001t0002 | 0/0 | 1573 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0001c0007t0001 | 0/0 | 1573 | 8 | 8 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0001c0016t0001 | 0/0 | 1573 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0001c0018t0001 | 0/0 | 1573 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0002c0002t0001 | 0/0 | 1576 | 46 | 1 | 9 | 24 | 3 | 9 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1571): Show |
chr11 | 18075292 | 18111082 |
| a0002c0008t0001 | 0/1 | 1576 | 2 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1571): Show |
chr11 | 18075292 | 18111082 |
| a0002c0013t0001 | 0/0 | 1576 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1571): Show |
chr11 | 18075292 | 18111082 |
| a0003c0003t0001 | 0/0 | 1573 | 29 | 16 | 5 | 2 | 2 | 4 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0004c0004t0001 | 0/0 | 1573 | 13 | 13 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0005c0005t0001 | 0/0 | 1579 | 10 | 0 | 0 | 10 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1574): Show |
chr11 | 18075292 | 18111082 |
| a0006c0006t0001 | 0/0 | 1573 | 10 | 9 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0007c0012t0001 | 0/0 | 1573 | 2 | 0 | 1 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0008c0009t0001 | 0/0 | 1573 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0009c0010t0001 | 0/0 | 1573 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0010c0011t0001 | 0/0 | 1573 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0011c0014t0001 | 0/0 | 1573 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0012c0019t0001 | 0/0 | 1573 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0013c0015t0001 | 0/0 | 1573 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| a0014c0017t0001 | 0/0 | 1573 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | AGCTT others(1568): Show |
chr11 | 18075292 | 18111082 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 46 | 7 | 13 | 17 | 2 | 6 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0005 | 0/0 | 9 | 2 | 4 | 2 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0007 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0007t0001g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0007t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0007t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0016t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0001c0018t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0002 | 0/0 | 16 | 1 | 5 | 7 | 1 | 2 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0004 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0008t0001g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0008t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0002c0013t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0009 | 0/0 | 6 | 0 | 2 | 1 | 0 | 3 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0012 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0004c0004t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0004c0004t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0004c0004t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0004c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0004c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0004c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0004c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0004c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0005c0005t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0005c0005t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0005c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0006c0006t0001g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0006c0006t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0006c0006t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0006c0006t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0006c0006t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0006c0006t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0007c0012t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0008c0009t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0009c0010t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0010c0011t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0011c0014t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0012c0019t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0013c0015t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| a0014c0017t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00099 | hp2 | a0003 | c0003 | t0001 | g0012 | EUR | GBR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00280 | hp1 | a0011 | c0014 | t0001 | g0060 | EUR | FIN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0024 | EUR | FIN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00323 | hp1 | a0003 | c0003 | t0001 | g0012 | EUR | FIN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00438 | hp2 | a0005 | c0005 | t0001 | g0006 | EAS | CHS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00733 | hp2 | a0003 | c0003 | t0001 | g0012 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01081 | hp1 | a0006 | c0006 | t0001 | g0014 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0057 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0012 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01257 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0009 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0012 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01433 | hp2 | a0007 | c0012 | t0001 | g0038 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01884 | hp2 | a0006 | c0006 | t0001 | g0065 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01891 | hp1 | a0004 | c0004 | t0001 | g0069 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0039 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02145 | hp1 | a0006 | c0006 | t0001 | g0063 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0037 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02258 | hp1 | a0001 | c0007 | t0001 | g0008 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02280 | hp1 | a0001 | c0007 | t0001 | g0071 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02280 | hp2 | a0012 | c0019 | t0001 | g0121 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0055 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02451 | hp1 | a0001 | c0007 | t0001 | g0008 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02572 | hp1 | a0001 | c0016 | t0001 | g0119 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02615 | hp1 | a0004 | c0004 | t0001 | g0067 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02615 | hp2 | a0008 | c0009 | t0001 | g0028 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0117 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02647 | hp2 | a0009 | c0010 | t0001 | g0032 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0009 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02717 | hp1 | a0004 | c0004 | t0001 | g0068 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02717 | hp2 | a0001 | c0007 | t0001 | g0008 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02723 | hp1 | a0003 | c0003 | t0001 | g0116 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02723 | hp2 | a0001 | c0007 | t0001 | g0008 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0009 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0049 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02809 | hp2 | a0001 | c0007 | t0001 | g0072 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02886 | hp1 | a0006 | c0006 | t0001 | g0014 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0111 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02895 | hp1 | a0006 | c0006 | t0001 | g0026 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0013 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0013 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02922 | hp1 | a0006 | c0006 | t0001 | g0026 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02922 | hp2 | a0006 | c0006 | t0001 | g0062 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02965 | hp1 | a0004 | c0004 | t0001 | g0066 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02970 | hp2 | a0001 | c0007 | t0001 | g0008 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02976 | hp1 | a0004 | c0004 | t0001 | g0017 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03195 | hp1 | a0003 | c0003 | t0001 | g0115 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03195 | hp2 | a0006 | c0006 | t0001 | g0014 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0114 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0110 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0037 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0118 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0041 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0013 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03491 | hp2 | a0001 | c0018 | t0001 | g0084 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03516 | hp1 | a0001 | c0007 | t0001 | g0008 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03516 | hp2 | a0004 | c0004 | t0001 | g0070 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03540 | hp1 | a0008 | c0009 | t0001 | g0028 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03540 | hp2 | a0004 | c0004 | t0001 | g0018 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03579 | hp2 | a0004 | c0004 | t0001 | g0027 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03688 | hp1 | a0007 | c0012 | t0001 | g0038 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0056 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0009 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18522 | hp1 | a0006 | c0006 | t0001 | g0014 | AFR | YRI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | CHB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18906 | hp2 | a0004 | c0004 | t0001 | g0017 | AFR | YRI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18945 | hp2 