Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79053 |
| ensemblid | ENSG00000159063.14 |
| hgncid | 23161 |
| symbol | ALG8 |
| name | ALG8 alpha-1,3-glucosyltransferase |
| refseq_nuc | NM_024079.5 |
| refseq_prot | NP_076984.2 |
| ensembl_nuc | ENST00000299626.10 |
| ensembl_prot | ENSP00000299626.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 78100946 |
| end | 78139626 |
| strand | - |
| ver | v1.2 |
| region | chr11:78100946-78139626 |
| region5000 | chr11:78095946-78144626 |
| regionname0 | ALG8_chr11_78100946_78139626 |
| regionname5000 | ALG8_chr11_78095946_78144626 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 526 | 338 | 77 | 55 | 161 | 8 | 36 | 129 | ALG8_chr11_78095946_78144626 | ALG8 | MAALT others(521): Show |
chr11 | 78095946 | 78144626 |
| a0002 | 0/1 | 526 | 53 | 4 | 16 | 23 | 4 | 5 | 14 | ALG8_chr11_78095946_78144626 | ALG8 | MAALT others(521): Show |
chr11 | 78095946 | 78144626 |
| a0003 | 0/0 | 526 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | MAALT others(521): Show |
chr11 | 78095946 | 78144626 |
| a0004 | 0/0 | 526 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | MAALT others(521): Show |
chr11 | 78095946 | 78144626 |
| a0005 | 0/0 | 526 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | MAALT others(521): Show |
chr11 | 78095946 | 78144626 |
| a0006 | 0/0 | 526 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | MAALT others(521): Show |
chr11 | 78095946 | 78144626 |
| a0007 | 0/0 | 526 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | MAALT others(521): Show |
chr11 | 78095946 | 78144626 |
| a0008 | 0/0 | 526 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | MAALT others(521): Show |
chr11 | 78095946 | 78144626 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1578 | 326 | 67 | 54 | 160 | 8 | 36 | ALG8_chr11_78095946_78144626 | ALG8 | ATGGC others(1573): Show |
chr11 | 78095946 | 78144626 | ||
| a0001c0003 | 0/0 | 1578 | 11 | 10 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | ATGGC others(1573): Show |
chr11 | 78095946 | 78144626 | ||
| a0001c0009 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | ATGGC others(1573): Show |
chr11 | 78095946 | 78144626 | ||
| a0002c0002 | 0/1 | 1578 | 53 | 4 | 16 | 23 | 4 | 5 | ALG8_chr11_78095946_78144626 | ALG8 | ATGGC others(1573): Show |
chr11 | 78095946 | 78144626 | ||
| a0003c0004 | 0/0 | 1578 | 5 | 5 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | ATGGC others(1573): Show |
chr11 | 78095946 | 78144626 | ||
| a0004c0005 | 0/0 | 1578 | 2 | 0 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | ATGGC others(1573): Show |
chr11 | 78095946 | 78144626 | ||
| a0005c0008 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | ATGGC others(1573): Show |
chr11 | 78095946 | 78144626 | ||
| a0006c0006 | 0/0 | 1578 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | ATGGC others(1573): Show |
chr11 | 78095946 | 78144626 | ||
| a0007c0007 | 0/0 | 1578 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | ATGGC others(1573): Show |
chr11 | 78095946 | 78144626 | ||
| a0008c0010 | 0/0 | 1578 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | ATGGC others(1573): Show |
chr11 | 78095946 | 78144626 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1637 | 326 | 67 | 54 | 160 | 8 | 36 | ALG8_chr11_78095946_78144626 | ALG8 | GTGGA others(1632): Show |
chr11 | 78095946 | 78144626 |
| a0001c0003t0001 | 0/0 | 1637 | 11 | 10 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | GTGGA others(1632): Show |
chr11 | 78095946 | 78144626 |
| a0001c0009t0001 | 0/0 | 1637 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | GTGGA others(1632): Show |
chr11 | 78095946 | 78144626 |
| a0002c0002t0001 | 0/1 | 1637 | 52 | 4 | 16 | 22 | 4 | 5 | ALG8_chr11_78095946_78144626 | ALG8 | GTGGA others(1632): Show |
chr11 | 78095946 | 78144626 |
| a0002c0002t0002 | 0/0 | 1637 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | GTGGA others(1632): Show |
chr11 | 78095946 | 78144626 |
| a0003c0004t0001 | 0/0 | 1637 | 5 | 5 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | GTGGA others(1632): Show |
chr11 | 78095946 | 78144626 |
| a0004c0005t0001 | 0/0 | 1637 | 2 | 0 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | GTGGA others(1632): Show |
chr11 | 78095946 | 78144626 |
| a0005c0008t0001 | 0/0 | 1637 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | GTGGA others(1632): Show |
chr11 | 78095946 | 78144626 |
| a0006c0006t0001 | 0/0 | 1637 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | GTGGA others(1632): Show |
chr11 | 78095946 | 78144626 |
| a0007c0007t0001 | 0/0 | 1637 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | GTGGA others(1632): Show |
chr11 | 78095946 | 78144626 |
| a0008c0010t0001 | 0/0 | 1637 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | GTGGA others(1632): Show |
chr11 | 78095946 | 78144626 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0002 | 0/0 | 7 | 1 | 0 | 5 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0001c0009t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0010 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0002c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0003c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0003c0004t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0003c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0003c0004t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0003c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0004c0005t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0004c0005t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0005c0008t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0006c0006t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0007c0007t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| a0008c0010t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0341 | EUR | GBR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0193 | EUR | GBR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0208 | EUR | GBR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | FIN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | FIN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00621 | hp1 | a0005 | c0008 | t0001 | g0203 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG00738 | hp2 | a0004 | c0005 | t0001 | g0257 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0111 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0207 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0196 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0200 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01358 | hp1 | a0006 | c0006 | t0001 | g0273 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0205 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0030 | EUR | IBS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | IBS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0199 | EUR | IBS | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0201 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02148 | hp1 | a0004 | c0005 | t0001 | g0258 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CDX | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | CDX | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0185 | AMR | PEL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02451 | hp1 | a0003 | c0004 | t0001 | g0244 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02630 | hp2 | a0003 | c0004 | t0001 | g0227 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0112 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0189 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0204 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02809 | hp1 | a0003 | c0004 | t0001 | g0226 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0110 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0105 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03098 | hp1 | a0003 | c0004 | t0001 | g0228 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0104 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03225 | hp2 | a0003 | c0004 | t0001 | g0224 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0113 | AFR | ESN | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0191 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0253 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0254 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04228 | hp1 | a0007 | c0007 | t0001 | g0098 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | STU | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | YRI | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0345 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18983 | hp2 | a0008 | c0010 | t0001 | g0087 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18986 | hp2 | a0001 | c0009 | t0001 | g0289 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0348 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0108 | AFR | LWK | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0346 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | YRI | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | GIH | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0195 | AMR | CLM | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0210 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | USA | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0036 | AFR | USA | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | USA | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0216 | REF | REF | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0162 | REF | REF | ALG8_chr11_78095946_78144626 | ALG8 | chr11 | 78095946 | 78144626 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:78101029 | C | T | 1 | a0007 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1516G>A | p.Ala506Thr | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 13/13 | 1554/1637 | 1516/1581 | 506/526 | chr11 | 78101029 | |||
| chr11:78101031 | T | C | 1 | a0005 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1514A>G | p.Tyr505Cys | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 13/13 | 1552/1637 | 1514/1581 | 505/526 | chr11 | 78101031 | |||
| chr11:78104013 | A | G | 1 | a0004 | 2 | HG00738.hp2 HG02148.hp1 |
missense_variant | MODERATE | c.1316T>C | p.Ile439Thr | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/13 | 1354/1637 | 1316/1581 | 439/526 | chr11 | 78104013 | |||
| chr11:78112652 | A | G | 1 | a0003 | 5 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.896T>C | p.Ile299Thr | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/13 | 934/1637 | 896/1581 | 299/526 | chr11 | 78112652 | |||
| chr11:78112745 | C | T | 1 | a0006 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.803G>A | p.Arg268Gln | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/13 | 841/1637 | 803/1581 | 268/526 | chr11 | 78112745 | |||
| chr11:78114274 | T | C | 2 | a0002 a0005 |
53 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(50): Show |
missense_variant | MODERATE | c.665A>G | p.Asn222Ser | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/13 | 703/1637 | 665/1581 | 222/526 | chr11 | 78114274 | |||
| chr11:78127378 | T | C | 1 | a0008 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.154A>G | p.Ile52Val | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/13 | 192/1637 | 154/1581 | 52/526 | chr11 | 78127378 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:78112686 | A | G | 1 | a0001c0003 | 11 | HG01081.hp2 HG02622.hp1 HG02647.hp2 others(8): Show |
synonymous_variant | LOW | c.862T>C | p.Leu288Leu | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/13 | 900/1637 | 862/1581 | 288/526 | chr11 | 78112686 | |||
| chr11:78121078 | T | C | 1 | a0001c0009 | 1 | NA18986.hp2 | synonymous_variant | LOW | c.465A>G | p.Leu155Leu | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/13 | 503/1637 | 465/1581 | 155/526 | chr11 | 78121078 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:78139595 | G | A | 1 | a0002c0002t0002 | 1 | NA19011.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/13 | chr11 | 78139595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:78101260 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1350-65A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101260 | |||||||
| chr11:78101277 | T | A | 6 | a0001c0003t0001g0104 a0001c0003t0001g0105 a0001c0003t0001g0110 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350-82A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101277 | |||||||
| chr11:78101474 | CA | C | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1350-280delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101474 | |||||||
| chr11:78101483 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1350-288C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101483 | |||||||
| chr11:78101516 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1350-321G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101516 | |||||||
| chr11:78101517 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1350-322A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101517 | |||||||
| chr11:78101597 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1350-402G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101597 | |||||||
| chr11:78101741 | G | A | 8 | a0001c0001t0001g0026 a0001c0001t0001g0298 a0001c0001t0001g0299 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1350-546C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101741 | |||||||
| chr11:78101775 | A | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
100 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1350-580T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101775 | |||||||
| chr11:78101801 | T | C | 1 | a0001c0001t0001g0342 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1350-606A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101801 | |||||||
| chr11:78101869 | C | T | 2 | a0002c0002t0001g0190 a0002c0002t0001g0199 |
2 | HG01070.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1350-674G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101869 | |||||||
| chr11:78101930 | C | G | 6 | a0001c0003t0001g0104 a0001c0003t0001g0105 a0001c0003t0001g0110 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350-735G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101930 | |||||||
| chr11:78101945 | G | A | 6 | a0001c0003t0001g0104 a0001c0003t0001g0105 a0001c0003t0001g0110 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350-750C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101945 | |||||||
| chr11:78101987 | G | A | 19 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(16): Show |
23 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1350-792C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78101987 | |||||||
| chr11:78102034 | G | T | 3 | a0001c0001t0001g0303 a0001c0001t0001g0305 a0001c0001t0001g0327 |
3 | HG01516.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1350-839C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102034 | |||||||
| chr11:78102154 | C | A | 1 | a0001c0001t0001g0337 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1350-959G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102154 | |||||||
| chr11:78102155 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1350-960C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102155 | |||||||
| chr11:78102161 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(90): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1350-966G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102161 | |||||||
| chr11:78102162 | G | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
100 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1350-967C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102162 | |||||||
| chr11:78102223 | A | G | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1350-1028T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102223 | |||||||
| chr11:78102696 | T | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1349+1284A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102696 | |||||||
| chr11:78102750 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1349+1230A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102750 | |||||||
| chr11:78102768 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1349+1212G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102768 | |||||||
| chr11:78102784 | T | A | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1349+1196A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102784 | |||||||
| chr11:78102803 | C | T | 261 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(258): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1349+1177G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102803 | |||||||
| chr11:78102820 | G | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0239 a0001c0001t0001g0240 |
4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1349+1160C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102820 | |||||||
| chr11:78102883 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1349+1097C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102883 | |||||||
| chr11:78102895 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1349+1085A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102895 | |||||||
| chr11:78102951 | C | CA | 19 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0133 others(16): Show |
21 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.1349+1028dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102951 | |||||||
| chr11:78102951 | CA | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(183): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1349+1028delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102951 | |||||||
| chr11:78102951 | CAA | C | 27 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(24): Show |
29 | HG00558.hp2 HG01081.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1349+1027_1349+102 others(6): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78102951 | |||||||
| chr11:78103158 | T | G | 1 | a0001c0001t0001g0343 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1349+822A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103158 | |||||||
| chr11:78103182 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1349+798C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103182 | |||||||