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18948 | hp1 | a0010 | c0011 | t0001 | g0025 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18968 | hp1 | a0013 | c0015 | t0001 | g0096 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18968 | hp2 | a0003 | c0003 | t0001 | g0112 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18986 | hp2 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18994 | hp2 | a0010 | c0011 | t0001 | g0025 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19001 | hp1 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19001 | hp2 | a0005 | c0005 | t0001 | g0059 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19043 | hp2 | a0004 | c0004 | t0001 | g0027 | AFR | LWK | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19060 | hp1 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19074 | hp1 | a0005 | c0005 | t0001 | g0058 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19076 | hp2 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19079 | hp1 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19079 | hp2 | a0002 | c0013 | t0001 | g0051 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19091 | hp1 | a0002 | c0008 | t0001 | g0047 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19091 | hp2 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0013 | AFR | YRI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA20129 | hp1 | a0009 | c0010 | t0001 | g0032 | AFR | ASW | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ASW | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA20752 | hp2 | a0014 | c0017 | t0001 | g0076 | EUR | TSI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0053 | EUR | TSI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0022 | SAS | GIH | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | GIH | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02109 | hp2 | a0004 | c0004 | t0001 | g0018 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02486 | hp1 | a0004 | c0004 | t0001 | g0018 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0113 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03471 | hp1 | a0003 | c0003 | t0001 | g0013 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG06807 | hp1 | a0004 | c0004 | t0001 | g0017 | AFR | USA | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | USA | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0039 | AFR | USA | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA20300 | hp2 | a0006 | c0006 | t0001 | g0064 | AFR | USA | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| homoSapiens | chm13v2 | a0002 | c0008 | t0001 | g0040 | REF | REF | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18080426 | G | T | 1 | a0008 | 2 | HG02615.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.1398C>A | p.Asn466Lys | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 12/12 | 1439/1573 | 1398/1425 | 466/474 | chr11 | 18080426 | |||
| chr11:18080467 | G | A | 1 | a0007 | 2 | HG01433.hp2 HG03688.hp1 |
missense_variant | MODERATE | c.1357C>T | p.Arg453Cys | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 12/12 | 1398/1573 | 1357/1425 | 453/474 | chr11 | 18080467 | |||
| chr11:18081467 | T | C | 2 | a0004 a0012 |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
missense_variant | MODERATE | c.1276A>G | p.Ser426Gly | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/12 | 1317/1573 | 1276/1425 | 426/474 | chr11 | 18081467 | |||
| chr11:18083666 | G | T | 1 | a0013 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.1108C>A | p.Pro370Thr | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/12 | 1149/1573 | 1108/1425 | 370/474 | chr11 | 18083666 | |||
| chr11:18086957 | T | G | 1 | a0006 | 10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
missense_variant | MODERATE | c.951A>C | p.Gln317His | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/12 | 992/1573 | 951/1425 | 317/474 | chr11 | 18086957 | |||
| chr11:18086965 | T | C | 2 | a0003 a0007 |
31 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(28): Show |
missense_variant | MODERATE | c.943A>G | p.Ile315Val | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/12 | 984/1573 | 943/1425 | 315/474 | chr11 | 18086965 | |||
| chr11:18086985 | T | C | 1 | a0014 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.923A>G | p.Gln308Arg | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/12 | 964/1573 | 923/1425 | 308/474 | chr11 | 18086985 | |||
| chr11:18087019 | A | T | 1 | a0010 | 2 | NA18948.hp1 NA18994.hp2 |
missense_variant | MODERATE | c.889T>A | p.Leu297Ile | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/12 | 930/1573 | 889/1425 | 297/474 | chr11 | 18087019 | |||
| chr11:18089375 | A | G | 1 | a0002 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.725T>C | p.Val242Ala | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/12 | 766/1573 | 725/1425 | 242/474 | chr11 | 18089375 | |||
| chr11:18090237 | C | T | 1 | a0009 | 2 | HG02647.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.527G>A | p.Arg176Lys | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/12 | 568/1573 | 527/1425 | 176/474 | chr11 | 18090237 | |||
| chr11:18105917 | C | T | 1 | a0011 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.125G>A | p.Gly42Glu | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/12 | 166/1573 | 125/1425 | 42/474 | chr11 | 18105917 | |||
| chr11:18105921 | T | G | 1 | a0012 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.121A>C | p.Ser41Arg | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/12 | 162/1573 | 121/1425 | 41/474 | chr11 | 18105921 | |||
| chr11:18105983 | A | ACCTCCT | 1 | a0005 | 10 | HG00438.hp2 NA18945.hp2 NA18986.hp2 others(7): Show |
conservative_inframe_insertion | MODERATE | c.53_58dupAGGAGG | p.Glu18_Glu19dup | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/12 | 99/1573 | 58/1425 | 20/474 | chr11 | 18105983 | |||
| chr11:18106011 | C | CCGG | 1 | a0002 | 48 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(45): Show |
conservative_inframe_insertion | MODERATE | c.28_30dupCCG | p.Pro10dup | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/12 | 71/1573 | 30/1425 | 10/474 | chr11 | 18106011 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18081470 | A | G | 1 | a0010c0011 | 2 | NA18948.hp1 NA18994.hp2 |
synonymous_variant | LOW | c.1273T>C | p.Leu425Leu | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/12 | 1314/1573 | 1273/1425 | 425/474 | chr11 | 18081470 | |||
| chr11:18083637 | C | T | 1 | a0001c0016 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1137G>A | p.Glu379Glu | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/12 | 1178/1573 | 1137/1425 | 379/474 | chr11 | 18083637 | |||
| chr11:18086945 | T | C | 2 | a0002c0002 a0002c0013 |
47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
synonymous_variant | LOW | c.963A>G | p.Thr321Thr | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/12 | 1004/1573 | 963/1425 | 321/474 | chr11 | 18086945 | |||
| chr11:18089491 | C | A | 2 | a0001c0018 a0012c0019 |
2 | HG02280.hp2 HG03491.hp2 |
synonymous_variant | LOW | c.609G>T | p.Val203Val | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/12 | 650/1573 | 609/1425 | 203/474 | chr11 | 18089491 | |||
| chr11:18103290 | C | T | 2 | a0001c0007 a0008c0009 |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
synonymous_variant | LOW | c.192G>A | p.Glu64Glu | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/12 | 233/1573 | 192/1425 | 64/474 | chr11 | 18103290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18080396 | G | A | 1 | a0001c0001t0002 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 12/12 | 3 | chr11 | 18080396 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:18080564 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1333-73G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/11 | chr11 | 18080564 | |||||||
| chr11:18080685 | C | T | 21 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0022 others(18): Show |
47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.1333-194G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/11 | chr11 | 18080685 | |||||||
| chr11:18080717 | G | A | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1333-226C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/11 | chr11 | 18080717 | |||||||
| chr11:18081164 | G | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(61): Show |
135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1332+247C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/11 | chr11 | 18081164 | |||||||
| chr11:18081182 | C | T | 71 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(68): Show |
153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1332+229G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/11 | chr11 | 18081182 | |||||||
| chr11:18081521 | T | C | 9 | a0002c0002t0001g0004 a0002c0002t0001g0022 a0002c0002t0001g0023 others(6): Show |
19 | HG02015.hp1 HG02129.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.1240-18A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081521 | |||||||
| chr11:18081546 | T | G | 1 | a0002c0002t0001g0041 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1240-43A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081546 | |||||||
| chr11:18081675 | C | T | 9 | a0003c0003t0001g0009 a0003c0003t0001g0012 a0003c0003t0001g0037 others(6): Show |
21 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1240-172G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081675 | |||||||
| chr11:18081702 | C | T | 1 | a0002c0002t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1240-199G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081702 | |||||||
| chr11:18081734 | T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-231A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081734 | |||||||
| chr11:18081783 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-280C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081783 | |||||||