| chr11:78103246 | C | T | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1349+734G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103246 | |||||||
| chr11:78103249 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1349+731G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103249 | |||||||
| chr11:78103378 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1349+602G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103378 | |||||||
| chr11:78103395 | C | T | 2 | a0001c0001t0001g0086 a0001c0003t0001g0113 |
2 | HG03516.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1349+585G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103395 | |||||||
| chr11:78103442 | C | T | 30 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(27): Show |
34 | HG01074.hp1 HG01081.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1349+538G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103442 | |||||||
| chr11:78103527 | C | G | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1349+453G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103527 | |||||||
| chr11:78103584 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1349+396G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103584 | |||||||
| chr11:78103589 | T | C | 6 | a0001c0003t0001g0104 a0001c0003t0001g0105 a0001c0003t0001g0110 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1349+391A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103589 | |||||||
| chr11:78103609 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1349+371G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103609 | |||||||
| chr11:78103637 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1349+343C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103637 | |||||||
| chr11:78103686 | CTGT | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1349+291_1349+293d others(5): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 12/12 | chr11 | 78103686 | |||||||
| chr11:78104096 | G | C | 1 | a0002c0002t0001g0180 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1277-44C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 11/12 | chr11 | 78104096 | |||||||
| chr11:78104150 | C | T | 41 | a0002c0002t0001g0004 a0002c0002t0001g0010 a0002c0002t0001g0019 others(38): Show |
48 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.1277-98G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 11/12 | chr11 | 78104150 | |||||||
| chr11:78104334 | T | C | 1 | a0002c0002t0001g0254 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1276+22A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 11/12 | chr11 | 78104334 | |||||||
| chr11:78104615 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1179-162C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104615 | |||||||
| chr11:78104643 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1179-190G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104643 | |||||||
| chr11:78104694 | T | C | 6 | a0001c0003t0001g0104 a0001c0003t0001g0105 a0001c0003t0001g0110 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1179-241A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104694 | |||||||
| chr11:78104730 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1179-277C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104730 | |||||||
| chr11:78104820 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1179-367A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104820 | |||||||
| chr11:78104951 | G | A | 5 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179-498C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104951 | |||||||
| chr11:78104963 | C | CA | 14 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(11): Show |
14 | HG01346.hp2 HG01981.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1179-511dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78104963 | |||||||
| chr11:78105058 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1179-605G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105058 | |||||||
| chr11:78105109 | G | C | 1 | a0001c0001t0001g0343 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1179-656C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105109 | |||||||
| chr11:78105172 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1179-719G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105172 | |||||||
| chr11:78105221 | G | C | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1179-768C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105221 | |||||||
| chr11:78105325 | T | C | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(214): Show |
254 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1179-872A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105325 | |||||||
| chr11:78105331 | A | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0219 a0001c0001t0001g0220 others(17): Show |
23 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1179-878T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105331 | |||||||
| chr11:78105481 | A | G | 41 | a0002c0002t0001g0004 a0002c0002t0001g0010 a0002c0002t0001g0019 others(38): Show |
48 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.1179-1028T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105481 | |||||||
| chr11:78105492 | T | C | 5 | a0002c0002t0001g0019 a0002c0002t0001g0186 a0002c0002t0001g0190 others(2): Show |
6 | HG00733.hp2 HG01069.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1179-1039A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105492 | |||||||
| chr11:78105503 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1179-1050C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105503 | |||||||
| chr11:78105595 | G | A | 3 | a0001c0001t0001g0316 a0001c0001t0001g0329 a0001c0001t0001g0330 |
3 | HG01928.hp1 HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1179-1142C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105595 | |||||||
| chr11:78105648 | T | TA | 84 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
99 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1178+1158dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105648 | |||||||
| chr11:78105648 | T | TAA | 7 | a0001c0001t0001g0045 a0001c0003t0001g0104 a0001c0003t0001g0105 others(4): Show |
7 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1178+1157_1178+115 others(6): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105648 | |||||||
| chr11:78105705 | CT | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1178+1101delA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105705 | |||||||
| chr11:78105718 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0274 a0001c0001t0001g0334 |
3 | HG00673.hp2 HG02738.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1178+1089G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105718 | |||||||
| chr11:78105718 | CT | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(91): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1178+1088delA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105718 | |||||||
| chr11:78105719 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0274 a0001c0001t0001g0334 |
3 | HG00673.hp2 HG02738.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1178+1088A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105719 | |||||||
| chr11:78105803 | G | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0237 |
3 | HG01884.hp2 HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1178+1004C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105803 | |||||||
| chr11:78105901 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1178+906T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78105901 | |||||||
| chr11:78106034 | G | T | 261 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(258): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1178+773C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106034 | |||||||
| chr11:78106157 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1178+650C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106157 | |||||||
| chr11:78106173 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1178+634G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106173 | |||||||
| chr11:78106182 | A | G | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(259): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1178+625T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106182 | |||||||
| chr11:78106185 | A | G | 3 | a0001c0001t0001g0281 a0001c0001t0001g0307 a0001c0001t0001g0308 |
3 | NA18941.hp1 NA18951.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1178+622T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106185 | |||||||
| chr11:78106260 | C | T | 47 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(44): Show |
54 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1178+547G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106260 | |||||||
| chr11:78106290 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1178+517G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106290 | |||||||
| chr11:78106323 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(2): Show |
7 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1178+484C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106323 | |||||||
| chr11:78106327 | A | G | 1 | a0002c0002t0001g0185 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1178+480T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106327 | |||||||
| chr11:78106347 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1178+460C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106347 | |||||||
| chr11:78106385 | G | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1178+422C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106385 | |||||||
| chr11:78106399 | A | G | 1 | a0001c0003t0001g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1178+408T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106399 | |||||||
| chr11:78106421 | T | C | 16 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(13): Show |
16 | HG00558.hp2 HG01081.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.1178+386A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106421 | |||||||
| chr11:78106465 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1178+342C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106465 | |||||||
| chr11:78106487 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1178+320C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106487 | |||||||
| chr11:78106513 | A | G | 5 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1178+294T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106513 | |||||||
| chr11:78106550 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1178+257C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106550 | |||||||
| chr11:78106573 | A | G | 22 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0219 others(19): Show |
26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1178+234T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106573 | |||||||
| chr11:78106681 | C | CATCT | 22 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0039 others(19): Show |
23 | HG01074.hp1 HG01081.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1178+122_1178+125d others(6): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 10/12 | chr11 | 78106681 | |||||||
| chr11:78106951 | A | G | 6 | a0001c0003t0001g0104 a0001c0003t0001g0105 a0001c0003t0001g0110 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1039-5T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78106951 | |||||||
| chr11:78107198 | A | AAT | 16 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0037 others(13): Show |
19 | HG01081.hp2 HG01975.hp1 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039-254_1039-253d others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | |||||||
| chr11:78107198 | A | AATAT | 42 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(39): Show |
50 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1039-256_1039-253d others(6): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | |||||||
| chr11:78107198 | A | AATATAT | 16 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0041 others(13): Show |
17 | HG01261.hp1 HG01346.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1039-258_1039-253d others(8): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | |||||||
| chr11:78107198 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1039-262_1039-253d others(12): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | |||||||
| chr11:78107198 | A | AATATATA others(5): Show |
1 | a0001c0001t0001g0046 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1039-264_1039-253d others(14): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | |||||||
| chr11:78107198 | AAT | A | 58 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0109 others(55): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.1039-254_1039-253d others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | |||||||
| chr11:78107198 | AATAT | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1039-256_1039-253d others(6): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | |||||||
| chr11:78107198 | AATATAT | A | 21 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0039 others(18): Show |
23 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1039-258_1039-253d others(8): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107198 | |||||||
| chr11:78107302 | C | T | 5 | a0001c0003t0001g0104 a0001c0003t0001g0110 a0001c0003t0001g0111 others(2): Show |
5 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-356G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107302 | |||||||
| chr11:78107324 | G | C | 6 | a0001c0003t0001g0104 a0001c0003t0001g0105 a0001c0003t0001g0110 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-378C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107324 | |||||||
| chr11:78107334 | C | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0305 |
2 | HG01516.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1039-388G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107334 | |||||||
| chr11:78107339 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1039-393T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107339 | |||||||
| chr11:78107377 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1039-431G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107377 | |||||||
| chr11:78107418 | AC | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-473delG | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107418 | |||||||
| chr11:78107500 | T | G | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1039-554A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107500 | |||||||
| chr11:78107515 | A | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1039-569T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107515 | |||||||
| chr11:78107694 | T | A | 1 | a0001c0003t0001g0015 | 2 | HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1039-748A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107694 | |||||||
| chr11:78107703 | G | C | 8 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0135 others(5): Show |
8 | NA18963.hp2 NA18965.hp2 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1039-757C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107703 | |||||||
| chr11:78107719 | G | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-773C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107719 | |||||||
| chr11:78107731 | A | G | 22 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0219 others(19): Show |
26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1039-785T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107731 | |||||||
| chr11:78107757 | G | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-811C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107757 | |||||||
| chr11:78107763 | A | T | 11 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0040 others(8): Show |
11 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1039-817T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107763 | |||||||
| chr11:78107839 | C | CA | 13 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0124 others(10): Show |
13 | HG00639.hp2 HG01175.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1039-894dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107839 | |||||||
| chr11:78107839 | CA | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(140): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1039-894delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107839 | |||||||
| chr11:78107839 | CAA | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0039 others(17): Show |
23 | HG01069.hp2 HG01070.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1039-895_1039-894d others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107839 | |||||||
| chr11:78107984 | A | G | 5 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039-1038T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78107984 | |||||||
| chr11:78108105 | C | A | 6 | a0001c0003t0001g0104 a0001c0003t0001g0105 a0001c0003t0001g0110 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-1159G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108105 | |||||||
| chr11:78108136 | C | T | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1039-1190G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108136 | |||||||
| chr11:78108209 | G | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+1233C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108209 | |||||||
| chr11:78108327 | C | T | 5 | a0003c0004t0001g0224 a0003c0004t0001g0226 a0003c0004t0001g0227 others(2): Show |
5 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+1115G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108327 | |||||||
| chr11:78108364 | T | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1038+1078A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108364 | |||||||
| chr11:78108391 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1038+1051G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108391 | |||||||
| chr11:78108486 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1038+956G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108486 | |||||||
| chr11:78108572 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1038+870T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108572 | |||||||
| chr11:78108844 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1038+598A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108844 | |||||||
| chr11:78108928 | G | A | 1 | a0002c0002t0001g0209 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1038+514C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78108928 | |||||||
| chr11:78109035 | A | G | 16 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0039 others(13): Show |
17 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1038+407T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78109035 | |||||||
| chr11:78109122 | T | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(94): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1038+320A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78109122 | |||||||
| chr11:78109123 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1038+319C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78109123 | |||||||
| chr11:78109182 | T | C | 1 | a0001c0003t0001g0015 | 2 | HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1038+260A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78109182 | |||||||
| chr11:78109217 | AAC | A | 5 | a0003c0004t0001g0224 a0003c0004t0001g0226 a0003c0004t0001g0227 others(2): Show |
5 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+223_1038+224d others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78109217 | |||||||
| chr11:78109270 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0138 |
2 | HG01258.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1038+172A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 9/12 | chr11 | 78109270 | |||||||
| chr11:78109624 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.899-43A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78109624 | |||||||
| chr11:78109627 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.899-46A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78109627 | |||||||
| chr11:78109702 | C | T | 11 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0040 others(8): Show |
11 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.899-121G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78109702 | |||||||
| chr11:78109749 | C | G | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.899-168G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78109749 | |||||||
| chr11:78109832 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.899-251C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78109832 | |||||||
| chr11:78109961 | G | A | 41 | a0002c0002t0001g0004 a0002c0002t0001g0010 a0002c0002t0001g0019 others(38): Show |
48 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.899-380C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78109961 | |||||||
| chr11:78110077 | C | T | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.899-496G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110077 | |||||||
| chr11:78110100 | T | G | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.899-519A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110100 | |||||||
| chr11:78110183 | C | CT | 7 | a0001c0001t0001g0080 a0001c0003t0001g0104 a0001c0003t0001g0105 others(4): Show |
7 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.899-603dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110183 | |||||||
| chr11:78110198 | A | C | 14 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0039 others(11): Show |
15 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.899-617T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110198 | |||||||
| chr11:78110246 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.899-665C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110246 | |||||||
| chr11:78110254 | A | G | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(259): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.899-673T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110254 | |||||||
| chr11:78110294 | C | T | 1 | a0002c0002t0001g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.899-713G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110294 | |||||||
| chr11:78110342 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.899-761G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110342 | |||||||
| chr11:78110353 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0239 a0001c0001t0001g0240 |
4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.899-772C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110353 | |||||||
| chr11:78110452 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.899-871T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110452 | |||||||
| chr11:78110501 | C | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0058 |
3 | HG01243.hp2 HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.899-920G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110501 | |||||||
| chr11:78110599 | T | C | 16 | a0002c0002t0001g0004 a0002c0002t0001g0173 a0002c0002t0001g0187 others(13): Show |
19 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.899-1018A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110599 | |||||||
| chr11:78110626 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.899-1045T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110626 | |||||||
| chr11:78110654 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.899-1073A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110654 | |||||||
| chr11:78110721 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0241 |
3 | HG02055.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.899-1140G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110721 | |||||||
| chr11:78110961 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.899-1380C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110961 | |||||||
| chr11:78110971 | C | A | 1 | a0001c0001t0001g0139 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.899-1390G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78110971 | |||||||
| chr11:78111010 | T | C | 1 | a0002c0002t0001g0199 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.899-1429A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111010 | |||||||
| chr11:78111023 | T | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.899-1442A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111023 | |||||||
| chr11:78111033 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.899-1452G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111033 | |||||||
| chr11:78111059 | G | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.899-1478C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111059 | |||||||
| chr11:78111175 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.898+1475C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111175 | |||||||
| chr11:78111183 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.898+1467A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111183 | |||||||
| chr11:78111346 | G | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0219 a0001c0001t0001g0220 others(17): Show |
23 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.898+1304C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111346 | |||||||
| chr11:78111397 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.898+1253C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111397 | |||||||
| chr11:78111417 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.898+1233G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111417 | |||||||
| chr11:78111498 | C | T | 2 | a0002c0002t0001g0198 a0002c0002t0001g0218 |
2 | HG02080.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.898+1152G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111498 | |||||||
| chr11:78111516 | C | T | 5 | a0001c0003t0001g0104 a0001c0003t0001g0110 a0001c0003t0001g0111 others(2): Show |
5 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.898+1134G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111516 | |||||||
| chr11:78111520 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.898+1130G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111520 | |||||||
| chr11:78111656 | ACACT | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
77 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.898+990_898+993del others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111656 | |||||||
| chr11:78111770 | A | C | 1 | a0001c0001t0001g0089 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.898+880T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111770 | |||||||
| chr11:78111779 | T | TTC | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.898+870_898+871ins others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111779 | |||||||
| chr11:78111786 | T | C | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.898+864A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111786 | |||||||
| chr11:78111842 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.898+808G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78111842 | |||||||
| chr11:78112182 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
114 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.898+468G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112182 | |||||||
| chr11:78112281 | A | C | 73 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0057 others(70): Show |
81 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.898+369T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112281 | |||||||
| chr11:78112444 | G | C | 1 | a0002c0002t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.898+206C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112444 | |||||||
| chr11:78112511 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.898+139C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112511 | |||||||
| chr11:78112562 | A | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.898+88T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112562 | |||||||
| chr11:78112614 | A | G | 5 | a0001c0003t0001g0104 a0001c0003t0001g0110 a0001c0003t0001g0111 others(2): Show |
5 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.898+36T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112614 | |||||||
| chr11:78112635 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.898+15A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112635 | |||||||
| chr11:78112642 | T | C | 1 | a0002c0002t0001g0192 | 1 | HG00733.hp2 | splice_region_variant&intron_variant | LOW | c.898+8A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 8/12 | chr11 | 78112642 | |||||||
| chr11:78112998 | C | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.778-228G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78112998 | |||||||
| chr11:78113063 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.778-293A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113063 | |||||||
| chr11:78113146 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.778-376A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113146 | |||||||
| chr11:78113148 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-378T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113148 | |||||||
| chr11:78113150 | T | C | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.778-380A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113150 | |||||||
| chr11:78113233 | C | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.778-463G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113233 | |||||||
| chr11:78113366 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+520A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113366 | |||||||
| chr11:78113371 | G | GTA | 79 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
91 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.777+513_777+514dup others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113371 | |||||||
| chr11:78113440 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.777+446G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113440 | |||||||
| chr11:78113441 | G | A | 6 | a0001c0001t0001g0140 a0002c0002t0001g0213 a0002c0002t0001g0214 others(3): Show |
6 | HG00544.hp1 HG02015.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+445C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113441 | |||||||
| chr11:78113450 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.777+436A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113450 | |||||||
| chr11:78113452 | C | T | 46 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(43): Show |
53 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.777+434G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113452 | |||||||
| chr11:78113523 | A | T | 2 | a0001c0001t0001g0336 a0001c0001t0001g0338 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.777+363T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113523 | |||||||
| chr11:78113667 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.777+219G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113667 | |||||||
| chr11:78113699 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.777+187A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113699 | |||||||
| chr11:78113712 | TAAACA | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.777+169_777+173del others(5): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113712 | |||||||
| chr11:78113712 | TAAACAA | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.777+168_777+173del others(6): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113712 | |||||||
| chr11:78113715 | ACAAAAAC | A | 4 | a0001c0001t0001g0084 a0001c0001t0001g0099 a0001c0001t0001g0245 others(1): Show |
4 | HG01070.hp1 HG01081.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+164_777+170del others(7): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113715 | |||||||
| chr11:78113716 | C | CA | 3 | a0001c0001t0001g0182 a0002c0002t0001g0217 a0002c0002t0001g0253 |
3 | HG02965.hp2 HG03831.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.777+169dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113716 | |||||||
| chr11:78113722 | C | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(259): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.777+164G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113722 | |||||||
| chr11:78113726 | A | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0161 |
2 | NA18953.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.777+160T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113726 | |||||||
| chr11:78113728 | A | C | 1 | a0001c0001t0001g0135 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.777+158T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113728 | |||||||
| chr11:78113861 | G | GA | 32 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0116 others(29): Show |
36 | HG01109.hp1 HG01891.hp2 HG02135.hp2 others(33): Show |
intron_variant | MODIFIER | c.777+24dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113861 | |||||||
| chr11:78113861 | G | GAAA | 11 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0058 others(8): Show |
13 | HG01081.hp2 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.777+22_777+24dupTT others(1): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113861 | |||||||
| chr11:78113861 | G | GAAAA | 79 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
92 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.777+21_777+24dupTT others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 7/12 | chr11 | 78113861 | |||||||
| chr11:78114011 | A | G | 1 | a0002c0002t0001g0188 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.674-22T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/12 | chr11 | 78114011 | |||||||
| chr11:78114016 | C | A | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0335 |
3 | HG00738.hp1 HG02559.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.674-27G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/12 | chr11 | 78114016 | |||||||
| chr11:78114018 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.674-29T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/12 | chr11 | 78114018 | |||||||
| chr11:78114020 | G | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0219 others(19): Show |
26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.674-31C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/12 | chr11 | 78114020 | |||||||
| chr11:78114203 | C | A | 1 | a0001c0001t0001g0318 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.673+63G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/12 | chr11 | 78114203 | |||||||
| chr11:78114229 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(94): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.673+37T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 6/12 | chr11 | 78114229 | |||||||
| chr11:78114462 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-70T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114462 | |||||||
| chr11:78114596 | A | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.547-204T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114596 | |||||||
| chr11:78114620 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.547-228A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114620 | |||||||
| chr11:78114629 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0058 |
3 | HG01243.hp2 HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.547-237A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114629 | |||||||
| chr11:78114651 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-259G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114651 | |||||||
| chr11:78114711 | A | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-319T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114711 | |||||||
| chr11:78114711 | A | G | 2 | a0001c0003t0001g0112 a0001c0003t0001g0113 |
2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.547-319T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114711 | |||||||
| chr11:78114714 | C | T | 5 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-322G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114714 | |||||||
| chr11:78114717 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.547-325C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114717 | |||||||
| chr11:78114835 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.547-443G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114835 | |||||||