| chr11:18081953 | T | C | 1 | a0002c0002t0001g0057 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1240-450A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081953 | |||||||
| chr11:18082155 | A | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1240-652T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082155 | |||||||
| chr11:18082229 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-726C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082229 | |||||||
| chr11:18082444 | A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-941T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082444 | |||||||
| chr11:18082476 | T | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1240-973A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082476 | |||||||
| chr11:18082518 | T | TTAAATTA others(29): Show |
1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1239+1016_1240-101 others(40): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082518 | |||||||
| chr11:18082544 | A | T | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1239+991T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082544 | |||||||
| chr11:18082547 | A | T | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1239+988T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082547 | |||||||
| chr11:18082589 | G | A | 9 | a0004c0004t0001g0017 a0004c0004t0001g0018 a0004c0004t0001g0027 others(6): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1239+946C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082589 | |||||||
| chr11:18082781 | G | A | 21 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0022 others(18): Show |
47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.1239+754C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082781 | |||||||
| chr11:18082876 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1239+659G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082876 | |||||||
| chr11:18082907 | A | G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1239+628T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082907 | |||||||
| chr11:18083084 | A | G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1239+451T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083084 | |||||||
| chr11:18083124 | G | A | 71 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(68): Show |
153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1239+411C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083124 | |||||||
| chr11:18083178 | G | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1239+357C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083178 | |||||||
| chr11:18083197 | TA | T | 65 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(62): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1239+337delT | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083197 | |||||||
| chr11:18083353 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1239+182C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083353 | |||||||
| chr11:18083396 | A | G | 1 | a0006c0006t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1239+139T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083396 | |||||||
| chr11:18083439 | A | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1239+96T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083439 | |||||||
| chr11:18083480 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1239+55C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083480 | |||||||
| chr11:18083755 | T | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1043-24A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18083755 | |||||||
| chr11:18083793 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0081 others(1): Show |
8 | HG00423.hp1 HG02129.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1043-62A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18083793 | |||||||
| chr11:18084101 | C | A | 1 | a0003c0003t0001g0039 | 2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1043-370G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084101 | |||||||
| chr11:18084179 | G | T | 1 | a0003c0003t0001g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1043-448C>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084179 | |||||||
| chr11:18084324 | C | T | 62 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1043-593G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084324 | |||||||
| chr11:18084350 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0075 |
5 | HG02083.hp2 NA18983.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1043-619T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084350 | |||||||
| chr11:18084357 | C | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(23): Show |
54 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.1043-626G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084357 | |||||||
| chr11:18084493 | T | C | 1 | a0003c0003t0001g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1043-762A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084493 | |||||||
| chr11:18084522 | C | T | 16 | a0001c0016t0001g0119 a0002c0002t0001g0002 a0002c0002t0001g0024 others(13): Show |
35 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1043-791G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084522 | |||||||
| chr11:18084544 | A | C | 1 | a0002c0002t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1043-813T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084544 | |||||||
| chr11:18084608 | C | T | 1 | a0003c0003t0001g0012 | 5 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043-877G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084608 | |||||||
| chr11:18084638 | A | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0036 others(5): Show |
21 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1043-907T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084638 | |||||||
| chr11:18084669 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043-938G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084669 | |||||||
| chr11:18084780 | G | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043-1049C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084780 | |||||||
| chr11:18084815 | G | C | 21 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0078 others(18): Show |
41 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1043-1084C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084815 | |||||||
| chr11:18084864 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1043-1133G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084864 | |||||||
| chr11:18084955 | A | G | 1 | a0005c0005t0001g0059 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1043-1224T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084955 | |||||||
| chr11:18085013 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043-1282C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085013 | |||||||
| chr11:18085050 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1043-1319C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085050 | |||||||
| chr11:18085141 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043-1410C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085141 | |||||||
| chr11:18085184 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043-1453G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085184 | |||||||
| chr11:18085187 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1043-1456A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085187 | |||||||
| chr11:18085202 | G | C | 1 | a0002c0002t0001g0043 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1043-1471C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085202 | |||||||
| chr11:18085383 | T | C | 72 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(69): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1042+1483A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085383 | |||||||
| chr11:18085437 | AT | A | 66 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(63): Show |
144 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.1042+1428delA | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085437 | |||||||
| chr11:18085476 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+1390G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085476 | |||||||
| chr11:18085560 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+1306C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085560 | |||||||
| chr11:18085657 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+1209C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085657 | |||||||
| chr11:18085718 | T | C | 2 | a0004c0004t0001g0068 a0004c0004t0001g0069 |
2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1042+1148A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085718 | |||||||
| chr11:18085725 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1042+1141T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085725 | |||||||
| chr11:18085940 | T | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+926A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085940 | |||||||
| chr11:18085967 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+899G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085967 | |||||||
| chr11:18086031 | T | C | 1 | a0001c0001t0001g0035 | 2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1042+835A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086031 | |||||||
| chr11:18086215 | C | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+651G>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086215 | |||||||
| chr11:18086381 | A | G | 62 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1042+485T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086381 | |||||||
| chr11:18086415 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+451G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086415 | |||||||
| chr11:18086516 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+350G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086516 | |||||||