| chr11:78114929 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-537A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114929 | |||||||
| chr11:78114933 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.547-541C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114933 | |||||||
| chr11:78114934 | A | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-542T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78114934 | |||||||
| chr11:78115021 | T | A | 47 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(44): Show |
54 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.547-629A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115021 | |||||||
| chr11:78115118 | C | T | 5 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG02071.hp2 NA18952.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-726G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115118 | |||||||
| chr11:78115128 | G | T | 1 | a0002c0002t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.547-736C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115128 | |||||||
| chr11:78115300 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.547-908G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115300 | |||||||
| chr11:78115313 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.547-921G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115313 | |||||||
| chr11:78115350 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-958A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115350 | |||||||
| chr11:78115446 | C | G | 1 | a0001c0001t0001g0280 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.547-1054G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115446 | |||||||
| chr11:78115447 | G | A | 6 | a0001c0003t0001g0104 a0001c0003t0001g0105 a0001c0003t0001g0110 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-1055C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115447 | |||||||
| chr11:78115454 | T | TC | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-1063_547-1062i others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115454 | |||||||
| chr11:78115726 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-1334G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115726 | |||||||
| chr11:78115749 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-1357T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115749 | |||||||
| chr11:78115814 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-1422A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115814 | |||||||
| chr11:78115939 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(94): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.547-1547G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115939 | |||||||
| chr11:78115951 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.547-1559A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115951 | |||||||
| chr11:78115995 | G | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0219 others(19): Show |
26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.547-1603C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78115995 | |||||||
| chr11:78116108 | C | G | 3 | a0001c0001t0001g0316 a0001c0001t0001g0329 a0001c0001t0001g0330 |
3 | HG01928.hp1 HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.547-1716G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116108 | |||||||
| chr11:78116113 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0297 a0001c0001t0001g0302 |
4 | HG00621.hp2 HG02129.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-1721T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116113 | |||||||
| chr11:78116185 | C | A | 1 | a0001c0001t0001g0090 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.547-1793G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116185 | |||||||
| chr11:78116211 | A | C | 1 | a0002c0002t0001g0346 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.547-1819T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116211 | |||||||
| chr11:78116325 | G | A | 10 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0003t0001g0036 others(7): Show |
10 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.547-1933C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116325 | |||||||
| chr11:78116428 | G | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0035 others(8): Show |
15 | HG00323.hp2 HG00609.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.547-2036C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116428 | |||||||
| chr11:78116451 | G | T | 1 | a0002c0002t0001g0193 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.547-2059C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116451 | |||||||
| chr11:78116474 | C | G | 1 | a0002c0002t0001g0193 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.547-2082G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116474 | |||||||
| chr11:78116479 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-2087T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116479 | |||||||
| chr11:78116563 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.547-2171G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116563 | |||||||
| chr11:78116606 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.547-2214G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116606 | |||||||
| chr11:78116653 | G | A | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.547-2261C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116653 | |||||||
| chr11:78116712 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.547-2320C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116712 | |||||||
| chr11:78116753 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0239 a0001c0001t0001g0240 |
4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-2361G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116753 | |||||||
| chr11:78116797 | TC | T | 7 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
7 | HG02071.hp2 NA18952.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.546+2384delG | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116797 | |||||||
| chr11:78116848 | A | G | 1 | a0001c0003t0001g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.546+2334T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116848 | |||||||
| chr11:78116910 | T | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.546+2272A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78116910 | |||||||
| chr11:78117102 | T | A | 1 | a0001c0001t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.546+2080A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117102 | |||||||
| chr11:78117173 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.546+2009G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117173 | |||||||
| chr11:78117302 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.546+1880G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117302 | |||||||
| chr11:78117410 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.546+1772T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117410 | |||||||
| chr11:78117412 | T | C | 22 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0219 others(19): Show |
26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.546+1770A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117412 | |||||||
| chr11:78117420 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.546+1762T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117420 | |||||||
| chr11:78117611 | C | CA | 14 | a0001c0001t0001g0106 a0001c0001t0001g0114 a0001c0001t0001g0116 others(11): Show |
14 | HG01081.hp2 HG01515.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.546+1570dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117611 | |||||||
| chr11:78117611 | C | CAA | 6 | a0001c0001t0001g0022 a0001c0001t0001g0239 a0001c0001t0001g0240 others(3): Show |
8 | HG02622.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+1569_546+1570d others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117611 | |||||||
| chr11:78117611 | C | CAAA | 76 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(73): Show |
89 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.546+1568_546+1570d others(5): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117611 | |||||||
| chr11:78117611 | CA | C | 51 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(48): Show |
58 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.546+1570delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117611 | |||||||
| chr11:78117634 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.546+1548G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117634 | |||||||
| chr11:78117709 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.546+1473A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117709 | |||||||
| chr11:78117779 | T | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.546+1403A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117779 | |||||||
| chr11:78117812 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.546+1370G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117812 | |||||||
| chr11:78117867 | G | C | 1 | a0001c0001t0001g0160 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.546+1315C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117867 | |||||||
| chr11:78117871 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.546+1311T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117871 | |||||||
| chr11:78117899 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.546+1283C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117899 | |||||||
| chr11:78117919 | A | C | 1 | a0001c0003t0001g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.546+1263T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117919 | |||||||
| chr11:78117943 | C | T | 1 | a0001c0003t0001g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.546+1239G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117943 | |||||||
| chr11:78117944 | G | A | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.546+1238C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117944 | |||||||
| chr11:78117964 | G | A | 24 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0259 others(21): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.546+1218C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117964 | |||||||
| chr11:78117976 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.546+1206G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78117976 | |||||||
| chr11:78118070 | C | CA | 6 | a0001c0001t0001g0096 a0001c0001t0001g0119 a0001c0001t0001g0179 others(3): Show |
6 | HG00621.hp1 NA18940.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.546+1111dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118070 | |||||||
| chr11:78118070 | CA | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
212 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.546+1111delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118070 | |||||||
| chr11:78118070 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.546+1102_546+1111d others(12): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118070 | |||||||
| chr11:78118126 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.546+1056A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118126 | |||||||
| chr11:78118132 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.546+1050A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118132 | |||||||
| chr11:78118242 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+940C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118242 | |||||||
| chr11:78118249 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.546+933A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118249 | |||||||
| chr11:78118250 | A | G | 264 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(261): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.546+932T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118250 | |||||||
| chr11:78118274 | C | A | 1 | a0001c0001t0001g0141 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.546+908G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118274 | |||||||
| chr11:78118283 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.546+899C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118283 | |||||||
| chr11:78118331 | C | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.546+851G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118331 | |||||||
| chr11:78118381 | T | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.546+801A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118381 | |||||||
| chr11:78118387 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.546+795C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118387 | |||||||
| chr11:78118399 | T | G | 1 | a0001c0001t0001g0306 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.546+783A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118399 | |||||||
| chr11:78118603 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0158 |
3 | HG00408.hp2 NA19005.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.546+579C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118603 | |||||||
| chr11:78118615 | C | CA | 12 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0001g0128 others(9): Show |
12 | HG01433.hp1 HG01981.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.546+566dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118615 | |||||||
| chr11:78118615 | CA | C | 37 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0183 others(34): Show |
41 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.546+566delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118615 | |||||||
| chr11:78118615 | CAA | C | 11 | a0001c0001t0001g0023 a0001c0001t0001g0068 a0001c0001t0001g0182 others(8): Show |
12 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.546+565_546+566del others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118615 | |||||||
| chr11:78118615 | CAAA | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(183): Show |
221 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.546+564_546+566del others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118615 | |||||||
| chr11:78118615 | CAAAA | C | 19 | a0001c0001t0001g0022 a0001c0001t0001g0055 a0001c0001t0001g0101 others(16): Show |
20 | HG01081.hp2 HG01975.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.546+563_546+566del others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118615 | |||||||
| chr11:78118628 | A | C | 1 | a0001c0003t0001g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.546+554T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118628 | |||||||
| chr11:78118671 | C | T | 42 | a0001c0001t0001g0197 a0002c0002t0001g0004 a0002c0002t0001g0010 others(39): Show |
49 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.546+511G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118671 | |||||||
| chr11:78118680 | A | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.546+502T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118680 | |||||||
| chr11:78118720 | G | C | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.546+462C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118720 | |||||||
| chr11:78118731 | G | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.546+451C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118731 | |||||||
| chr11:78118878 | C | T | 47 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(44): Show |
54 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.546+304G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118878 | |||||||
| chr11:78118898 | C | G | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0003t0001g0036 others(1): Show |
4 | HG03225.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+284G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118898 | |||||||
| chr11:78118912 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.546+270A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78118912 | |||||||
| chr11:78119002 | G | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(94): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.546+180C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 5/12 | chr11 | 78119002 | |||||||
| chr11:78119417 | TTTTTTTT others(4): Show |
T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0239 a0001c0001t0001g0240 |
4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-179_479-169del others(11): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119417 | |||||||
| chr11:78119418 | TTTTTTTT others(3): Show |
T | 14 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0039 others(11): Show |
14 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.479-179_479-170del others(10): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119418 | |||||||
| chr11:78119419 | TTTTTTTT others(2): Show |
T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
91 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.479-179_479-171del others(9): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119419 | |||||||
| chr11:78119543 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.479-294A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119543 | |||||||
| chr11:78119553 | C | T | 10 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0003t0001g0036 others(7): Show |
10 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.479-304G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119553 | |||||||
| chr11:78119617 | G | C | 6 | a0001c0003t0001g0104 a0001c0003t0001g0105 a0001c0003t0001g0110 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-368C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119617 | |||||||
| chr11:78119650 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.479-401G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119650 | |||||||
| chr11:78119684 | T | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(210): Show |
250 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.479-435A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119684 | |||||||
| chr11:78119724 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.479-475G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119724 | |||||||
| chr11:78119940 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.479-691C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119940 | |||||||
| chr11:78119995 | G | C | 2 | a0002c0002t0001g0188 a0002c0002t0001g0201 |
2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.479-746C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78119995 | |||||||
| chr11:78120010 | G | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0219 others(19): Show |
26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.479-761C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120010 | |||||||
| chr11:78120019 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.479-770G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120019 | |||||||
| chr11:78120093 | A | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.479-844T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120093 | |||||||
| chr11:78120237 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.478+828G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120237 | |||||||
| chr11:78120285 | T | C | 10 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0003t0001g0036 others(7): Show |
10 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.478+780A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120285 | |||||||
| chr11:78120316 | T | A | 1 | a0001c0001t0001g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.478+749A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120316 | |||||||
| chr11:78120408 | G | A | 1 | a0002c0002t0001g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.478+657C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120408 | |||||||
| chr11:78120425 | T | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(259): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.478+640A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120425 | |||||||
| chr11:78120429 | TCTTTAGA others(4): Show |
T | 1 | a0001c0001t0001g0171 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.478+625_478+635del others(11): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120429 | |||||||
| chr11:78120492 | TA | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0219 others(19): Show |
26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.478+572delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120492 | |||||||
| chr11:78120552 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.478+513C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120552 | |||||||
| chr11:78120623 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478+442T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120623 | |||||||
| chr11:78120712 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.478+353G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120712 | |||||||
| chr11:78120744 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+321C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120744 | |||||||
| chr11:78120822 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0157 a0001c0001t0001g0175 |
3 | NA18942.hp1 NA19072.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.478+243G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 4/12 | chr11 | 78120822 | |||||||
| chr11:78121287 | C | CT | 10 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0070 others(7): Show |
10 | HG01175.hp2 HG01255.hp1 NA18972.hp1 others(7): Show |
intron_variant | MODIFIER | c.369-114dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121287 | |||||||
| chr11:78121423 | T | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.369-249A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121423 | |||||||
| chr11:78121531 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.369-357G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121531 | |||||||
| chr11:78121548 | C | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.369-374G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121548 | |||||||
| chr11:78121555 | G | GA | 7 | a0001c0001t0001g0022 a0001c0001t0001g0092 a0001c0001t0001g0144 others(4): Show |
9 | HG02071.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.369-382dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121555 | |||||||
| chr11:78121588 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.369-414T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121588 | |||||||
| chr11:78121611 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.369-437G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78121611 | |||||||
| chr11:78122089 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.369-915C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122089 | |||||||
| chr11:78122146 | C | A | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0003t0001g0036 others(1): Show |
4 | HG03225.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-972G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122146 | |||||||
| chr11:78122342 | A | AT | 21 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0039 others(18): Show |
24 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.369-1169dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122342 | |||||||
| chr11:78122342 | A | ATT | 71 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(68): Show |
83 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.369-1170_369-1169d others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122342 | |||||||
| chr11:78122342 | AT | A | 6 | a0001c0001t0001g0127 a0001c0001t0001g0145 a0001c0001t0001g0157 others(3): Show |
6 | HG01993.hp2 HG02738.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.369-1169delA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122342 | |||||||
| chr11:78122460 | G | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.369-1286C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122460 | |||||||
| chr11:78122514 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0164 |
2 | HG00280.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.369-1340C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122514 | |||||||
| chr11:78122726 | C | T | 8 | a0001c0003t0001g0036 a0001c0003t0001g0104 a0001c0003t0001g0105 others(5): Show |
8 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.368+1295G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122726 | |||||||
| chr11:78122791 | C | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0068 |
3 | HG03942.hp2 NA18962.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.368+1230G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122791 | |||||||
| chr11:78122835 | A | T | 1 | a0001c0001t0001g0041 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.368+1186T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122835 | |||||||
| chr11:78122857 | C | A | 1 | a0006c0006t0001g0273 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.368+1164G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122857 | |||||||
| chr11:78122858 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.368+1163C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122858 | |||||||
| chr11:78122866 | TA | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.368+1154delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122866 | |||||||
| chr11:78122874 | T | A | 1 | a0001c0001t0001g0284 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.368+1147A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78122874 | |||||||
| chr11:78123011 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.368+1010T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123011 | |||||||
| chr11:78123012 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.368+1009C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123012 | |||||||
| chr11:78123029 | T | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(94): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.368+992A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123029 | |||||||
| chr11:78123030 | C | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(94): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.368+991G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123030 | |||||||
| chr11:78123031 | G | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(94): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.368+990C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123031 | |||||||
| chr11:78123032 | G | GAA | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(94): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.368+988_368+989ins others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123032 | |||||||
| chr11:78123074 | G | A | 10 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0003t0001g0036 others(7): Show |
10 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.368+947C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123074 | |||||||
| chr11:78123078 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.368+943G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123078 | |||||||
| chr11:78123084 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.368+937C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123084 | |||||||
| chr11:78123112 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0339 a0001c0001t0001g0344 |
4 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.368+909G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123112 | |||||||
| chr11:78123257 | C | T | 64 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
75 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.368+764G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123257 | |||||||
| chr11:78123272 | T | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.368+749A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123272 | |||||||
| chr11:78123303 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.368+718T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123303 | |||||||
| chr11:78123315 | G | GA | 90 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(87): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.368+705dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123315 | |||||||
| chr11:78123315 | G | GAA | 41 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0256 others(38): Show |
44 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.368+704_368+705dup others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123315 | |||||||
| chr11:78123315 | GA | G | 29 | a0001c0001t0001g0197 a0001c0001t0001g0229 a0002c0002t0001g0004 others(26): Show |
35 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.368+705delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123315 | |||||||
| chr11:78123315 | GAA | G | 6 | a0002c0002t0001g0020 a0002c0002t0001g0193 a0002c0002t0001g0194 others(3): Show |
7 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.368+704_368+705del others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123315 | |||||||
| chr11:78123322 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0086 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.368+684_368+698del others(15): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123322 | |||||||
| chr11:78123323 | AAAAAAAA others(7): Show |
A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
85 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.368+684_368+697del others(14): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123323 | |||||||
| chr11:78123324 | AAAAAAAA others(6): Show |
A | 21 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0039 others(18): Show |
23 | HG01074.hp1 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.368+684_368+696del others(13): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123324 | |||||||
| chr11:78123325 | AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.368+684_368+695del others(12): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123325 | |||||||
| chr11:78123338 | A | G | 1 | a0002c0002t0001g0215 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.368+683T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123338 | |||||||
| chr11:78123654 | A | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.368+367T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123654 | |||||||
| chr11:78123734 | G | C | 3 | a0001c0001t0001g0275 a0001c0001t0001g0282 a0001c0001t0001g0291 |
3 | HG00558.hp1 NA19058.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.368+287C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123734 | |||||||
| chr11:78123756 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.368+265A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123756 | |||||||
| chr11:78123760 | C | G | 1 | a0001c0001t0001g0069 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.368+261G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123760 | |||||||
| chr11:78123831 | C | G | 1 | a0001c0001t0001g0327 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.368+190G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123831 | |||||||
| chr11:78123832 | C | A | 1 | a0001c0001t0001g0327 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.368+189G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123832 | |||||||
| chr11:78123948 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.368+73C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 3/12 | chr11 | 78123948 | |||||||
| chr11:78124227 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.175-13A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124227 | |||||||
| chr11:78124232 | G | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-18C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124232 | |||||||
| chr11:78124301 | TCTTTAAA others(6): Show |
T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.175-100_175-88delT others(12): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124301 | |||||||
| chr11:78124453 | C | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.175-239G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124453 | |||||||
| chr11:78124805 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.175-591G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124805 | |||||||
| chr11:78124831 | G | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-617C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124831 | |||||||
| chr11:78124852 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-638T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124852 | |||||||
| chr11:78124854 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.175-640A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124854 | |||||||
| chr11:78124892 | A | G | 1 | a0002c0002t0001g0206 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.175-678T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124892 | |||||||
| chr11:78124967 | C | T | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(264): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.175-753G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78124967 | |||||||
| chr11:78125021 | T | TCTAA | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-808_175-807ins others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125021 | |||||||
| chr11:78125039 | C | CT | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(97): Show |
118 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.175-826dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125039 | |||||||
| chr11:78125125 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-911G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125125 | |||||||
| chr11:78125195 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.175-981C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125195 | |||||||
| chr11:78125247 | C | T | 4 | a0001c0001t0001g0223 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
4 | HG02145.hp1 HG02922.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-1033G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125247 | |||||||
| chr11:78125274 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-1060G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125274 | |||||||
| chr11:78125351 | C | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.175-1137G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125351 | |||||||
| chr11:78125367 | G | A | 52 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(49): Show |
59 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.175-1153C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125367 | |||||||
| chr11:78125434 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.175-1220G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125434 | |||||||
| chr11:78125435 | G | A | 1 | a0002c0002t0002g0348 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.175-1221C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125435 | |||||||
| chr11:78125512 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-1298A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125512 | |||||||
| chr11:78125519 | A | C | 3 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | HG01891.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.175-1305T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125519 | |||||||
| chr11:78125565 | A | T | 1 | a0001c0001t0001g0297 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.175-1351T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125565 | |||||||
| chr11:78125582 | G | A | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(264): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.175-1368C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125582 | |||||||
| chr11:78125611 | C | CA | 32 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(29): Show |
36 | HG00738.hp2 HG01081.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.175-1398dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125611 | |||||||
| chr11:78125692 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.175-1478C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125692 | |||||||
| chr11:78125843 | T | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0053 others(2): Show |
7 | HG02080.hp1 NA18942.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+1515A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125843 | |||||||
| chr11:78125881 | C | T | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG00738.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.174+1477G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125881 | |||||||
| chr11:78125888 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.174+1470T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78125888 | |||||||