| chr11:18086524 | A | C | 65 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(62): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1042+342T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086524 | |||||||
| chr11:18086527 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+339G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086527 | |||||||
| chr11:18086608 | C | T | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1042+258G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086608 | |||||||
| chr11:18086653 | A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+213T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086653 | |||||||
| chr11:18086676 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0078 a0001c0001t0001g0079 others(9): Show |
21 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1042+190C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086676 | |||||||
| chr11:18086677 | T | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+189A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086677 | |||||||
| chr11:18086777 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+89C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086777 | |||||||
| chr11:18086798 | A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+68T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086798 | |||||||
| chr11:18087138 | C | A | 1 | a0003c0003t0001g0113 | 1 | HG02559.hp1 | splice_region_variant&intron_variant | LOW | c.853+5G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 8/11 | chr11 | 18087138 | |||||||
| chr11:18087317 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.771-92G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087317 | |||||||
| chr11:18087468 | A | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.771-243T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087468 | |||||||
| chr11:18087510 | A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.771-285T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087510 | |||||||
| chr11:18087512 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.771-287G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087512 | |||||||
| chr11:18087524 | T | G | 1 | a0003c0003t0001g0012 | 5 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.771-299A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087524 | |||||||
| chr11:18087606 | G | A | 1 | a0012c0019t0001g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.771-381C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087606 | |||||||
| chr11:18087606 | G | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.771-381C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087606 | |||||||
| chr11:18087761 | A | G | 4 | a0001c0007t0001g0008 a0001c0007t0001g0071 a0001c0007t0001g0072 others(1): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.771-536T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087761 | |||||||
| chr11:18087796 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0036 others(5): Show |
21 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.771-571C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087796 | |||||||
| chr11:18087888 | A | G | 1 | a0006c0006t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.771-663T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087888 | |||||||
| chr11:18087893 | C | G | 21 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0022 others(18): Show |
47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.771-668G>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087893 | |||||||
| chr11:18087928 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.771-703C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087928 | |||||||
| chr11:18088084 | A | G | 1 | a0002c0002t0001g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.771-859T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088084 | |||||||
| chr11:18088136 | C | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.771-911G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088136 | |||||||
| chr11:18088136 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.771-911G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088136 | |||||||
| chr11:18088148 | A | G | 1 | a0010c0011t0001g0025 | 2 | NA18948.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.771-923T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088148 | |||||||
| chr11:18088436 | T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+894A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088436 | |||||||
| chr11:18088459 | T | C | 1 | a0002c0002t0001g0022 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.770+871A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088459 | |||||||
| chr11:18088562 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0108 |
2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.770+768G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088562 | |||||||
| chr11:18088592 | T | A | 71 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(68): Show |
153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.770+738A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088592 | |||||||
| chr11:18088720 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+610C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088720 | |||||||
| chr11:18088797 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+533C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088797 | |||||||
| chr11:18088887 | A | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0036 others(5): Show |
21 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.770+443T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088887 | |||||||
| chr11:18088906 | T | C | 1 | a0010c0011t0001g0025 | 2 | NA18948.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.770+424A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088906 | |||||||
| chr11:18088934 | C | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0108 others(1): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.770+396G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088934 | |||||||
| chr11:18088956 | A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+374T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088956 | |||||||
| chr11:18089095 | G | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.770+235C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18089095 | |||||||
| chr11:18089216 | G | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+114C>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18089216 | |||||||
| chr11:18089241 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.770+89A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18089241 | |||||||
| chr11:18089289 | T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+41A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18089289 | |||||||
| chr11:18089531 | A | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.590-21T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089531 | |||||||
| chr11:18089592 | T | G | 6 | a0006c0006t0001g0014 a0006c0006t0001g0026 a0006c0006t0001g0062 others(3): Show |
10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.590-82A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089592 | |||||||
| chr11:18089670 | C | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.590-160G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089670 | |||||||
| chr11:18089699 | C | T | 1 | a0006c0006t0001g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.590-189G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089699 | |||||||
| chr11:18089794 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.590-284G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089794 | |||||||
| chr11:18089841 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.590-331G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089841 | |||||||
| chr11:18089927 | A | G | 4 | a0002c0002t0001g0024 a0002c0002t0001g0055 a0002c0002t0001g0056 others(1): Show |
5 | HG00280.hp2 HG01081.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.589+248T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089927 | |||||||
| chr11:18089970 | A | C | 65 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(62): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.589+205T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089970 | |||||||
| chr11:18089971 | T | C | 65 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(62): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.589+204A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089971 | |||||||
| chr11:18090084 | T | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.589+91A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18090084 | |||||||
| chr11:18090145 | A | AT | 64 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(61): Show |
135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.589+29dupA | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18090145 | |||||||
| chr11:18090145 | A | ATT | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.589+28_589+29dupAA | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18090145 | |||||||
| chr11:18090325 | C | CA | 4 | a0001c0001t0001g0010 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
8 | HG01255.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.474-36dupT | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 5/11 | chr11 | 18090325 | |||||||
| chr11:18090325 | CA | C | 5 | a0001c0001t0001g0020 a0002c0002t0001g0044 a0002c0002t0001g0045 others(2): Show |
7 | HG01099.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-36delT | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 5/11 | chr11 | 18090325 | |||||||
| chr11:18090326 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.474-36T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 5/11 | chr11 | 18090326 | |||||||
| chr11:18090417 | T | TAAAAGGA others(23): Show |
1 | a0012c0019t0001g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.460_473+16dupCTGGA others(25): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 5/11 | chr11 | 18090417 | |||||||