| chr11:78126000 | A | T | 1 | a0002c0002t0001g0215 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.174+1358T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126000 | |||||||
| chr11:78126020 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.174+1338T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126020 | |||||||
| chr11:78126163 | A | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.174+1195T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126163 | |||||||
| chr11:78126268 | C | T | 7 | a0001c0003t0001g0015 a0001c0003t0001g0034 a0002c0002t0001g0019 others(4): Show |
9 | HG00733.hp2 HG01069.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.174+1090G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126268 | |||||||
| chr11:78126351 | G | T | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(259): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.174+1007C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126351 | |||||||
| chr11:78126456 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.174+902G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126456 | |||||||
| chr11:78126516 | G | C | 11 | a0001c0001t0001g0022 a0001c0001t0001g0239 a0001c0001t0001g0240 others(8): Show |
12 | HG01081.hp2 HG02630.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+842C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126516 | |||||||
| chr11:78126523 | A | C | 1 | a0001c0001t0001g0268 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.174+835T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126523 | |||||||
| chr11:78126532 | C | CA | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(91): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.174+825dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126532 | |||||||
| chr11:78126532 | C | CAA | 112 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(109): Show |
130 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.174+824_174+825dup others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126532 | |||||||
| chr11:78126532 | C | CAAA | 10 | a0001c0001t0001g0022 a0001c0001t0001g0054 a0001c0001t0001g0065 others(7): Show |
11 | HG02257.hp1 HG02630.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+823_174+825dup others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126532 | |||||||
| chr11:78126547 | G | T | 2 | a0001c0003t0001g0036 a0001c0003t0001g0108 |
2 | NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.174+811C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126547 | |||||||
| chr11:78126715 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.174+643G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126715 | |||||||
| chr11:78126815 | T | C | 2 | a0001c0003t0001g0036 a0001c0003t0001g0108 |
2 | NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.174+543A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126815 | |||||||
| chr11:78126940 | C | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.174+418G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126940 | |||||||
| chr11:78126965 | G | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(94): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.174+393C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126965 | |||||||
| chr11:78126972 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+386C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126972 | |||||||
| chr11:78126984 | AT | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(98): Show |
116 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.174+373delA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126984 | |||||||
| chr11:78126991 | T | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.174+367A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78126991 | |||||||
| chr11:78127041 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.174+317C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127041 | |||||||
| chr11:78127043 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.174+315C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127043 | |||||||
| chr11:78127090 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.174+268G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127090 | |||||||
| chr11:78127098 | G | GC | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.174+259dupG | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127098 | |||||||
| chr11:78127120 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0239 a0001c0001t0001g0240 |
4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+238T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127120 | |||||||
| chr11:78127203 | C | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.174+155G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127203 | |||||||
| chr11:78127222 | C | A | 1 | a0001c0001t0001g0288 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.174+136G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127222 | |||||||
| chr11:78127295 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.174+63G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127295 | |||||||
| chr11:78127327 | TA | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(213): Show |
253 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.174+30delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 2/12 | chr11 | 78127327 | |||||||
| chr11:78127611 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0167 |
3 | NA18994.hp2 NA19063.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.96-175T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127611 | |||||||
| chr11:78127634 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-198G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127634 | |||||||
| chr11:78127699 | C | T | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(264): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.96-263G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127699 | |||||||
| chr11:78127712 | C | CTTTT | 16 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0055 others(13): Show |
18 | HG01081.hp2 HG02622.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.96-280_96-277dupAA others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127712 | |||||||
| chr11:78127712 | C | CTTTTT | 75 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(72): Show |
88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.96-281_96-277dupAA others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127712 | |||||||
| chr11:78127792 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-356A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127792 | |||||||
| chr11:78127812 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-376G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127812 | |||||||
| chr11:78127992 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.96-556T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127992 | |||||||
| chr11:78127999 | G | C | 1 | a0001c0001t0001g0175 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.96-563C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78127999 | |||||||
| chr11:78128214 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-778G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128214 | |||||||
| chr11:78128231 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-795A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128231 | |||||||
| chr11:78128384 | C | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-948G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128384 | |||||||
| chr11:78128612 | C | CT | 110 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
125 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.96-1177dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128612 | |||||||
| chr11:78128617 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.96-1181A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128617 | |||||||
| chr11:78128642 | C | T | 1 | a0005c0008t0001g0203 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.96-1206G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128642 | |||||||
| chr11:78128643 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1207C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128643 | |||||||
| chr11:78128743 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1307A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128743 | |||||||
| chr11:78128760 | G | A | 3 | a0001c0001t0001g0316 a0001c0001t0001g0329 a0001c0001t0001g0330 |
3 | HG01928.hp1 HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.96-1324C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128760 | |||||||
| chr11:78128771 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1335A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128771 | |||||||
| chr11:78128847 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1411G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128847 | |||||||
| chr11:78128865 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.96-1429G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128865 | |||||||
| chr11:78128866 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1430C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128866 | |||||||
| chr11:78128960 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1524C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78128960 | |||||||
| chr11:78129010 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1574G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129010 | |||||||
| chr11:78129011 | A | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1575T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129011 | |||||||
| chr11:78129012 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1576C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129012 | |||||||
| chr11:78129034 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1598C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129034 | |||||||
| chr11:78129046 | T | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1610A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129046 | |||||||
| chr11:78129047 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1611C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129047 | |||||||
| chr11:78129049 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1613G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129049 | |||||||
| chr11:78129050 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1614G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129050 | |||||||
| chr11:78129052 | A | AAGCTGAG others(6): Show |
1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1617_96-1616ins others(13): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129052 | |||||||
| chr11:78129053 | T | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1617A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129053 | |||||||
| chr11:78129054 | C | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1618G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129054 | |||||||
| chr11:78129057 | T | G | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1621A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129057 | |||||||
| chr11:78129059 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1623G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129059 | |||||||
| chr11:78129067 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1631T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129067 | |||||||
| chr11:78129071 | A | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1635T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129071 | |||||||
| chr11:78129072 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1636G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129072 | |||||||
| chr11:78129075 | A | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1639T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129075 | |||||||
| chr11:78129077 | A | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1641T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129077 | |||||||
| chr11:78129079 | C | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1643G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129079 | |||||||
| chr11:78129090 | G | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1654C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129090 | |||||||
| chr11:78129092 | A | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1656T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129092 | |||||||
| chr11:78129099 | G | A | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.96-1663C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129099 | |||||||
| chr11:78129112 | C | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1676G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129112 | |||||||
| chr11:78129114 | C | G | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1678G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129114 | |||||||
| chr11:78129115 | G | A | 50 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(47): Show |
57 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.96-1679C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129115 | |||||||
| chr11:78129115 | G | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1679C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129115 | |||||||
| chr11:78129116 | T | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1680A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129116 | |||||||
| chr11:78129122 | A | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1686T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129122 | |||||||
| chr11:78129123 | A | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1687T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129123 | |||||||
| chr11:78129128 | G | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1692C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129128 | |||||||
| chr11:78129135 | G | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1699C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129135 | |||||||
| chr11:78129141 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1705G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129141 | |||||||
| chr11:78129143 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.96-1707C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129143 | |||||||
| chr11:78129146 | C | G | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1710G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129146 | |||||||
| chr11:78129147 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.96-1711C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129147 | |||||||
| chr11:78129147 | G | C | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1711C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129147 | |||||||
| chr11:78129148 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1712G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129148 | |||||||
| chr11:78129159 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1723T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129159 | |||||||
| chr11:78129180 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96-1744C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129180 | |||||||
| chr11:78129195 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1759G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129195 | |||||||
| chr11:78129196 | G | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1760C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129196 | |||||||
| chr11:78129202 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.96-1766G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129202 | |||||||
| chr11:78129231 | T | A | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.96-1795A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129231 | |||||||
| chr11:78129255 | G | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(94): Show |
112 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.96-1819C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129255 | |||||||
| chr11:78129280 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1844A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129280 | |||||||
| chr11:78129345 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-1909T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129345 | |||||||
| chr11:78129375 | G | A | 1 | a0003c0004t0001g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.96-1939C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129375 | |||||||
| chr11:78129419 | CA | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(166): Show |
194 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.96-1984delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129419 | |||||||
| chr11:78129419 | CAA | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.96-1985_96-1984del others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129419 | |||||||
| chr11:78129494 | C | A | 1 | a0001c0003t0001g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.96-2058G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129494 | |||||||
| chr11:78129599 | T | C | 22 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0219 others(19): Show |
26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.96-2163A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129599 | |||||||
| chr11:78129672 | T | C | 1 | a0002c0002t0001g0238 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.96-2236A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129672 | |||||||
| chr11:78129680 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2244A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129680 | |||||||
| chr11:78129710 | CA | C | 5 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.96-2275delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129710 | |||||||
| chr11:78129760 | A | G | 12 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(9): Show |
12 | HG00558.hp2 HG01081.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.96-2324T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129760 | |||||||
| chr11:78129876 | A | AG | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2441_96-2440ins others(1): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129876 | |||||||
| chr11:78129896 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2460A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129896 | |||||||
| chr11:78129906 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2470C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129906 | |||||||
| chr11:78129921 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0239 a0001c0001t0001g0240 |
4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.96-2485G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129921 | |||||||
| chr11:78129962 | T | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0061 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.96-2526A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129962 | |||||||
| chr11:78129966 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2530A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78129966 | |||||||
| chr11:78130014 | A | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2578T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130014 | |||||||
| chr11:78130052 | G | A | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(279): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.96-2616C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130052 | |||||||
| chr11:78130163 | G | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.96-2727C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130163 | |||||||
| chr11:78130236 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.96-2800G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130236 | |||||||
| chr11:78130248 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-2812A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130248 | |||||||
| chr11:78130266 | C | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.96-2830G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130266 | |||||||
| chr11:78130333 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0058 |
3 | HG01243.hp2 HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.96-2897T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130333 | |||||||
| chr11:78130348 | C | CAAAAAAA others(2): Show |
8 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0183 others(5): Show |
8 | HG00280.hp2 HG01070.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.96-2921_96-2913dup others(9): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130348 | |||||||
| chr11:78130348 | C | CAAAAAAA others(3): Show |
105 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(102): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.96-2922_96-2913dup others(10): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130348 | |||||||
| chr11:78130348 | C | CAAAAAAA others(4): Show |
51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0028 others(48): Show |
59 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.96-2923_96-2913dup others(11): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130348 | |||||||
| chr11:78130348 | C | CAAAAAAA others(5): Show |
6 | a0001c0001t0001g0222 a0001c0001t0001g0331 a0001c0001t0001g0332 others(3): Show |
6 | HG02300.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.96-2924_96-2913dup others(12): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130348 | |||||||
| chr11:78130348 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0235 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.96-2925_96-2913dup others(13): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130348 | |||||||
| chr11:78130361 | A | AAAAAAAA others(18): Show |
3 | a0001c0001t0001g0106 a0001c0001t0001g0237 a0001c0001t0001g0241 |
3 | HG02055.hp2 HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.96-2926_96-2925ins others(25): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130361 | |||||||
| chr11:78130361 | A | AAAAAAAA others(17): Show |
11 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0057 others(8): Show |
13 | HG01884.hp2 HG02976.hp1 HG03225.hp1 others(10): Show |
intron_variant | MODIFIER | c.96-2926_96-2925ins others(24): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130361 | |||||||
| chr11:78130361 | A | AAAAAAAA others(16): Show |
3 | a0001c0001t0001g0022 a0001c0001t0001g0239 a0001c0001t0001g0240 |
4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.96-2926_96-2925ins others(23): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130361 | |||||||
| chr11:78130361 | A | AAAAAAAA others(16): Show |
74 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(71): Show |
85 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.96-2926_96-2925ins others(23): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130361 | |||||||
| chr11:78130361 | A | AAAAAAAA others(11): Show |
2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.96-2926_96-2925ins others(18): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130361 | |||||||
| chr11:78130361 | A | AAAAAAAA others(15): Show |
3 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0003t0001g0111 |
3 | HG01070.hp1 HG01081.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.96-2926_96-2925ins others(22): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130361 | |||||||
| chr11:78130622 | T | C | 2 | a0002c0002t0001g0180 a0002c0002t0001g0210 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.96-3186A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130622 | |||||||
| chr11:78130748 | T | C | 2 | a0001c0001t0001g0336 a0001c0001t0001g0338 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.96-3312A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130748 | |||||||
| chr11:78130875 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-3439A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130875 | |||||||
| chr11:78130881 | CTCTTA | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.96-3450_96-3446del others(5): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78130881 | |||||||
| chr11:78131069 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.96-3633A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131069 | |||||||
| chr11:78131086 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.96-3650A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131086 | |||||||
| chr11:78131114 | G | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.96-3678C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131114 | |||||||
| chr11:78131116 | T | TTTAG | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-3681_96-3680ins others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131116 | |||||||
| chr11:78131122 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.96-3686A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131122 | |||||||
| chr11:78131160 | T | G | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.96-3724A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131160 | |||||||
| chr11:78131170 | G | A | 52 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(49): Show |
59 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.96-3734C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131170 | |||||||
| chr11:78131264 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-3828T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131264 | |||||||
| chr11:78131282 | T | TAAAC | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-3847_96-3846ins others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131282 | |||||||
| chr11:78131332 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-3896T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131332 | |||||||
| chr11:78131360 | T | C | 8 | a0001c0003t0001g0036 a0001c0003t0001g0104 a0001c0003t0001g0105 others(5): Show |
8 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.96-3924A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131360 | |||||||
| chr11:78131499 | AGGCTGAG others(10): Show |
A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4080_96-4064del others(17): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131499 | |||||||
| chr11:78131568 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(90): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4132T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131568 | |||||||
| chr11:78131586 | G | A | 52 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(49): Show |
59 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.96-4150C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131586 | |||||||
| chr11:78131694 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4258T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131694 | |||||||
| chr11:78131769 | T | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.96-4333A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131769 | |||||||
| chr11:78131817 | A | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4381T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131817 | |||||||
| chr11:78131868 | T | C | 1 | a0002c0002t0001g0211 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.96-4432A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131868 | |||||||
| chr11:78131917 | A | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.96-4481T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131917 | |||||||
| chr11:78131932 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4496G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131932 | |||||||
| chr11:78131985 | A | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4549T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78131985 | |||||||
| chr11:78132028 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4592G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132028 | |||||||
| chr11:78132158 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4722A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132158 | |||||||
| chr11:78132169 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-4733G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132169 | |||||||
| chr11:78132202 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.96-4766G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132202 | |||||||
| chr11:78132213 | C | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.96-4777G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132213 | |||||||
| chr11:78132305 | C | A | 1 | a0001c0001t0001g0274 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.96-4869G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132305 | |||||||
| chr11:78132357 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.96-4921A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132357 | |||||||
| chr11:78132514 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-5078C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132514 | |||||||
| chr11:78132602 | T | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.96-5166A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132602 | |||||||
| chr11:78132605 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-5169G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132605 | |||||||
| chr11:78132643 | A | G | 2 | a0002c0002t0001g0185 a0002c0002t0001g0189 |
2 | HG02300.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.96-5207T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132643 | |||||||
| chr11:78132673 | T | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-5237A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132673 | |||||||
| chr11:78132682 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.96-5246G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132682 | |||||||
| chr11:78132683 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-5247A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132683 | |||||||
| chr11:78132692 | C | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
88 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.96-5256G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132692 | |||||||
| chr11:78132740 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.96-5304T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132740 | |||||||
| chr11:78132819 | GTTC | G | 91 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
106 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.96-5386_96-5384del others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132819 | |||||||
| chr11:78132828 | CTT | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0003t0001g0036 others(1): Show |
4 | NA19030.hp2 NA19058.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.96-5394_96-5393del others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132828 | |||||||
| chr11:78132831 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.96-5395G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132831 | |||||||
| chr11:78132832 | C | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0003t0001g0036 others(1): Show |
4 | NA19030.hp2 NA19058.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.96-5396G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132832 | |||||||
| chr11:78132832 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.96-5396G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132832 | |||||||
| chr11:78132833 | A | AT | 44 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0197 others(41): Show |
51 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.96-5398dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132833 | |||||||
| chr11:78132833 | A | ATT | 10 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(7): Show |
10 | HG01069.hp2 HG01978.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.96-5399_96-5398dup others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132833 | |||||||
| chr11:78132833 | A | T | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0068 others(2): Show |
5 | HG03942.hp2 NA19030.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.96-5397T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132833 | |||||||
| chr11:78132833 | AT | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.96-5398delA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132833 | |||||||
| chr11:78132833 | ATTT | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
17 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.96-5400_96-5398del others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132833 | |||||||
| chr11:78132833 | ATTTTTTT | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0117 a0001c0001t0001g0118 others(2): Show |
6 | NA18944.hp2 NA18956.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.96-5404_96-5398del others(7): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132833 | |||||||
| chr11:78132876 | G | A | 1 | a0001c0003t0001g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.96-5440C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132876 | |||||||
| chr11:78132877 | A | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-5441T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132877 | |||||||
| chr11:78132906 | G | A | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(12): Show |
19 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.96-5470C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132906 | |||||||
| chr11:78132956 | C | A | 1 | a0001c0001t0001g0059 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.96-5520G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78132956 | |||||||
| chr11:78133018 | G | A | 3 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 |
3 | HG00099.hp1 HG01361.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.96-5582C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133018 | |||||||
| chr11:78133065 | G | A | 17 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(14): Show |
21 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.96-5629C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133065 | |||||||
| chr11:78133079 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.96-5643G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133079 | |||||||
| chr11:78133082 | G | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
111 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.96-5646C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133082 | |||||||
| chr11:78133115 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.96-5679C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133115 | |||||||
| chr11:78133233 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.96-5797G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133233 | |||||||
| chr11:78133346 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.96-5910T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133346 | |||||||
| chr11:78133351 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.96-5915G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133351 | |||||||
| chr11:78133449 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.96-6013A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133449 | |||||||
| chr11:78133449 | T | G | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(12): Show |
19 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.96-6013A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133449 | |||||||
| chr11:78133451 | C | T | 5 | a0001c0001t0001g0225 a0003c0004t0001g0224 a0003c0004t0001g0226 others(2): Show |
5 | HG02451.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.96-6015G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133451 | |||||||
| chr11:78133566 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.95+5928A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133566 | |||||||
| chr11:78133623 | C | A | 1 | a0001c0001t0001g0172 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.95+5871G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133623 | |||||||
| chr11:78133644 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.95+5850C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133644 | |||||||
| chr11:78133675 | C | T | 3 | a0001c0003t0001g0036 a0001c0003t0001g0108 a0001c0003t0001g0110 |
3 | HG02922.hp2 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.95+5819G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133675 | |||||||
| chr11:78133697 | G | A | 5 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.95+5797C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133697 | |||||||
| chr11:78133708 | G | A | 47 | a0001c0001t0001g0197 a0002c0002t0001g0004 a0002c0002t0001g0010 others(44): Show |
54 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.95+5786C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133708 | |||||||