| chr11:18090515 | C | T | 6 | a0006c0006t0001g0014 a0006c0006t0001g0026 a0006c0006t0001g0062 others(3): Show |
10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-22G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18090515 | |||||||
| chr11:18090650 | C | T | 9 | a0003c0003t0001g0009 a0003c0003t0001g0012 a0003c0003t0001g0037 others(6): Show |
21 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.414-157G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18090650 | |||||||
| chr11:18090659 | G | A | 62 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.414-166C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18090659 | |||||||
| chr11:18090779 | T | C | 1 | a0003c0003t0001g0114 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.414-286A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18090779 | |||||||
| chr11:18091137 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.414-644G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091137 | |||||||
| chr11:18091137 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.414-644G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091137 | |||||||
| chr11:18091226 | T | C | 3 | a0002c0002t0001g0023 a0002c0002t0001g0044 a0002c0002t0001g0045 |
4 | NA18981.hp1 NA19009.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-733A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091226 | |||||||
| chr11:18091235 | G | C | 1 | a0003c0003t0001g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414-742C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091235 | |||||||
| chr11:18091253 | A | ACTATT | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.414-761_414-760ins others(5): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091253 | |||||||
| chr11:18091318 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.414-825G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091318 | |||||||
| chr11:18091329 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.414-836G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091329 | |||||||
| chr11:18091781 | T | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.413+464A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091781 | |||||||
| chr11:18091802 | G | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.413+443C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091802 | |||||||
| chr11:18091908 | G | A | 3 | a0004c0004t0001g0017 a0004c0004t0001g0066 a0004c0004t0001g0067 |
5 | HG02615.hp1 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+337C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091908 | |||||||
| chr11:18092071 | G | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.413+174C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18092071 | |||||||
| chr11:18092114 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.413+131T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18092114 | |||||||
| chr11:18092116 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.413+129A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18092116 | |||||||
| chr11:18092406 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-82C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18092406 | |||||||
| chr11:18092653 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-329C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18092653 | |||||||
| chr11:18092891 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-567C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18092891 | |||||||
| chr11:18092960 | T | TAAAAGTA others(303): Show |
1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-637_334-636ins others(310): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18092960 | |||||||
| chr11:18092991 | A | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-667T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18092991 | |||||||
| chr11:18092992 | A | C | 1 | a0012c0019t0001g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.334-668T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18092992 | |||||||
| chr11:18093000 | T | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.334-676A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093000 | |||||||
| chr11:18093032 | G | A | 34 | a0001c0007t0001g0008 a0001c0007t0001g0071 a0001c0007t0001g0072 others(31): Show |
71 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.334-708C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093032 | |||||||
| chr11:18093087 | T | A | 4 | a0001c0007t0001g0008 a0001c0007t0001g0071 a0001c0007t0001g0072 others(1): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.334-763A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093087 | |||||||
| chr11:18093099 | G | A | 71 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(68): Show |
153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.334-775C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093099 | |||||||
| chr11:18093147 | G | A | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-823C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093147 | |||||||
| chr11:18093153 | C | T | 20 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0078 others(17): Show |
40 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.334-829G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093153 | |||||||
| chr11:18093154 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-830C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093154 | |||||||
| chr11:18093157 | A | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(57): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.334-833T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093157 | |||||||
| chr11:18093170 | C | T | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-846G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093170 | |||||||
| chr11:18093250 | A | T | 1 | a0001c0001t0001g0108 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.334-926T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093250 | |||||||
| chr11:18093329 | T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-1005A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093329 | |||||||
| chr11:18093463 | C | A | 1 | a0012c0019t0001g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.334-1139G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093463 | |||||||
| chr11:18093574 | G | T | 60 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(57): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.334-1250C>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093574 | |||||||
| chr11:18093619 | T | C | 4 | a0001c0001t0001g0007 a0004c0004t0001g0017 a0004c0004t0001g0066 others(1): Show |
13 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.334-1295A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093619 | |||||||
| chr11:18093669 | G | A | 1 | a0002c0002t0001g0054 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.334-1345C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093669 | |||||||
| chr11:18093720 | C | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-1396G>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093720 | |||||||
| chr11:18094073 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0073 others(4): Show |
19 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.334-1749A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094073 | |||||||
| chr11:18094106 | TTTCCAGG others(13): Show |
T | 1 | a0003c0003t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.334-1802_334-1783d others(22): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094106 | |||||||
| chr11:18094210 | A | G | 1 | a0010c0011t0001g0025 | 2 | NA18948.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.334-1886T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094210 | |||||||
| chr11:18094278 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0108 others(1): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.334-1954A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094278 | |||||||
| chr11:18094464 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-2140C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094464 | |||||||
| chr11:18094526 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.334-2202C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094526 | |||||||
| chr11:18094567 | A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+2204T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094567 | |||||||
| chr11:18094603 | T | C | 21 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0022 others(18): Show |
47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.333+2168A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094603 | |||||||
| chr11:18094631 | T | C | 1 | a0005c0005t0001g0059 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.333+2140A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094631 | |||||||
| chr11:18094689 | A | C | 1 | a0002c0002t0001g0050 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.333+2082T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094689 | |||||||
| chr11:18094725 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.333+2046G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094725 | |||||||
| chr11:18094749 | G | A | 6 | a0006c0006t0001g0014 a0006c0006t0001g0026 a0006c0006t0001g0062 others(3): Show |
10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.333+2022C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094749 | |||||||
| chr11:18094913 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+1858C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094913 | |||||||
| chr11:18094913 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.333+1858C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094913 | |||||||
| chr11:18094955 | C | T | 1 | a0004c0004t0001g0018 | 3 | HG02109.hp2 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.333+1816G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094955 | |||||||
| chr11:18094956 | T | C | 1 | a0001c0001t0001g0021 | 3 | HG00735.hp1 HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.333+1815A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094956 | |||||||
| chr11:18095106 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+1665C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095106 | |||||||
| chr11:18095159 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+1612G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095159 | |||||||
| chr11:18095168 | T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+1603A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095168 | |||||||
| chr11:18095210 | G | A | 1 | a0001c0007t0001g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.333+1561C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095210 | |||||||
| chr11:18095220 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+1551C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095220 | |||||||
| chr11:18095331 | T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+1440A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095331 | |||||||
| chr11:18095333 | A | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.333+1438T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095333 | |||||||
| chr11:18095347 | A | G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.333+1424T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095347 | |||||||
| chr11:18095386 | G | A | 13 | a0001c0007t0001g0008 a0001c0007t0001g0071 a0001c0007t0001g0072 others(10): Show |
24 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.333+1385C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095386 | |||||||
| chr11:18095463 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.333+1308G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095463 | |||||||
| chr11:18095530 | A | G | 1 | a0010c0011t0001g0025 | 2 | NA18948.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.333+1241T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095530 | |||||||
| chr11:18095622 | C | T | 1 | a0006c0006t0001g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.333+1149G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095622 | |||||||
| chr11:18095701 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
12 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.333+1070A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095701 | |||||||
| chr11:18095815 | A | G | 21 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0022 others(18): Show |
47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.333+956T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095815 | |||||||
| chr11:18095855 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+916C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095855 | |||||||
| chr11:18095947 | G | A | 1 | a0006c0006t0001g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.333+824C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095947 | |||||||
| chr11:18095969 | C | T | 20 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0078 others(17): Show |
40 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.333+802G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095969 | |||||||
| chr11:18095998 | A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+773T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095998 | |||||||
| chr11:18096011 | G | A | 9 | a0003c0003t0001g0009 a0003c0003t0001g0012 a0003c0003t0001g0037 others(6): Show |
21 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.333+760C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096011 | |||||||
| chr11:18096077 | T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+694A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096077 | |||||||
| chr11:18096096 | A | AGGGGGGG others(18): Show |
1 | a0003c0003t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.333+674_333+675ins others(25): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096096 | |||||||
| chr11:18096098 | A | G | 1 | a0003c0003t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.333+673T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096098 | |||||||
| chr11:18096101 | A | G | 1 | a0003c0003t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.333+670T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096101 | |||||||
| chr11:18096102 | A | G | 1 | a0003c0003t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.333+669T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096102 | |||||||
| chr11:18096103 | T | G | 1 | a0003c0003t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.333+668A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096103 | |||||||
| chr11:18096224 | C | T | 1 | a0002c0002t0001g0055 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.333+547G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096224 | |||||||
| chr11:18096250 | T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+521A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096250 | |||||||
| chr11:18096274 | A | G | 21 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0022 others(18): Show |
47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.333+497T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096274 | |||||||
| chr11:18096281 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.333+490T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096281 | |||||||
| chr11:18096318 | G | A | 2 | a0001c0001t0001g0061 a0001c0016t0001g0119 |
2 | HG02572.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.333+453C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096318 | |||||||
| chr11:18096329 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0090 |
6 | NA18963.hp1 NA19011.hp2 NA19057.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+442G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096329 | |||||||
| chr11:18096334 | C | A | 1 | a0003c0003t0001g0116 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.333+437G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096334 | |||||||
| chr11:18096353 | G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+418C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096353 | |||||||
| chr11:18096463 | C | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+308G>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096463 | |||||||
| chr11:18096532 | G | A | 20 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0078 others(17): Show |
40 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.333+239C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096532 | |||||||
| chr11:18096575 | C | A | 1 | a0001c0018t0001g0084 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.333+196G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096575 | |||||||
| chr11:18096599 | T | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.333+172A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096599 | |||||||
| chr11:18096615 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.333+156T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096615 | |||||||
| chr11:18096906 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.250-52G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18096906 | |||||||
| chr11:18096915 | C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.250-61G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18096915 | |||||||
| chr11:18096953 | A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.250-99T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18096953 | |||||||
| chr11:18096954 | C | T | 5 | a0002c0002t0001g0024 a0002c0002t0001g0049 a0002c0002t0001g0055 others(2): Show |
6 | HG00280.hp2 HG01081.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.250-100G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18096954 | |||||||
| chr11:18096961 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0073 others(4): Show |
19 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.250-107G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18096961 | |||||||
| chr11:18096991 | A | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.250-137T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18096991 | |||||||
| chr11:18097092 | C | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0073 others(4): Show |
19 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.250-238G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097092 | |||||||
| chr11:18097094 | G | A | 4 | a0001c0007t0001g0008 a0001c0007t0001g0071 a0001c0007t0001g0072 others(1): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.250-240C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097094 | |||||||
| chr11:18097132 | G | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(38): Show |
85 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.250-278C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097132 | |||||||
| chr11:18097177 | C | T | 15 | a0003c0003t0001g0009 a0003c0003t0001g0012 a0003c0003t0001g0013 others(12): Show |
31 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.250-323G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097177 | |||||||
| chr11:18097266 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
9 | HG01255.hp1 HG02451.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-412T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097266 | |||||||
| chr11:18097343 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0036 others(5): Show |
21 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.250-489A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097343 | |||||||
| chr11:18097684 | C | T | 1 | a0003c0003t0001g0112 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.250-830G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097684 | |||||||
| chr11:18097773 | A | G | 65 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(62): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.250-919T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097773 | |||||||