| chr11:78133744 | C | G | 5 | a0001c0003t0001g0104 a0001c0003t0001g0110 a0001c0003t0001g0111 others(2): Show |
5 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.95+5750G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133744 | |||||||
| chr11:78133758 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.95+5736G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133758 | |||||||
| chr11:78133835 | A | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+5659T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133835 | |||||||
| chr11:78133857 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.95+5637G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133857 | |||||||
| chr11:78133900 | C | CA | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
109 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.95+5593dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133900 | |||||||
| chr11:78133970 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+5524G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133970 | |||||||
| chr11:78133999 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | NA18947.hp1 NA18960.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.95+5495C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78133999 | |||||||
| chr11:78134099 | T | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+5395A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134099 | |||||||
| chr11:78134139 | G | GT | 12 | a0001c0001t0001g0116 a0001c0001t0001g0121 a0001c0001t0001g0122 others(9): Show |
12 | HG00280.hp2 HG00544.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.95+5354dupA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134139 | |||||||
| chr11:78134210 | T | C | 2 | a0001c0003t0001g0015 a0001c0003t0001g0034 |
3 | HG02622.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.95+5284A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134210 | |||||||
| chr11:78134296 | C | T | 1 | a0002c0002t0001g0180 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.95+5198G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134296 | |||||||
| chr11:78134312 | A | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.95+5182T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134312 | |||||||
| chr11:78134325 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | NA18968.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.95+5169T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134325 | |||||||
| chr11:78134326 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95+5168G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134326 | |||||||
| chr11:78134369 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+5125G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134369 | |||||||
| chr11:78134402 | C | A | 1 | a0001c0001t0001g0334 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.95+5092G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134402 | |||||||
| chr11:78134413 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+5081G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134413 | |||||||
| chr11:78134525 | C | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.95+4969G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134525 | |||||||
| chr11:78134597 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0239 a0001c0001t0001g0240 |
4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.95+4897C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134597 | |||||||
| chr11:78134652 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0117 a0001c0001t0001g0118 others(2): Show |
6 | NA18944.hp2 NA18956.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.95+4842T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134652 | |||||||
| chr11:78134878 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.95+4616C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134878 | |||||||
| chr11:78134946 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.95+4548C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78134946 | |||||||
| chr11:78135031 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0007c0007t0001g0098 |
3 | HG01070.hp1 HG01071.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.95+4463C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135031 | |||||||
| chr11:78135149 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+4345A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135149 | |||||||
| chr11:78135218 | G | A | 52 | a0001c0001t0001g0109 a0001c0001t0001g0181 a0001c0001t0001g0182 others(49): Show |
59 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.95+4276C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135218 | |||||||
| chr11:78135233 | A | G | 22 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0219 others(19): Show |
26 | HG01891.hp2 HG02145.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.95+4261T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135233 | |||||||
| chr11:78135354 | CA | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(100): Show |
122 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.95+4139delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135354 | |||||||
| chr11:78135373 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95+4121T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135373 | |||||||
| chr11:78135518 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0239 a0001c0001t0001g0240 |
4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.95+3976G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135518 | |||||||
| chr11:78135559 | A | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+3935T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135559 | |||||||
| chr11:78135639 | G | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.95+3855C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135639 | |||||||
| chr11:78135660 | C | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(94): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.95+3834G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135660 | |||||||
| chr11:78135711 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.95+3783C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135711 | |||||||
| chr11:78135779 | C | T | 2 | a0001c0001t0001g0278 a0001c0001t0001g0343 |
2 | HG03239.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.95+3715G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135779 | |||||||
| chr11:78135840 | T | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): Show |
89 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.95+3654A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135840 | |||||||
| chr11:78135864 | G | GA | 115 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(112): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.95+3629dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135864 | |||||||
| chr11:78135864 | G | GAAA | 7 | a0001c0001t0001g0066 a0001c0003t0001g0104 a0001c0003t0001g0105 others(4): Show |
7 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.95+3627_95+3629dup others(3): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135864 | |||||||
| chr11:78135864 | G | GAAAA | 82 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
95 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.95+3626_95+3629dup others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135864 | |||||||
| chr11:78135869 | A | AAAAG | 4 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.95+3624_95+3625ins others(4): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135869 | |||||||
| chr11:78135894 | T | G | 6 | a0001c0003t0001g0104 a0001c0003t0001g0105 a0001c0003t0001g0110 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.95+3600A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135894 | |||||||
| chr11:78135897 | A | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+3597T>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135897 | |||||||
| chr11:78135971 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95+3523G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78135971 | |||||||
| chr11:78136071 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95+3423C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136071 | |||||||
| chr11:78136073 | G | C | 1 | a0001c0001t0001g0339 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.95+3421C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136073 | |||||||
| chr11:78136126 | T | C | 3 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 |
3 | HG00099.hp1 HG01361.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.95+3368A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136126 | |||||||
| chr11:78136227 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.95+3267G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136227 | |||||||
| chr11:78136275 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
110 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.95+3219G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136275 | |||||||
| chr11:78136306 | G | GA | 8 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0237 others(5): Show |
10 | HG00642.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.95+3187dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136306 | |||||||
| chr11:78136306 | GA | G | 91 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
104 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.95+3187delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136306 | |||||||
| chr11:78136317 | A | T | 1 | a0001c0003t0001g0015 | 2 | HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.95+3177T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136317 | |||||||
| chr11:78136319 | C | A | 1 | a0002c0002t0001g0218 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.95+3175G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136319 | |||||||
| chr11:78136430 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): Show |
89 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.95+3064C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136430 | |||||||
| chr11:78136605 | T | C | 6 | a0001c0003t0001g0104 a0001c0003t0001g0105 a0001c0003t0001g0110 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.95+2889A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136605 | |||||||
| chr11:78136738 | G | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.95+2756C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136738 | |||||||
| chr11:78136766 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.95+2728A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136766 | |||||||
| chr11:78136905 | CT | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
109 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.95+2588delA | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136905 | |||||||
| chr11:78136925 | G | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.95+2569C>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136925 | |||||||
| chr11:78136994 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.95+2500G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78136994 | |||||||
| chr11:78137040 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.95+2454G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137040 | |||||||
| chr11:78137138 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | NA18978.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.95+2356G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137138 | |||||||
| chr11:78137177 | C | T | 6 | a0001c0001t0001g0109 a0001c0003t0001g0104 a0001c0003t0001g0110 others(3): Show |
6 | HG01081.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.95+2317G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137177 | |||||||
| chr11:78137191 | T | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0066 others(36): Show |
44 | HG00408.hp1 HG00597.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.95+2303A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137191 | |||||||
| chr11:78137207 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.95+2287C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137207 | |||||||
| chr11:78137261 | A | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
108 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.95+2233T>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137261 | |||||||
| chr11:78137452 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.95+2042G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137452 | |||||||
| chr11:78137554 | T | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): Show |
89 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.95+1940A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137554 | |||||||
| chr11:78137809 | G | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
101 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.95+1685C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137809 | |||||||
| chr11:78137821 | G | T | 2 | a0001c0001t0001g0272 a0006c0006t0001g0273 |
2 | HG00280.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.95+1673C>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78137821 | |||||||
| chr11:78138029 | C | A | 1 | a0002c0002t0001g0238 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.95+1465G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138029 | |||||||
| chr11:78138045 | T | G | 1 | a0001c0001t0001g0271 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.95+1449A>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138045 | |||||||
| chr11:78138062 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0268 a0001c0001t0001g0269 others(2): Show |
7 | HG00544.hp2 HG01975.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.95+1432G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138062 | |||||||
| chr11:78138073 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.95+1421G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138073 | |||||||
| chr11:78138149 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.95+1345A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138149 | |||||||
| chr11:78138274 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18982.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.95+1220C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138274 | |||||||
| chr11:78138351 | C | CA | 77 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0024 others(74): Show |
89 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.95+1142dupT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138351 | |||||||
| chr11:78138351 | CA | C | 15 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0109 others(12): Show |
15 | HG01081.hp1 HG01081.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.95+1142delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138351 | |||||||
| chr11:78138351 | CAA | C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
98 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.95+1141_95+1142del others(2): Show |
ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138351 | |||||||
| chr11:78138373 | CA | C | 4 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(1): Show |
4 | NA18940.hp2 NA18944.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.95+1120delT | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138373 | |||||||
| chr11:78138378 | A | C | 1 | a0001c0001t0001g0032 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.95+1116T>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138378 | |||||||
| chr11:78138462 | AC | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0239 a0001c0001t0001g0240 |
4 | HG02630.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.95+1031delG | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138462 | |||||||
| chr11:78138539 | C | G | 2 | a0002c0002t0001g0030 a0002c0002t0001g0031 |
2 | HG01433.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.95+955G>C | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138539 | |||||||
| chr11:78138569 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0241 |
3 | HG02055.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.95+925G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138569 | |||||||
| chr11:78138676 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.95+818G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138676 | |||||||
| chr11:78138712 | T | A | 1 | a0001c0001t0001g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.95+782A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138712 | |||||||
| chr11:78138807 | C | T | 2 | a0004c0005t0001g0257 a0004c0005t0001g0258 |
2 | HG00738.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.95+687G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138807 | |||||||
| chr11:78138808 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.95+686C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138808 | |||||||
| chr11:78138815 | T | C | 2 | a0001c0001t0001g0024 a0003c0004t0001g0244 |
3 | HG02280.hp1 HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.95+679A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78138815 | |||||||
| chr11:78139051 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.95+443G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78139051 | |||||||
| chr11:78139143 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.95+351G>A | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78139143 | |||||||
| chr11:78139170 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.95+324A>G | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78139170 | |||||||
| chr11:78139414 | G | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
9 | HG01099.hp2 HG01175.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.95+80C>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78139414 | |||||||
| chr11:78139430 | T | A | 2 | a0002c0002t0001g0253 a0002c0002t0001g0254 |
2 | HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.95+64A>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78139430 | |||||||
| chr11:78139471 | C | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(98): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.95+23G>T | ALG8 | ENSG00000159063.14 | transcript | ENST00000299626.10 | protein_coding | 1/12 | chr11 | 78139471 |