| chr11:18097826 | C | G | 2 | a0001c0001t0001g0007 a0001c0016t0001g0119 |
9 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-972G>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097826 | |||||||
| chr11:18097838 | GA | G | 59 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(56): Show |
122 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(119): Show |
intron_variant | MODIFIER | c.250-985delT | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097838 | |||||||
| chr11:18097838 | GAA | G | 10 | a0001c0001t0001g0108 a0003c0003t0001g0009 a0003c0003t0001g0012 others(7): Show |
22 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.250-986_250-985del others(2): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097838 | |||||||
| chr11:18097851 | A | C | 21 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0022 others(18): Show |
47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.250-997T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097851 | |||||||
| chr11:18097872 | AGGT | A | 62 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.250-1021_250-1019d others(5): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097872 | |||||||
| chr11:18097894 | T | C | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-1040A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097894 | |||||||
| chr11:18097963 | T | C | 13 | a0001c0007t0001g0008 a0001c0007t0001g0071 a0001c0007t0001g0072 others(10): Show |
24 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.250-1109A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097963 | |||||||
| chr11:18097983 | A | C | 6 | a0006c0006t0001g0014 a0006c0006t0001g0026 a0006c0006t0001g0062 others(3): Show |
10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.250-1129T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097983 | |||||||
| chr11:18098199 | G | C | 21 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0022 others(18): Show |
47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.250-1345C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098199 | |||||||
| chr11:18098202 | A | T | 1 | a0001c0001t0001g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.250-1348T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098202 | |||||||
| chr11:18098337 | C | T | 28 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(25): Show |
61 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.250-1483G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098337 | |||||||
| chr11:18098341 | A | G | 1 | a0003c0003t0001g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.250-1487T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098341 | |||||||
| chr11:18098348 | G | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.250-1494C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098348 | |||||||
| chr11:18098447 | C | A | 1 | a0002c0002t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.250-1593G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098447 | |||||||
| chr11:18098605 | G | A | 1 | a0004c0004t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.250-1751C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098605 | |||||||
| chr11:18098661 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.250-1807C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098661 | |||||||
| chr11:18098789 | C | A | 1 | a0001c0001t0001g0036 | 2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.250-1935G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098789 | |||||||
| chr11:18098969 | T | C | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-2115A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098969 | |||||||
| chr11:18099079 | C | CAT | 65 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(62): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.250-2227_250-2226d others(4): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099079 | |||||||
| chr11:18099100 | T | C | 22 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0022 others(19): Show |
48 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.250-2246A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099100 | |||||||
| chr11:18099278 | C | A | 2 | a0004c0004t0001g0017 a0004c0004t0001g0066 |
4 | HG02965.hp1 HG02976.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-2424G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099278 | |||||||
| chr11:18099325 | T | C | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-2471A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099325 | |||||||
| chr11:18099371 | T | C | 4 | a0002c0002t0001g0024 a0002c0002t0001g0055 a0002c0002t0001g0056 others(1): Show |
5 | HG00280.hp2 HG01081.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-2517A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099371 | |||||||
| chr11:18099537 | C | T | 1 | a0001c0001t0001g0015 | 4 | HG02132.hp2 NA18963.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-2683G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099537 | |||||||
| chr11:18099547 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.250-2693A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099547 | |||||||
| chr11:18099601 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.250-2747C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099601 | |||||||
| chr11:18099721 | GACATTGA others(1): Show |
G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.250-2875_250-2868d others(10): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099721 | |||||||
| chr11:18099745 | A | G | 1 | a0004c0004t0001g0066 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250-2891T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099745 | |||||||
| chr11:18099943 | G | A | 21 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0022 others(18): Show |
47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.250-3089C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099943 | |||||||
| chr11:18099992 | G | A | 12 | a0002c0002t0001g0002 a0002c0002t0001g0024 a0002c0002t0001g0048 others(9): Show |
28 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.250-3138C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099992 | |||||||
| chr11:18100006 | A | G | 1 | a0002c0002t0001g0048 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.250-3152T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18100006 | |||||||
| chr11:18100047 | G | A | 1 | a0001c0007t0001g0072 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.249+3186C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18100047 | |||||||
| chr11:18100402 | A | G | 1 | a0002c0002t0001g0022 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.249+2831T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18100402 | |||||||
| chr11:18100452 | G | A | 1 | a0004c0004t0001g0069 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.249+2781C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18100452 | |||||||
| chr11:18100888 | A | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+2345T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18100888 | |||||||
| chr11:18100958 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.249+2275T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18100958 | |||||||
| chr11:18101000 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.249+2233G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101000 | |||||||
| chr11:18101252 | C | CGT | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+1979_249+1980d others(4): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101252 | |||||||
| chr11:18101253 | G | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+1980C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101253 | |||||||
| chr11:18101351 | G | C | 1 | a0001c0001t0001g0102 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.249+1882C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101351 | |||||||
| chr11:18101379 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+1854G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101379 | |||||||
| chr11:18101384 | G | A | 21 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0022 others(18): Show |
47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.249+1849C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101384 | |||||||
| chr11:18101450 | G | A | 12 | a0002c0002t0001g0002 a0002c0002t0001g0024 a0002c0002t0001g0048 others(9): Show |
28 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.249+1783C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101450 | |||||||
| chr11:18101467 | C | T | 12 | a0002c0002t0001g0002 a0002c0002t0001g0024 a0002c0002t0001g0048 others(9): Show |
28 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.249+1766G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101467 | |||||||
| chr11:18101506 | C | T | 8 | a0004c0004t0001g0017 a0004c0004t0001g0018 a0004c0004t0001g0027 others(5): Show |
13 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.249+1727G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101506 | |||||||
| chr11:18101530 | T | C | 4 | a0001c0007t0001g0008 a0001c0007t0001g0071 a0001c0007t0001g0072 others(1): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+1703A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101530 | |||||||
| chr11:18101579 | A | G | 1 | a0004c0004t0001g0027 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.249+1654T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101579 | |||||||
| chr11:18101820 | TAA | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0036 others(56): Show |
124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.249+1411_249+1412d others(4): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101820 | |||||||
| chr11:18101820 | TAAA | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
9 | HG02257.hp2 HG02258.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+1410_249+1412d others(5): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101820 | |||||||
| chr11:18101857 | GGAT | G | 21 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0022 others(18): Show |
47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.249+1373_249+1375d others(5): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101857 | |||||||
| chr11:18102005 | G | A | 1 | a0003c0003t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.249+1228C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102005 | |||||||
| chr11:18102045 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+1188G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102045 | |||||||
| chr11:18102083 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0085 others(1): Show |
14 | HG00408.hp2 HG00438.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+1150T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102083 | |||||||
| chr11:18102127 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.249+1106A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102127 | |||||||
| chr11:18102167 | C | T | 1 | a0005c0005t0001g0058 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.249+1066G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102167 | |||||||
| chr11:18102171 | GA | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0083 a0001c0018t0001g0084 |
4 | HG01257.hp1 HG01258.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+1061delT | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102171 | |||||||
| chr11:18102179 | A | C | 6 | a0006c0006t0001g0014 a0006c0006t0001g0026 a0006c0006t0001g0062 others(3): Show |
10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+1054T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102179 | |||||||
| chr11:18102212 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.249+1021C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102212 | |||||||
| chr11:18102239 | T | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+994A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102239 | |||||||
| chr11:18102261 | G | A | 1 | a0010c0011t0001g0025 | 2 | NA18948.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.249+972C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102261 | |||||||
| chr11:18102271 | T | G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+962A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102271 | |||||||
| chr11:18102299 | C | G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+934G>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102299 | |||||||
| chr11:18102313 | A | C | 1 | a0003c0003t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.249+920T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102313 | |||||||
| chr11:18102333 | C | T | 1 | a0010c0011t0001g0025 | 2 | NA18948.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.249+900G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102333 | |||||||
| chr11:18102356 | C | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0073 others(39): Show |
91 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.249+877G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102356 | |||||||
| chr11:18102446 | G | GT | 21 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0077 others(18): Show |
42 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.249+786dupA | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102446 | |||||||
| chr11:18102562 | A | C | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+671T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102562 | |||||||
| chr11:18102572 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.249+661C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102572 | |||||||
| chr11:18102575 | T | TG | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+657dupC | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102575 | |||||||
| chr11:18102940 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.249+293G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102940 | |||||||
| chr11:18103002 | T | A | 1 | a0004c0004t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.249+231A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18103002 | |||||||
| chr11:18103177 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.249+56A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18103177 | |||||||
| chr11:18103441 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.136-95C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18103441 | |||||||
| chr11:18103497 | T | C | 1 | a0001c0001t0001g0035 | 2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.136-151A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18103497 | |||||||
| chr11:18103571 | A | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.136-225T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18103571 | |||||||
| chr11:18103585 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.136-239C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18103585 | |||||||
| chr11:18103696 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.136-350G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18103696 | |||||||
| chr11:18103905 | A | T | 1 | a0002c0002t0001g0041 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.136-559T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18103905 | |||||||
| chr11:18104126 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.136-780A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104126 | |||||||
| chr11:18104347 | A | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0108 others(1): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-1001T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104347 | |||||||
| chr11:18104390 | A | T | 1 | a0011c0014t0001g0060 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.136-1044T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104390 | |||||||
| chr11:18104401 | T | C | 12 | a0002c0002t0001g0002 a0002c0002t0001g0024 a0002c0002t0001g0048 others(9): Show |
28 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.136-1055A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104401 | |||||||
| chr11:18104440 | C | CT | 56 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(53): Show |
122 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.136-1095dupA | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104440 | |||||||
| chr11:18104440 | C | CTT | 4 | a0004c0004t0001g0018 a0004c0004t0001g0068 a0004c0004t0001g0069 others(1): Show |
6 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-1096_136-1095d others(4): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104440 | |||||||
| chr11:18104550 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0108 others(1): Show |
9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-1204T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104550 | |||||||
| chr11:18104744 | T | C | 58 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0036 others(55): Show |
124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.135+1163A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104744 | |||||||
| chr11:18104753 | G | A | 1 | a0003c0003t0001g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.135+1154C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104753 | |||||||
| chr11:18104944 | G | A | 60 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0011 others(57): Show |
134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.135+963C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104944 | |||||||
| chr11:18104947 | G | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0011 others(57): Show |
134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.135+960C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104947 | |||||||
| chr11:18105222 | T | C | 1 | a0003c0003t0001g0118 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.135+685A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105222 | |||||||
| chr11:18105332 | C | CT | 9 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0073 others(6): Show |
21 | HG00733.hp1 HG01106.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+574dupA | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105332 | |||||||
| chr11:18105332 | CTT | C | 5 | a0001c0001t0001g0007 a0006c0006t0001g0014 a0006c0006t0001g0064 others(2): Show |
16 | HG00639.hp1 HG01081.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.135+573_135+574del others(2): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105332 | |||||||
| chr11:18105359 | G | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0108 others(16): Show |
40 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.135+548C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105359 | |||||||
| chr11:18105385 | G | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.135+522C>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105385 | |||||||
| chr11:18105454 | TG | T | 12 | a0001c0007t0001g0008 a0001c0007t0001g0071 a0001c0007t0001g0072 others(9): Show |
23 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.135+452delC | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105454 | |||||||
| chr11:18105671 | T | C | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+236A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105671 | |||||||
| chr11:18105705 | T | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.135+202A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105705 | |||||||
| chr11:18105723 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.135+184C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105723 | |||||||
| chr11:18105724 | G | T | 6 | a0006c0006t0001g0014 a0006c0006t0001g0026 a0006c0006t0001g0062 others(3): Show |
10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+183C>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105724 | |||||||
| chr11:18105762 | C | T | 2 | a0001c0001t0001g0007 a0010c0011t0001g0025 |
10 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+145G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105762 | |||||||
| chr11:18105885 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.135+22G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105885 |